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高温对成年及发育中大鼠脑、睾丸和胸腺细胞死亡诱导的影响。

The effect of hyperthermia on the induction of cell death in brain, testis, and thymus of the adult and developing rat.

作者信息

Khan Vania R, Brown Ian R

机构信息

Centre for the Neurobiology of Stress, Division of Life Sciences, University of Toronto at Scarborough, Ontario, Canada.

出版信息

Cell Stress Chaperones. 2002 Jan;7(1):73-90. doi: 10.1379/1466-1268(2002)007<0073:teohot>2.0.co;2.

DOI:10.1379/1466-1268(2002)007<0073:teohot>2.0.co;2
PMID:11892990
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC514805/
Abstract

Stressful stimuli can elicit 2 distinct reactive cellular responses, the heat shock (stress) response and the activation of cell death pathways. Most studies on the effects of hyperthermia on the mammalian nervous system have focused on the heat shock response, characterized by the transient induction of Hsps, which play roles in repair and protective mechanisms. This study examines the effect of hyperthermia on the induction of cell death via apoptosis, assayed by terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick-end labeling and active caspase 3 cytochemistry, in the adult rat brain, testis, and thymus. Results show that a fever-like increase in temperature triggered apoptosis in dividing cell populations of testis and thymus, but not in mature, postmitotic cells of the adult cerebellum. These differential apoptotic responses did not correlate with whole-tissue levels of Hsp70 induction. We further investigated whether dividing neural cells were more sensitive to heat-induced apoptosis by examining the external granule cell layer of the cerebellum at postnatal day 7 and the neuroepithelial layers of the neocortex and tectum at embryonic day 17. These proliferative neural regions were highly susceptible to hyperthermia-induced apoptosis, suggesting that actively dividing cell populations are more prone to cell death induced by hyperthermia than fully differentiated postmitotic neural cells.

摘要

应激刺激可引发两种不同的细胞反应,即热休克(应激)反应和细胞死亡途径的激活。大多数关于热疗对哺乳动物神经系统影响的研究都集中在热休克反应上,其特征是热休克蛋白(Hsps)的短暂诱导,这些蛋白在修复和保护机制中发挥作用。本研究通过末端脱氧核苷酸转移酶介导的脱氧尿苷三磷酸缺口末端标记和活性半胱天冬酶3细胞化学分析,检测热疗对成年大鼠脑、睾丸和胸腺中细胞凋亡诱导细胞死亡的影响。结果表明,类似发热的体温升高引发了睾丸和胸腺中分裂细胞群体的凋亡,但未引发成年小脑成熟的、有丝分裂后的细胞凋亡。这些不同的凋亡反应与Hsp70诱导的全组织水平无关。我们进一步通过检查出生后第7天小脑的外颗粒细胞层以及胚胎第17天新皮层和顶盖的神经上皮层,研究分裂的神经细胞是否对热诱导的凋亡更敏感。这些增殖性神经区域对热疗诱导的凋亡高度敏感,表明活跃分裂的细胞群体比完全分化的有丝分裂后神经细胞更容易因热疗而发生细胞死亡。

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