J.H. is supported by NIH K99/R00 Pathway to Independence Award (5K99CA172700) and NCI Brain Cancer SPORE Career Development Award (2P50CA127001).

NOTE: All the steps in this protocol have been approved by UT MD Anderson Cancer Center.
1. Generation of mTERT-ER Allele
<ol>
	<li>Introduce knock-in targeting vector containing the ERT2-LBD (Ligand Binding Domain) upstream and in frame with the mTERT genomic sequence (exon 1 through intron 2) and a Lox-pgk-Neo-Lox fragment (Figure 1A) into mouse ES cells with electroporation.</li>
	<li>Culture the ES cells in neomycin for 6-10 days. Pick neomycin-resistant clones and expand in 48 well plates. Extract the genomic DNA using a commercial kit and confirm the knock-in allele by southern blot.</li>
	<li>Inject two ES lines with over 95% normal karyotypes into C57BL/6 blastocysts with a micromanipulation kit under an inverted microscope. Implant the blastocysts into the uterus of surrogate mothers23. Mate the high-grade male chimaeras (70-90%) to C57BL/6 females.</li>
	<li>Confirm the genotyping of heterozygous mTERT-ERneo animals by southern blot.</li>
	<li>Mate the heterozygous mTERT-ERneo animals and EIIa-Cre animals to delete the NeoR cassette. Mate the heterozygous animals to C57BL/6 animals for at least three times, and further inter-breed heterozygous mTERT-ER animals to generate homozygosity.</li>
</ol>
2. Generation of LSL-mTERT Allele
<ol>
	<li>Introduce the knock-in targeting vector containing a LoxP-triple Stopper-Neo-LoxP fragment and the mTERT genomic sequence (between exon 1 and intron 2, Figure 1B) into mouse ES cells with electroporation23.</li>
	<li>Culture the ES cells in neomycin for 6-10 days. Pick neomycin-resistant clones and expand in 48 well plates. Extract the genomic DNA using a commercial kit and confirm the knock-in allele by southern blot23.</li>
	<li>Inject two ES lines with over 95% normal karyotypes into C57BL/6 blastocysts with a micromanipulation kit under an inverted microscope. Implant the blastocysts into the uterus of surrogate mothers23. Mate the high-grade male chimaeras (70-90%) to C57BL/6 females.</li>
	<li>Confirm the genotyping of heterozygous LSL-mTERT animals by southern blot.</li>
	<li>Mate the heterozygous animals to C57BL/6 animals for at least three times, and further inter-breed heterozygous LSL-mTERT animals to generate homozygosity.</li>
</ol>
3. Reactivation of Telomerase in mTERT-ER and LSL-mTERT Mice In Vivo
 For mTERT-ER
<ol>
	<li>Sterilize all the surgical tools before the injection.</li>
	<li>Anesthetize the mice with isoflurane chamber (4% for induction, 2% for maintaining) in 50% (v/v) oxygen/50% (v/v) dinitrogen monoxide gas mixture. Or anesthetize mice by a ketamine-xylazine mixture (100 mg/kg bodyweight + 10 mg/kg bodyweight).</li>
	<li>After deep anesthesia is reached, remove the anesthetized animal from the induction chamber, and keep their head inside the tube connected to the isoflurane chamber (2%).</li>
	<li>Pinch the foot pads of the mice to ensure the animal is deeply anaesthetized. Put ointment on both eyes in order to prevent the eyes from drying out. Wipe the back of the mice with povidone-iodine solution.</li>
	<li>Inject the slow-releasing 4-OHT pellet with precision trochar (10 G) under the skin of the back and push the pellet all the way to the midline between two shoulders.</li>
	<li>Seal the incision with wound clip applier and monitor the mice for recovery from anesthesia. Remove the clips 10 days later.&#160;Supplemental heat is not necessary because the procedure is finished shortly.</li>
	<li>Period of treatment with 4-OHT pellet should be optimized according to the purpose of the study.</li>
</ol>
For LSL-mTERT
<ol>
	<li>Tamoxifen (10 mg/ml, dissolved in corn oil) is injected intraperitoneally two consecutive days (200 ul/25 g/day).
	</li>
</ol>
4. Isolation of Neural Stem Cells and Reactivation of Telomerase In Vitro
<ol>
	<li>Mice are euthanized with carbon dioxide and the brains are removed.&#160;Follow the protocol of commercially available neural tissue dissociation kit as per manufacturer.&#160;</li>
	<li>Resuspend the lyophilized powder in the vial labeled Solution 4 with 1 ml of cell culture medium for Solution 4. Do not vortex. This solution should then be aliquoted and stored at &#8211;20 &#176;C for later use.</li>
	<li>Pre-Heat the mixture at 37 &#176;C for 15 min before use.</li>
	<li>Make Enzyme Mix 1: Solution 1 (50 &#181;l) and Solution 2 (1,900 &#181;l). Make Enzyme Mix 2: Solution 3 (20 &#181;l) and Solution 4 (10 &#181;l).</li>
	<li>Prepare 1,950 &#181;l enzyme mix 1 for up to 400 mg tissue and vortex. Pre-heat the mixture at 37 &#176;C for 15 min before use.</li>
	<li>Take out the 1-day mouse brains, and keep the forebrains by removing the olfactory bulbs and the cerebellum. Keep the forebrain tissues in 1 ml of cold culture medium since removal and store in 4 &#176;C. Make sure to process the neural tissue within 1 hr.</li>
	<li>Determine the weight of tissue to make sure the 400 mg limit per digestion is not exceeded. Place the brain on the lid of a 35 mm diameter Petri dish, and crush the brain using a scalpel.</li>
	<li>Using a 1 ml pipette tip, add 1 ml of HBSS (w/o Ca/Mg) and pipette pieces back into a 15 ml tube. Rinse with HBSS (w/o Ca/Mg). Centrifuge at 300 &#215; g for 2 min at room temperature and aspirate the supernatant carefully.</li>
	<li>Add 1,950 &#181;l of pre-heated enzyme mix 1 (Solutions 1 and 2) per up to 400 mg tissue. Incubate in the 15 ml tube for 15 min at 37 &#176;C, mixing by inverting or shaking the tube every 5 min.</li>
	<li>Prepare 30 &#181;l enzyme mix 2 per tissue sample by adding 20 &#956;l of Solution 3 to 10 &#956;l of Solution 4. Then add to sample. Invert gently to mix. Do not vortex.</li>
	<li>Dissociate tissue mechanically using a wide-tipped, fire-polished Pasteur pipette by pipetting up and down 10 times slowly. Avoid forming air bubbles.</li>
	<li>Incubate at 37 &#176;C for 10 min, inverting the tube every 3 min.</li>
	<li>Repeat the step 4.11 and step 4.12 if the tissues are bigger than 200 mg.</li>
	<li>Apply the cell suspension to a 70 &#956;m cell strainer, placed on a 50 ml tube. Apply 10 ml of PBS through cell strainer. Discard cell strainer and centrifuge cell suspension at 300 g for 20 min at room temperature. Aspirate supernatant completely.</li>
	<li>Resuspend cells with stem cell medium to the required volume for further applications.</li>
	<li>To activate telomerase in LSL-mTERT NSCs, treat the cells with 100 &#181;M 4-OHT for two days. To activate telomerase in mTERT-ER NSCs, keep the cells in culture medium with 100 &#181;M 4-OHT.</li>
</ol>
5. Telomere FISH
<ol>
	<li>Prepare the metaphase chromosomes from cultured cells.</li>
	<li>For FFPE (Formalin Fixed and Paraffin Embedded) tissue sections, deparaffinize in xylene and rehydrate in ethanol series for 5 minutes each (100%, 90%, 70%, 50% ethanol) and PBS for 5 min.</li>
	<li>Post-fix in the methanol: acetic acid (3:1) for 1-2 hr. Dehydrate in cold ethanol series for 5 min each (70%, 90%, 100% ethanol) and air dry. Wash in 1x PBS at 37 &#176;C for 5 min.</li>
	<li>Denature chromosomes in 4% formaldehyde at 37 &#176;C for 2 min. Dehydrate in cold ethanol series 5 min each (70%, 90%, 100% ethanol) and air dry.</li>
	<li>Apply 12 to 25 &#181;l of the PNA hybridization mixture to each slide. (Hybridization mix: 70% formamide, 0.06x SSC, 0.2% BSA, 0.5 ng/&#181;l tRNA, 0.5 ng/&#181;l telomere or centromere probes)</li>
	<li>Seal the cover slip with rubber cement. Post-denature chromosomal preps and tissue sections at 80 &#176;C for 4 min. Hybridize at room temperature or 37 &#176;C for 2-4 hr in humid chamber.</li>
	<li>Wash at room temperature with washing buffer 2 x 15 min. (Wash buffer: 70% formamide, 0.06x SSC, pH 7.2). Wash at room temperature 3 x 5 min with PBST. Counter-stain slides with DAPI or far-red fluorescence for microscopic examination.</li>
</ol>

