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AdvancesinMicroscopy
THEPROTOTYPICALNEURON
TheSoma
TheNucleus
RoughEndoplasmicReticulum
SmoothEndoplasmicReticulumandtheGolgiApparatus
TheMitochondrion
TheNeuronalMembrane
TheCytoskeleton
Microtubules
Box2.2OfSpecialInterestAlzheimer'
sDiseaseandtheNeuronalCytoskeleton
Microfilaments
Neurofilaments
TheAxon
TheAxonTerminal
TheSynapse,
AxoplasmicTransport
Box2.3OfSpecialInterestHitchingaRideon"
Retrorail"
Dendrites
Box2.4OfSpecialInterestMentalRetardationandDendriticSpines
Box2.5PathofDiscoveryTheStoryofDendriticProteinSynthesis,byOswaldSteward
CLASSIFYINGNEURONS
ClassificationBasedontheNumberofNeurites
ClassificationBasedonDendrites
ClassificationBasedonConnections
ClassificationBasedonAxonLength
ClassificationBasedonNeurotransmitter
GLlA
Astrocytes
MyelinatingGlia
OtherNon-NeuronalCells
CONCLUDINGREMARKS
Alltissuesandorgansinthebodyconsistofcells.Thespecializedfunctionsofcellsandhowtheyinteractdeterminethefunctionsoforgans.Thebrainisanorgan--tobesure,themostsophisticatedandcomplexorganthatnaturehasdevised.Butthebasicstrategyforunravelingitsfunctionisnodifferentfromthatusedtoinvestigatethepancreasorthelung.Wemustbeginbylearninghowbraincellsworkindividuallyandthenseehowtheyareassembledtoworktogether.Inneuroscience,thereisnoneedtoseparatemindfrombrain:
oncewefullyunderstandtheindividualandconcertedactionsofbraincells,wewillunderstandtheoriginsofourmentalabilities.Theorganizationofthisbookreflectsthis"
neurophilosophy."
Webeginwiththecellsofthenervoussystemtheirstructure,function,andmeansofcommunication.Inlaterchapters,wewillexplorehowthesecellsareassembledintocircuitsthatmediatesensation,perception,movement,speech,andemotion.
Inthischapter,wefocusonthestructureofthedifferenttypesofcellsinthenervoussystem:
neuronsandglia.Thesearebroadcategories,withinwhicharemanytypesofcellsthatdifferbasedontheirstructure,chemistry,andfunction.Nonetheless,thedistinctionbetweenneuronsandgliaisimportant.Althoughtherearemanyneuronsinthehumanbrain(about100billion),gliaoutnumberneuronsbytenfold.Basedonthesenumbers,itmightappearthatweshouldfocusourattentionongliaforinsightsintothecellularfunctionsofthenervoussystem.However,neuronsarethemostimportantcellsfortheuniquefunctionsofthebrain.Itistheneuronsthatsensechangesintheenvironment,communicatethesechangestootherneurons,andcommandthebody'
sresponsestothesesensations.Gliaarethoughttocontributetobrainfunctionmainlybyinsulating,supporting,andnourishingneighboringneurons.Ifthebrainwereachocolate-chipcookieandtheneuronswerechocolatechips,thegliawouldbethecookiedoughthatfillsalltheotherspaceandensuresthatthechipsaresuspendedintheirappropriatelocations.Indeed,thetermgliaisderivedfromtheGreekwordfor‘glue’,I'
mgivingtheimpressionthatthemainfunctionofthesecellsistokeepthebrainfromrunningoutofourears!
Asweshallseelaterinthechapter,thesimplicityofthisviewisprobablyagoodindicationofthedepthofourignoranceaboutglialfunction.However,westillareconfidentthatneuronsperformthebulkofinformationprocessinginthebrain.Therefore,wewillfocus90%ofourattentionon10%ofbraincells:
theneurons.
Neuroscience,likeotherfields,hasalanguageallitsown.Tousethislanguage,youmustlearnthevocabulary.Afteryouhavereadthischapter,takeafewminutestoreviewthekeytermslistandmakesureyouunderstandthemeaningofeachterm.Yourneurosciencevocabularywillgrowasyouworkyourwaythroughthebook.
Tostudythestructureofbraincells,scientistshavehadtoovercomeseveralobstacles.Thefirstwasthesmallsize.Mostcellsareintherangeof0.01-0.05mmindiameter.Thetipofanunsharpenedpencilleadisabout2mmacross;
neuronsare40-200timessmaller.(Forareviewofthemetricsystem,seeTable2.1.)Thissizeisatorbeyondthelimitofwhatcanbeseenbythenakedeye.Therefore,progressincellularneurosciencewasnotpossiblebeforethedevelopmentofthecompoundmicroscopeinthelateseventeenthcentury.Eventhen,obstaclesremained.Toobservebraintissueusingamicroscope,itwasnecessarytomakeverythinslices,ideallynotmuchthickerthanthediameterofthecells.However,braintissuehasaconsistencylikeabowlofJello:
notfirmenoughtomakethinslices.Thus,thestudyoftheanatomyofbraincellshadtoawaitthedevelopmentofamethodtohardenthetissuewithoutdisturbingitsstructureandaninstrumentthatcouldproduceverythinslices.Earlyinthenineteenthcentury,scientistsdiscoveredhowtoharden,or"
fix,"
tissuesbyimmersingtheminformaldehyde,andtheydevelopedaspecialdevicecalledamicrotometomakeverythinslices.
