Name: studying wnt signaling during patterning of conducting airways
Uploaded: 2016-10-16T13:00:00
Description: Watch this Scientific Journal Video about Studying Wnt Signaling During Patterning of Conducting Airways at JoVE.com

Vi anerkender bistand fra Mike Muntifering og Matt Kofron med konfokal billedbehandling og Gail Macke med histologiske procedurer. Dette arbejde blev delvist støttet af National Institutes of Health-NHLBI (K01HL115447 til DS).

Dyrene blev huset i patogenfrie betingelser. Musene blev håndteret i overensstemmelse med protokoller godkendt af CCHMC Institutional Animal Care og brug Udvalg (Cincinnati, OH USA). Mus anvendt i alle disse undersøgelser blev opretholdt i en blandet baggrund. 1. Whole Mount X-galactosidasefarvning <ol><li> Euthanize gravide kvinder ved E11.5 til E14.5 ved CO2 inhalation. Placer dyr i CO 2 kammer, oplade kammer med CO 2. Oprethold dyr i kammer til mindst ...

<ol>
	<li>Maeda, Y., Dave, V., Whitsett, J. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Transcriptional+control+of+lung+morphogenesis.">Transcriptional control of lung morphogenesis.</a> Physiol Rev. 87, 219-244 (2007).</li><li>Morrisey, E. E., Hogan, B. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Preparing+for+the+first+breath:+genetic+and+cellular+mechanisms+in+lung+development.">Preparing for the first breath: genetic and cellular mechanisms in lung development.</a> Dev Cell. 18, 8-23 (2010).</li><li>Fausett, S. R., Klingensmith, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Compartmentalization+of+the+foregut+tube:+developmental+origins+of+the+trachea+and+esophagus.">Compartmentalization of the foregut tube: developmental origins of the trachea and esophagus.</a> Wiley Interdiscip Rev Dev Biol. 1, 184-202 (2012).</li><li>Goss, A. 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=Wnt2/2b+and+beta-catenin+signaling+are+necessary+and+sufficient+to+specify+lung+progenitors+in+the+foregut.">Wnt2/2b and beta-catenin signaling are necessary and sufficient to specify lung progenitors in the foregut.</a> Dev Cell. 17, 290-298 (2009).</li><li>Harris-Johnson, K. S., Domyan, E. T., Vezina, C. M., Sun, X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=beta-Catenin+promotes+respiratory+progenitor+identity+in+mouse+foregut.">beta-Catenin promotes respiratory progenitor identity in mouse foregut.</a> Proc Natl Acad Sci U S A. 106, 16287-16292 (2009).</li><li>Cornett, 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=Wntless+is+required+for+peripheral+lung+differentiation+and+pulmonary+vascular+development.">Wntless is required for peripheral lung differentiation and pulmonary vascular development.</a> Dev Biol. 379, 38-52 (2013).</li><li>Snowball, J., Ambalavanan, M., Whitsett, J., Sinner, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=34;Endodermal+Wnt+signaling+is+required+for+tracheal+cartilage+formation&amp;#34;.">34;Endodermal Wnt signaling is required for tracheal cartilage formation&amp;#34;.</a> Dev Biol. , (2015).</li><li>Shannon, J. M., Hyatt, B. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Epithelial-mesenchymal+interactions+in+the+developing+lung.">Epithelial-mesenchymal interactions in the developing lung.</a> Annu Rev Physiol. 66, 625-645 (2004).</li><li>Shannon, J. M., Nielsen, L. D., Gebb, S. A., Randell, S. H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mesenchyme+specifies+epithelial+differentiation+in+reciprocal+recombinants+of+embryonic+lung+and+trachea.">Mesenchyme specifies epithelial differentiation in reciprocal recombinants of embryonic lung and trachea.</a> Dev Dyn. 212, 482-494 (1998).</li><li>Li, C., 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=Wnt5a+regulates+Shh+and+Fgf10+signaling+during+lung+development.">Wnt5a regulates Shh and Fgf10 signaling during lung development.</a> Dev Biol. 287, 86-97 (2005).</li><li>Loscertales, M., Mikels, A. J., Hu, J. K., Donahoe, P. K., Roberts, D. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Chick+pulmonary+Wnt5a+directs+airway+and+vascular+tubulogenesis.">Chick pulmonary Wnt5a directs airway and vascular tubulogenesis.</a> Development. 135, 1365-1376 (2008).</li><li>Yin, Y., 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=An+FGF-WNT+gene+regulatory+network+controls+lung+mesenchyme+development.">An FGF-WNT gene regulatory network controls lung mesenchyme development.</a> Dev Biol. 319, 426-436 (2008).</li><li>Shu, 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=Wnt/beta-catenin+signaling+acts+upstream+of+N-myc,+BMP4,+and+FGF+signaling+to+regulate+proximal-distal+patterning+in+the+lung.">Wnt/beta-catenin signaling acts upstream of N-myc, BMP4, and FGF signaling to regulate proximal-distal patterning in the lung.</a> Dev Biol. 283, 226-239 (2005).