Yamashita N, Schroeder J I, Umbach J A, Gundersen C B
Department of Physiology and Pharmacology, University of California School of Medicine, Los Angeles 90024.
Biochem Biophys Res Commun. 1992 May 15;184(3):1235-40. doi: 10.1016/s0006-291x(05)80014-2.
Poly(A)+ mRNA extracted from rat calcitonin-secreting cells (rMTC 44-2) was injected into Xenopus oocytes. In mRNA-injected oocytes the intracellular Ca2+ concentration ([Ca2+]i), measured with the Ca2+ indicator dye, fura2, increased in response to an elevation of the extracellular Ca2+ ions ([Ca2+]o). In some oocytes [Ca2+]i transiently increased in high [Ca2+]o but it did not respond to the subsequent alterations of [Ca2+]o. The addition of 10 microM carbonyl cyanide m-chlorphenylhydrazone (CCCP) to the extracellular medium restored the dependence of [Ca2+]i on [Ca2+]o in such cells. It was concluded that rMTC 44-2 cells possessed a receptor which recognizes changes in [Ca2+]o and that these receptors can be functionally expressed by microinjection of messenger RNA from rMTC 44-2 cells into Xenopus oocytes.
从大鼠降钙素分泌细胞(rMTC 44-2)中提取的多聚腺苷酸(Poly(A))+信使核糖核酸(mRNA)被注射到非洲爪蟾卵母细胞中。在用钙离子指示剂染料fura2测量的mRNA注射卵母细胞中,细胞内钙离子浓度([Ca2+]i)随着细胞外钙离子浓度([Ca2+]o)的升高而增加。在一些卵母细胞中,[Ca2+]i在高[Ca2+]o时短暂增加,但对随后[Ca2+]o的变化没有反应。向细胞外培养基中添加10微摩尔羰基氰化物间氯苯腙(CCCP)可恢复此类细胞中[Ca2+]i对[Ca2+]o的依赖性。得出的结论是,rMTC 44-2细胞拥有一种识别[Ca2+]o变化的受体,并且这些受体可以通过将rMTC 44-2细胞的信使核糖核酸显微注射到非洲爪蟾卵母细胞中进行功能性表达。