Name: ovarian tissue culture to visualize phenomena in mouse ovary
Uploaded: 2018-06-19T14:30:00
Description: Watch this Scientific Journal Video about Ovarian Tissue Culture to Visualize Phenomena in Mouse Ovary at JoVE.com

oog1pro 3.9 चूहों को उपलब्ध कराने के लिए हम डॉ॰ Naojiro Minami (क्योटो विश्वविद्यालय) को धन्यवाद देते हैं । इस शोध को JSPS (KAKENHI # JP15H06275) और Nitto फाउंडेशन ने सपोर्ट किया था ।

चूहों एक 12 ज प्रकाश/12 एच अंधेरे चक्र के साथ 23 ± 1 ° c में एक पर्यावरण की दृष्टि से नियंत्रित कमरे में स्थित थे । पशु देखभाल प्रोटोकॉल और प्रयोगों के अनुसार आईची चिकित्सा विश्वविद्यालय में पशु प्रयोग के लिए द...

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J., Srsen, V., Lapping, R., Spears, N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Combined+effect+of+follicle-follicle+interactions+and+declining+follicle-stimulating+hormone+on+murine+follicle+health+in+vitro.">Combined effect of follicle-follicle interactions and declining follicle-stimulating hormone on murine follicle health in vitro.</a> Biol Reprod. 65 (4), 1304-1310 (2001).</li><li>Komatsu, 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=Analysis+of+the+Effect+of+Leukemia+Inhibitory+Factor+on+Follicular+Growth+in+Cultured+Murine+Ovarian+Tissue.">Analysis of the Effect of Leukemia Inhibitory Factor on Follicular Growth in Cultured Murine Ovarian Tissue.</a> Biol Reprod. 93 (1), 18 (2015).</li><li>Komatsu, K., Masubuchi, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+concentration-dependent+effect+of+progesterone+on+follicle+growth+in+the+mouse+ovary.">The concentration-dependent effect of progesterone on follicle growth in the mouse ovary.</a> J Reprod Dev. 63 (3), 271-277 (2017).</li><li>Murase, 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=Follicle+dynamics:+visualization+and+analysis+of+follicle+growth+and+maturation+using+murine+ovarian+tissue+culture.">Follicle dynamics: visualization and analysis of follicle growth and maturation using murine ovarian tissue culture.</a> J Assist Reprod Genet. , 1-5 (2017).</li><li>Ishida, 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=The+promoter+of+the+oocyte-specific+gene,+Oog1,+functions+in+both+male+and+female+meiotic+germ+cells+in+transgenic+mice.">The promoter of the oocyte-specific gene, Oog1, functions in both male and female meiotic germ cells in transgenic mice.</a> PLoS One. 8 (7), 68686 (2013).</li><li>Minami, N., 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=Oogenesin+is+a+novel+mouse+protein+expressed+in+oocytes+and+early+cleavage-stage+embryos.">Oogenesin is a novel mouse protein expressed in oocytes and early cleavage-stage embryos.</a> Biol Reprod. 69 (5), 1736-1742 (2003).</li><li>Nilsson, E. E., Skinner, M. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Growth+and+differentiation+factor-9+stimulates+progression+of+early+primary+but+not+primordial+rat+ovarian+follicle+development.">Growth and differentiation factor-9 stimulates progression of early primary but not primordial rat ovarian follicle development.</a> Biol Reprod. 67 (3), 1018-1024 (2002).</li><li>Nilsson, E. E., Kezele, P., Skinner, M. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Leukemia+inhibitory+factor+(LIF)+promotes+the+primordial+to+primary+follicle+transition+in+rat+ovaries.">Leukemia inhibitory factor (LIF) promotes the primordial to primary follicle transition in rat ovaries.</a> Mol Cell Endocrinol. 188 (1-2), 65-73 (2002).</li><li>Nilsson, E. E., Skinner, M. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Bone+morphogenetic+protein-4+acts+as+an+ovarian+follicle+survival+factor+and+promotes+primordial+follicle+development.">Bone morphogenetic protein-4 acts as an ovarian follicle survival factor and promotes primordial follicle development.</a> Biol Reprod. 69 (4), 1265-1272 (2003).</li><li>Nilsson, E. E., Skinner, M. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Kit+ligand+and+basic+fibroblast+growth+factor+interactions+in+the+induction+of+ovarian+primordial+to+primary+follicle+transition.">Kit ligand and basic fibroblast growth factor interactions in the induction of ovarian primordial to primary follicle transition.</a> Mol Cell Endocrinol. 214 (1-2), 19-25 (2004).</li><li>Abe, 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=Establishment+of+conditional+reporter+mouse+lines+at+ROSA26+locus+for+live+cell+imaging.">Establishment of conditional reporter mouse lines at ROSA26 locus for live cell imaging.</a> Genesis. 49 (7), 579-590 (2011).</li><li>Lan, Z. J., Xu, X., Cooney, A. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Differential+oocyte-specific+expression+of+Cre+recombinase+activity+in+GDF-9-iCre,+Zp3cre,+and+Msx2Cre+transgenic+mice.">Differential oocyte-specific expression of Cre recombinase activity in GDF-9-iCre, Zp3cre, and Msx2Cre transgenic mice.</a> Biol Reprod. 71 (5), 1469-1474 (2004).</li><li>Payer, B., 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=Generation+of+stella-GFP+transgenic+mice:+a+novel+tool+to+study+germ+cell+development.">Generation of stella-GFP transgenic mice: a novel tool to study germ cell development.</a> Genesis. 44 (2), 75-83 (2006).</li><li>Ohinata, Y., Sano, M., Shigeta, M., Yamanaka, K., Saitou, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+comprehensive,+non-invasive+visualization+of+primordial+germ+cell+development+in+mice+by+the+Prdm1-mVenus+and+Dppa3-ECFP+double+transgenic+reporter.">A comprehensive, non-invasive visualization of primordial germ cell development in mice by the Prdm1-mVenus and Dppa3-ECFP double transgenic reporter.</a> Reproduction. 136 (4), 503-514 (2008).</li></ol>