</li><li>Bretholz, A., Morrisey, R., Hoffman, R. 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+use+of+OpdA+in+rat+models+of+organic+phosphorus+(OP)+poisoning.">The use of OpdA in rat models of organic phosphorus (OP) poisoning.</a> Toxicology. 257, (2009).</li><li>Goss, A. 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=Wnt2+signaling+is+necessary+and+sufficient+to+activate+the+airway+smooth+muscle+program+in+the+lung+by+regulating+myocardin/Mrtf-B+and+Fgf10+expression.">Wnt2 signaling is necessary and sufficient to activate the airway smooth muscle program in the lung by regulating myocardin/Mrtf-B and Fgf10 expression.</a> Dev Biol. 356, 541-552 (2011).</li><li>Mucenski, M. 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=beta-Catenin+is+required+for+specification+of+proximal/distal+cell+fate+during+lung+morphogenesis.">beta-Catenin is required for specification of proximal/distal cell fate during lung morphogenesis.</a> J Biol Chem. 278, 40231-40238 (2003).</li><li>Hyatt, B. A., Shangguan, X., Shannon, J. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=FGF-10+induces+SP-C+and+Bmp4+and+regulates+proximal-distal+patterning+in+embryonic+tracheal+epithelium.">FGF-10 induces SP-C and Bmp4 and regulates proximal-distal patterning in embryonic tracheal epithelium.</a> Am J Physiol Lung Cell Mol Physiol. 287, L1116-L1126 (2004).</li><li>Del Moral, P. 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=VEGF-A+signaling+through+Flk-1+is+a+critical+facilitator+of+early+embryonic+lung+epithelial+to+endothelial+crosstalk+and+branching+morphogenesis.">VEGF-A signaling through Flk-1 is a critical facilitator of early embryonic lung epithelial to endothelial crosstalk and branching morphogenesis.</a> Dev Biol. 290, 177-188 (2006).</li><li>Ott, S. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Confocal+microscopy+in+large+insect+brains:+zinc-formaldehyde+fixation+improves+synapsin+immunostaining+and+preservation+of+morphology+in+whole-mounts.">Confocal microscopy in large insect brains: zinc-formaldehyde fixation improves synapsin immunostaining and preservation of morphology in whole-mounts.</a> J Neurosci Methods. 172, 220-230 (2008).</li><li>Jahrling, N., Becker, K., Dodt, H. U. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=3D-reconstruction+of+blood+vessels+by+ultramicroscopy.">3D-reconstruction of blood vessels by ultramicroscopy.</a> Organogenesis. 5, 145-148 (2009).</li><li>Park, 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=Regulation+of+Sox9+by+Sonic+Hedgehog+(Shh)+is+essential+for+patterning+and+formation+of+tracheal+cartilage.">Regulation of Sox9 by Sonic Hedgehog (Shh) is essential for patterning and formation of tracheal cartilage.</a> Dev Dyn. 239, 514-526 (2010).</li><li>Elluru, R. G., Thompson, F., Reece, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fibroblast+growth+factor+18+gives+growth+and+directional+cues+to+airway+cartilage.">Fibroblast growth factor 18 gives growth and directional cues to airway cartilage.</a> Laryngoscope. 119, 1153-1165 (2009).</li><li>Ahnfelt-Ronne, 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=An+improved+method+for+three-dimensional+reconstruction+of+protein+expression+patterns+in+intact+mouse+and+chicken+embryos+and+organs.">An improved method for three-dimensional reconstruction of protein expression patterns in intact mouse and chicken embryos and organs.</a> J Histochem Cytochem. 55, 925-930 (2007).</li><li>Yang, 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=Single-cell+phenotyping+within+transparent+intact+tissue+through+whole-body+clearing.">Single-cell phenotyping within transparent intact tissue through whole-body clearing.</a> Cell. 158, 945-958 (2014).</li><li>Gillotte, D. M., Fox, P. L., Mjaatvedt, C. H., Hoffman, S., Capehart, A. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=An+in+vitro+method+for+analysis+of+chondrogenesis+in+limb+mesenchyme+from+individual+transgenic+(hdf)+embryos.">An in vitro method for analysis of chondrogenesis in limb mesenchyme from individual transgenic (hdf) embryos.</a> Methods Cell Sci. 25, 97-104 (2003).</li><li>Cohen, E. D., 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=Wnt+signaling+regulates+smooth+muscle+precursor+development+in+the+mouse+lung+via+a+tenascin+C/PDGFR+pathway.">Wnt signaling regulates smooth muscle precursor development in the mouse lung via a tenascin C/PDGFR pathway.</a> J Clin Invest. 119, 2538-2549 (2009).</li><li>Boucherat, O., 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=Partial+functional+redundancy+between+Hoxa5+and+Hoxb5+paralog+genes+during+lung+morphogenesis.">Partial functional redundancy between Hoxa5 and Hoxb5 paralog genes during lung morphogenesis.</a> Am J Physiol Lung Cell Mol Physiol. 304, L817-L830 (2013).</li></ol>

