Department of Neurophysiology & Neural Repair, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.
Research Program for Neural Signaling, Division of Endocrinology, Metabolism and Signal Research, Gunma University Initiative for Advanced Research, Maebashi, Gunma, Japan.
Cerebellum. 2018 Feb;17(1):23-27. doi: 10.1007/s12311-017-0898-x.
Protein kinase C (PKC), a family of serine/threonine protein kinases, mediates a myriad of patho-physiological cellular events in various tissues. The originally discovered PKC (conventional) requires the binding of diacylglycerol and Ca for full activation. The conventional PKC consists of four isoforms, PKCα, PKCβI/βII, and PKCγ. PKCα and PKCβI/βII are expressed in the cells of various tissues including the brain, while PKCγ is present specifically in neurons of the brain and spinal cord. The cerebellum expresses the largest amount of PKC with all its four isoforms. Purkinje cells express PKCα and PKCγ. Previous studies have shown that PKCα is involved in the induction of long-term depression (LTD) at parallel fiber-Purkinje cell synapses. On the other hand, analysis of PKCγ-deficient mice has revealed that PKCγ plays a critical role in eliminating supernumerary climbing fiber synapses from developing Purkinje cells. Although why PKCα has no compensatory action in climbing fiber pruning in PKCγ-deficient Purkinje cells had so far remained unclear, we have recently demonstrated that PKCα is also capable of pruning supernumerary climbing fiber synapses, but the expression levels of PKCα are too low to achieve pruning in PKCγ-null Purkinje cells. Notably, although PKCγ is most abundant in Purkinje cells, its physiological role in mature Purkinje cells remained totally unknown. In addition to a concise review of the physiological and pathological roles of conventional PKCs in Purkinje cells, this report postulates a contribution of PKCα in developing Purkinje cells and a possible involvement of PKCγ in motor coordination in the mature cerebellum.
蛋白激酶 C(PKC)是丝氨酸/苏氨酸蛋白激酶家族的一员,在各种组织中介导多种病理生理细胞事件。最初发现的 PKC(传统型)需要二酰基甘油和 Ca 的结合才能完全激活。传统的 PKC 由四种同工型组成,即 PKCα、PKCβI/βII 和 PKCγ。PKCα 和 PKCβI/βII 在包括大脑在内的各种组织的细胞中表达,而 PKCγ 则特异性存在于大脑和脊髓的神经元中。小脑表达所有四种同工型的 PKC 量最大。浦肯野细胞表达 PKCα 和 PKCγ。先前的研究表明,PKCα 参与平行纤维-浦肯野细胞突触的长时程抑制(LTD)诱导。另一方面,对 PKCγ 缺陷小鼠的分析表明,PKCγ 在消除发育中的浦肯野细胞中超数的 climbing 纤维突触中发挥关键作用。尽管 PKCα 在 PKCγ 缺陷的浦肯野细胞中在 climbing 纤维修剪中没有代偿作用,但迄今为止仍不清楚原因,我们最近证明 PKCα 也能够修剪超数的 climbing 纤维突触,但 PKCα 的表达水平太低,无法在 PKCγ 缺失的浦肯野细胞中实现修剪。值得注意的是,尽管 PKCγ 在浦肯野细胞中含量最丰富,但它在成熟浦肯野细胞中的生理作用仍完全未知。除了简要综述传统 PKC 在浦肯野细胞中的生理和病理作用外,本报告还假设 PKCα 在发育中的浦肯野细胞中发挥作用,PKCγ 可能参与成熟小脑的运动协调。