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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Activation of calpain-1 in myelin and microglia in the white matter of the aged rhesus monkey.
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Activation of calpain-1 in myelin and microglia in the white matter of the aged rhesus monkey.

机译:老年猕猴白质中髓鞘和小胶质细胞中calpain-1的激活。

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Abstract Ultrastructural disruption of myelin sheaths and a loss of myelin with age are well-documented phenomena in both the human and rhesus monkey. Age-dependent activation of calpain-1 (EC 3.4.22.52) has been suggested as a plausible mechanism for increased proteolysis in the white matter of the rhesus monkey. The present study documents activation of calpain-1 throughout brain white matter in aged animals, evidenced by immunodetection of the activated enzyme as well as a calpain-derived spectrin fragment in both tissue section and Triton X-100-soluble homogenate of subcortical white matter from the frontal, temporal, and parietal lobes. Separation of myelin fractions from brain stem tissue into intact and floating myelin confirmed previous reports of an age-related increase in activated calpain-1 in the floating fraction. Measurements of calpain-1 activity using a fluorescent substrate revealed an age-related increase in calpain-1 proteolytic activity in the floating myelin fraction consistent with immunodetection of the activated enzyme in this fraction. Double-immunofluorescence demonstrated co-localization of activated calpain-1 with human leukocyte antigen-DR (HLA-DR), a marker for activated microglia, suggesting that these cells represent the major source of the increase in activated calpain-1 in the aging brain. These data solidify the role of calpain-1 in myelin protein metabolism and further implicate activated microglia in the pathology of the aging brain.
机译:摘要不论是人类还是恒河猴,髓鞘的超微结构破坏和随着年龄的增长髓磷脂的丢失都是有据可查的现象。钙蛋白酶-1(EC 3.4.22.52)的年龄依赖性激活已被认为是增加恒河猴白质蛋白水解的合理机制。本研究记录了老年动物大脑白质中calpain-1的活化,这是通过免疫检测组织切片和来自皮层下白质的Triton X-100可溶性匀浆的活化酶以及钙蛋白酶衍生的血影蛋白片段来证明的。额叶,颞叶和顶叶将髓磷脂级分从脑干组织中分离成完整的和漂浮的髓磷脂,证实了以前有关漂浮级分中激活的calpain-1的年龄增加的报道。使用荧光底物对calpain-1活性进行的测量显示,与漂浮部分髓磷脂级分中的calpain-1蛋白水解活性呈年龄相关性增加,与该级分中活化酶的免疫检测相一致。双重免疫荧光显示活化的calpain-1与活化的小胶质细胞标记物人白细胞抗原-DR(HLA-DR)共定位,表明这些细胞代表了衰老大脑中活化的calpain-1增加的主要来源。 。这些数据巩固了钙蛋白酶1在髓磷脂蛋白代谢中的作用,并进一步将活化的小胶质细胞牵连到衰老的大脑病理中。

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