Mirkes P E, Doggett B
Department of Pediatrics, University of Washington, Seattle 98195.
Teratology. 1992 Sep;46(3):301-9. doi: 10.1002/tera.1420460315.
A monoclonal antibody to the 72 kDa heat shock protein and Western blot analysis were used to determine the induction, accumulation and turnover of hsp 72 after day 10 rat embryos were exposed to elevated temperatures (40 degrees-43 degrees C) for various lengths of time (2.5 minutes to 18 hours). Embryos exposed to temperatures that exceed the normal culture temperature (37 degrees C) by 4 degrees C or more for as little as 2.5 minutes (43 degrees C) or 15 minutes (41, 42 degrees C) synthesized and accumulated detectable amounts of heat-inducible hsp 72. Hsp 72 could not be detected by Western blot analysis of proteins from embryos cultured at 40 degrees C or below. Once induced, hsp 72 can be detected in embryos for 24-48 hours after they are removed from the hyperthermic conditions and returned to normothermic conditions. Our results also indicate that hsp 72 is induced by all hyperthermic exposures that induce alterations in rat embryo growth and development; therefore, hsp 72 is a potential biomarker for heat-induced embryotoxicity.
利用一种针对72 kDa热休克蛋白的单克隆抗体和蛋白质印迹分析,来确定在第10天的大鼠胚胎暴露于高温(40摄氏度至43摄氏度)不同时长(2.5分钟至18小时)后,热休克蛋白72(hsp 72)的诱导、积累和周转情况。暴露于比正常培养温度(37摄氏度)高出4摄氏度或更多温度的胚胎,即便仅暴露2.5分钟(43摄氏度)或15分钟(41、42摄氏度),也会合成并积累可检测量的热诱导型hsp 72。通过对在40摄氏度或更低温度下培养的胚胎蛋白质进行蛋白质印迹分析,无法检测到hsp 72。一旦诱导产生,hsp 72在胚胎从高温环境移除并恢复到正常体温环境后24至48小时内都能被检测到。我们的结果还表明,所有能诱导大鼠胚胎生长和发育发生改变的高温暴露都会诱导hsp 72产生;因此,hsp 72是热诱导胚胎毒性的一个潜在生物标志物。