Heat-shock gene expression and cell cycle changes during mammalian embryonic development.

D Walsh, K Li, J Wass, A Dolnikov, F Zeng, L Zhe, M Edwards
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引用次数: 56

Abstract

Synchronized regulation of cell division during gastrulation is essential for the regional proliferation of cells and pattern formation of the early CNS. The neural plate and neuroectoderm cells are a rapidly dividing and differentiating population of cells with a unique and rapid heat-shock response. Heat shock and the heat-shock genes were studied during neural plate development in a whole rat embryo culture system at 9.5-11.5 days. A lethal shock can cause cell death and severe developmental defects to the forebrain and eye during organogenesis. Heat shock can also result in acquired thermotolerance whereby cell progression is delayed at the G1/S and S/G2 boundaries of the cell cycle. This delay in cell cycle progression caused an overall lengthening of the cell cycle time of at least 2 hr. The heat shock genes may therefore function as cell cycle regulators in neuroectoderm induction and differentiation. The kinetics and expression of the hsp genes were examined in neuroectodermal cells by flow cytometry and Northern analysis. The levels of hsp mRNA 27, 71, 73, and 88 were identified following exposure at 42 degrees C (nonlethal), 43 degrees C (lethal) and 42 degrees/43 degrees C (thermotolerant) heat shock. Examination of hsp gene expression in the neural plate showed tight regulation in the cell cycle phases. Hsp 88 expression was enhanced at Go and hsp71 induction at G2 + M of the cell cycle. Cells exposed to a thermotolerant heat shock of 42 degrees C induced hsp71 mRNA expression in all phases of the cell cycle with the mRNA levels of hsp27, 73, and 88 increased but relatively constant. Following a lethal heat shock, dramatic changes in hsp expression were seen especially enhanced hsp71 induction in late S phase. The regulated expression of hsps during the cell cycle at various phases could play a unique and important role in the fate and recovery of neuroectoderm cells during early mammalian embryo development.

哺乳动物胚胎发育过程中热休克基因表达与细胞周期变化。
原肠胚形成过程中细胞分裂的同步调控对于早期中枢神经系统细胞的区域增殖和模式形成至关重要。神经板细胞和神经外胚层细胞是一种快速分裂和分化的细胞群,具有独特和快速的热休克反应。研究了9.5 ~ 11.5 d大鼠胚胎培养系统中神经板发育过程中的热休克及热休克基因。在器官形成过程中,致命的休克可导致细胞死亡和严重的前脑和眼睛发育缺陷。热休克还可以导致获得性热耐受性,从而在细胞周期的G1/S和S/G2边界延迟细胞进程。这种细胞周期进展的延迟导致细胞周期时间至少延长2小时。因此,热休克基因可能在神经外胚层诱导和分化中起细胞周期调节作用。用流式细胞术和Northern分析检测了热休克蛋白基因在神经外胚层细胞中的表达和表达动力学。在42℃(非致死)、43℃(致死)和42℃/43℃(耐热)热休克条件下,确定热休克蛋白mRNA 27、71、73和88的水平。神经板中热休克蛋白基因的表达在细胞周期阶段表现出严格的调控。hsp88在Go时表达增强,hsp71在G2 + M时表达增强。42℃的耐热热休克诱导细胞在细胞周期的各个阶段表达hsp71 mRNA, hsp27、73和88 mRNA水平升高,但相对稳定。在致死性热休克后,热休克蛋白表达发生显著变化,尤其是在S期晚期,热休克蛋白71的诱导增强。在哺乳动物早期胚胎发育过程中,细胞周期各阶段对热休克蛋白表达的调控在神经外胚层细胞的命运和恢复中发挥着独特而重要的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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