Pitts J D, Hamilton A E, Kam E, Burk R R, Murphy J P
Carcinogenesis. 1986 Jun;7(6):1003-10. doi: 10.1093/carcin/7.6.1003.
Retinoic acid inhibits junctional communication between a variety of vertebrate cell types in culture. It reduces the intercellular transfer of 3H-nucleotides between Syrian hamster kidney fibroblasts (BHK 21/13), Chinese hamster lung fibroblasts (V79), rat liver epithelial cells (BRL), Swiss mouse embryo fibroblasts (3T3), rainbow trout gonadal fibroblasts (RTG2) and Xenopus embryo fibroblasts (Xen). It also reduces metabolic cooperation between hypoxanthine-guanine phosphoribosyl transferase deficient mutant and wild-type BHK cells. The inhibition is rapid (intercellular transfer of iontophoretically injected Lucifer Yellow CH between BRL cells is completely blocked after the cells have been exposed to 10(-4) M retinoic acid for 5 min), and is fully reversed when the drug is removed. Based on these results and the observation that the amount of gap junctional protein isolated from cells grown in the presence of retinoic acid for 1 h is the same and after 24 h is increased (1.3- to 3.1-fold) compared with the amount isolated from untreated cells, we suggest that the inhibitory effect is mediated by the reversible closure of junctional channels.
视黄酸抑制培养的多种脊椎动物细胞类型之间的连接通讯。它减少了叙利亚仓鼠肾成纤维细胞(BHK 21/13)、中国仓鼠肺成纤维细胞(V79)、大鼠肝上皮细胞(BRL)、瑞士小鼠胚胎成纤维细胞(3T3)、虹鳟性腺成纤维细胞(RTG2)和非洲爪蟾胚胎成纤维细胞(Xen)之间3H-核苷酸的细胞间转移。它还减少了次黄嘌呤-鸟嘌呤磷酸核糖基转移酶缺陷型突变体与野生型BHK细胞之间的代谢合作。这种抑制作用迅速(在细胞暴露于10(-4) M视黄酸5分钟后,BRL细胞之间离子电渗注入的荧光黄CH的细胞间转移被完全阻断),并且当去除药物时完全逆转。基于这些结果以及观察到从在视黄酸存在下培养1小时的细胞中分离出的间隙连接蛋白的量与从未经处理的细胞中分离出的量相同,而在24小时后增加(1.3至3.1倍),我们认为这种抑制作用是由连接通道的可逆关闭介导的。