इस अध्ययन में, हम माउस अंडाशय में कूप विकास के अध्ययन के लिए दो नए तरीके विकसित की है । पहली विधि कटा हुआ डिम्बग्रंथि वयस्क चूहों कूप विकास के विश्लेषण के द्वारा पीछा ऊतकों की संस्कृति शामिल है, और दूसरा ...

महिला माउस अंडाशय कई हजार रोम1होते हैं, और आवधिक ovulation प्रत्येक मद चक्र में लगभग दस अंडाणुओं परिपक्व होती है । रोम कई विकास चरणों में वर्गीकृत कर रहे हैं: मौलिक, प्राथमिक, माध्यमिक, कोटरीय, और Graafian कूप, granulosa सेलुलर प्रत्येक oocyte के आसपास परत के रूप पर निर्भर करता है । अधिकांश मौलिक कूप निष्क्रिय कर रहे हैं, और उनमें से कुछ सक्रिय और प्रत्येक मद चक्र2में प्राथमिक कूप में विकसित कर रहे हैं । माध्यमिक तोंसिल्लितिस चरण के बाद, कूप विकास मुख्य रूप से गोनैडोट्रॉपिंस, तोंसिल्लितिस उत्तेजक हार्मोन (FSH), और luteinizing हार्मोन (LH) द्वारा विनियमित है । हालांकि, मौलिक और प्राथमिक कूप विकास गोनॉडोट्रॉफिन से स्वतंत्र है, और विनियामक तंत्र है कि इन चरणों को नियंत्रित3,4,5inderstood खराब रहते हैं । वृद्धि कारकों और हार्मोन के अलावा, मौलिक और प्राथमिक कूप रोम6,7के बीच बातचीत के द्वारा विनियमित है । इसलिए, हम माउस अंडाशय के ऊतकों में कूप गतिशीलता का विश्लेषण किया, और डिम्बग्रंथि ऊतक संस्कृतियों8,9,10का उपयोग कर जुड़े विनियामक तंत्र की जांच की ।
साथ ही, हम दो डिंबग्रंथि ऊतक संस्कृति मॉडल तरीकों परिचय । पहले के लिए फुफ्फुसीय क्षेत्रों की माप द्वारा कूप विकास का विश्लेषण किया जाता है, और दूसरा ट्रांसजेनिक चूहों के साथ माध्यमिक कूप चरण के लिए मौलिक से जल्दी कूप विकास के दौरान विनियामक तंत्र का अध्ययन करने के लिए प्रयोग किया जाता है । कूप विकास विश्लेषण के लिए, हम मुख्य रूप से 4 सप्ताह पुराने मादा चूहों के अंडाशय का इस्तेमाल किया, क्योंकि वे रोम के आसान दृश्य के लिए अनुमति देते हैं । vivo कूप विकास में आवधिक ovulation और मॉडल प्रेरित करने के लिए, हम LH वृद्धि reproduced और ovulation मनाया, कूप अविवरता, और ऊतक संस्कृति की स्थिति के तहत एस्ट्राडियोल के स्राव । संस्कृतिपूर्ण अंडाशय की छवियाँ कैप्चर किए गए थे, और कूप विकास प्रक्रियाओं को तोंसिल्लितिस क्षेत्र में परिवर्तन अनुरेखण द्वारा विश्लेषण किया गया । हालांकि, चमकीले क्षेत्र माइक्रोस्कोपी विश्लेषण में, मौलिक और प्रारंभिक प्राथमिक कूप के बीच भेद अस्पष्ट था । इस प्रकार, हम छोटे रोम का पता लगाने के लिए एक विधि विकसित की है, और मौलिक, प्राथमिक, और Oogenesin1 (Oog1) pro3 का उपयोग कर संस्कृतिपूर्ण डिम्बग्रंथि ऊतकों में माध्यमिक कूप के बीच भेद । 9 और R26-H2B-mCherry ट्रांसजेनिक चूहों अंडाशय के दिनों में 0 और 4 जन्म के बाद11. Oog1 अभिव्यक्ति अंडाणुओं में अर्धसूत्रीविभाजन में प्रवेश के बाद पता लगाने में है, और धीरे से कूप विकास के साथ बढ़ जाती है, मौलिक से प्राथमिक कूप के लिए संक्रमण के अवलोकन की अनुमति समय का उपयोग करते हुए, संस्कृतिपूर्ण अंडाशय ऊतक 11 के चूक छवियों ,12. हालांकि रूपात्मक तरीके कारकों है कि निष्क्रियमौलिक कूप13,14,15,16, अंडाशय में शारीरिक कूप विकास सक्रिय अध्ययन करने के लिए इस्तेमाल किया गया है मुश्किल निरीक्षण करने के लिए, और विभिंन कारकों के प्रभाव के लक्षण रहते हैं । वर्तमान संस्कृति के तरीकों को लक्षित कारकों में से वास्तविक समय विश्लेषण में इस धनाभाव का पता डिजाइन किए गए थे ।
वर्तमान अध्ययन में, हम एक समय चूक इमेजिंग विधि का उपयोग कर तोंसिल्लितिस के विकास पर नज़र रखी और कूप विकास की प्रक्रिया की विशेषता । हमारे उपंयास तरीकों अंडाशय के फिजियोलॉजी की जांच के लिए एक अभूतपूर्व उपकरण प्रदान करते हैं ।

