Kato K, Ito H, Hasegawa K, Inaguma Y, Kozawa O, Asano T
Department of Biochemistry, Aichi Human Service Center, Japan.
J Neurochem. 1996 Mar;66(3):946-50. doi: 10.1046/j.1471-4159.1996.66030946.x.
The possible participation of cyclic AMP in the stress-induced synthesis of two small stress proteins, hsp27 and alpha B-crystallin, in C6 rat glioma cells was examined by specific immunoassays, western blot analysis, and northern blot analysis. When C6 cells were exposed to arsenite (50-100 microM for 1 h) or heat (42 degrees C for 30 min), expression of hsp27 and alpha B-crystallin was stimulated, with levels of the two proteins reaching a maximum after 10-16 h of culture. Induction of hsp27 was markedly enhanced when cells were exposed to arsenite in the presence of isoproterenol (20 microM) or epinephrine (20 microM) but not in the presence of phenylephrine. The stimulatory effects of isoproterenol and epinephrine were blocked completely by propranolol, an antagonist of beta-adrenergic receptors. Cholera toxin (2 micrograms/ml), forskolin (20 microM), and dibutyryl cyclic AMP (2.5 mM), all of which are known to increase intracellular levels of cyclic AMP, also stimulated the arsenite- or heat-induced accumulation of hsp27. Treatment of cells with each of these modulators alone did not result in the induction of hsp27. The level of hsp70 in C6 cells, as estimated by western blot analysis, was also enhanced by arsenite or heat stress. However, induction of hsp70 by stress was barely stimulated by isoproterenol. By contrast, induction of alpha B-crystallin by heat or arsenite stress was suppressed when isoproterenol, cholera toxin, forskolin, or dibutyryl cyclic AMP was present during the stress period. Northern blot analysis of the expression of mRNAs for hsp70, hsp27, and alpha B-crystallin showed that the modulation of the stress-induced accumulation of the three hsps by the various agents was regulated at the level of the corresponding mRNA. These results indicate that stress responses of hsp70, hsp27, and alpha B-crystallin in C6 rat glioma cells are regulated differently and, moreover, that when the level of cyclic AMP increases in cells, the response to stress of hsp27 is stimulated but that of alpha B-crystallin is suppressed.
通过特异性免疫分析、蛋白质印迹分析和Northern印迹分析,研究了环磷酸腺苷(cAMP)在应激诱导的C6大鼠胶质瘤细胞中两种小应激蛋白hsp27和αB-晶状体蛋白合成过程中可能发挥的作用。当C6细胞暴露于亚砷酸盐(50 - 100微摩尔/升,1小时)或热(42℃,30分钟)时,hsp27和αB-晶状体蛋白的表达受到刺激,两种蛋白的水平在培养10 - 16小时后达到最高。当细胞在异丙肾上腺素(20微摩尔/升)或肾上腺素(20微摩尔/升)存在的情况下暴露于亚砷酸盐时,hsp27的诱导显著增强,但在去氧肾上腺素存在时则不然。异丙肾上腺素和肾上腺素的刺激作用被β-肾上腺素能受体拮抗剂普萘洛尔完全阻断。霍乱毒素(2微克/毫升)、福斯高林(20微摩尔/升)和二丁酰环磷酸腺苷(2.5毫摩尔/升),所有这些都已知会增加细胞内环磷酸腺苷的水平,它们也刺激了亚砷酸盐或热诱导的hsp27积累。单独用这些调节剂中的每一种处理细胞并不会导致hsp27的诱导。通过蛋白质印迹分析估计,C6细胞中hsp70的水平也因亚砷酸盐或热应激而升高。然而,异丙肾上腺素几乎不能刺激应激诱导的hsp70诱导。相比之下,当应激期间存在异丙肾上腺素、霍乱毒素、福斯高林或二丁酰环磷酸腺苷时,热或亚砷酸盐应激诱导的αB-晶状体蛋白的诱导受到抑制。对hsp70、hsp27和αB-晶状体蛋白mRNA表达的Northern印迹分析表明,各种试剂对三种热休克蛋白应激诱导积累的调节是在相应mRNA水平上进行的。这些结果表明,C6大鼠胶质瘤细胞中hsp70、hsp27和αB-晶状体蛋白的应激反应受到不同的调节,此外,当细胞内环磷酸腺苷水平升高时,hsp27的应激反应受到刺激,而αB-晶状体蛋白的应激反应则受到抑制。