<ol>
	<li>Bass, A. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Genomic+sequencing+of+colorectal+adenocarcinomas+identifies+a+recurrent+VTI1A-TCF7L2+fusion.">Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion.</a> Nat Genet. 43, 964-968 (2011).</li><li>Beroukhim, R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+landscape+of+somatic+copy-number+alteration+across+human+cancers.">The landscape of somatic copy-number alteration across human cancers.</a> Nature. 463, 899-905 (2010).</li><li>Blasco, M. A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Telomere+shortening+and+tumor+formation+by+mouse+cells+lacking+telomerase+RNA.">Telomere shortening and tumor formation by mouse cells lacking telomerase RNA.</a> Cell. 91, 25-34 (1997).</li><li>Lee, H. W., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Essential+role+of+mouse+telomerase+in+highly+proliferative+organs.">Essential role of mouse telomerase in highly proliferative organs.</a> Nature. 392, 569-574 (1998).</li><li>Rossi, D. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Deficiencies+in+DNA+damage+repair+limit+the+function+of+haematopoietic+stem+cells+with+age.">Deficiencies in DNA damage repair limit the function of haematopoietic stem cells with age.</a> Nature. 447, 725-729 (2007).</li><li>Wong, K. K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Telomere+dysfunction+and+Atm+deficiency+compromises+organ+homeostasis+and+accelerates+ageing.">Telomere dysfunction and Atm deficiency compromises organ homeostasis and accelerates ageing.</a> Nature. 421, 643-648 (2003).</li><li>Rudolph, K. L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Longevity,+stress+response,+and+cancer+in+aging+telomerase-deficient+mice.">Longevity, stress response, and cancer in aging telomerase-deficient mice.</a> Cell. 96, 701-712 (1999).</li><li>Wong, K. K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Telomere+dysfunction+impairs+DNA+repair+and+enhances+sensitivity+to+ionizing+radiation.">Telomere dysfunction impairs DNA repair and enhances sensitivity to ionizing radiation.</a> Nat Genet. 26, 85-88 (2000).</li><li>Ferron, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Telomere+shortening+and+chromosomal+instability+abrogates+proliferation+of+adult+but+not+embryonic+neural+stem+cells.">Telomere shortening and chromosomal instability abrogates proliferation of adult but not embryonic neural stem cells.</a> Development. 131, 4059-4070 (2004).</li><li>Savage, S. A., Alter, B. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dyskeratosis+congenita.">Dyskeratosis congenita.</a> Hematol Oncol Clin North Am. 23, 215-231 (2009).</li><li>Armanios, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Syndromes+of+telomere+shortening.">Syndromes of telomere shortening.</a> Annu Rev Genomics Hum Genet. 10, 45-61 (2009).</li><li>Vulliamy, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+RNA+component+of+telomerase+is+mutated+in+autosomal+dominant+dyskeratosis+congenita.">The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita.</a> Nature. 413, 432-435 (2001).</li><li>Harley, C. B., Harley, S. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Telomerase,+checkpoints+and+cancer.">Telomerase, checkpoints and cancer.</a> Cancer surveys. 29, 263-284 (1997).</li><li>Karlseder, J., Broccoli, D., Dai, Y., Hardy, S., de Lange, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=p53-+and+ATM-dependent+apoptosis+induced+by+telomeres+lacking+TRF2.">p53- and ATM-dependent apoptosis induced by telomeres lacking TRF2.</a> Science (New York, N.Y.). 283, 1321-1325 (1999).</li><li>Steensel, B., Smogorzewska, A., de Lange, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=TRF2+protects+human+telomeres+from+end-to-end+fusions.">TRF2 protects human telomeres from end-to-end fusions.</a> Cell. 92, 401-413 (1998).</li><li>Chin, L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=p53+deficiency+rescues+the+adverse+effects+of+telomere+loss+and+cooperates+with+telomere+dysfunction+to+accelerate+carcinogenesis.">p53 deficiency rescues the adverse effects of telomere loss and cooperates with telomere dysfunction to accelerate carcinogenesis.</a> Cell. 97, 527-538 (1999).</li><li>Artandi, S. E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Telomere+dysfunction+promotes+non-reciprocal+translocations+and+epithelial+cancers+in+mice.">Telomere dysfunction promotes non-reciprocal translocations and epithelial cancers in mice.</a> Nature. 406, 641-645 (2000).</li><li>Rudolph, K. L., Millard, M., Bosenberg, M. W., DePinho, R. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Telomere+dysfunction+and+evolution+of+intestinal+carcinoma+in+mice+and+humans.">Telomere dysfunction and evolution of intestinal carcinoma in mice and humans.</a> Nat Genet. 28, 155-159 (2001).</li><li>Greenberg, R. A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Short+dysfunctional+telomeres+impair+tumorigenesis+in+the+INK4a(delta2/3)+cancer-prone+mouse.">Short dysfunctional telomeres impair tumorigenesis in the INK4a(delta2/3) cancer-prone mouse.</a> Cell. 97, 515-525 (1999).</li><li>Jaskelioff, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Telomerase+reactivation+reverses+tissue+degeneration+in+aged+telomerase-deficient+mice.">Telomerase reactivation reverses tissue degeneration in aged telomerase-deficient mice.</a> Nature. 469, 102-106 (2011).</li><li>Hu, J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Antitelomerase+therapy+provokes+ALT+and+mitochondrial+adaptive+mechanisms+in+cancer.">Antitelomerase therapy provokes ALT and mitochondrial adaptive mechanisms in cancer.</a> Cell. 148, 651-663 (2012).</li><li>Ding, Z., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Telomerase+reactivation+following+telomere+dysfunction+yields+murine+prostate+tumors+with+bone+metastases.">Telomerase reactivation following telomere dysfunction yields murine prostate tumors with bone metastases.</a> Cell. 148, 896-907 (2012).</li><li>Nagy, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Manipulating the mouse embryo : a laboratory manual. , (2003).</li></ol>