<table border="0" cellpadding="0" cellspacing="0" style="width:1176px;" width="1175">
	<colgroup>
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		<col />
		<col />
		<col />
	</colgroup>
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:383px;">Follicle stimulating hormone from human pituitary</td>
			<td style="width:224px;">SIGMA</td>
			<td style="width:119px;">F4021</td>
			<td style="width:451px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Lutenizing hormone from equine pituitary</td>
			<td>SIGMA</td>
			<td>L9773</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Penicillin-streptomycin solution</td>
			<td>Wako Pure Chemical Industries</td>
			<td>168-23191</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">MEM a, GlutaMax, no nucleotides</td>
			<td>Thermo Fisher</td>
			<td>32561037</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Glass bottom dish</td>
			<td>MatTek</td>
			<td>P35G-0-10-C</td>
			<td>35mm dish, No. 0 coverslip, 10mm glass diameter</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Millicell cell culture insert</td>
			<td>Merck Millipore</td>
			<td>PICM0RG50</td>
			<td>Diameter: 315 mm, pore size: 0.4 mm, material: hydrophilic PTTE</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:383px;">3.5cm cell culture dishes</td>
			<td style="width:224px;">greiner bio-one</td>
			<td style="width:119px;">627160</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:383px;">50ml / centrifuge tube with triple seal cap</td>
			<td style="width:224px;">IWAKI</td>
			<td style="width:119px;">2345-050</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:383px;">Low-profile disposable blades 819</td>
			<td style="width:224px;">Leica</td>
			<td style="width:119px;">14035838925</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">LSM 710</td>
			<td>Carl Zeiss</td>
			<td style="width:119px;"></td>
			<td>Confocal microscope</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">CellVoyager, CV1000</td>
			<td>Yokogawa Electric Corporation</td>
			<td style="width:119px;"></td>
			<td>Time-lapse imaging</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">BZ-X700</td>
			<td>KEYENCE</td>
			<td style="width:119px;"></td>
			<td>Time-lapse imaging</td>
		</tr>
	</tbody>
</table>

ovarian tissue culture to visualize phenomena in mouse ovary

स्तनधारी महिलाओं को समय पर प्रत्येक मद चक्र के दौरान अंडाणुओं की एक लगभग निरंतर संख्या ovulation । इस तरह की नियमितता और आवधिकता बनाए रखने के लिए, विनियमन हाइपोथैलेमस-पिट्यूटरी-जननांगों अक्ष स्तर पर और अंडाशय में विकसित कूप पर होता है । सक्रिय अध्ययन के बावजूद, कूप विकास तंत्र कई कदम निष्क्रिय मौलिक कूप सक्रियण से ovulation के लिए शामिल की वजह से स्पष्ट नहीं हैं, और विनियमन जटिलता की वजह से है कि प्रत्येक तोंसिल्लितिस मंच पर अलग है । कूप विकास के तंत्र की जांच करने के लिए, और मद चक्र भर में रोम के गतिशीलता, हम एक माउस डिम्बग्रंथि ऊतक संस्कृति मॉडल है कि एक खुर्दबीन का उपयोग कूप विकास का पालन किया जा सकता है विकसित की है । व्यवस्थित कूप विकास, आवधिक ovulation, और कूप अविवरता सभी प्रसंस्कृत अंडाशय मॉडल में reproduced किया जा सकता है, और संस्कृति की स्थिति प्रयोग संग्राहक किया जा सकता है । यहां, हम कूप विकास और अंय डिंबग्रंथि घटना के विनियामक तंत्र के अध्ययन में इस पद्धति की उपयोगिता का प्रदर्शन ।

