2013
Paracrine Loop of Keratinocyte Proliferation and Directed Neuritic Outgrowth in a Neuroepithelial Coculture
Radtke C, Rennekampff H, Reimers K, Vogt P, Kocsis J. Paracrine Loop of Keratinocyte Proliferation and Directed Neuritic Outgrowth in a Neuroepithelial Coculture. Annals Of Plastic Surgery 2013, Publish Ahead of Print: &na;. DOI: 10.1097/sap.0b013e318276d946.Peer-Reviewed Original ResearchNerve growth factorNeuritic outgrowthDRG neuronsHuman keratinocytesNeurotrophin nerve growth factorDorsal root ganglion neuronsCutaneous afferent axonsKeratinocyte proliferationAnti-NGF antibodyWound healingChronic nonhealing woundsProliferation of keratinocytesNGF levelsSkin innervationPrimary human keratinocytesNeurotrophic factorGanglion neuronsAfferent axonsParacrine loopNonhealing woundsMitogenic effectCell bodiesNeuritic processesGrowth factorNeurons
2000
Excitability changes of dorsal root axons following nerve injury: implications for injury-induced changes in axonal Na+ channels
Nonaka T, Honmou O, Sakai J, Hashi K, Kocsis J. Excitability changes of dorsal root axons following nerve injury: implications for injury-induced changes in axonal Na+ channels. Brain Research 2000, 859: 280-285. PMID: 10719075, DOI: 10.1016/s0006-8993(00)01979-x.Peer-Reviewed Original ResearchConceptsDorsal root axonsNerve injuryDorsal rootsAction potentialsCutaneous afferent axonsSciatic nerve ligationAfferent cell bodiesInjury-induced changesRat dorsal rootSucrose gap chamberTarget disconnectionNerve ligationExcitability changesSpinal cordAfferent axonsTrophic supportRoot ligationRefractory periodCell bodiesElectrophysiological recordingsAxonsInjuryDepolarizationLigationPrevious studies
1998
The delayed depolarization in rat cutaneous afferent axons is reduced following nerve transection and ligation, but not crush: Implications for injury‐induced axonal NA + channel reorganization
Sakai J, Honmou O, Kocsis J, Hashi K. The delayed depolarization in rat cutaneous afferent axons is reduced following nerve transection and ligation, but not crush: Implications for injury‐induced axonal NA + channel reorganization. Muscle & Nerve 1998, 21: 1040-1047. PMID: 9655122, DOI: 10.1002/(sici)1097-4598(199808)21:8<1040::aid-mus8>3.0.co;2-8.Peer-Reviewed Original ResearchConceptsCutaneous afferent axonsNerve injurySural nerveNerve transectionAfferent axonsAction potentialsCell bodiesCutaneous afferent neuronsPeripheral nerve injuryAfferent cell bodiesSucrose gap chamberRat sural nerveTarget disconnectionAfferent neuronsPeripheral targetsAxonal NaNerveRefractory periodAxonsTransectionCompound actionDepolarizationSimilar changesInjuryTarget connections
1991
Differential sensitivity to hypoxia of the peripheral versus central trajectory of primary afferent axons
Utzschneider D, Kocsis J, Waxman S. Differential sensitivity to hypoxia of the peripheral versus central trajectory of primary afferent axons. Brain Research 1991, 551: 136-141. PMID: 1913145, DOI: 10.1016/0006-8993(91)90924-k.Peer-Reviewed Original ResearchConceptsDorsal columnsDorsal rootsAfferent fibersCentral nervous system componentsPrimary afferent fibersSucrose gap chamberAction potential amplitudePrimary afferent axonsCompound action potentialDorsal spinal rootsNervous system componentsAxonal trunksPeripheral nervesSpinal cordSpinal rootsAfferent axonsCNS portionSchwann cellsAdult ratsPotential amplitudeAxon branchesAction potentialsHypoxiaMembrane potential changesMembrane depolarization