The authors have nothing to disclose.

Here, we report the generation of two inducible murine telomerase alleles and how to reactivate telomerase in vivo and in vitro. The critical step for reactivating mTERT-ER activity is to keep a continuous concentration of tamoxifen, so we choose to use 4-OHT time-release pellets manufactured by Innovative Research of America. The pellets keep releasing 4OHT at a steady state blood level of 1&#8201;ng/ml for up to 60 days. In a previous study, we showed that reactivating telomerase activity with this strategy was able to ameliorate the degenerative phenotypes such as stem cell exhaustion, impairment of tissue injury responses and organ failure in multiple organs that were induced by telomere dysfunction in G4mTERTER/ER mice20.
Other than studying the function of telomerase in ageing, these two inducible telomerase alleles can also be used to study cancer. Previous studies took advantage of these alleles to explore the role of telomere attrition and telomerase reactivation in shaping the genomes and impacting the biology of T-cell thymic lymphoma21 and prostate cancer22. These two studies showed that telomere dysfunction in late generation G4 Atm-/- mTERTER/ER and G4 PB-Cre4 PtenL/L p53L/L LSL-mTERTL/L mice provides a mechanism fueling the acquisition of early mutagenic events for tumor initiation, yet preventing progression of fully malignant tumors. When telomerase was reactivated in the context of telomere dysfunction-induced genomic instability, DNA damage checkpoints and rampant chromosomal instability were suppressed , which allowed the full progression of malignant tumors with new biological properties such as bone metastasis of prostate cancer21 and brain infiltration of thymic lymphoma21. Similar phenomena were also observed in other cancer types including colon cancer and pancreatic cancer (personal communications with Drs. Haoqiang Ying, Adam Boutin and Ronald DePinho).
Because TERT-ER protein can be easily toggled between on and off states depending on whether the animals are treated with tamoxifen or vehicle, the tumor models generated by mTERT-ER allele can be utilized to test anti-telomerase therapy. In previous study, tumors generated in G4 Atm-/- mTERTER/ER animals were released from 4-OHT; upon telomerase depletion, tumors eventually shrank due to the reinstatement of telomere dysfunction-induced checkpoints21. However, some of the tumors acquired resistance in response to telomerase extinction by activating an Alternative Lengthening of Telomeres (ALT) mechanism. Further characterization of these ALT+ resistant tumors showed that they have aberrant transcription of genes involved in mitochondrial biology and oxidative defense including a master regulator of mitochondrial synthesis and oxidative defense PGC-1&#946;. Knockdown of PGC-1&#946; or SOD2 (another regulator of oxidative defense) significantly eliminates ALT+ tumor cells while keep telomerase+ tumor cells remain relatively intact21 .
One limitation of these two knock-in alleles is that they can only afford reactivation of telomerase at endogenous level because they are in the native locus of the telomerase gene. In most human cancers, telomerase is actually overexpressed at a much higher level. In order to enhance the level of telomerase, one modification we can consider is to insert the mTERT-ER construct with a stronger promoter such as PGK (phosphoglycerate kinase) promoter into Rosa26 locus.
In conclusion, these two novel inducible murine telomerase alleles provide unprecedented genetic tools to study the functions of telomerase in ageing and tissue homeostasis as well as the tumor progression, especially under the background of pre-acquired telomere dysfunction-induced genomic instability. The mTERT-ER allele can also be used to study anti-telomerase therapy by crossing into other tumor-prone mouse models.