Arrangementer ligger til grund for morfogenese i luftvejene forstås ikke til fulde, navnlig de processer, der er nødvendige for mønsterdannelse af de ledende luftveje. Tidligere undersøgelser har anvendt ex vivo-teknikker, hvor udviklingslande eksplantater dyrkes ved luft-væske interfase eller indlejret i matrigel 21,22. Disse undersøgelser har vist, hvordan vækstfaktorer påvirker mønsterdannelse af den udviklende luftrøret og dannelsen af ​​tracheal brusk. En begrænsning til disse und...

Udvikling luftvejene er initieret af embryonale dag 9 (E9) med fremkomsten af Nkx2.1 positive celler i den ventrale endodermal fortarm 1,2. Esophageal-trachealtube separation vil løse ved E11.5 når rørene kan skelnes som særskilte enheder, hver omgivet af mesenkymale væv 3. Wnt signalering spiller en central rolle i specifikationen af luftvejene som sletning af Wnt2 og Wnt2b ved splanknisk mesenkym og sletning af β-catenin fra endodermal respiratorisk epitel udtrykt vil resultere i lunge agenesi 4,5. Vores tidligere undersøgelser fastslået, at sletning af WLS, en last receptor medierer sekretion af alle Wnt-ligander, fra endodermale resultater luftveje i lungehypoplasi, defekter i pulmonal vaskulær udvikling og mis-mønster af tracheal mesenchym 6,7. Disse data understøtter betydningen af ​​epitel-mesenchymale cross taler i celledifferentiering og specifikation, som det også er blevet vist i andre undersøgelser 8,9. Undersøgelsen af de tidligste stadier af lunge udvikling er afhængig af genetiske, in vitro og ex vivo teknikker, der har givet os mulighed for bedre at forstå mekanismerne kørsel respiratorisk identitet 10-16. Hele lunge eksplantatkulturer på Air Liquide interfase er ofte blevet anvendt til at undersøge virkningerne af vækstfaktorer i tidlige stadier af pulmonal forgrening morfogenese 10,17,18. Mens denne metode anvendes som udlæsning af morfologiske ændringer, såsom forgrening morfogenese og genekspression modulation, det er begrænset til studiet af tidlige stadier af udviklingsprocessen, da kulturen ikke selv støtte udviklingen af karrene 17. Udvikling af tracheal brusk kræver længere inkubationstider, der kan være ikke kompatibel med denne kultur teknik. at analyze rolle Wnt signalering under dannelsen luftveje, har vi tilpasset standardteknikker til at opfylde de behov, vores embryonale undersøgelser. Vi har ændret volumener, farvning gange, forarbejdning cykling for paraffin indlejring og timing for rydning af tracheal-lungevæv. Det vigtigste mål for at optimere de beskrevne teknikker i nærværende undersøgelse var at analysere de tidligste stadier af trachea udvikling hos mus, der finder sted fra E11 til E14.5. Brug af reporter mus linje Axin2LacZ vi præcist bestemte steder i Wnt / β-catenin aktivitet i udviklingslandene tracheal mesenkym. Vi har også tilpasset lectin farvningsprocedure for hele mount luftrør væv. Således var vi i stand til at visualisere mesenkymale fortætninger og forudsige steder, hvor chondrogenese vil finde sted. Farvning af hele mount og sektioner af fostervæv opnået fra WlsShhCre mus, kombineret med avancerede mikroskopi-teknikker, tilladt os at afsløre rolle Wnt ligander produceret af traCheal epitel i tracheal mønster.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Anti Sox9 ab.</td>
			<td>Millipore</td>
			<td>AB5535</td>
			<td>1:400 , rabbit</td>
		</tr>
		<tr>
			<td>Anti Sox9 ab.</td>
			<td>Santa Cruz</td>
			<td>Sc-20095</td>
			<td>1:50, rabbit</td>
		</tr>
		<tr>
			<td>Anti Smooth Muscle Actin ab.</td>
			<td>Sigma</td>
			<td>A5228</td>
			<td>1:2k, mouse</td>
		</tr>
		<tr>
			<td>Anti NKX2.1 ab.</td>
			<td>Seven Hills</td>
			<td>n/a</td>
			<td>1:100, guinea pig</td>
		</tr>
		<tr>
			<td>Anti NKX2.1 ab.</td>
			<td>Seven Hills</td>
			<td>n/a</td>
			<td>1:400, mouse</td>
		</tr>
		<tr>
			<td>Anti Brdu ab.</td>
			<td>Abcam</td>
			<td>AB1893</td>
			<td>1:200, sheep</td>
		</tr>
		<tr>
			<td>Anti Brdu ab.</td>
			<td>Santa Cruz</td>
