Acheson A, Conover J C, Fandl J P, DeChiara T M, Russell M, Thadani A, Squinto S P, Yancopoulos G D, Lindsay R M
Regeneron Pharmaceuticals Inc., Tarrytown, New York 10591-6707, USA.
Nature. 1995 Mar 30;374(6521):450-3. doi: 10.1038/374450a0.
During the initial phase of their development, sensory neurons of the dorsal root ganglion (DRG) require target-derived trophic support for their survival, but as they mature they lose this requirement. Because many of these neurons express BDNF (brain-derived neurotrophic factor) messenger RNA, we hypothesized that BDNF might act as an autocrine survival factor in adult DRG neurons, thus explaining their lack of dependence on exogenous growth factors. When cultured adult DRG cells were treated with antisense oligonucleotides to BDNF, expression of BDNF protein was reduced by 80%, and neuronal survival was reduced by 35%. These neurons could be rescued by exogenous BDNF or neurotrophin-3, but not by other growth factors. Similar results were obtained with single-neuron microcultures, whereas microcultures derived from mutant mice lacking BDNF were unaffected by antisense oligonucleotides. Our results strongly support an autocrine role for BDNF in mediating the survival of a subpopulation of adult DRG neurons.
在背根神经节(DRG)感觉神经元发育的初始阶段,它们需要靶源性营养支持来维持存活,但随着神经元成熟,它们对这种支持的需求逐渐消失。由于这些神经元中的许多都表达脑源性神经营养因子(BDNF)信使核糖核酸,我们推测BDNF可能作为成年DRG神经元的自分泌存活因子,从而解释了它们对外源性生长因子的不依赖性。当用针对BDNF的反义寡核苷酸处理培养的成年DRG细胞时,BDNF蛋白的表达降低了80%,神经元存活率降低了35%。这些神经元可以通过外源性BDNF或神经营养因子-3挽救,但不能通过其他生长因子挽救。在单神经元微培养中也获得了类似结果,而来自缺乏BDNF的突变小鼠的微培养不受反义寡核苷酸的影响。我们的结果有力地支持了BDNF在介导成年DRG神经元亚群存活中的自分泌作用。