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随着年龄增长神经丝重亚基的渐进性过度磷酸化:可能参与神经丝积累的机制。

Progressive hyperphosphorylation of neurofilament heavy subunits with aging: possible involvement in the mechanism of neurofilament accumulation.

作者信息

Gou J P, Eyer J, Leterrier J F

机构信息

U 298 INSERM, Angers, France.

出版信息

Biochem Biophys Res Commun. 1995 Oct 4;215(1):368-76. doi: 10.1006/bbrc.1995.2475.

Abstract

Abnormal accumulations of phosphorylated neurofilaments occur both in normal senescence and in age-associated neurodegenerative diseases. In the present work, we study the physicochemical properties of neurofilaments isolated from rats of controlled ages. Aging induces in vivo hyperphosphorylation of the heavy neurofilament subunit without affecting in vitro neurofilament phosphorylation by the neurofilament-associated protein kinase. Interactions in vitro between neurofilaments from very old rats occur at higher rate and extent than that of neurofilaments from younger animals. These results support the hypothesis that the abnormal accumulation of neurofilaments observed in nervous tissues from aging mammals results from an altered equilibrium in situ between interconnected and independent neurofilaments.

摘要

磷酸化神经丝的异常积累既发生在正常衰老过程中,也发生在与年龄相关的神经退行性疾病中。在本研究中,我们研究了从不同年龄的大鼠中分离出的神经丝的物理化学性质。衰老在体内诱导重神经丝亚基的过度磷酸化,但不影响神经丝相关蛋白激酶对神经丝的体外磷酸化。非常年老的大鼠的神经丝之间的体外相互作用比年轻动物的神经丝之间的相互作用发生得更快、程度更大。这些结果支持了这样一种假说,即在衰老哺乳动物的神经组织中观察到的神经丝异常积累是由于相互连接和独立的神经丝之间原位平衡的改变所致。

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