			<td>Sc-32323</td>
			<td>1:4k, mouse</td>
		</tr>
		<tr>
			<td>PNA Lectin</td>
			<td>Sigma</td>
			<td>L 7381</td>
			<td></td>
		</tr>
		<tr>
			<td>Secondary antibodies</td>
			<td>Life technologies</td>
			<td></td>
			<td>Alexa fluor Molecular probes</td>
		</tr>
		<tr>
			<td>K3Fe(CN)6</td>
			<td>Sigma</td>
			<td>P8131</td>
			<td></td>
		</tr>
		<tr>
			<td>K4Fe(CN)6</td>
			<td>Sigma-Aldrich</td>
			<td>P3289</td>
			<td></td>
		</tr>
		<tr>
			<td>MgCl2</td>
			<td>Sigma-Aldrich</td>
			<td>M9272</td>
			<td></td>
		</tr>
		<tr>
			<td>NaDOC</td>
			<td>Life Technologies</td>
			<td>89905</td>
			<td></td>
		</tr>
		<tr>
			<td>NP4O</td>
			<td>Life Technologies</td>
			<td>85124</td>
			<td></td>
		</tr>
		<tr>
			<td>Alcian Blue 8GX</td>
			<td>Sigma</td>
			<td>A-3157</td>
			<td></td>
		</tr>
		<tr>
			<td>Fisher brand super-frost plus</td>
			<td>Fisher</td>
			<td>12-550-15</td>
			<td></td>
		</tr>
		<tr>
			<td>PFA (16%)</td>
			<td>EMS</td>
			<td>15710</td>
			<td></td>
		</tr>
		<tr>
			<td>PBS</td>
			<td>Gibco</td>
			<td>70011-044</td>
			<td></td>
		</tr>
		<tr>
			<td>Fetal Calf Serum</td>
			<td>Sigma</td>
			<td>11K413</td>
			<td></td>
		</tr>
		<tr>
			<td>Blocking reagent</td>
			<td>Invitrogen</td>
			<td></td>
			<td>Component of TSA kit #2&#160;&#160;&#160; ( T20932)</td>
		</tr>
		<tr>
			<td>BrDu</td>
			<td>Sigma</td>
			<td>B5002-5g</td>
			<td></td>
		</tr>
		<tr>
			<td>Vectashield mounting medium</td>
			<td>Vector labs</td>
			<td>H-1000</td>
			<td></td>
		</tr>
		<tr>
			<td>Permount</td>
			<td>Fisher</td>
			<td>SP15-500</td>
			<td></td>
		</tr>
		<tr>
			<td>Tissue-loc cassettes Histoscreen</td>
			<td>Fisher</td>
			<td>C-0250-GR</td>
			<td></td>
		</tr>
		<tr>
			<td>Biopsy cassettes</td>
			<td>Premiere</td>
			<td>BC0109</td>
			<td>Available in different colors</td>
		</tr>
		<tr>
			<td>Nuclear fast red&#160; Kernechtrot 0.1%</td>
			<td>Sigma</td>
			<td>N3020</td>
			<td></td>
		</tr>
		<tr>
			<td>Citric acid</td>
			<td>Sigma</td>
			<td>C1909-500G</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium citrate tribasic dihydrate</td>
			<td>Sigma</td>
			<td>S4641-1Kg</td>
			<td></td>
		</tr>
		<tr>
			<td>Trizma hydrochloride</td>
			<td>Sigma</td>
			<td>T5941-500G</td>
			<td></td>
		</tr>
		<tr>
			<td>Xylene</td>
			<td>Pharmco-AAPER</td>
			<td>399000000</td>
			<td></td>
		</tr>
		<tr>
			<td>Ethanol</td>
			<td>Pharmco-AAPER</td>
			<td>111000200</td>
			<td></td>
		</tr>
		<tr>
			<td>Micro knives</td>
			<td>FST</td>
			<td>10318-14</td>
			<td></td>
		</tr>
		<tr>
			<td>Dumont #5 ceramic coated</td>
			<td>FST</td>
			<td>11252-50</td>
			<td></td>
		</tr>
		<tr>
			<td>Dumont #5CO</td>
			<td>FST</td>
			<td>11295-20</td>
			<td></td>
		</tr>
		<tr>
			<td>Dumont # 5</td>
			<td>FST</td>
			<td>91150-20</td>
			<td></td>
		</tr>
		<tr>
			<td>Thermo/Shandon Excelsior ES</td>
			<td>Thermo Fisher</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Microtome</td>
			<td>Leica</td>
			<td>RM2135</td>
			<td></td>
		</tr>
		<tr>
			<td>Nikon i90</td>
			<td>Nikon</td>
			<td></td>
			<td>Wide field microscope</td>
		</tr>
		<tr>
			<td>NikonA1Rsi</td>
			<td>Nikon</td>
			<td></td>
			<td>Confocal microscopy. Settings:NikonA1 plus camera, scanner: Galvano, detector:DU4. Optics Plan Apo lambda 10x. Modality: Widefield fluorescence laser confocal.&#160;</td>
		</tr>
		<tr>
			<td>Leica MS 16 FA</td>
			<td>Leica</td>
			<td></td>
			<td>Fluorescence Dissecting microscope</td>
		</tr>
		<tr>
			<td>Zeiss</td>
			<td>Zeiss</td>
			<td></td>
			<td>Automated fluorescence microscope</td>
		</tr>
		<tr>
			<td>Leica Application suite</td>
			<td>Leica</td>
			<td></td>
			<td>Leica imaging software</td>
		</tr>
		<tr>
			<td>NIS</td>
			<td>Nikon</td>
			<td></td>
			<td>Nikon imaging software</td>
		</tr>
		<tr>
			<td>IMARIS</td>
			<td>Bitplane</td>
			<td></td>
			<td>Imaging processing software</td>
		</tr>
	</tbody>
</table>

