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PMID: 8332899 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Induction of apoptosis by the low-affinity NGF receptor.

Science (New York, N.Y.) ·Vol. 261 ·No. 5119 ·1993-07-16 ·Pages 345-8

Rabizadeh S, Oh J, Zhong LT, Yang J, Bitler CM, Butcher LL, Bredesen DE

Abstract

Nerve growth factor (NGF) binding to cellular receptors is required for the survival of some neural cells. In contrast to TrkA, the high-affinity NGF receptor that transduces NGF signals for survival and differentiation, the function of the low-affinity NGF receptor, p75NGFR, remains uncertain. Expression of p75NGFR induced neural cell death constitutively when p75NGFR was unbound; binding by NGF or monoclonal antibody, however, inhibited cell death induced by p75NGFR. Thus, expression of p75NGFR may explain the dependence of some neural cells on NGF for survival. These findings also suggest that p75NGFR has some functional similarities to other members of a superfamily of receptors that include tumor necrosis factor receptors, Fas (Apo-1), and CD40.

MeSH Terms
Animals Apoptosis/drug effects Cell Line Cell Survival/drug effects Culture Media, Serum-Free Nerve Growth Factors/metabolism,pharmacology Neurons/cytology,drug effects,metabolism PC12 Cells Receptors, Nerve Growth Factor/metabolism,physiology Transfection
Chemicals
Culture Media, Serum-Free Nerve Growth Factors Receptors, Nerve Growth Factor
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Rabizadeh S
Department of Neurology, University of California, Los Angeles 90024.
Oh J
Zhong L T
Yang J
Bitler C M
Butcher L L
Bredesen D E
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1993-07-16
Pages
345-8
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIA NIH HHS · AG10671 · United States
NINDS NIH HHS · NS10928 · United States
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