FromthevariousmicrosurgicalproceduresofSpemannandothers,severaldevelopmentalprincipleshaveemergedaboutamphibianembryos.Oneofthemostimportantdiscoverieswastheunderstandingthatthedevelopmentalfatesofvariousgroupsofcellsarenotrigidlydeterminedearlyindevelopment.Inmanycases,ifamulticellularfragmentofanearlyfroggastrulaistransplantedfromoneregionoftheembryotoanother,thecellswillbehaveasiftheywerecellsfromtheinsertedsite,producingstructuresthatwouldnormallydevelopinthatpartoftheembryo.Laterindevelopment,however,cellsoftransplantedfragmentsdevelopdifferently.Theytendtocontinuealongthesamedevelopmentalpathwaysthattheywouldhavefollowedintheiroriginallocation.Theydifferentiateasiftheyhadnotbeentransplanted,thusproducingananomalouspatchofmisplacedtissue.ExperimentsbyDuShaneinthe1930srevealedthattheneuralcrestelementsareprecursorsofpigmentcells.Todemonstratethatthepigmentcellsarederivedfromtheneuralcrest,weplantotransplantthecrestmaterialtoanotherregionofthefrog\"sbody.Neuralcrestcellsformadorsallyplacedwedgebetweenthelateralwalloftheneuralfoldandtheectodermoneachsideoftheembryo,thustheremovalofthelateralneuralfoldremovesaportionoftheneuralcrest. Ayoungaxolotlembryo. Objective Inthisexperimentwewilltransplantneuralcrestelementsfromoneembryointotheventralsurfaceofanotherembryoandobservehowthetransplantationeffectsthedevelopmentoftheembryo.Becausepigmentcellsdevelopfromtheneuralcrestregion,asuccessfultransplantationwouldresultinagroupofpigmentcellsarisingwheretheneuralcrestcellsaretransplantedto.Finallywewillobservewhetherthedonorembryocanrecoverfromthesurgeryandstillmaketheneuralcrestafterwehaveremovedthelateralneuraltube. Anaxolotlembryo,anexampleofwhatwasusedinthislab. Protocol I.PreparationofMicrosurgeryTools Followprotocolfoundonthegeneralprotocolwebpage. II.Microsurgerypreparation: 1.Manuallydejellyembryoofstage14andkeepinHSBtcontainingantibioticsuntiluse.Formicrosurgery,alsoremovemembranearoundtheembryo. 2.Prepare2%agarose-coatedoperatingdish.RinsewithHBStandantibiotics. 3.Placeembryosintooperatingdishcontaining1XHBStandantibiotics. 4.Usecleantechniquewhileperformingmicrosurgery(i.e.dipalltools,Pipettes,andglassbridgesinto70%ethanolandthenintosterileHBStbeforeusing). III.Transplantationoftheneuralcrest 1.Prepareasmallpocketintheventralsurfaceofthehostembryo.Onlyaslitisrequiredbycuttingwithaglassneedle.Thepocketcanbeenlargedtoreceivethetransplantbycarefullyremovingsomeofthemesodermcellswiththetipoftheglassneedle. 2.Usingafine-tippedneedle,removepartoftheneuralfoldontherightsideoftheembryo.Withasinglemotionfromtheanteriortotheposterior,usetheglassneedletomakeathintearinthepigmentedepidermisveryclosetotheouteredgeoftherightneuralfold.Now,tearcarefullythroughthewhitishmesodermalcellsthatlieunderneath.Whenthegrayish-tanendodermalcellsbecomevisIBLe,stopcutting.Followthefirstlongitudinalcutwithasecondparallelcutattheinneredgeoftherightneuralfold.Next,maketwotransversecuts,anteriortoposterior,tocompletearectangularareaofneuralfoldtissue. 3.Lifttheentirerectangularareaofneuraltissueawayfromtheembryowiththetipoftheglassneedle.Thepieceshouldincludeawhitishmesodermwiththeoverlyingpigmentedectoderm. 4.Transfertheneuralfoldtransplantonthetipoftheglassneedletotheventralpocketontherecipientembryo.Gentlyandfirmlypushthewholemassthroughthenarrowincisionandanchoritagainsttheyolk.Atightfittingtransplantisdesirable. 5.Quicklycovertheimplantwiththeflatsurfaceofapiecefromathin-gradecoverslip.Waitonehour. 6.Carefullyremovethecoverslip.Ifthetransplanthasnothealedproperly,placeitunderpressureagainforanotherhalfhour.Afterhealingiscomplete,transferboththedonorandthehostembryostoaglassdishcontainingspringwater. 7.Observethedifferentiationoftheimplantedtissue.Notewhethergraftwassuccessfullytransplanted,howtheembryorespondedtothegraft,andwhethertherehavebeenanydifferenceswhichhaveoccurredinthedevelopmentoftheembryo. Results Twentyembryosweresurgicallymanipulated.Ofthose20,eightweredeemedpossiblysuccessfultransplants.However,uponcheckingtheembryosafter48hours,itwasdeterminedthatnoneoftheembryosuccessfullyacceptedthegrafts.Whydidthishappen?Itwasmostlikelybecausewedidnotpossessthemanualdexteritywhichwasrequiredtoperformmicrosurgeryonthesmallembryos.Additionally,theglasscoverplateswhichwereplacedontopoftheembryospost-surgerycausedtheembryostobepulledapartafterweattemptedtoremovethem48hourspost-op.Wefeelthatthislabwouldbebettertoperformwithlaterstageembryosorbyapersonwiththenecessarydexteritytomanipulatethedelicateembryos.