Suzuki Shingo, Kiyosue Kazuyuki, Hazama Shunsuke, Ogura Akihiko, Kashihara Megumi, Hara Tomoko, Koshimizu Hisatsugu, Kojima Masami
Research Institute for Cell Engineering, National Institute of Advanced Industrial Science and Technology, Ikeda, Osaka 563-8577, Japan.
J Neurosci. 2007 Jun 13;27(24):6417-27. doi: 10.1523/JNEUROSCI.0690-07.2007.
Brain-derived neurotrophic factor (BDNF) exerts multiple biological functions in the CNS. Although BDNF can control transcription and protein synthesis, it still remains open to question whether BDNF regulates lipid biosynthesis. Here we show that BDNF elicits cholesterol biosynthesis in cultured cortical and hippocampal neurons. Importantly, BDNF elicited cholesterol synthesis in neurons, but not in glial cells. Quantitative reverse transcriptase-PCR revealed that BDNF stimulated the transcription of enzymes in the cholesterol biosynthetic pathway. BDNF-induced cholesterol increases were blocked by specific inhibitors of cholesterol synthesis, mevastatin and zaragozic acid, suggesting that BDNF stimulates de novo synthesis of cholesterol rather than the incorporation of extracellular cholesterol. Because cholesterol is a major component of lipid rafts, we investigated whether BDNF would increase the cholesterol content in lipid rafts or nonraft membrane domains. Interestingly, the BDNF-mediated increase in cholesterol occurred in rafts, but not in nonrafts, suggesting that BDNF promotes the development of neuronal lipid rafts. Consistent with this notion, BDNF raised the level of the lipid raft marker protein caveolin-2 in rafts. Remarkably, BDNF increased the levels of presynaptic proteins in lipid rafts, but not in nonrafts. An electrophysiological study revealed that BDNF-dependent cholesterol biosynthesis plays an important role for the development of a readily releasable pool of synaptic vesicles. Together, these results suggest a novel role for BDNF in cholesterol metabolism and synapse development.
脑源性神经营养因子(BDNF)在中枢神经系统中发挥多种生物学功能。尽管BDNF可以控制转录和蛋白质合成,但BDNF是否调节脂质生物合成仍存在疑问。在此我们表明,BDNF可诱导培养的皮质和海马神经元中的胆固醇生物合成。重要的是,BDNF在神经元中而非神经胶质细胞中诱导胆固醇合成。定量逆转录聚合酶链反应显示,BDNF刺激胆固醇生物合成途径中酶的转录。BDNF诱导的胆固醇增加被胆固醇合成的特异性抑制剂美伐他汀和扎伐司特酸所阻断,这表明BDNF刺激胆固醇的从头合成而非细胞外胆固醇的掺入。由于胆固醇是脂筏的主要成分,我们研究了BDNF是否会增加脂筏或非脂筏膜结构域中的胆固醇含量。有趣的是,BDNF介导的胆固醇增加发生在脂筏中,而非非脂筏中,这表明BDNF促进神经元脂筏的发育。与此观点一致,BDNF提高了脂筏中脂筏标记蛋白小窝蛋白-2的水平。值得注意的是,BDNF增加了脂筏中突触前蛋白的水平,但在非脂筏中未增加。一项电生理研究表明,BDNF依赖的胆固醇生物合成对突触小泡的易释放池的发育起重要作用。总之,这些结果表明BDNF在胆固醇代谢和突触发育中具有新的作用。