Telomerase is an enzyme responsible for maintaining telomeres. These are repetitive sequences at the ends of chromosomes that protect their integrity. The core components of telomerase holoenzyme are a reverse transcriptase catalytic subunit (TERT) and an RNA subunit (TERC) that serves as the template for adding the telomeric repeats1,2. While generally suppressed in differentiated somatic cells, telomerase exhibits robust activity and plays important roles in germ cells, cancer cells and stem cells.
mTERC and mTERT knockout mice provide great in vivo model systems to study the functions of telomerase in both stem cells and cancer. The mTERC and mTERT knockout mice (G1) did not show any obvious phenotypes due to the long reserve of telomeres in mice3. However, serially intercrossing mTERC and mTERT knockout mice to late generation (G5-G6) resulted in progressive erosion of telomeres and eventually provoked severe degeneration of highly proliferative tissues4. Late generation (G5-G6) mTERC-/- mice are infertile due to the high rates of apoptosis in testis and germ cell depletion. G5-G6 mTERC-/- mice also exhibit degenerative phenotypes in highly proliferative tissues including bone marrow, intestine and skin due to high rates of apoptosis and defective self-renewal capability in tissue stem/progenitor cell compartments4. Hematopoietic stem cells in the bone marrow of late generation mTERC-/- mice exhibit loss of proliferative potential, compromised self-renewal capability, enhanced apoptosis and, eventually functional exhaustion5,6. Similarly, progressively increased apoptotic bodies in intestinal crypts were observed in each successive generation of G1-G6 mTERC-/- mice7,8. The deleterious effect of dysfunctional telomeres doesn&#8217;t seem to be limited to high turnover tissues since both the proliferation of adult neural stem cells in vitro and the neurogenesis in vivo were severely impaired in late generation (G4-G5) mTERC-/- mice9. The role of telomerase in stem cells is further supported by the findings in a rare human genetic disorder dyskeratosis congenita (DKC), which in some ways resembles premature ageing10,11. DKC is caused by mutations in TERC, TERT, and genes that encode dyskerin, a core telomerase subunit, and other dyskerin associated proteins12. In average, telomeres in DKC patients are shorter than 99% of age-matched controls. The major morbidity of the disease is due to aplastic anemia, which is caused by defective maintenance of hematopoietic stem cells. Other aspects of the disease such as oral leukoplakia, nail dystrophy, mental retardation, testes atrophy and pulmonary complications all suggest impaired functions of tissue stem cells and progenitor cells10, findings in close agreement with those in late generation of telomerase knockout mice. DKC patients are prone to myelodysplastic syndrome and have an increased prevalence of malignant mucosal neoplasms. Thus, deficiency of telomerase in human patients recapitulates the defects of stem cell functions and tumor predisposition that are observed in late generation telomerase knockout mice.
Short telomeres and high telomerase activity are hallmarks of cancer. As normal or premalignant cells divide, the low or absent telomerase activity results in the eventual erosion of telomeres and activation of cellular checkpoints similar to those provoked by DNA double-stranded-breaks (DSBs)13. Like classical DSBs, telomere dysfunction has been shown to induce p53 and associated cellular responses, such as senescence and/or apoptosis14,15. Upon mutational inactivation of p53, cell cycling and cell survival are enhanced in cells with telomere dysfunction, which provides a pro-carcinogenic mutator mechanism characterized by translocations and regional amplifications and deletions16,17. At the same time, continued telomere dysfunction and associated rampant chromosomal instability (even in p53 null cells) appear to constrain full malignant progression of such cancers. For instance, late generation G4-G5 mTERC-/- Ink4a/Arf-/- mice showed significantly reduced lymphoma incidence compared with Ink4a/Arf null mice due to telomere attrition. In another study, more advanced adenomatous lesions in G4 mTERT-/- APCmin mice were greatly suppressed in comparison with APCmin mice due to significant growth arrest and apoptosis18,19. The observation that telomere dysfunction-induced genomic instability inhibits tumor progression prompts the speculation that the activation of telomerase may enable malignant progression in part by quelling genomic instability to a level compatible with cancer cell viability and/or neutralizing p53-dependent or -independent checkpoint mechanisms.
In order to study whether telomerase reactivation can stop or even reverse ageing of stem cells, and whether telomerase reactivation can promote the tumorigenesis against the backdrop of genomic instability, we generated two inducible murine telomerase alleles. The first one is 4-Hydroxytamoxifen (4-OHT)-inducible TERT-Estrogen Receptor (mTERT-ER) fusion knock-in allele. In the absence of 4-OHT, mice homozygous for mTERT-ER (designated mTERTER/ER) are telomerase activity deficient and sustain same cytogenetic and cellular phenotypes as conventional mTERT or mTERC knockout model. Upon 4-OHT treatment, TERT-ER protein activity can be restored to levels comparable to the native TERT protein20, 21. The second allele is a novel inducible TERT knock-in allele containing an intronic LoxP-Stopper-LoxP cassette (LSL-mTERT); upon Cre-mediated excision of LSL, mTERT is re-expressed under endogenous expression control mechanisms22.

