培养基

In vitro culture of embryonic lungs

Whatyouneed:

  • E11-12mouseembryos
  • DMEMwith5%fetalbovineserum
  • petridishesfordissectionsandwashes
  • Tyrode-Ringer"ssolution,pH7.6-7.7(recipebelow)
  • pancreatin-trypsinsolution(recipebelow)

1.DissectE11-12lungsinDMEMand5%serumonice.Younglungs(E11to11.5)arebest.

2.Washthelungs3x5minutesoniceinTyrode-Ringer"sSolution,pH7.6-7.7tooptimizephysiologicalconditionsforpancreatin-trypsinactivity.

3.Incubatewholelungsforappoximately5minutesinpancreatin-trypsinsolutiononice.ThetimerequiredwillvarydependingonthebatchofPT.

4.Washlungs3x5minutesinDMEM+serumtosaturatepancreatin-trypsinactivity.

5.Usingtungstenneedles,dissectoffthemesenchymeandcutoffthebuds.Alternatively,cutoffthebudsfirstandremovethemesenchymesurroundingthem.

6.Placeintomatrigelmatrixandcultureforthreetofivedays(seeaccompanyingprotocol).Isolatedendodermwillnotsurvivewithoutgrowthfactoraddedtotheculturemedium.

Solutions

Tyrode-Ringer"sSolution,pH7.6-7.7

componentg/liter

  • NaCl8.0
  • KCl0.3
  • NaH2PO4.5H2O0.093
  • KH2PO40.025
  • NaHCO31.0
  • Glucose2.0

Pancreatin/TrypsinSolution

componentg/20mlfinalconcentration

  • pancreatin0.502.5%
  • trypsin0.100.5%
  • polyvinylpyrrolidone(PVP)0.100.5%
  • Tyrode-Ringer"sSolution20ml

SUSPendbymixingforabout30minutes.Centrifugeat3000XgintheSorvallhangingbucketrotorfor5minutes.Filtersterilizethesupernatantusing.8micronMilliporefilter(s).Storeinaliquotsat-80C.Thisprocessisabigpainandtimeconsuming,mainlybecausethesupernatantdoesnotfilterefficientlyandtheMilliporefiltersmustbeswitchedoften.

CollagenGels

Whatyouneed:

  • Collagen,typeIrattail(catno40236,CollaborativeBiomedicalProducts)
  • 10XDMEM,lowglucose(catnoD6921,SigmaCellCulture)
  • 0.8MNaHCO3insterilewater
  • four-well(1.5cmdiameter/well)Nunctissueculturedishes(catno176740,NalgeNuncInternational)
  • culturemedium(forlungbuds)
  • tissuecultureincubator

Tissuestobeculturedareplacedinto50uldropsofcollageninfour-wellNuncdishes.Foreachtreatment,makeaseparate50ulaliquotofcollagengelasdescribedintheprotocolbelowandstoreonice.Directlybeforeaddingsamples,addtheNaHCO3andmixwell.ItisnecessarytoprepareeachcollagengelseparatelybecauseadditionofNaHCO3makesthecollagenpolymerizequickly.

1.Placecollagen,10XDMEMandonice.Alsochillthefour-welldishesintherfridgebeforeuse.

2.Mix45ulcollagenand5ul10XDMEM.Mixwellonice.Thecollagenwillnotgelifkeptcold.

3.Add1.9ulofNaHCO3.Mixwell.Thisstepbeginspolymerizationofthecollagengel.

4.Addthe50ulcollagenmixturetoachilledfour-welldish.

5.Firstprepareabedofcollagenandallowittosetat37篊.Afterithaspolymerized,addyoursampletothebedofcollagenandaddcoldunpolymerizedcollageninalayeroverthetopofthesample.

6.Placeat37篊forapproximately10minutestoallowcompletepolymerization.

  • Addculturemediumtocoverthebeadofcollagenandtissueandincubatethesampleat37?C.
  • Replacemediadaily.

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