Hatayama T, Nishiyama E, Yasuda K
Department of Biochemistry, Kyoto Pharmaceutical University, Japan.
Biochem Biophys Res Commun. 1994 May 16;200(3):1367-73. doi: 10.1006/bbrc.1994.1602.
We have previously prepared an antiserum raised against hsp105 of murine FM3A cells. The anti-hsp105 serum reacted to two isoforms of high-molecular-mass heat shock protein (HMM-HSP) having a molecular mass of 105,000 Da (hsp105A and hsp105B) in FM3A cells. While hsp105A and hsp105B were both synthesized and accumulated under non-stressed conditions, upon exposure to heat shock much more hsp105B was induced than hsp105A. When the cellular distribution of these hsp105s in murine 3T3 Swiss albino and C3H 10T1/2 cells was examined by immunofluorescence methods using the anti-hsp105 serum, the HMM-HSPs were localized in the cytoplasm and nuclei and were never found in the nucleoli of both 3T3 and C3H cells under non-stressed and stressed conditions.
我们之前制备了一种针对小鼠FM3A细胞hsp105的抗血清。该抗hsp105血清与FM3A细胞中分子量为105,000 Da的两种高分子量热休克蛋白(HMM-HSP)同工型(hsp105A和hsp105B)发生反应。虽然hsp105A和hsp105B在非应激条件下均能合成并积累,但在热休克处理后,hsp105B的诱导量比hsp105A多得多。当使用抗hsp105血清通过免疫荧光方法检测这些hsp105在小鼠3T3瑞士白化细胞和C3H 10T1/2细胞中的细胞分布时,在非应激和应激条件下,HMM-HSP均定位于细胞质和细胞核中,在3T3和C3H细胞的核仁中均未发现。