<table border="0" cellpadding="0" cellspacing="0">
	<tbody>
		<tr>
			<td>Leica AM6000 Micromanipulation Kit</td>
			<td>Leica</td>
			<td>Per quote</td>
			<td></td>
		</tr>
		<tr>
			<td>Leica DMI6000 B inverted microscope</td>
			<td>Leica</td>
			<td>Per quote</td>
			<td></td>
		</tr>
		<tr>
			<td>Neomycin</td>
			<td>Life technologies</td>
			<td>21810031</td>
			<td></td>
		</tr>
		<tr>
			<td>isoflurane vaporizer</td>
			<td>Veterinary Anesthesia Systems</td>
			<td>911103</td>
			<td></td>
		</tr>
		<tr>
			<td>isoflurane</td>
			<td>Henry Schein</td>
			<td>1005796</td>
			<td></td>
		</tr>
		<tr>
			<td>ketamine-xylazine mixture</td>
			<td>Sigma-Aldrich</td>
			<td>K113-10ML</td>
			<td></td>
		</tr>
		<tr>
			<td>4-OHT powder</td>
			<td>Sigma-Aldrich</td>
			<td>H7904-5MG</td>
			<td></td>
		</tr>
		<tr>
			<td>Tamoxfien</td>
			<td>Sigma-Aldrich</td>
			<td>T5648-1G</td>
			<td></td>
		</tr>
		<tr>
			<td>4-OHT pellet</td>
			<td>Innovative Research of America</td>
			<td>Custermized</td>
			<td></td>
		</tr>
		<tr>
			<td>Precision Trochar (10 Gauge)</td>
			<td>Innovative Research of America</td>
			<td>MP-182</td>
			<td></td>
		</tr>
		<tr>
			<td>wound clip applier</td>
			<td>Fischer Scientific</td>
			<td>01-804</td>
			<td></td>
		</tr>
		<tr>
			<td>clip</td>
			<td>Fischer Scientific</td>
			<td>01-804-5</td>
			<td></td>
		</tr>
		<tr>
			<td>Neural Tissue Dissociation Kit</td>
			<td>Miltenyi Biotec</td>
			<td>130-092-628</td>
			<td></td>
		</tr>
		<tr>
			<td>HBSS</td>
			<td>Life technologies</td>
			<td>14025092</td>
			<td></td>
		</tr>
		<tr>
			<td>PBS</td>
			<td>Life technologies</td>
			<td>10010023</td>
			<td></td>
		</tr>
		<tr>
			<td>xylene</td>
			<td>Fischer Scientific</td>
			<td>X3P-1GAL</td>
			<td></td>
		</tr>
		<tr>
			<td>methanol</td>
			<td>Fischer Scientific</td>
			<td>A-433S4</td>
			<td></td>
		</tr>
		<tr>
			<td>acetic acid</td>
			<td>Fischer Scientific</td>
			<td>A38-500</td>
			<td></td>
		</tr>
		<tr>
			<td>ethanol</td>
			<td>Fischer Scientific</td>
			<td>22-032-104</td>
			<td></td>
		</tr>
		<tr>
			<td>formamide</td>
			<td>Fischer Scientific</td>
			<td>F84-1</td>
			<td></td>
		</tr>
		<tr>
			<td>PNA telomere probe</td>
			<td>Panagene</td>
			<td>F1001-5</td>
			<td></td>
		</tr>
		<tr>
			<td>PNA centromere probe</td>
			<td>Panagene</td>
			<td>F3003-5</td>
			<td></td>
		</tr>
		<tr>
			<td>20X SSC</td>
			<td>Fischer Scientific</td>
			<td>BP1325-4</td>
			<td></td>
		</tr>
		<tr>
			<td>BSA</td>
			<td>Sigma-Aldrich</td>
			<td>A2153-10G</td>
			<td></td>
		</tr>
		<tr>
			<td>tRNA</td>
			<td>Sigma-Aldrich</td>
			<td>R5636-1ML</td>
			<td></td>
		</tr>
		<tr>
			<td>Tween 20</td>
			<td>Fischer Scientific</td>
			<td>BP337-100</td>
			<td></td>
		</tr>
		<tr>
			<td>rubber cement</td>
			<td>Walmart</td>
			<td>Elmer&#39;s</td>
			<td></td>
		</tr>
		<tr>
			<td>DAPI</td>
			<td>Sigma-Aldrich</td>
			<td>D9542</td>
			<td></td>
		</tr>
	</tbody>
</table>

utilizing murine inducible telomerase alleles in the studies of tissue degeneration/regeneration and cancer

Telomere dysfunction-induced loss of genome integrity and its associated DNA damage signaling and checkpoint responses are well-established drivers that cause tissue degeneration during ageing. Cancer, with incidence rates greatly increasing with age, is characterized by short telomere lengths and high telomerase activity. To study the roles of telomere dysfunction and telomerase reactivation in ageing and cancer, the protocol shows how to generate two murine inducible telomerase knock-in alleles 4-Hydroxytamoxifen (4-OHT)-inducible TERT-Estrogen Receptor (mTERT-ER) and Lox-Stopper-LoxTERT (LSL-mTERT). The protocol describes the procedures to induce telomere dysfunction and reactivate telomerase activity in mTERT-ER and LSL-mTERT mice in vivo. The representative data show that reactivation of telomerase activity can ameliorate the tissue degenerative phenotypes induced by telomere dysfunction. In order to determine the impact of telomerase reactivation on tumorigenesis, we generated prostate tumor model G4 PB-Cre4 PtenL/L p53L/L LSL-mTERTL/L and thymic T-cell lymphoma model G4 Atm-/- mTERTER/ER. The representative data show that telomerase reactivation in the backdrop of genomic instability induced by telomere dysfunction can greatly enhance tumorigenesis. The protocol also describes the procedures used to isolate neural stem cells (NSCs) from mTERT-ER and LSL-mTERT mice and reactivate telomerase activity in NSCs in vitro. The representative data show that reactivation of telomerase can enhance the self-renewal capability and neurogenesis in vitro. Finally, the protocol describes the procedures for performing telomere FISH (Fluorescence In Situ Hybridization) on both mouse FFPE (Formalin Fixed and Paraffin Embedded) brain tissues and metaphase chromosomes of cultured cells.