चित्रा 1 डिम्बग्रंथि ऊतक संस्कृति के दौरान मीडिया में परिवर्तन के लिए प्रोटोकॉल से पता चलता है. इस कार्यक्रम के बाद, 4 सप्ताह पुराने ICR चूहों अंडाशय और संस्कृति 24-एच में imaged थे फोकल ?...

Watch this Scientific Journal Video about Ovarian Tissue Culture to Visualize Phenomena in Mouse Ovary at JoVE.com

Ovarian Tissue Culture to Visualize Phenomena in Mouse Ovary

डिम्बग्रंथि ऊतक संस्कृति माउस अंडाशय में घटनाएं कल्पना करने के लिए

डिम्बग्रंथि ऊतक संस्कृतियों कूप विकास, ovulation, और कूप अविवरता के मॉडल के रूप में इस्तेमाल किया जा सकता है और गतिशील डिम्बग्रंथि प्रक्रियाओं के विनियामक तंत्र से संकेत मिलता है ।

Mammalian females periodically ovulate an almost constant number of oocytes during each estrus cycle. To sustain such regularity and periodicity, ...

This method can help answer key questions in the ovary research field about follicle development, follicle atresia and operation. The main advantage of this technique is that we can reproduce the ovarian phenomena under controlled culture conditions for the observation in real time. To prepare the ovaries from a four week old Institute of Cancer Research mouse for culture:Use scissors and tweezers to trim the surrounding tissue from the ovaries under a stereo microscope, and place the cleaned ovaries into a dish of fresh culture medium.When all of the ovaries have been trimmed, transfer the individual ovaries onto a piece of filter paper moistened with 37 degrees Celsius PBS, and use a microtome blade to slice each ovary into four pieces. Transfer the slices into a 3.5 centimeter dish of 37 degrees Celsius culture medium, and use a micropipette to add an about 0.5 micrometer droplet of culture medium onto one cell culture insert per ovarian tissue section. In a second 3.5 centimeter glass bottom cell culture dish containing one millimeter of medium:Using tweezers, transfer one tissue specimen into each droplet and place the plate in a cell culture incubator.Replace the supernatant in the dish with fresh 37 degrees Celsius culture medium every two days and treat the ovaries with 100 milliunits per milliliter of FSH and LH for 12 hours every fourth day. Begin imaging the cultured ovaries every 24 hours after one day of culture to allow sufficient follicle growth between imaging sessions;capturing images at 30 minute intervals using a time-lapse imaging system under the appropriate experimental conditions. To analyze ovarian follicle development:Open the images in ImageJ and open the analyze menu to select set scale.Enter the side lengths of the captured images and the corresponding numbers of pixels in the known distance and distance in pixels fields, respectively. Then, use the free-hand tool to outline the follicles and click measure. During a three week ovarian tissue slice culture period, most antral and secondary follicles are degenerated by follicle atresia, and some are ovulated.Some follicles develop in groups during each LH surge cycle. While the timing of ovulation and the number of ovulated oocytes differs between mouse ovaries, ovulation from cultured ovaries predominantly occurs within 48 hours of each LH surge. Note that not all ovulated oocytes release first polar bodies after ovulation.Primordial and primary follicles are present simultaneously in postnatal day four mouse ovaries. Whereas, only primordial follicles are present in postnatal day zero ovaries. However, primary follicles become detectable in cultured postnatal day zero ovaries after 30 to 40 hours of culture as demonstrated.Primordial and primary follicles can also be distinguished in the cultured ovaries isolated from mCherry transgenic animals by the mCherry positive nuclei of granulosa cells;allowing the tracking of the follicle stages in the ovary slice cultures. I hope that this technique paves the way for researchers in the field of reproductive technology to explore new techniques for fertility treatment.

