TY - JOUR
T1 - Neurotrophin‐3 affects proliferation and differentiation of distinct neural crest cells and is present in the early neural tube of avian embryos
AU - Pinco, Ofrit
AU - Carmeli, Chana
AU - Rosenthal, Arnon
AU - Kalcheim, Chaya
PY - 1993/12
Y1 - 1993/12
N2 - Neurotrophin‐3 is mitogenic for cultured quail neural crest cells (Kalcheim et al., 1992, Proc. Natl. Acad. Sci. USA 89:1661–1665). We now report that neurotrophin‐3 also influences the survival and/or differentiation of a subset of postmitotic neural crest precursors into neurons, provided these progenitors are grown on a cellular substrate. When cultured for 1 day on monolayers of NT‐3‐producing, chinese hamster ovary cells, 59% of the neural crest clusters growing on the transfected line revealed the presence of intense neuronal outgrowht, compared to 25% of that in controls. Moreover, dissociated neural crest cells grown for 20 h on top of mesodermal cells in the presence of various concentrations of purified recombinant neurotrophin‐3 displayed a dose‐dependent increase in neuronal number. Localization experiments using specific polyclonal antibodies, revealed that neurotrophin‐3 is confined to neuroepithelial cells of quail neural tubes in situ on E2 and E3, and to E2 neural tubes grown in culture for 24 h. At this stage, neural crest cells and somites were negative. At later stages, staining was likewise apparent in peripheral nerves and dorsal root ganglia. We, therefore, propose that NT‐3, a factor that is expressed in the early avian central nervous system, has multiple effects both on the proliferation and differentiation of distinct neural crest cells, which depend on the state of committment of the responsive progenitors. © 1993 John Wiley & Sons, Inc.
AB - Neurotrophin‐3 is mitogenic for cultured quail neural crest cells (Kalcheim et al., 1992, Proc. Natl. Acad. Sci. USA 89:1661–1665). We now report that neurotrophin‐3 also influences the survival and/or differentiation of a subset of postmitotic neural crest precursors into neurons, provided these progenitors are grown on a cellular substrate. When cultured for 1 day on monolayers of NT‐3‐producing, chinese hamster ovary cells, 59% of the neural crest clusters growing on the transfected line revealed the presence of intense neuronal outgrowht, compared to 25% of that in controls. Moreover, dissociated neural crest cells grown for 20 h on top of mesodermal cells in the presence of various concentrations of purified recombinant neurotrophin‐3 displayed a dose‐dependent increase in neuronal number. Localization experiments using specific polyclonal antibodies, revealed that neurotrophin‐3 is confined to neuroepithelial cells of quail neural tubes in situ on E2 and E3, and to E2 neural tubes grown in culture for 24 h. At this stage, neural crest cells and somites were negative. At later stages, staining was likewise apparent in peripheral nerves and dorsal root ganglia. We, therefore, propose that NT‐3, a factor that is expressed in the early avian central nervous system, has multiple effects both on the proliferation and differentiation of distinct neural crest cells, which depend on the state of committment of the responsive progenitors. © 1993 John Wiley & Sons, Inc.
KW - avian embryo
KW - baby hamster kidney cells
KW - brain‐derived neurotrophic factor
KW - central nervous system
KW - dorsal root ganglia
KW - neural tube
KW - peripheral nervous system
KW - sympathetic ganglia
KW - trophic factors
UR - http://www.scopus.com/inward/record.url?scp=0027427443&partnerID=8YFLogxK
U2 - 10.1002/neu.480241207
DO - 10.1002/neu.480241207
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 8301270
AN - SCOPUS:0027427443
SN - 0022-3034
VL - 24
SP - 1626
EP - 1641
JO - Journal of Neurobiology
JF - Journal of Neurobiology
IS - 12
ER -