TY - JOUR
T1 - Neurofibromin negatively regulates neurotrophin signaling through p21(ras) in embryonic sensory neurons
AU - Vogel, Kristine S.
AU - El-Afandi, Mary
AU - Parada, Luis F.
N1 - Funding Information:
We thank Dr. Ellen Vitetta for providing Y13-259 and rat IgG2b control Fab fragments and Dr. Guy James for providing the H-ras E. coli strains. This work was supported by NIH Grants R01 NS33199 to L.F.P. and P30AR41940 to the Skin Disease Research Center, UTSWMC.
PY - 2000/4
Y1 - 2000/4
N2 - Embryonic sensory and sympathetic neurons that lack neurofibromin, the protein product of the neurofibromatosis type 1 (Nfl) gene, survive and extend neurites in the absence of neurotrophins. To determine whether neurofibromin negatively regulates neurotrophin signaling through its interaction with p21(ras), we used Fab antibody fragments to block Ras function in DRG, trigeminal, nodose, and SCG neurons isolated from Nfl-/- and wild-type mouse embryos. We show that introduction of anti-Ras Fab fragments significantly reduces the ability of neurofibromin-deficient neurons to survive in the absence of neurotrophins. Moreover, addition of H-ras protein enhances the survival of Nfl-/-, but not wild-type, DRG neurons. Our results are consistent with a major role for neurofibromin in modulating Trk signaling through p21(ras) during neuronal development.
AB - Embryonic sensory and sympathetic neurons that lack neurofibromin, the protein product of the neurofibromatosis type 1 (Nfl) gene, survive and extend neurites in the absence of neurotrophins. To determine whether neurofibromin negatively regulates neurotrophin signaling through its interaction with p21(ras), we used Fab antibody fragments to block Ras function in DRG, trigeminal, nodose, and SCG neurons isolated from Nfl-/- and wild-type mouse embryos. We show that introduction of anti-Ras Fab fragments significantly reduces the ability of neurofibromin-deficient neurons to survive in the absence of neurotrophins. Moreover, addition of H-ras protein enhances the survival of Nfl-/-, but not wild-type, DRG neurons. Our results are consistent with a major role for neurofibromin in modulating Trk signaling through p21(ras) during neuronal development.
UR - http://www.scopus.com/inward/record.url?scp=0034103390&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0034103390&partnerID=8YFLogxK
U2 - 10.1006/mcne.2000.0836
DO - 10.1006/mcne.2000.0836
M3 - Article
C2 - 10845775
AN - SCOPUS:0034103390
SN - 1044-7431
VL - 15
SP - 398
EP - 407
JO - Molecular and Cellular Neuroscience
JF - Molecular and Cellular Neuroscience
IS - 4
ER -