ovarian-tissue-culture-to-visualize-phenomena-in-mouse-ovary

Research

JoVE Journal

Developmental Biology

Culture and Co-Culture of Mouse Ovaries and Ovarian Follicles

The mammalian ovary is composed of ovarian follicles, each follicle consisting of a single oocyte surrounded by somatic granulosa cells, enclosed together within a basement membrane. A finite pool of follicles is laid down during embryonic development, when oocytes in meiotic arrest form a close association with flattened granulosa cells, forming primordial follicles. By or shortly after birth, mammalian ovaries contain their lifetime&#8217;s supply of primordial follicles, from which point onwards there is a steady release of follicles into the growing follicular pool.
The ovary is particularly amenable to development in vitro, with follicles growing in a highly physiological manner in culture. This work describes the culture of whole neonatal ovaries containing primordial follicles, and the culture of individual ovarian follicles, a method which can support the development of follicles from an immature through to the preovulatory stage, after which their oocytes are able to undergo fertilization in vitro. The work outlined here uses culture systems to determine how the ovary is affected by exposure to external compounds. We also describe a co-culture system, which allows investigation of the interactions that occur between growing follicles and the non-growing pool of primordial follicles.

This protocol describes the primary culture/co-culture of mouse ovarian tissue, using ovaries from neonatal mice and individual ovarian follicles from prepubertal mice. The culture techniques support development in a highly physiological manner, allowing investigation of the effect of extrinsic agents on the ovary, and of interactions between ovarian follicles.

संस्कृति और सह संस्कृति माउस के अंडाशय और डिम्बग्रंथि

The mammalian ovary is composed of ovarian follicles, each follicle consisting of a single oocyte surrounded by somatic granulosa cells, enclosed together ...

Ex Utero Electroporation and Organotypic Slice Culture of Mouse Hippocampal Tissue

Mouse genetics offers a powerful tool determining the role of specific genes during development. Analyzing the resulting phenotypes by immunohistochemical and molecular methods provides information of potential target genes and signaling pathways. To further elucidate specific regulatory mechanisms requires a system allowing the manipulation of only a small number of cells of a specific tissue by either overexpression, ablation or re-introduction of specific genes and follow their fate during development. To achieve this ex utero electroporation of hippocampal structures, especially the dentate gyrus, followed by organotypic slice culture provides such a tool. Using this system to generate mosaic deletions allows determining whether the gene of interest regulates cell-autonomously developmental processes like progenitor cell proliferation or neuronal differentiation. Furthermore it facilitates the rescue of phenotypes by re-introducing the deleted gene or its target genes. In contrast to in utero electroporation the ex utero approach improves the rate of successfully targeting deeper layers of the brain like the dentate gyrus. Overall ex utero electroporation and organotypic slice culture provide a potent tool to study regulatory mechanisms in a semi-native environment mirroring endogenous conditions.

Ex Utero Electroporation and Organotypic Slice Culture of Mouse Hippocampal Tissue

Here we present a protocol providing a tool to examine regulatory mechanisms of specific genes during hippocampal development. Employing ex utero electroporation and organotypic slice culture allows the up- and down-regulation of the expression of genes of interest in single cells and follow their fate during development.

माउस hippocampal ऊतक के पूर्व utero Electroporation और Organotypic स्लाइस संस्कृति

Mouse genetics offers a powerful tool determining the role of specific genes during development. Analyzing the resulting phenotypes by immunohistochemical ...

Loss- and Gain-of-function Approach to Investigate Early Cell Fate Determinants in Preimplantation Mouse Embryos

Gene silencing and overexpression techniques are instrumental for the identification of genes involved in embryonic development. Direct target gene modification in preimplantation embryos provides a means to study the underlying mechanisms of genes implicated in, for instance, cellular differentiation into the trophectoderm (TE) and the inner cell mass (ICM). Here, we describe a protocol that examines the role of neogenin as an authentic receptor for initial cell fate determination in preimplantation mouse embryos. First, we discuss the experimental manipulations that were used to produce gain and loss of neogenin function by microinjecting neogenin cDNA and shRNA; the effectiveness of this approach was confirmed by a strong correlation between the pair-wise expression levels of either red fluorescent protein (RFP) or green fluorescent protein (GFP) and the immunocytochemical quantification of neogenin expression. Secondly, overexpression of neogenin in preimplantation mouse embryos leads to normal ICM development while neogenin knockdown causes the ICM to develop abnormally, implying that neogenin could be a receptor that relays extracellular cues to drive blastomeres to early cell fates. Given the success of this detailed protocol in investigating the function of a novel embryonic developmental stage-specific receptor, we propose that it has the potential to aid in exploration and identification of other stage-specific genes during embryogenesis.

The goal of this protocol is to describe a loss- and gain-of function method that is applicable to identify neogenin as a stage-specific receptor that leads to trophectoderm and inner cell mass differentiation in preimplantation mouse embryos.

नुकसान और लाभ के समारोह दृष्टिकोण Preimplantation माउस भ्रूण के प्रारंभिक दिनों में सेल भाग्य अवधारक जांच

 Gene silencing and overexpression techniques are instrumental for the identification of genes involved in embryonic development. Direct target gene ...

