Division of Neurobiology, Department of Molecular and Cell Biology, Helen Wills Neuroscience Institute, University of California, Berkeley, CA 94720, USA.
Proc Natl Acad Sci U S A. 2011 Nov 8;108(45):18430-5. doi: 10.1073/pnas.1115907108. Epub 2011 Oct 24.
A critical step in neuronal development is the formation of axon/dendrite polarity, a process involving symmetry breaking in the newborn neuron. Local self-amplifying processes could enhance and stabilize the initial asymmetry in the distribution of axon/dendrite determinants, but the identity of these processes remains elusive. We here report that BDNF, a secreted neurotrophin essential for the survival and differentiation of many neuronal populations, serves as a self-amplifying autocrine factor in promoting axon formation in embryonic hippocampal neurons by triggering two nested positive-feedback mechanisms. First, BDNF elevates cytoplasmic cAMP and protein kinase A activity, which triggers further secretion of BDNF and membrane insertion of its receptor TrkB. Second, BDNF/TrkB signaling activates PI3-kinase that promotes anterograde transport of TrkB in the putative axon, further enhancing local BDNF/TrkB signaling. Together, these self-amplifying BDNF actions ensure stable elevation of local cAMP/protein kinase A activity that is critical for axon differentiation and growth.
神经元发育的关键步骤是轴突/树突极性的形成,这一过程涉及新生神经元中对称性的破坏。局部自我放大过程可以增强和稳定轴突/树突决定因素分布的初始不对称性,但这些过程的身份仍然难以捉摸。我们在这里报告说,BDNF 是一种分泌性神经生长因子,对许多神经元群体的存活和分化至关重要,它通过触发两个嵌套的正反馈机制,作为促进胚胎海马神经元轴突形成的自我放大自分泌因子。首先,BDNF 升高细胞质 cAMP 和蛋白激酶 A 活性,这进一步触发 BDNF 的分泌和其受体 TrkB 的膜插入。其次,BDNF/TrkB 信号激活 PI3-激酶,促进 TrkB 在假定的轴突中的顺行运输,进一步增强局部 BDNF/TrkB 信号。总之,这些自我放大的 BDNF 作用确保了局部 cAMP/蛋白激酶 A 活性的稳定升高,这对于轴突分化和生长至关重要。