Chrétien P, Landry J
Département de Médecine, Université Laval, Québec, Canada.
J Cell Physiol. 1988 Oct;137(1):157-66. doi: 10.1002/jcp.1041370119.
Four heat-resistant variants were isolated after treatment of Chinese hamster lung cells with the mutagen ethyl methane sulfonate, followed by a single-step selection procedure consisting in a severe hyperthermic treatment of 4 h at 44 degrees C. The isolated clones had a stable resistant phenotype for at least 150 generations during which they showed a 5,000-fold increased survival to a 4-h treatment at 44 degrees C when compared to wild-type cells. Comparative two-dimensional electrophoretic analyses of proteins revealed that, like induced thermotolerant wild-type cells (i.e., cells induced to a transient physiological state of thermotolerance by a sublethal heat conditioning treatment administered 18 h before), the heat-resistant variants had, at normal temperature, an increased content of a heat-shock protein with Mr of 27,000 (HSP27). In three of the four heat-resistant variants, the increased content of HSP27 was correlated with a two-fold increase in the constitutive level of the mRNA encoding HSP27. Chinese hamster HSP27 is composed of three species that differ in their relative isoelectric point, among which the two most acidic forms are phosphoproteins. In both the heat-resistant variant and wild-type cells, heat shock induces a rapid enhancement of the phosphorylation of HSP27: maximal phosphorylation occurs within 10 min upon changing the incubation temperature from 35 degrees to 44 degrees C. A concomitant shift in silver-staining intensity is rapidly detectable between the three isoforms, which seems to indicate that the two phosphorylated species represent post-translational modifications of the more basic species. It is concluded that most likely the enhanced expression of HSP27 is linked to the resistant phenotype of the variants. The study provides supporting evidence that both the content and phosphorylation status of HSP27 are determining factors in the ability of cells to survive hyperthermic treatments.
用诱变剂甲磺酸乙酯处理中国仓鼠肺细胞,然后进行一步选择程序,即在44℃下进行4小时的严格高温处理,之后分离出四个耐热变体。分离出的克隆在至少150代中具有稳定的抗性表型,在此期间,与野生型细胞相比,它们在44℃下进行4小时处理后的存活率提高了5000倍。蛋白质的二维电泳比较分析表明,与诱导耐热的野生型细胞(即通过18小时前给予的亚致死热预处理诱导至短暂耐热生理状态的细胞)一样,耐热变体在正常温度下,分子量为27,000的热休克蛋白(HSP27)含量增加。在四个耐热变体中的三个中,HSP27含量的增加与编码HSP27的mRNA组成型水平的两倍增加相关。中国仓鼠HSP27由三种相对等电点不同的物种组成,其中两种酸性最强的形式是磷蛋白。在耐热变体和野生型细胞中,热休克均会导致HSP27磷酸化迅速增强:将孵育温度从35℃变为44℃后10分钟内发生最大磷酸化。在三种同工型之间可迅速检测到银染强度的伴随变化,这似乎表明两种磷酸化形式代表了更碱性形式的翻译后修饰。得出的结论是,HSP27表达增强很可能与变体的抗性表型有关。该研究提供了支持性证据,即HSP27的含量和磷酸化状态都是细胞在高温处理下存活能力的决定因素。