A Novel Mammary Fat Pad Transplantation Technique to Visualize the Vessel Generation of Vascular Endothelial Stem Cells

Endothelial cells (ECs) are the fundamental building blocks of the vascular architecture and mediate vascular growth and remodeling to ensure proper vessel development and homeostasis. However, studies on endothelial lineage hierarchy remain elusive due to the lack of tools to gain access as well as to directly evaluate their behavior in vivo. To address this shortcoming, a new tissue model to study angiogenesis using the mammary fat pad has been developed. The mammary gland develops mostly in the postnatal stages, including puberty and pregnancy, during which robust epithelium proliferation is accompanied by extensive vascular remodeling. Mammary fat pads provide space, matrix, and rich angiogenic stimuli from the growing mammary epithelium. Furthermore, mammary fat pads are located outside the peritoneal cavity, making them an easily accessible grafting site for assessing the angiogenic potential of exogenous cells. This work also describes an efficient tracing approach using fluorescent reporter mice to specifically label the targeted population of vascular endothelial stem cells (VESCs) in vivo. This lineage tracing method, coupled with subsequent tissue whole-mount microscopy, enable the direct visualization of targeted cells and their descendants, through which the proliferation capability can be quantified and the differentiation commitment can be fate-mapped. Using these methods, a population of bipotent protein C receptor (Procr) expressing VESCs has recently been identified in multiple vascular systems. Procr+ VESCs, giving rise to both new ECs and pericytes, actively contribute to angiogenesis during development, homeostasis, and injury repair. Overall, this manuscript describes a new mammary fat pad transplantation and in vivo lineage tracing techniques that can be used to evaluate the stem cell properties of VESCs.

This work demonstrates a novel approach to assess the proliferation, differentiation, and vessel-forming potential of vascular endothelial stem cells (VESCs) through mammary fat pad transplantation followed by whole-mount tissue preparation for microscopic observation. A lineage tracing strategy to investigate the behavior of VESCs in vivo is also presented.

संवहनी एंडोथिलियल स्टेम सेल के पोत जनरेशन को विज़ुअलाइज़ करने के लिए एक उपन्यास स्तनधारी फैट पैड ट्रांसप्लांटेशन तकनीक

Endothelial cells (ECs) are the fundamental building blocks of the vascular architecture and mediate vascular growth and remodeling to ensure proper ...

Live Imaging of Mouse Secondary Palate Fusion

The fusion of the secondary palatal shelves to form the intact secondary palate is a key process in mammalian development and its disruption can lead to cleft secondary palate, a common congenital anomaly in humans. Secondary palate fusion has been extensively studied leading to several proposed cellular mechanisms that may mediate this process. However, these studies have been mostly performed on fixed embryonic tissues at progressive timepoints during development or in fixed explant cultures analyzed at static timepoints. Static analysis is limited for the analysis of dynamic morphogenetic processes such a palate fusion and what types of dynamic cellular behaviors mediate palatal fusion is incompletely understood. Here we describe a protocol for live imaging of ex vivo secondary palate fusion in mouse embryos. To examine cellular behaviors of palate fusion, epithelial-specific Keratin14-cre was used to label palate epithelial cells in ROSA26-mTmGflox reporter embryos. To visualize filamentous actin, Lifeact-mRFPruby reporter mice were used. Live imaging of secondary palate fusion was performed by dissecting recently-adhered secondary palatal shelves of embryonic day (E) 14.5 stage embryos and culturing in agarose-containing media on a glass bottom dish to enable imaging with an inverted confocal microscope. Using this method, we have detected a variety of novel cellular behaviors during secondary palate fusion. An appreciation of how distinct cell behaviors are coordinated in space and time greatly contributes to our understanding of this dynamic morphogenetic process. This protocol can be applied to mutant mouse lines, or cultures treated with pharmacological inhibitors to further advance understanding of how secondary palate fusion is controlled.

Here, we present a protocol for live imaging of mouse secondary palate fusion using confocal microscopy. This protocol can be used in combination with a variety of fluorescent reporter mouse lines, and with pathway inhibitors for mechanistic insight. This protocol can be adapted for live imaging in other developmental systems.

माउस द्वितीयक ताललेट फ्यूजन की लाइव इमेजिंग

The fusion of the secondary palatal shelves to form the intact secondary palate is a key process in mammalian development and its disruption can lead to ...

