Miyazaki Taisuke, Hashimoto Kouichi, Uda Atsushi, Sakagami Hiroyuki, Nakamura Yoshitaka, Saito Shin-ya, Nishi Miyuki, Kume Hideaki, Tohgo Akira, Kaneko Izumi, Kondo Hisatake, Fukunaga Kohji, Kano Masanobu, Watanabe Masahiko, Takeshima Hiroshi
Department of Anatomy, Hokkaido University, School of Medicine, Sapporo, Japan.
FEBS Lett. 2006 Jul 24;580(17):4057-64. doi: 10.1016/j.febslet.2006.06.043. Epub 2006 Jun 27.
By DNA cloning, we have identified the BSRP (brain-specific receptor-like proteins) family of three members in mammalian genomes. BSRPs were predominantly expressed in the soma and dendrites of neurons and localized in the endoplasmic reticulum (ER). Expression levels of BSRPs seemed to fluctuate greatly during postnatal cerebellar maturation. Triple-knockout mice lacking BSRP members exhibited motor discoordination, and Purkinje cells (PCs) were often innervated by multiple climbing fibers with different neuronal origins in the mutant cerebellum. Moreover, the phosphorylation levels of protein kinase Calpha (PKCalpha) were significantly downregulated in the mutant cerebellum. Because cerebellar maturation and plasticity require metabotropic glutamate receptor signaling and resulting PKC activation, BSRPs are likely involved in ER functions supporting PKCalpha activation in PCs.
通过DNA克隆,我们在哺乳动物基因组中鉴定出了由三个成员组成的脑特异性受体样蛋白(BSRP)家族。BSRP主要在神经元的胞体和树突中表达,并定位于内质网(ER)。在出生后小脑成熟过程中,BSRP的表达水平似乎波动很大。缺乏BSRP成员的三敲除小鼠表现出运动失调,并且在突变体小脑中,浦肯野细胞(PC)常常被来自不同神经元起源的多条攀缘纤维支配。此外,突变体小脑中蛋白激酶Cα(PKCα)的磷酸化水平显著下调。由于小脑成熟和可塑性需要代谢型谷氨酸受体信号传导以及由此导致的PKC激活,因此BSRP可能参与支持PC中PKCα激活的内质网功能。