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细胞周期蛋白依赖性激酶5在小鼠胚胎神经系统中的活性与表达模式

Activity and expression pattern of cyclin-dependent kinase 5 in the embryonic mouse nervous system.

作者信息

Tsai L H, Takahashi T, Caviness V S, Harlow E

机构信息

Massachusetts General Hospital Cancer Center, Charlestown 02129.

出版信息

Development. 1993 Dec;119(4):1029-40. doi: 10.1242/dev.119.4.1029.

Abstract

Cyclin-dependent kinase 5 (cdk5) was originally isolated on the basis of its close primary sequence homology to the human cdc2 serine/threonine kinase, the prototype of the cyclin-dependent kinases. While kinase activities of both cdc2 and cdk2 are detected in proliferating cells and are essential for cells to progress through the key transition points of the cell cycle, cdk5 kinase activity has been observed only in lysates of adult brain. In this study, we compared the activity and expression of cdk5 with that of cdc2 and cdk2 in the embryonic mouse forebrain. The expression and activity of cdk5 increased progressively as increasing numbers of cells exited the proliferative cycle. In contrast, the expression and activity of cdc2 and cdk2 were maximum at gestational day 11 (E11) when the majority of cells were proliferating and fell to barely detectable levels at E17 at the end of the cytogenetic period. Immunohistochemical studies showed that cdk5 is expressed in postmitotic neurons but not in glial cells or mitotically active cells. Expression of cdk5 was concentrated in fasciculated axons of postmitotic neurons. In contrast to other cell division cycle kinases to which it is closely related, cdk5 appears not to be expressed in dividing cells in the developing brain. These observations suggest that cdk5 may have a role in neuronal differentiation but not in the cell division cycle in the embryonic nervous system.

摘要

细胞周期蛋白依赖性激酶5(cdk5)最初是根据其与人类细胞周期蛋白依赖性激酶原型——细胞周期蛋白依赖性激酶2(cdc2)丝氨酸/苏氨酸激酶的紧密一级序列同源性分离出来的。虽然在增殖细胞中可检测到cdc2和cdk2的激酶活性,且这些活性对于细胞通过细胞周期的关键转换点至关重要,但仅在成年脑裂解物中观察到cdk5激酶活性。在本研究中,我们比较了胚胎小鼠前脑中cdk5与cdc2和cdk2的活性及表达情况。随着越来越多的细胞退出增殖周期,cdk5的表达和活性逐渐增加。相比之下,cdc2和cdk2的表达及活性在妊娠第11天(E11)达到最高,此时大多数细胞正在增殖,而在细胞遗传学时期结束时的E17降至几乎检测不到的水平。免疫组织化学研究表明,cdk5在有丝分裂后的神经元中表达,但在神经胶质细胞或有丝分裂活跃的细胞中不表达。cdk5的表达集中在有丝分裂后神经元的成束轴突中。与它密切相关的其他细胞分裂周期激酶不同,cdk5似乎在发育中的大脑中的分裂细胞中不表达。这些观察结果表明,cdk5可能在神经元分化中起作用,但在胚胎神经系统的细胞分裂周期中不起作用。

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