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大鼠脑中钙调蛋白依赖性酶的差异定位:特定神经元中选择性表达环核苷酸磷酸二酯酶的证据。

Differential localization of calmodulin-dependent enzymes in rat brain: evidence for selective expression of cyclic nucleotide phosphodiesterase in specific neurons.

作者信息

Kincaid R L, Balaban C D, Billingsley M L

出版信息

Proc Natl Acad Sci U S A. 1987 Feb;84(4):1118-22. doi: 10.1073/pnas.84.4.1118.

Abstract

High-affinity antibodies against calmodulin (CaM)-dependent cyclic nucleotide phosphodiesterase and protein phosphatase (calcineurin) were purified and characterized. Rabbit anti-phosphodiesterase antibody did not react with other phosphodiesterases or with the regulatory subunits of cAMP-dependent protein kinase. Affinity-purified goat anti-calcineurin antibody recognized both the 61-kDa catalytic subunit and the 18-kDa Ca2+-binding subunit of the phosphatase. Neither antibody reacted with CaM, several CaM-binding proteins (calmodulin-dependent protein kinase, myosin light chain kinase, fodrin), or other cytosolic proteins from brain. The antibodies were used to compare the cellular localization of these two CaM-dependent enzymes in rat brain. Both calcineurin and phosphodiesterase were found predominantly in nerve cells; however, phosphodiesterase was restricted to very specific neuronal populations. Phosphodiesterase was prominent in the somatic cytoplasm and dendrites of regional output neurons--e.g., cerebellar Purkinje cells and hippocampal and cortical pyramidal cells. The extensive and uniform staining in the dendrites was consistent with postsynaptic localization and suggested an important function for this enzyme in neurons that integrate multiple convergent inputs. Calcineurin was present in virtually all classes of neurons, with immunoreactivity confined primarily to cell bodies. Both diffuse cytoplasmic staining and characteristic punctate staining of cell bodies were observed; the latter suggested compartmentalization of calcineurin at or near the plasma membrane. The results of this study demonstrate that calcineurin and phosphodiesterase are differentially localized in the central nervous system. Thus, the expression and compartmentalization of CaM-binding proteins may be highly regulated and specific for particular differentiated nerve cell types.

摘要

针对钙调蛋白(CaM)依赖性环核苷酸磷酸二酯酶和蛋白磷酸酶(钙调神经磷酸酶)的高亲和力抗体被纯化并进行了表征。兔抗磷酸二酯酶抗体不与其他磷酸二酯酶或环磷酸腺苷依赖性蛋白激酶的调节亚基发生反应。亲和纯化的山羊抗钙调神经磷酸酶抗体识别该磷酸酶的61 kDa催化亚基和18 kDa钙结合亚基。两种抗体均不与CaM、几种CaM结合蛋白(钙调蛋白依赖性蛋白激酶、肌球蛋白轻链激酶、血影蛋白)或来自大脑的其他胞质蛋白发生反应。这些抗体被用于比较这两种CaM依赖性酶在大鼠脑中的细胞定位。钙调神经磷酸酶和磷酸二酯酶主要存在于神经细胞中;然而,磷酸二酯酶仅限于非常特定的神经元群体。磷酸二酯酶在区域输出神经元的体细胞胞质和树突中很突出——例如,小脑浦肯野细胞以及海马和皮质锥体细胞。树突中广泛而均匀的染色与突触后定位一致,并表明该酶在整合多个汇聚输入的神经元中具有重要功能。钙调神经磷酸酶几乎存在于所有类型的神经元中,免疫反应性主要局限于细胞体。观察到细胞体既有弥漫性胞质染色又有特征性点状染色;后者表明钙调神经磷酸酶在质膜处或附近存在区室化。这项研究的结果表明,钙调神经磷酸酶和磷酸二酯酶在中枢神经系统中的定位存在差异。因此,CaM结合蛋白的表达和区室化可能受到高度调控,并且对特定分化的神经细胞类型具有特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b161/304374/73d5fe4c8dc3/pnas00269-0226-a.jpg

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