Carter B D, Kaltschmidt C, Kaltschmidt B, Offenhäuser N, Böhm-Matthaei R, Baeuerle P A, Barde Y A
Department of Neurobiochemistry, Max-Planck Institute for Psychiatry, Martinsried, Germany.
Science. 1996 Apr 26;272(5261):542-5. doi: 10.1126/science.272.5261.542.
Nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and neurotrophin-3 (NT-3) selectively bind to distinct members of the Trk family of tyrosine kinase receptors, but all three bind with similar affinities to the neurotrophin receptor p75 (p75NTR). The biological significance of neurotrophin binding to p75NTR in cells that also express Trk receptors has been difficult to ascertain. In the absence of TrkA, NGF binding to p75NGR activated the transcription factor nuclear factor kappa B (NF-kappa B) in rat Schwann cells. This activation was not observed in Schwann cells isolated from mice that lacked p75NTR. The effect was selective for NGF; NF-kappa B was not activated by BDNF or NT-3.
神经生长因子(NGF)、脑源性神经营养因子(BDNF)和神经营养素-3(NT-3)选择性地与酪氨酸激酶受体Trk家族的不同成员结合,但这三种因子都以相似的亲和力与神经营养素受体p75(p75NTR)结合。在同时表达Trk受体的细胞中,神经营养素与p75NTR结合的生物学意义一直难以确定。在缺乏TrkA的情况下,NGF与p75NGR的结合激活了大鼠雪旺细胞中的转录因子核因子κB(NF-κB)。在从缺乏p75NTR的小鼠中分离出的雪旺细胞中未观察到这种激活。这种效应是NGF特有的;BDNF或NT-3不会激活NF-κB。