Orthotopic Ovarian Transplantation Procedures to Investigate the Life- and Health-span Influence of Ovarian Senescence in Female Mice

Ovarian transplantation was first conducted at Utah State University in 1963. In more recent work, heterochronic transplantation of mammalian ovaries is being used to investigate the health-protective effects of young ovaries in young females. The current procedures employ an orthotopic transplantation method, where allogenic ovaries are transplanted back to their original position in the ovarian bursa. This is in contrast to the more commonly used heterotopic transplantation of ovaries/ovarian tissue subcutaneously or under the kidney capsule. All three locations provide efficient revascularization of the transplanted tissues. However, orthotopic transplantation provides the ovary with the most natural signaling environment and is the only procedure that provides the opportunity for the animal to reproduce naturally post-operatively. One must take care to remove all endogenous ovarian tissue during the ovariectomy procedure. If any endogenous tissue remains or if only one ovary is removed, the transplanted tissue will remain dormant until the existing tissue becomes senescent. While revascularization of the transplanted ovaries occurs very quickly, the transplant recipient can take a considerable amount of time to adapt to a new hypothalamic/pituitary/gonadal/adrenal (HPG/A) axis signaling regime associated with the transplanted tissue. This normally takes about 100 days in the mouse. Therefore, transplantation experiments should be designed to accommodate this adaptation period. Typical results with ovarian transplantation will include changes in the health of the recipient that reflect the age of the transplanted ovary, rather than the chronological age of the recipient.

Described here are orthotopic ovarian transplantation protocols for modifying ovarian influence on the physiology of the recipient mouse. This surgical procedure is used to expose female mice to various types of ovarian influence and may include heterochronic transplantations and transplantation of ovaries that have undergone various ex vivo treatments.

Orthotopic डिम्बग्रंथि प्रत्यारोपण प्रक्रियाओं मादा चूहों में डिम्बग्रंथि वार्धक्य के जीवन और स्वास्थ्य अवधि के प्रभाव की जांच करने के लिए

Ovarian transplantation was first conducted at Utah State University in 1963. In more recent work, heterochronic transplantation of mammalian ovaries is ...

A Hyperandrogenic Mouse Model to Study Polycystic Ovary Syndrome

Hyperandrogenemia plays a critical role in reproductive and metabolic function in females and is the hallmark of polycystic ovary syndrome. Developing a lean PCOS-like mouse model that mimics women with PCOS is clinically meaningful. In this protocol, we describe such a model. By inserting a 4 mm length of DHT (dihydrotestosterone) crystal powder pellet (total length of pellet is 8 mm), and replacing it monthly, we are able to produce a PCOS-like mouse model with serum DHT levels 2 fold higher than mice not implanted with DHT (no-DHT). We observed reproductive and metabolic dysfunction without changing body weight and body composition. While exhibiting a high degree of infertility, a small subset of these PCOS-like female mice can get pregnant and their offspring show delayed puberty and increased testosterone as adults. This PCOS-like lean mouse model is a useful tool to study the pathophysiology of PCOS and the offspring from these PCOS-like dams.

We describe the development of a lean PCOS-like mouse model with&#160;dihydrotestosterone pellet to study the pathophysiology of PCOS and the offspring from these PCOS-like dams.

पॉलीसिस्टिक अंडाशय सिंड्रोम का अध्ययन करने के लिए एक Hyperandrogenic माउस मॉडल

Hyperandrogenemia plays a critical role in reproductive and metabolic function in females and is the hallmark of polycystic ovary syndrome. Developing a ...

Assessment of Oxidative Damage in the Primary Mouse Ocular Surface Cells/Stem Cells in Response to Ultraviolet-C (UV-C) Damage

The ocular surface is subjected to regular wear and tear due to various environmental factors. Exposure to UV-C radiation constitutes an occupational health hazard. Here, we demonstrate the exposure of primary stem cells from the mouse ocular surface to UV-C radiation. Reactive oxygen species (ROS) formation is the readout of the extent of oxidative stress/damage. In an experimental in vitro setting, it is also essential to assess the percentage of dead cells generated due to oxidative stress. In this article, we will demonstrate the 2&#39;,7&#39;-Dichlorofluoresceindiacetate (DCFDA) staining of UV-C exposed mouse primary ocular surface stem cells and their quantification based on the fluorescent images of DCFDA staining. DCFDA staining directly corresponds to ROS generation. We also demonstrate the quantification of dead and live cells by simultaneous staining with propidium iodide (PI) and Hoechst 3332 respectively and the percentage of DCFDA (ROS positive) and PI positive cells.

Assessment of Oxidative Damage in the Primary Mouse Ocular Surface Cells/Stem Cells in Response to Ultraviolet-C UV-C Damage

This protocol demonstrates the simultaneous detection of reactive oxygen species (ROS), live cells, and dead cells in live primary cultures from mouse ocular surface cells. 2&#39;,7&#39;-Dichlorofluoresceindiacetate, propidium iodide, and Hoechst staining are used to assess the ROS, dead cells, and live cells, respectively, followed by imaging and analysis.

