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热休克转录因子调控大鼠组织细胞瘤中的热诱导细胞死亡。

Heat shock transcription factors regulate heat induced cell death in a rat histiocytoma.

作者信息

Prasad Kolla V, Taiyab Aftab, Jyothi D, Srinivas Usha K, Sreedhar Amere S

机构信息

Centre for Cellular and Molecular Biology, Hyderabad 500 007, India.

出版信息

J Biosci. 2007 Apr;32(3):585-93. doi: 10.1007/s12038-007-0058-4.

Abstract

Heat shock response is associated with the synthesis of heat shock proteins (Hsps) which is strictly regulated by different members of heat shock transcription factors (HSFs). We previously reported that a rat histiocytoma, BC-8 failed to synthesize Hsps when subjected to typical heat shock conditions (42 degrees C, 60 min). The lack of Hsp synthesis in these cells was due to a failure in HSF1 DNA binding activity. In the present study we report that BC-8 tumor cells when subjected to heat shock at higher temperature (43 degrees C, 60 min) or incubation for longer time at 42 degrees C, exhibited necrosis characteristics; however,under mild heat shock (42 degrees C, 30 min) conditions cells showed activation of autophagy. Mild heat shock treatment induced proteolysis of HSF1, and under similar conditions we observed an increase in HSF2 expression followed by its enhanced DNA binding activity. Inhibiting HSF1 proteolysis by reversible proteasome inhibition failed to inhibit heat shock induced autophagy. Compromising HSF2 expression but not HSF1 resulted in the inhibition of autophagy, suggesting HSF2 dependent activation of autophagy. We are reporting for the first time that HSF2 is heat inducible and functions in heat shock induced autophagic cell death in BC-8 tumor cells.

摘要

热休克反应与热休克蛋白(Hsps)的合成相关,而热休克蛋白的合成受到热休克转录因子(HSFs)不同成员的严格调控。我们之前报道过,大鼠组织细胞瘤BC - 8在典型热休克条件(42摄氏度,60分钟)下无法合成Hsps。这些细胞中Hsp合成的缺乏是由于HSF1 DNA结合活性的缺失。在本研究中,我们报道BC - 8肿瘤细胞在较高温度(43摄氏度,60分钟)下受到热休克或在42摄氏度下孵育更长时间时,表现出坏死特征;然而,在轻度热休克(42摄氏度,30分钟)条件下,细胞显示出自噬激活。轻度热休克处理诱导了HSF1的蛋白水解,在类似条件下,我们观察到HSF2表达增加,随后其DNA结合活性增强。通过可逆蛋白酶体抑制来抑制HSF1蛋白水解未能抑制热休克诱导的自噬。降低HSF2而非HSF1的表达导致自噬受到抑制,这表明自噬的激活依赖于HSF2。我们首次报道HSF2是热诱导的,并在BC - 8肿瘤细胞的热休克诱导自噬性细胞死亡中发挥作用。

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