The strategies to generate murine mTERT-ER and LSL-mTERT knock-in alleles were described in Figure 1A and 1B. Specifically, a LoxP-triple Stopper-Neo-LoxP fragment was inserted between exon 1 and exon 2 of mTERT locus to generate LSL-mTERT allele. To generate mTERT-ER allele, ERT2-LBD domain in frame with the mTERT gene was inserted into the N-terminus of exon 1. We showed that when telomerase was transiently reactivated in telomere dysfunction mice by treating them with 4-OHT pellets for 4 weeks, the degenerative phenotype could be ameliorated in multiple organs such as brain (Figure 2A) and testes (Figure 2B).&#160;In order to determine the impact of telomerase reactivation on cells cultured in vitro, we isolated neural stem cells (NSCs) from late generation G4 LSL-mTERT and G4 mTERT-ER mice. We showed that when telomerase was reactivated in telomere dysfunctional NSCs, the self-renewal capability of NSCs was greatly increased (Figure 3A), and in vitro neurogenesis was also significantly enhanced (Figure 3B). In order to determine the impact of telomerase reactivation on tumorigenesis in the context of telomere dysfunction, we generated PB-Cre4 PtenL/L p53L/L LSL-mTERTL/L (prostate tumor model) and Atm-/- mTERTER/ER (thymic T-cell lymphoma model) late generation cohorts. When telomerase was reactivated by tamoxifen treatment in these mice with injection (Figure 4A) or 4-OHT pellets for 8 weeks (Figure 4B), the tumorigenesis was greatly enhanced in both prostate tumor model (Figure 4A) and thymic T-cell lymphoma model (Figure 4B). Lastly, we reported the protocols of performing telomere FISH on FFPE mouse brain tissues (Figure 5) and metaphase chromosomes (Figure 5, inset).
<img alt="Figure 1" src="/files/ftp_upload/52599/52599fig1.jpg" /> 
Figure 1: (A) mTERT-ER knock-in strategy. TV, targeting vector; WT, wild type allele; KI, knock-in allele; LA, left arm; RA, right arm; E1, exon 1; E2, exon 2; neo, pgk promoter-driven neomycin resistant gene; ER, modified estrogen receptor (ERT2) ligand binding domain; DT, dyphteria toxin gene. (B) LSL-mTERT knock-in strategy. TV, targeting vector; WT, wild type allele; KI, knock-in allele; LA, left arm; RA, right arm; E1, exon 1; E2, exon 2; neo, pgk promoter-driven neomycin resistant gene; STOPPER, three repetitive transcriptional stop sequences; DT, dyphteria toxin gene.
<img alt="Figure 2" src="/files/ftp_upload/52599/52599fig2.jpg" /> 
Figure 2: Representative data to show telomerase reactivation ameliorates degenerative phenotypes of organs. Representative images of brains (left) and testes (right) of G0 and G4 mTERT-ER mice treated with placebo or 4-OHT for 4 weeks. Scale bars indicate 50 &#181;m. Re-print with permission from 20. <a href="https://www.jove.com/files/ftp_upload/52599/52599fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" src="/files/ftp_upload/52599/52599fig3.jpg" /> 
Figure 3: Representative data to show telomerase reactivation enhances self-renewal and neurogenesis of neural stem cells in vitro. (A) Representative images of neural stem cells isolated from G4 LSL-mTERT (upper panel) and G4 mTERT-ER (lower panel) growing in stem cell medium treated with vehicle or 4-OHT. (B) Representative images of in vitro neurogenesis (Tuj1+) of neural stem cells isolated from G4 mTERT-ER cultured in differentiation medium (with 1% FBS) treated with vehicle or 4-OHT. Scale bars indicate 100 &#181;m.
<img alt="Figure 4" src="/files/ftp_upload/52599/52599fig4.jpg" /> 
Figure 4: Representative data to show telomerase reactivation enhances tumorigenesis against the backdrop of genomic instability. (A) Representative images of prostate tumors dissected from G0 PB-Cre4 PtenL/L p53L/L LSL-mTERT+/-, G4 PB-Cre4 PtenL/L p53L/L LSL-mTERT-/-, and G4 PB-Cre4 PtenL/L p53L/L LSL-mTERTL/L treated with tamoxifen. Re-print with permission from 22. (B) Representative images of thymic T-cell lymphomas dissected from G0 Atm-/- mTERT+/ER, G4 Atm-/- mTERTER/ER treated with vehicle, and G4 Atm-/- mTERTER/ER treated with 4-OHT for 8 weeks. Scale bars indicate 1 cm.
<img alt="Figure 5" src="/files/ftp_upload/52599/52599fig5.jpg" /> 
Figure 5: Representative images of telomeric and centromeric FISH on FFPE mouse brain tissue and metaphase (inset). Red indicates DNA, green indicates telomere staining, and cyan indicates centromere staining. Scale bars indicate 1 mm.

Watch this Scientific Journal Video about Utilizing Murine Inducible Telomerase Alleles in the Studies of Tissue Degeneration/Regeneration and Cancer at JoVE.com

Utilizing Murine Inducible Telomerase Alleles in the Studies of Tissue Degeneration/Regeneration and Cancer

Telomere and telomerase play essential roles in ageing and tumorigenesis. The goal of this protocol is to show how to generate two murine inducible telomerase knock-in alleles and how to utilize them in the studies of tissue degeneration/regeneration and cancer.

Telomere dysfunction-induced loss of genome integrity and its associated DNA damage signaling and checkpoint responses are well-established drivers that ...

utilizing-murine-inducible-telomerase-alleles-studies-tissue

Research

JoVE Journal

Medicine

9.9K Views.  UT MD Anderson Cancer Center. Telomere and telomerase play essential roles in ageing and tumorigenesis. The goal of this protocol is to show how to generate two murine inducible telomerase knock-in alleles and how to utilize them in the studies of tissue degeneration/regeneration and cancer. 

Video: Utilizing Murine Inducible Telomerase Alleles in the Studies of Tissue Degeneration/Regeneration and Cancer

A Method for Murine Islet Isolation and Subcapsular Kidney Transplantation

Since the early pioneering work of Ballinger and Reckard demonstrating that transplantation of islets of Langerhans into diabetic rodents could normalize their blood glucose levels, islet transplantation has been proposed to be a potential treatment for type 1 diabetes 1,2. More recently, advances in human islet transplantation have further strengthened this view 1,3. However, two major limitations prevent islet transplantation from being a widespread clinical reality: (a) the requirement for large numbers of islets per patient, which severely reduces the number of potential recipients, and (b) the need for heavy immunosuppression, which significantly affects the pediatric population of patients due to their vulnerability to long-term immunosuppression. Strategies that can overcome these limitations have the potential to enhance the therapeutic utility of islet transplantation.
Islet transplantation under the mouse kidney capsule is a widely accepted model to investigate various strategies to improve islet transplantation. This experiment requires the isolation of high quality islets and implantation of islets to the diabetic recipients. Both procedures require surgical steps that can be better demonstrated by video than by text. Here, we document the detailed steps for these procedures by both video and written protocol. We also briefly discuss different transplantation models: syngeneic, allogeneic, syngeneic autoimmune, and allogeneic autoimmune.

Transplantation of isolated islets has been proposed to be a potential treatment for type 1 diabetes. Here we describe a method to isolate islets from mouse pancreata and transplant them to the subcapsular space of the kidney.

Since the early pioneering work of Ballinger and Reckard demonstrating that transplantation of islets of Langerhans into diabetic rodents could normalize ...

An Orthotopic Model of Murine Bladder Cancer

In this straightforward procedure, bladder tumors are established in female C57 mice through the use of catheterization, local cauterization, and subsequent cell adhesion. After their bladders are transurethrally catheterized and drained, animals are again catheterized to permit insertion of a platinum wire into bladders without damaging the urethra or bladder. The catheters are made of Teflon to serve as an insulator for the wire, which will conduct electrical current into the bladder to create a burn injury. An electrocautery unit is used to deliver 2.5W to the exposed end of the wire, burning away extracellular layers and providing attachment sites for carcinoma cells that are delivered in suspension to the bladder through a subsequent catheterization. Cells remain in the bladder for 90 minutes, after which the catheters are removed and the bladders allowed to drain naturally. The development of tumor is monitored via ultrasound. Specific attention is paid to the catheterization technique in the accompanying video.

Bladder tumors are established in female mice in a minimally invasive fashion through catheterization, local cauterization, and subsequent adhesion of carcinoma cells to the burn sites.

In this straightforward procedure, bladder tumors are established in female C57 mice through the use of catheterization, local cauterization, and ...