studying wnt signaling during patterning of conducting airways

Wnt signaling pathways play critical roles during development of the respiratory tract. Defining precise mechanisms of differentiation and morphogenesis controlled by Wnt signaling is required to understand how tissues are patterned during normal development. This knowledge is also critical to determine the etiology of birth defects such as lung hypoplasia and tracheobronchomalacia. Analysis of earliest stages of development of respiratory tract imposes challenges, as the limited amount of tissue prevents the performance of standard protocols better suited for postnatal studies. In this paper, we discuss methodologies to study cell differentiation and proliferation in the respiratory tract. We describe techniques such as whole mount staining, processing of the tissue for confocal microscopy and immunofluorescence in paraffin sections applied to developing tracheal lung. We also discuss methodologies for the study of tracheal mesenchyme differentiation, in particular cartilage formation. Approaches and techniques discussed in the current paper circumvent the limitation of material while working with embryonic tissue, allowing for a better understanding of the patterning process of developing conducting airways.

Wnt / β-catenin-aktivitet Whole mount Lac-Z farvning blev påvist i trakeal-lungevæv af embryoner isoleret fra reporter Axin2 Lac-Z mus 11. Lokaliteter af farvning indikerer Wnt / β-catenin-aktivitet. Analyse af sektioner af hele mount-farvning bestemmes, at Wnt / β-catenin-aktivitet var til stede i mesenkym af luftrøret og i mesenkym af randområder i udviklingslandene lungerne. ...

