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大鼠和恒河猴淋巴细胞中热休克蛋白70的表达随年龄增长而降低。

The expression of heat shock protein 70 decreases with age in lymphocytes from rats and rhesus monkeys.

作者信息

Pahlavani M A, Harris M D, Moore S A, Weindruch R, Richardson A

机构信息

Geriatric Research, Education and Clinical Center, Audie L. Murphy Memorial Veterans Hospital, University of Texas Health Science Center, San Antonio 78284, USA.

出版信息

Exp Cell Res. 1995 May;218(1):310-8. doi: 10.1006/excr.1995.1160.

Abstract

The ability of cells to express heat shock proteins in response to a stress such as heat is universal to all organisms and is believed to play a critical protective role. Therefore, it was of interest to determine the influence of aging on the ability of lymphocytes to express the heat shock protein hsp70 in response to a heat shock (42.5 degrees C for 1 h). Splenic lymphocytes isolated from old (24-26 months) rats showed a marked decrease in the induction of hsp70 protein levels or hsp70 synthesis when compared to lymphocytes isolated from young (4-5 months) rats. An age-related decrease in the induction of hsp70 levels by heat also was observed in peripheral lymphocytes isolated from rhesus monkeys. The decline with age in the induction of hsp70 by lymphocytes from rats was paralleled by a decrease in the induction of hsp70 mRNA and the nuclear transcription of hsp70. In addition, it was found that the ability of extracts from heat-shocked lymphocytes to bind the heat shock element (HSE) decreased approximately 50% with age. Therefore, it appears that the reduced ability of lymphocytes from old rats to express hsp70 in response to a heat shock occurs at the level of transcription because of an alteration in the ability of the heat shock transcription factor to bind the HSE on the promoter of the hsp70 gene. The age-related decrease in the induction of hsp70 appears to be physiologically important because the viability of spleen lymphocytes exposed to high temperatures decreases significantly with age.

摘要

细胞响应诸如热等应激而表达热休克蛋白的能力在所有生物体中都是普遍存在的,并且被认为起着关键的保护作用。因此,确定衰老对淋巴细胞响应热休克(42.5摄氏度,1小时)而表达热休克蛋白hsp70能力的影响是很有意义的。与从年轻(4 - 5个月)大鼠分离的淋巴细胞相比,从老年(24 - 26个月)大鼠分离的脾淋巴细胞在hsp70蛋白水平诱导或hsp70合成方面显著降低。在从恒河猴分离的外周淋巴细胞中也观察到热诱导hsp70水平随年龄的下降。大鼠淋巴细胞热诱导hsp70随年龄的下降与hsp70 mRNA的诱导以及hsp70的核转录下降平行。此外,发现热休克淋巴细胞提取物结合热休克元件(HSE)的能力随年龄下降约50%。因此,似乎老年大鼠淋巴细胞响应热休克而表达hsp70的能力降低发生在转录水平,这是由于热休克转录因子结合hsp70基因启动子上HSE的能力发生了改变。热诱导hsp70随年龄的下降似乎在生理上很重要,因为暴露于高温的脾淋巴细胞的活力随年龄显著降低。

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