Immunohistochemical Staining of B7-H1 (PD-L1) on Paraffin-embedded Slides of Pancreatic Adenocarcinoma Tissue

B7-H1/PD-L1, a member of the B7 family of immune-regulatory cell-surface proteins, plays an important role in the negative regulation of cell-mediated immune responses through its interaction with its receptor, programmed death-1 (PD-1) 1,2. Overexpression of B7-H1 by tumor cells has been noted in a number of human cancers, including melanoma, glioblastoma, and carcinomas of the lung, breast, colon, ovary, and renal cells, and has been shown to impair anti-tumor T-cell immunity3-8.
Recently, B7-H1 expression by pancreatic adenocarcinoma tissues has been identified as a potential prognostic marker9,10. Additionally, blockade of B7-H1 in a mouse model of pancreatic cancer has been shown to produce an anti-tumor response11. These data suggest the importance of B7-H1 as a potential therapeutic target. Anti-B7-H1 blockade antibodies are therefore being tested in clinical trials for multiple human solid tumors including melanoma and cancers of lung, colon, kidney, stomach and pancreas12.
In order to eventually be able to identify the patients who will benefit from B7-H1 targeting therapies, it is critical to investigate the correlation between expression and localization of B7-H1 and patient response to treatment with B7-H1 blockade antibodies. Examining the expression of B7-H1 in human pancreatic adenocarcinoma tissues through immunohistochemistry will give a better understanding of how this co-inhibitory signaling molecule contributes to the suppression of antitumor immunity in the tumor's microenvironment. The anti-B7-H1 monoclonal antibody (clone 5H1) developed by Chen and coworkers has been shown to produce reliable staining results in cryosections of multiple types of human neoplastic tissues4,8, but staining on paraffin-embedded slides had been a challenge until recently13-18. We have developed the B7-H1 staining protocol for paraffin-embedded slides of pancreatic adenocarcinoma tissues. The B7-H1 staining protocol described here produces consistent membranous and cytoplasmic staining of B7-H1 with little background.

Immunohistochemical Staining of B7-H1 PD-L1 on Paraffin-embedded Slides of Pancreatic Adenocarcinoma Tissue

B7-H1 (PD-L1) and its binding to PD-1 provide a major tumor-induced immunosuppressive signal in the tumor&#x2019;s microenvironment. An immunohistochemical staining technique to characterize the expression and localization of B7-H1 in pancreatic adenocarcinoma is described here.

B7-H1/PD-L1, a member  of the B7 family of immune-regulatory cell-surface proteins, plays an important  role in the negative regulation of cell-mediated ...

A Preclinical Murine Model of Hepatic Metastases

Numerous murine models have been developed to study human cancers and advance the understanding of cancer treatment and development. Here, a preclinical, murine pancreatic tumor model of hepatic metastases via a hemispleen injection of syngeneic murine pancreatic tumor cells is described. This model mimics many of the clinical conditions in patients with metastatic disease to the liver. Mice consistently develop metastases in the liver allowing for investigation of the metastatic process, experimental therapy testing, and tumor immunology research.

A preclinical, murine model of hepatic metastases performed via a hemispleen injection technique.

Numerous murine models have been developed to study human cancers and advance the understanding of cancer treatment and development. Here, a preclinical, ...

An In Vitro Dormancy Model of Estrogen-sensitive Breast Cancer in the Bone Marrow: A Tool for Molecular Mechanism Studies and Hypothesis Generation

The study of breast cancer dormancy in the bone marrow is an exceptionally difficult undertaking due to the complexity of the interactions of dormant cells with their microenvironment, their rarity and the overwhelming excess of hematopoietic cells. Towards this end, we developed an in vitro 2D clonogenic model of dormancy of estrogen-sensitive breast cancer cells in the bone marrow. The model consists of a few key elements necessary for dormancy. These include 1) the use of estrogen sensitive breast cancer cells, which are the type likely to remain dormant for extended periods, 2) incubation of cells at clonogenic density, where the structural interaction of each cell is primarily with the substratum, 3) fibronectin, a key structural element of the marrow and 4) FGF-2, a growth factor abundantly synthesized by bone marrow stromal cells and heavily deposited in the extracellular matrix. Cells incubated with FGF-2 form dormant clones after 6 days, which consist of 12 or less cells that have a distinct flat appearance, are significantly larger and more spread out than growing cells and have large cytoplasm to nucleus ratios. In contrast, cells incubated without FGF-2 form primarily growing colonies consisting of >30 relatively small cells. Perturbations of the system with antibodies, inhibitors, peptides or nucleic acids on day 3 after incubation can significantly affect various phenotypic and molecular aspects of the dormant cells at 6 days and can be used to assess the roles of membrane-localized or intracellular molecules, factors or signaling pathways on the dormant state or survival of dormant cells. While recognizing the in vitro nature of the assay, it can function as a highly useful tool to glean significant information about the molecular mechanisms necessary for establishment and survival of dormant cells. This data can be used to generate hypotheses to be tested in vivo models.

An In Vitro Dormancy Model of Estrogen-sensitive Breast Cancer in the Bone Marrow: A Tool for Molecular Mechanism Studies and Hypothesis Generation

We developed an in vitro model of dormancy in the bone marrow for estrogen-sensitive breast cancer cells. The goal of this protocol is to demonstrate use of the model for the study of the molecular and cellular biology of dormancy and for generation of hypotheses for subsequent testing in vivo.

The study of breast cancer dormancy in the bone marrow is an exceptionally difficult undertaking due to the complexity of the interactions of dormant ...

The bm12 Inducible Model of Systemic Lupus Erythematosus (SLE) in C57BL/6 Mice

Systemic lupus erythematosus (SLE) is an autoimmune disease with diverse clinical and immunological manifestations. Several spontaneous and inducible animal models mirror common components of human disease, including the bm12 transfer model. Upon transfer of bm12 splenocytes or purified CD4 T cells, C57BL/6 mice rapidly develop large frequencies of T follicular helper cells (Tfh), germinal center (GC) B cells, and plasma cells followed by high levels of circulating anti-nuclear antibodies. Since this model utilizes mice on a pure C57BL/6 background, researchers can quickly and easily study disease progression in transgenic or knockout mouse strains in a relatively short period of time. Here we describe protocols for the induction of the model and the quantitation Tfh, GC B cells, and plasma cells by multi-color flow cytometry. Importantly, these protocols can also be used to characterize disease in most mouse models of SLE and identify Tfh, GC B cells, and plasma cells in other disease models.

