Diethylstilbestrol-induced estrogen receptor-dependent [Ca2+](i) rises and apoptosis in chinese hamster ovary (CHO) cells

作者：Roan Cherng Jau; Huang Chorng Chih; Cheng He Hsiung; Chien Jau Min; Chou Chiang Ting; Lin Ko Long; Liu Shiuh Inn; Lu Yih Chau; Chang Hong Tai; Huang Jong Khing; Jan Chung Ren^*

来源：Journal of Receptors and Signal Transduction, 2008, 28(3): 307-322.

DOI：10.1080/10799890802092237

• Ca2+
• CHO-K1 cells
• DES
• fura-2
• WST-1

The effect of the synthetic estrogen diethylstilbestrol (DES) on cytosolic free Ca2+ concentrations ([Ca2+](i)) and cell viability was explored in Chinese hamster ovary (CHO-K1). [Ca2+](i) and cell viability were measured by using the fluorescent dyes fura-2 and WST-1, respectively. DES at concentrations >= 1 alpha increased [Ca2+](i) in a concentration-dependent manner. The Ca2+ signal was reduced partly by removing extracellular Ca2+. In Ca2+-free medium, after pretreatment with 50 alpha DES, 1 alpha thapsigargin (an endoplasmic reticulum Ca2+ pump inhibitor)-induced [Ca2+](i) rises were abolished. Conversely, thapsigargin pretreatment abolished DES-induced [Ca2+](i) rises. Inhibition of phospholipase C with U73122 did not alter DES-induced [Ca2+](i) rises. At a concentration of 5 alpha, DES increased cell viability. At concentrations of 100-200 mu M, DES decreased viabilityin a concentration-dependent manner. The effect of 5 and 100 mu M DES on viability was partly reversed by prechelating cytosolic Ca2+ with 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid (BAPTA). DES-induced cell death was induced via apoptosis as demonstrated by propidium iodide staining. DES (100 mu M)-induced [Ca2+](i) rises were largely inhibited by pretreatment with the estrogen receptor antagonist ICI-182,780 (100 mu M). ICI-182,780 did not affect 5 mu M DES-induced increase in viability but partly reversed 100 AM DES-induced cell death. Collectively, in CHO-K1 cells, DES induced [Ca2+](i) rises by stimulating estrogen receptors leading to Ca2+ release from the endoplasmic reticulum in a phospholipase C-independent manner, and Ca2+ influx. DES-caused cytotoxicity was mediated by an estrogen receptor- and Ca2+-dependent pathway.

• 出版日期2008