the Department of Neuroscience, Ohio State University, Columbus, Ohio 43210, the Department of Integrative Biology and Pharmacology, University of Texas Health Science Center at Houston, Houston, Texas 77030.
From the Department of Molecular and Cellular Biochemistry, the Biochemistry Program, and.
J Biol Chem. 2014 Nov 7;289(45):31458-72. doi: 10.1074/jbc.M114.589937. Epub 2014 Sep 24.
p75 is expressed among Purkinje cells in the adult cerebellum, but its function has remained obscure. Here we report that p75 is involved in maintaining the frequency and regularity of spontaneous firing of Purkinje cells. The overall spontaneous firing activity of Purkinje cells was increased in p75(-/-) mice during the phasic firing period due to a longer firing period and accompanying reduction in silence period than in the wild type. We attribute these effects to a reduction in small conductance Ca(2+)-activated potassium (SK) channel activity in Purkinje cells from p75(-/-) mice compared with the wild type littermates. The mechanism by which p75 regulates SK channel activity appears to involve its ability to activate Rac1. In organotypic cultures of cerebellar slices, brain-derived neurotrophic factor increased RacGTP levels by activating p75 but not TrkB. These results correlate with a reduction in RacGTP levels in synaptosome fractions from the p75(-/-) cerebellum, but not in that from the cortex of the same animals, compared with wild type littermates. More importantly, we demonstrate that Rac1 modulates SK channel activity and firing patterns of Purkinje cells. Along with the finding that spine density was reduced in p75(-/-) cerebellum, these data suggest that p75 plays a role in maintaining normalcy of Purkinje cell firing in the cerebellum in part by activating Rac1 in synaptic compartments and modulating SK channels.
p75 在成年小脑浦肯野细胞中表达,但它的功能仍然不清楚。在这里,我们报告 p75 参与维持浦肯野细胞自发放电的频率和规律性。由于放电周期延长和沉默期伴随的减少,p75(-/-) 小鼠在相期间的总体自发放电活性高于野生型。我们将这些效应归因于与野生型同窝仔相比,p75(-/-) 小鼠浦肯野细胞中小电导钙激活钾 (SK) 通道活性降低。p75 调节 SK 通道活性的机制似乎涉及它激活 Rac1 的能力。在小脑切片器官型培养物中,脑源性神经营养因子通过激活 p75 而不是 TrkB 增加 RacGTP 水平。这些结果与 p75(-/-) 小脑突触体部分 RacGTP 水平降低相关,但与同一动物的皮质部分相比,与野生型同窝仔相比,这些结果与 RacGTP 水平降低相关。更重要的是,我们证明 Rac1 调节 SK 通道活性和浦肯野细胞的放电模式。与发现 p75(-/-) 小脑中的棘密度降低有关,这些数据表明 p75 通过在突触区激活 Rac1 并调节 SK 通道,在维持小脑浦肯野细胞放电正常性方面发挥作用。