पराबैंगनी-सी (यूवी-सी) क्षति के जवाब में प्राथमिक माउस नेत्र सतह कोशिकाओं/स्टेम सेल में ऑक्सीडेटिव क्षति का आकलन

The ocular surface is subjected to regular wear and tear due to various environmental factors. Exposure to UV-C radiation constitutes an occupational ...

Isolation, Culture, and Adipogenic Induction of Neural Crest Original Adipose-Derived Stem Cells from Periaortic Adipose Tissue

An excessive amount of adipose tissue surrounding the blood vessels (perivascular adipose tissue, also known as PVAT) is associated with a high risk of cardiovascular disease. ADSCs derived from different adipose tissues show distinct features, and those from the PVAT have not been well characterized. In a recent study, we reported that some ADSCs in the periaortic arch adipose tissue (PAAT) descend from the neural crest cells (NCCs), a transient population of migratory cells originating from the ectoderm.
In this paper, we describe a protocol for isolating red fluorescent protein (RFP)-labeled NCCs from the PAAT of Wnt-1 Cre+/-;Rosa26RFP/+ mice and inducing their adipogenic differentiation in vitro. Briefly, the stromal vascular fraction (SVF) is enzymatically dissociated from the PAAT, and the RFP+ neural crest derived ADSCs (NCADSCs) are isolated by fluorescence activated cell sorting (FACS). The NCADSCs differentiate into both brown and white adipocytes, can be cryopreserved, and retain their adipogenic potential for ~3&#8211;5 passages. Our protocol can generate abundant ADSCs from the PVAT for modeling PVAT adipogenesis or lipogenesis in vitro. Thus, these NCADSCs can provide a valuable system for studying the molecular switches involved in PVAT differentiation.

We present a protocol for the isolation, culture, and adipogenic induction of neural crest derived adipose-derived stem cells (NCADSCs) from the periaortic adipose tissue of Wnt-1 Cre+/-;Rosa26RFP/+ mice. The NCADSCs can be an easily accessible source of ADSCs for modeling adipogenesis or lipogenesis in vitro.

पेरियाऑर्टिक एडीपोज ऊतक से न्यूरल क्रेस्ट मूल आदिपोज-व्युत्पन्न स्टेम सेल का अलगाव, संस्कृति और एडिपोजेनिक प्रेरण

An excessive amount of adipose tissue surrounding the blood vessels (perivascular adipose tissue, also known as PVAT) is associated with a high risk of ...

Whole Ovary Immunofluorescence, Clearing, and Multiphoton Microscopy for Quantitative 3D Analysis of the Developing Ovarian Reserve in Mouse

Female fertility and reproductive lifespan depend on the quality and quantity of the ovarian oocyte reserve. An estimated 80% of female germ cells entering meiotic prophase I are eliminated during Fetal Oocyte Attrition (FOA) and the first week of postnatal life. Three major mechanisms regulate the number of oocytes that survive during development and establish the ovarian reserve in females entering puberty. In the first wave of oocyte loss, 30-50% of the oocytes are eliminated during early FOA, a phenomenon that is attributed to high Long interspersed nuclear element-1 (LINE-1) expression. The second wave of oocyte loss is the elimination of oocytes with meiotic defects by a meiotic quality checkpoint. The third wave of oocyte loss occurs perinatally during primordial follicle formation when some oocytes fail to form follicles. It remains unclear what regulates each of these three waves of oocyte loss and how they shape the ovarian reserve in either mice or humans.
Immunofluorescence and 3D visualization have opened a new avenue to image and analyze oocyte development in the context of the whole ovary rather than in less informative 2D sections. This article provides a comprehensive protocol for whole ovary immunostaining and optical clearing, yielding preparations for imaging using multiphoton microscopy and 3D modeling using commercially available software. It shows how this method can be used to show the dynamics of oocyte attrition during ovarian development in C57BL/6J mice and quantify oocyte loss during the three waves of oocyte elimination. This protocol can be applied to prenatal and early postnatal ovaries for oocyte visualization and quantification, as well as other quantitative approaches. Importantly, the protocol was strategically developed to accommodate high-throughput, reliable, and repeatable processing that can meet the needs in toxicology, clinical diagnostics, and genomic assays of ovarian function.

Here, we present an optimized protocol for imaging entire ovaries for quantitative and qualitative analyses using whole-mount immunostaining, multiphoton microscopy, and 3D visualization and analysis. This protocol accommodates high-throughput, reliable, and repeatable processing that is applicable for toxicology, clinical diagnostics, and genomic assays of ovarian function.

माउस में डिम्बग्रंथि रिजर्व के विकासशील डिम्बग्रंथि रिजर्व के मात्रात्मक 3 डी विश्लेषण के लिए पूरे अंडाशय Immunofluorescence, समाशोधन, और Multiphoton माइक्रोस्कोपी