Watch this Scientific Journal Video about Studying Wnt Signaling During Patterning of Conducting Airways at JoVE.com

Studying Wnt Signaling During Patterning of Conducting Airways

Anvendelsen af reporter mus koblet til hele mount og sektion farvning, mikroskopi og in vivo assays letter analysen af mekanismer bag den normale mønsterdannelse i luftvejene. Her beskriver vi, hvordan disse teknikker bidraget til analyse af Wnt-signalering under tracheal udvikling.

Studere Wnt Signaling Under mønster af ledende Airways

Wnt signaling pathways play critical roles during development of the respiratory tract. Defining precise mechanisms of differentiation and morphogenesis ...

Research

JoVE Journal

Developmental Biology

Method of Studying Palatal Fusion using Static Organ Culture

Metode til at studere Palatal Fusion hjælp Statisk Organ Culture

Cleft lip and palate are among the most common of all birth defects. The secondary palate forms from mesenchymal shelves covered with epithelium that ...

Using Confocal Analysis of Xenopus laevis to Investigate Modulators of Wnt and Shh Morphogen Gradients

Using Confocal Analysis of Xenopus laevis to Investigate Modulators of Wnt and Shh Morphogen Gradients

Brug af Konfokal Analyse af<em&gt; Xenopus laevis</em&gt; At Undersøg Modulatorer af Wnt og Shh Morfogen Gradienter

This protocol describes a method to visualise ligands distributed across a field of cells. The ease of expressing exogenous proteins, together with the ...

The Power of Simplicity: Sea Urchin Embryos as in Vivo Developmental Models for Studying Complex Cell-to-cell Signaling Network Interactions

The Power of Simplicity: Sea Urchin Embryos as in Vivo Developmental Models for Studying Complex Cell-to-cell Signaling Network Interactions

The Power of Simplicity: Søpindsvin embryoner som<em&gt; I Vivo</em&gt; Developmental modeller til undersøgelser Complex celle-til-cellesignalering netværksinteraktioner

Remarkably few cell-to-cell signal transduction pathways are necessary during embryonic development to generate the large variety of cell types and ...

Stimulation of Notch Signaling in Mouse Osteoclast Precursors

Stimulering af Notch signalering i Mouse osteoklastpræcursorer

Notch signaling is a key component of multiple physiological and pathological processes. The nature of Notch signaling, however, makes in vitro ...

In Vitro Ovule Cultivation for Live-cell Imaging of Zygote Polarization and Embryo Patterning in Arabidopsis thaliana

In Vitro Ovule Cultivation for Live-cell Imaging of Zygote Polarization and Embryo Patterning in Arabidopsis thaliana

In Vitro Ovule dyrkning for Live-celle Imaging af Zygote polarisering og Embryo mønstre i Arabidopsis thaliana

In most flowering plants, the zygote and embryo are hidden deep in the mother tissue, and thus it has long been a mystery of how they develop dynamically; ...

Live Cell Imaging of Chromosome Segregation During Mitosis

Levende celle billeddannelse af kromosom Segregation under mitosen

Chromosomes must be reliably and uniformly segregated into daughter cells during mitotic cell division. Fidelity of chromosomal segregation is controlled ...

Visualization of the Superior Ocular Sulcus during Danio rerio Embryogenesis

Visualization of the Superior Ocular Sulcus during Danio rerio Embryogenesis

Visualisering af Superior okulær Sulcus under Danio rerio embryogenese

Congenital ocular coloboma is a genetic disorder that is typically observed as a cleft in the inferior aspect of the eye resulting from incomplete choroid ...

Genotyping of Sea Anemone during Early Development

Genotypebestemmelse af Havanemone under den tidlige udvikling

Described here is a PCR-based protocol to genotype the gastrula stage embryo of the anthozoan cnidarian Nematostella vectensis without sacrificing the ...

A Layered Mounting Method for Extended Time-Lapse Confocal Microscopy of Whole Zebrafish Embryos

En lagdelt monteringsmetode til forlænget tidsforskudt Konfokal mikroskopi af hele Zebrafish-embryoner

Dynamics of development can be followed by confocal time-lapse microscopy of live transgenic zebrafish embryos expressing fluorescence in specific tissues ...

Real-time Bioluminescence Imaging of Notch Signaling Dynamics during Murine Neurogenesis

Real-time bioluminescens billeddannelse af notch signalering dynamik under murine Neurogenesis

Notch signaling regulates the maintenance of neural stem/progenitor cells by cell-cell interactions. The components of Notch signaling exhibit dynamic ...