Yamanaka I, Kuraoka A, Inai T, Ishibashi T, Shibata Y
Department of Ophthalmology, Faculty of Medicine, Kyushu University, 3-1-1 Maidashi, Fukuoka 812-8582, Japan.
Histochem Cell Biol. 2001 Apr;115(4):277-84. doi: 10.1007/s004180100256.
We examined the expression pattern of two major gap junction proteins, connexin 26 (Cx26) and connexin 32 (Cx32), in rat mammary glands during pregnancy and lactation. Immunohistochemically the two different Cxs were coexpressed in acinar cells and were independently modulated according to the physiological cell activity. Western blot analysis demonstrated that Cx26 gradually increased from early pregnancy, while Cx32 rapidly and dramatically increased at 16 h after parturition, and that both Cxs reached a maximum early in lactation. Increased expression of both Cxs was confirmed by Northern blot analysis showing that their mRNA transcripts were significantly induced on the day of parturition. We also analyzed double-immunofluorescent staining for Cx26 and Cx32 on a confocal laser scanning microscope, in order to examine colocalization of these Cxs in situ. Cx26 immunoreactivity mostly overlapped with Cx32-positive sites in acinar cells of lactating mammary glands, indicating that both Cxs were colocalized together in the same gap junctional plaques in lactation. These results suggest that upregulation of Cx26 and Cx32 in acinar cells at lactating stages, with colocalization in the same gap junctional plaques, may be important for control of secretion by acinar cells in rat mammary glands.
我们研究了两种主要的缝隙连接蛋白,即连接蛋白26(Cx26)和连接蛋白32(Cx32)在大鼠乳腺妊娠和哺乳期的表达模式。免疫组织化学显示,这两种不同的连接蛋白在腺泡细胞中共表达,并根据生理细胞活性独立调节。蛋白质印迹分析表明,Cx26从妊娠早期开始逐渐增加,而Cx32在分娩后16小时迅速且显著增加,并且两种连接蛋白在泌乳早期均达到最大值。Northern印迹分析证实了两种连接蛋白的表达增加,表明它们的mRNA转录本在分娩当天被显著诱导。我们还在共聚焦激光扫描显微镜上分析了Cx26和Cx32的双重免疫荧光染色,以检查这些连接蛋白在原位的共定位。在泌乳期乳腺的腺泡细胞中,Cx26免疫反应性大多与Cx32阳性位点重叠,表明两种连接蛋白在泌乳期的同一缝隙连接斑块中共定位。这些结果表明,泌乳期腺泡细胞中Cx26和Cx32的上调以及在同一缝隙连接斑块中的共定位,可能对大鼠乳腺腺泡细胞的分泌控制很重要。