Pipkin J L, Anson J F, Hinson W G, Burns E R, Casciano D A, Sheehan D M
Biochim Biophys Acta. 1987 Mar 11;927(3):334-44. doi: 10.1016/0167-4889(87)90097-8.
Cultured mouse lymphoma cells incorporated [3H]leucine and [32P]phosphate into nuclear stress proteins within 3 h after exposure to either elevated temperature (45 degrees C) or sodium arsenite. Radiolabeled proteins were detected by autoradiography after two-dimensional polyacrylamide gel electrophoresis. To determine the cell cycle stage specificity of labeling, nuclei were isolated and sorted into two cell cycle phases using a fluorescent activated cell sorter. After either heat shock or sodium arsenite treatment, the majority of [3H]leucine incorporation into stress proteins occurred during the G0 + G1 phase with minimal labeling in the G2 phase. On the other hand, 32P labeling of stress proteins occurred in both the G0 + G1 and G2 phases after exposure to sodium arsenite, while incorporation of 32P was limited after heat stress. Following sodium arsenite treatment, a distinct set of four stress proteins (80-84 kDa) was detected with [3H]leucine only in G0 + G1 phase, but with [32P]phosphate these stress proteins were labeled in both G0 + G1 and G2. There was differential [32P]phosphate labeling between proteins of the 80-84 kDa set during cell cycling. Individual proteins of this set were isolated from gel plugs after sodium arsenite or heat-shock treatment. Coelectrophoresis of proteins from the two treatment groups showed that they had similar electrophoretic mobilities. All four proteins of the 80-84 kDa set (sodium arsenite induced) possessed similar polypeptide maps after digestion with V8 protease. Cytofluorometric analysis demonstrated a reduction in the number of nuclei in both S and G2 phases of the cell cycle two h after heat shock, but not following sodium arsenite treatment. However, there was a significant depression in the number of nuclei in S and G2 4 h after exposure to sodium arsenite and very modest labeling with 32P of stress proteins was observed at this time.
培养的小鼠淋巴瘤细胞在暴露于高温(45℃)或亚砷酸钠后3小时内将[3H]亮氨酸和[32P]磷酸盐掺入核应激蛋白中。二维聚丙烯酰胺凝胶电泳后,通过放射自显影检测放射性标记的蛋白质。为了确定标记的细胞周期阶段特异性,使用荧光激活细胞分选仪分离细胞核并将其分为两个细胞周期阶段。热休克或亚砷酸钠处理后,应激蛋白中大部分[3H]亮氨酸掺入发生在G0 + G1期,G2期标记最少。另一方面,暴露于亚砷酸钠后,应激蛋白的32P标记在G0 + G1和G2期均有发生,而热应激后32P掺入受限。亚砷酸钠处理后,仅在G0 + G1期用[3H]亮氨酸检测到一组独特的四种应激蛋白(80 - 84 kDa),但用[32P]磷酸盐标记时,这些应激蛋白在G0 + G1和G2期均有标记。细胞周期中80 - 84 kDa组蛋白质之间存在差异[32P]磷酸盐标记。在亚砷酸钠或热休克处理后,从凝胶块中分离出该组中的单个蛋白质。两个处理组蛋白质的共电泳显示它们具有相似的电泳迁移率。用V8蛋白酶消化后,80 - 84 kDa组(亚砷酸钠诱导)的所有四种蛋白质具有相似的多肽图谱。细胞荧光分析表明,热休克后2小时,细胞周期S期和G2期的细胞核数量减少,但亚砷酸钠处理后未减少。然而,暴露于亚砷酸钠4小时后,S期和G2期的细胞核数量显著减少,此时观察到应激蛋白的32P标记非常少。