馈源细胞与受体正常上皮细胞之间的间隙功能交流与生长刺激相关。

U K Ehmann, S K Calderwood, M A Stevenson
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引用次数: 5

摘要

LA7大鼠乳腺肿瘤细胞在培养过程中能刺激三种正常上皮细胞(即小鼠乳腺细胞、大鼠乳腺细胞和小鼠胸腺细胞)的增殖。通过显微注射荧光素黄,荧光素黄从 LA7 进入周围的小鼠乳腺细胞,证明了 LA7 饲养细胞和小鼠乳腺细胞之间的间隙功能通讯。供体与受体小鼠乳腺细胞、大鼠乳腺细胞和小鼠胸腺细胞之间的3H-尿苷交换量与供体诱导的生长率相关。马汀达比犬肾(MDCK)系细胞在用作供体细胞时不会明显刺激小鼠乳腺细胞的生长,但它们之间的 3H 尿苷交换量也很少。通过免疫细胞化学法研究了所有这些细胞系和品系中连接蛋白 Cx43、32 和 26 的表达情况。小鼠乳腺细胞表达 Cx26,少数小鼠胸腺细胞表达 Cx32。LA7、小鼠乳腺细胞、小鼠胸腺细胞和大鼠乳腺细胞都表达了很容易检测到的间隙连接蛋白 Cx43,而 MDCK 细胞只表达了少量该蛋白。这些结果表明,由 Cx43 组成的间隙连接是正常上皮细胞与 LA 饲养细胞进行沟通的途径。因此,供体细胞刺激受体细胞增殖的能力与供体/受体细胞对中双方的 Cx43 表达以及这些细胞之间形成功能性间隙连接的能力有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gap-junctional communication between feeder cells and recipient normal epithelial cells correlates with growth stimulation.

LA7 rat mammary tumor cells stimulate the proliferation, in culture, of three normal epithelial cell types, namely mouse mammary, rat mammary, and mouse thymic cells. Gap-junctional communication between LA7 feeders and mouse mammary cells was demonstrated by microinjection of lucifer yellow, which traveled from LA7 to the surrounding mouse mammary cells. The amount of 3H-uridine exchange between feeder and recipient mouse mammary, rat mammary, and mouse thymus cells correlated with the growth rate induced by the feeders. Cells of the Madin Darby canine kidney (MDCK) line, which do not appreciably stimulate mouse mammary cell growth when used as feeder cells, also exchange little 3H-uridine with them. Expression of connexins Cx43, 32, and 26 was studied in all these cell lines and strains by immunocytochemistry. Mouse mammary cells expressed Cx26, and a few mouse thymic cells expressed Cx32. LA7, mouse mammary, mouse thymic, and rat mammary cells all expressed easily detectable amounts of the gap-junction protein Cx43, in contrast to MDCK cells, which expressed only a hint of the protein. These results suggest that gap junctions composed of Cx43 are those by which the normal epithelial cells communicate with the LA feeders. Thus, the ability of feeder cells to stimulate proliferation in recipients correlates with the expression of Cx43 in both members of the feeder/recipient pair and the capacity to form functional gap junctions between these cells.

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