The bm12 Inducible Model of Systemic Lupus Erythematosus SLE in C57BL/6 Mice

The transfer of bm12 lymphocytes into a C57BL/6 recipient is an established model of systemic lupus erythematosus. Here we describe how to initiate disease using this model and how to characterize T follicular helper cells, germinal center B cells and plasma cells by flow cytometry.

Systemic lupus erythematosus (SLE) is an autoimmune disease with diverse clinical and immunological manifestations. Several spontaneous and inducible ...

Pre-clinical Orthotopic Murine Model of Human Prostate Cancer

To study the multifaceted biology of prostate cancer, pre-clinical in vivo models offer a range of options to uncover critical biological information about this disease. The human orthotopic prostate cancer xenograft mouse model provides a useful alternative approach for understanding the specific interactions between genetically and molecularly altered tumor cells, their organ microenvironment, and for evaluation of efficacy of therapeutic regimens. This is a well characterized model designed to study the molecular events of primary tumor development and it recapitulates the early events in the metastatic cascade prior to embolism and entry of tumor cells into the circulation. Thus it allows elucidation of molecular mechanisms underlying the initial phase of metastatic disease. In addition, this model can annotate drug targets of clinical relevance and is a valuable tool to study prostate cancer progression. In this manuscript we describe a detailed procedure to establish a human orthotopic prostate cancer xenograft mouse model.

Prostate cancer is the second most common cause of cancer-related deaths in the United States. An orthotopic cancer model provides a useful approach to understand the biology of prostate cancer and to evaluate the efficacy of therapeutic regimens. This protocol describes detailed steps necessary to establish an orthotopic prostate cancer mouse model.

To study the multifaceted biology of prostate cancer, pre-clinical in vivo models offer a range of options to uncover critical biological information ...

Analyzing Beneficial Effects of Nutritional Supplements on Intestinal Epithelial Barrier Functions During Experimental Colitis

Inflammatory bowel diseases (IBD), including Crohn&#39;s disease and ulcerative colitis, are chronic relapsing disorders of the intestines. They cause severe problems, such as abdominal cramping, bloody diarrhea, and weight loss, in affected individuals. Unfortunately, there is no cure yet, and treatments only aim to alleviate symptoms. Current treatments include anti-inflammatory and immunosuppressive drugs that may cause severe side effects. This warrants the search for alternative treatment options, such as nutritional supplements, that do not cause side effects. Before their application in clinical studies, such compounds must be rigorously tested for effectiveness and security in animal models. A reliable experimental model is the dextran sulfate sodium (DSS) colitis model in mice, which reproduces many of the clinical signs of ulcerative colitis in humans. We recently applied this model to test the beneficial effects of a nutritional supplement containing vitamins C and E, L-arginine, and &#969;3-polyunsaturated fatty acids (PUFA). We analyzed various disease parameters and found that this supplement was able to ameliorate edema formation, tissue damage, leukocyte infiltration, oxidative stress, and the production of pro-inflammatory cytokines, leading to an overall improvement in the disease activity index. In this article, we explain in detail the correct application of nutritional supplements using the DSS colitis model in C57Bl/6 mice, as well as how disease parameters such as histology, oxidative stress, and inflammation are assessed. Analyzing the beneficial effects of different diet supplements may then eventually open new avenues for the development of alternative treatment strategies that alleviate IBD symptoms and/or that prolong the phases of remission without causing severe side effects.

Current treatments of inflammatory bowel diseases (IBD) aim at alleviating disease symptoms but may cause severe side effects. Thus, alternative strategies are being investigated in animal colitis models. Here, we explain how the beneficial effects of diet supplements on clinical IBD signs are analyzed in such a colitis model.

Inflammatory bowel diseases (IBD), including Crohn&#39;s disease and ulcerative colitis, are chronic relapsing disorders of the intestines. They cause ...

Generating a Murine Orthotopic Metastatic Breast Cancer Model and Performing Murine Radical Mastectomy

In vivo mouse models to assess breast cancer progression are essential for cancer research, including preclinical drug developments. However, the majority of the practical and technical details are commonly omitted in published manuscripts which, therefore, makes it challenging to reproduce the models, particularly when it involves surgical techniques. Bioluminescence technology allows for the evaluation of small amounts of cancer cells even when a tumor is not palpable. Utilizing luciferase-expressing cancer cells, we establish a breast cancer orthotopic inoculation technique with a high tumorigenesis rate. Lung metastasis is assessed utilizing an ex vivo technique. We, then, establish a mastectomy model with a low local recurrence rate to assess the metastatic tumor burden. Herein, we describe, in detail, the surgical techniques of orthotopic implantation and mastectomy for breast cancer with a high tumorigenesis rate and low local recurrence rates, respectively, to improve breast cancer model efficiency.

We introduce a murine orthotopic breast cancer model and radical mastectomy model with bioluminescence technology to quantify the tumor burden to mimic human breast cancer progression.

In vivo mouse models to assess breast cancer progression are essential for cancer research, including preclinical drug developments. However, the majority ...

Murine Precision-Cut Liver Slices as an Ex Vivo Model of Liver Biology

Understanding the mechanisms of liver injury, hepatic fibrosis, and cirrhosis that underlie chronic liver diseases (i.e., viral hepatitis, non-alcoholic fatty liver disease, metabolic liver disease, and liver cancer) requires experimental manipulation of animal models and in vitro cell cultures. Both techniques have limitations, such as the requirement of large numbers of animals for in vivo manipulation. However, in vitro cell cultures do not reproduce the structure and function of the multicellular hepatic environment. The use of precision-cut liver slices is a technique in which uniform slices of viable mouse liver are maintained in laboratory tissue culture for experimental manipulation. This technique occupies an experimental niche that exists between animal studies and in vitro cell culture methods. The presented protocol describes a straightforward and reliable method to isolate and culture precision-cut liver slices from mice. As an application of this technique, ex vivo liver slices are treated with bile acids to simulate cholestatic liver injury and ultimately assess the mechanisms of hepatic fibrogenesis.

This protocol provides a simple and reliable method for the production of viable precision-cut liver slices from mice. The ex vivo tissue samples can be maintained under laboratory tissue culture conditions for multiple days, providing a flexible model to examine liver pathobiology.

Understanding the mechanisms of liver injury, hepatic fibrosis, and cirrhosis that underlie chronic liver diseases (i.e., viral hepatitis, non-alcoholic ...