UNITABBREVIATIONMETEREQUIVALENTREAL-WORLDEOUIVALENT
Kilomoterkm103mAbouttwo-thirdsofamile.
Meterm1mAbout3feet.
Centimetercm10-2mThicknessofyourlittlefinger,
Millimetermm10-3mThicknessofyourtoenail.
Micrometerpm10-6mNearthelimitofresolutionforthelightmicroscope.
Nanometernm10-9mNearthelimitofresolutionfor
theelectronmicroscope.
Thesetechnicaladvancesspawnedthefieldofhistology,themicroscopystudyofthestructureoftissues.Butscientistsstudyingbrainstructurefacedyetanotherobstacle.Freshlypreparedbrainhasauniform,cream-coloredappearanceunderthemicroscope:
thetissuehasnodifferencesinpigmentationtoenablehistologiststoresolveindividualcells.Thus,thefinalbreakthroughinneurohistologywastheintroductionofstainsthatcouldselectivelycolorsome,butnotall,partsofthecellsinbraintissue.
Onestain,stillusedtoday,wasintroducedbytheGermanneurologistFranzNisslinthelatenineteenthcentury.Nisslshowedthataclassofbasicdyeswouldstainthenucleiofallcellsandalsostainclumpsofmaterialsurroundingthenucleiofneurons(Figure2.1).TheseclumpsarecalledNisslbodies,andthestainisknownastheNisslstain.TheNisslstainisextremelyusefulfortworeasons.First,itdistinguishesneuronsandgliafromoneanother.Second,itenableshistologiststostudythearrangement,orcytoarchitecture,ofneuronsindifferentpartsofthebrain.(Theprefixcyto-isfromtheGreekwordfor"
cell."
)Thestudyofcytoarchitectureledtotherealizationthatthebrainconsistsofmanyspecializedregions.Wenowknowthateachregionperformsadifferentfunction.
TheNisslstain,however,doesnottellthewholestory.ANissl-stainedneuronlookslikelittlemorethanalumpofprotoplasmcontaininganucleus,Neuronsaremuchmorethanthat,buthowmuchmorewasnotrecognizeduntilthepublicationoftheworkofItalianhistologistCamilloGolgi(Figure2.2).In1873,Golgidiscoveredthatbysoakingbraintissueinasilverchromatesolution,nowcalledtheGolgistain,asmallpercentageofneuronsbecamedarklycoloredintheirentirety(Figure2.3).Thisrevealedthattheneuronalcellbody,theregionoftheneuronaroundthenucleusthatisshownwiththeNisslstain,isactuallyonlyasmallfractionofthetotalstructureoftheneuron.NoticeinFigures2.1and2.3howdifferenthistologicalstainscanprovidestrikinglydifferentviewsofthesametissue.Today,neurohistologyremainsanactivefieldinneuroscience,alongwithitscredo:
"
Thegaininbrainismainlyinthestain."
TheGolgistainshowsthatneuronshaveatleasttwodistinguishableparts:
acentralregionthatcontainsthecellnucleus,andnumerousthintubesthatradiateawayfromthecentralregion.Theswollenregioncontainingthecellnucleushasseveralnamesthatareusedinterchangeably:
cellbody,soma(plural:
somata),andperikaryon(plural:
perikarya).Thethintubesthatradiateawayfromthesomaarecalledneuritesandareoftwotypes:
axonsanddendrites(Figure2.4).
Thecellbodyusuallygivesrisetoasingleaxon.Theaxonisofuniformdiameterthroughoutitslength,andifitbranches,thebranchesgenerallyextendatrightangles.Becauseaxonscantravelovergreatdistancesinthebody(ameterormore),itwasimmediatelyrecognizedbythehistologistsofthedaythataxonsmustactlike"
wires'
thatcarrytheoutputoftheneurons.Dendrites,ontheotherhand,rarelyextendmorethan2mminlength.Manydendritesextendfromthecellbodyandgenerallytapertoafinepoint.Earlyhistologistsrecognizedthatbecausedendritescomeincontactwithmanyaxons,theymustactastheantennaeoftheneurontoreceiveincomingsignals,orinput.
Golgiinventedthestain,butitwasaSpanishcontemporaryofGolgiwhousedittogreatesteffect.SantiagoRamenyCajalwasaskilledhistologistandartistwholearnedaboutGolgi'
smethodin1888(Figure2.5).Inaremarkableseriesofpublicationsoverthenext25years,CajalusedtheGolgistaintoworkoutthecircuitryofmanyregionsofthebrain(Figure2.6).Ironically,GolgiandCajaldrewcompletelyoppositeconclusionsaboutneurons.Golgichampionedtheviewthattheneuritesofdifferentcellsarefusedtogethertoformacontinuousreticulum,ornetwork,similartothearteriesandveinsofthecirculatorysystem.Accordingtothisreticulartheory,thebrainisanexceptiontothecelltheory,whichst