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首页> 外文期刊>Journal of biosciences >Heat shock transcription factors regulate heat induced cell death in a rat histiocytoma
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Heat shock transcription factors regulate heat induced cell death in a rat histiocytoma

机译:热休克转录因子调节大鼠组织细胞瘤中热诱导的细胞死亡

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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?°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?°C, 60 min) or incubation for longer time at 42?°C, exhibited necrosis characteristics; however, under mild heat shock (42?°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.
机译:热休克反应与热休克蛋白(Hsps)的合成有关,热休克蛋白(Hsps)的合成受到热休克转录因子(HSFs)不同成员的严格调控。我们先前曾报道过,大鼠组织细胞瘤BC-8在典型的热休克条件下(42°C,60分钟)无法合成Hsps。这些细胞中缺乏Hsp合成是由于HSF1 DNA结合活性失败。在本研究中,我们报道了BC-8肿瘤细胞在较高温度(43°C,60分钟)下受到热激或在42°C下温育更长的时间表现出坏死特征。然而,在温和的热休克(42°C,30分钟)条件下,细胞显示出自噬激活。温和的热激处理诱导了HSF1的蛋白水解,在相似的条件下,我们观察到HSF2表达增加,随后DNA结合活性增强。通过可逆的蛋白酶体抑制抑制HSF1蛋白水解不能抑制热激诱导的自噬。损害HSF2表达但不损害HSF1导致自噬的抑制,表明HSF2依赖自噬的激活。我们首次报道HSF2是可热诱导的,并且在BC-8肿瘤细胞中由热休克诱导自噬细胞死亡中起作用。

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