Sato Masaaki, Suzuki Kazunori, Nakanishi Shigetada
Department of Molecular and Systems Biology, Graduate School of Biostudies, Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan.
Biochem Biophys Res Commun. 2006 Mar 10;341(2):304-9. doi: 10.1016/j.bbrc.2005.12.184. Epub 2006 Jan 10.
With the aid of microarray and PCR analysis, this investigation sought expression profiles of BDNF-regulated genes in cultured mouse cerebellar granule cells and addressed their relevance to gene regulation in developing granule cells in vivo. Many of the BDNF-upregulated and downregulated genes identified were upregulated and downregulated, respectively, during cerebellar development. This developmental change was, at least partly, prevented in the TrkB receptor-deficient cerebellum. The BDNF-upregulated genes were distributed in either postmigratory or both premigratory and postmigratory granule cells at postnatal day 8 (P8) and were still present in mature granule cells at P21. In contrast, the BDNF-downregulated genes were predominantly expressed in premigratory granule cells at P8 and disappeared at P21. Furthermore, many of the BDNF-upregulated gene products are implicated in signaling cascades of N-methyl-D-aspartate receptors and MAP kinase. The results indicate that BDNF signaling plays a pivotal role in promoting gene expression in granule cell development and maturation.
借助微阵列和聚合酶链反应分析,本研究探寻了脑源性神经营养因子(BDNF)调控的基因在培养的小鼠小脑颗粒细胞中的表达谱,并探讨了这些基因与体内发育中小脑颗粒细胞基因调控的相关性。在小脑发育过程中,许多鉴定出的BDNF上调基因和下调基因分别出现了上调和下调。这种发育变化在缺乏TrkB受体的小脑中至少部分受到了抑制。BDNF上调基因在出生后第8天(P8)分布于迁移后的颗粒细胞或迁移前和迁移后的颗粒细胞中,并且在P21的成熟颗粒细胞中仍然存在。相比之下,BDNF下调基因在P8时主要表达于迁移前的颗粒细胞中,并在P21时消失。此外,许多BDNF上调的基因产物与N-甲基-D-天冬氨酸受体和丝裂原活化蛋白激酶的信号级联反应有关。结果表明,BDNF信号在促进颗粒细胞发育和成熟过程中的基因表达方面起着关键作用。