Nerve growth factor signaling, neuroprotection, and neural repair

被引:1040
作者
Sofroniew, MV [1 ]
Howe, CL
Mobley, WC
机构
[1] Univ Calif Los Angeles, Dept Neurobiol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Inst Brain Res, Los Angeles, CA 90095 USA
[3] Stanford Univ, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
关键词
neurotrophins; NGF; TrkA; p75(NTR); neurodegeneration; neuroregeneration; excitotoxicity; tyrosine kinase;
D O I
10.1146/annurev.neuro.24.1.1217
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nerve growth factor (NGF) was discovered 50 years ago as a molecule that promoted the survival and differentiation of sensory and sympathetic neurons. Its roles in neural development have been characterized extensively, but recent findings point to an unexpected diversity of NGF actions and indicate that developmental effects are only one aspect of the biology of NGF. This article considers expanded roles for NGF that are associated with the dynamically regulated production of NGF and its receptors that begins in development, extends throughout adult life and aging, and involves a surprising variety of neurons, glia, and nonneural cells. Particular attention is given to a growing body of evidence that suggests that among other roles, endogenous NGF signaling subserves neuroprotective and repair functions. The analysis points to many interesting unanswered questions and to the potential for continuing research on NGF to substantially enhance our understanding of the mechanisms and treatment of neurological disorders.
引用
收藏
页码:1217 / 1281
页数:65
相关论文
共 506 条
  • [41] Boise L H, 1995, Curr Top Microbiol Immunol, V200, P107
  • [42] A NOVEL PROTEIN THAT INTERACTS WITH THE DEATH DOMAIN OF FAS/APO1 CONTAINS A SEQUENCE MOTIF RELATED TO THE DEATH DOMAIN
    BOLDIN, MP
    VARFOLOMEEV, EE
    PANCER, Z
    METT, IL
    CAMONIS, JH
    WALLACH, D
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (14) : 7795 - 7798
  • [43] SELF-ASSOCIATION OF THE DEATH DOMAINS OF THE P55 TUMOR-NECROSIS-FACTOR (TNF) RECEPTOR AND FAS/APO1 PROMPTS SIGNALING FOR TNF AND FAS/APO1 EFFECTS
    BOLDIN, MP
    METT, IL
    VARFOLOMEEV, EE
    CHUMAKOV, I
    SHEMERAVNI, Y
    CAMONIS, JH
    WALLACH, D
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (01) : 387 - 391
  • [44] BONIECE IR, 1993, J NEUROSCI, V13, P4220
  • [45] Nerve growth factor: An important molecule in allergic inflammation and tissue remodelling
    Bonini, S
    Lambiase, A
    Bonini, S
    Levi-Schaffer, F
    Aloe, L
    [J]. INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1999, 118 (2-4) : 159 - 162
  • [46] SERINE 133-PHOSPHORYLATED CREB INDUCES TRANSCRIPTION VIA A COOPERATIVE MECHANISM THAT MAY CONFER SPECIFICITY TO NEUROTROPHIN SIGNALS
    BONNI, A
    GINTY, DD
    DUDEK, H
    GREENBERG, ME
    [J]. MOLECULAR AND CELLULAR NEUROSCIENCE, 1995, 6 (02) : 168 - 183
  • [47] BOTHWELL M, 1995, ANNU REV NEUROSCI, V18, P223, DOI 10.1146/annurev.ne.18.030195.001255
  • [48] Brann AB, 1999, J NEUROSCI, V19, P8199
  • [49] p75(NTR) and apoptosis: Trk-dependent and Trk-independent effects
    Bredesen, DE
    Rabizadeh, S
    [J]. TRENDS IN NEUROSCIENCES, 1997, 20 (07) : 287 - 290
  • [50] The p75 neurotrophin receptor influences NT-3 responsiveness of sympathetic neurons in vivo
    Brennan, C
    Rivas-Plata, K
    Landis, SC
    [J]. NATURE NEUROSCIENCE, 1999, 2 (08) : 699 - 705