Chin Andrew R, Yan Wei, Cao Minghui, Liu Xuxiang, Wang Shizhen Emily
Department of Pathology, University of California San Diego, 9500 Gilman Drive, La Jolla, CA, 92093-0612, USA.
City of Hope Irell & Manella Graduate School of Biological Sciences, Duarte, CA, 91010, USA.
J Mammary Gland Biol Neoplasia. 2018 Sep;23(3):165-176. doi: 10.1007/s10911-018-9402-6. Epub 2018 Jul 3.
Extracellular vesicles (EVs) are secreted by many cell types and are increasingly investigated for their role in human diseases including cancer. Here we focus on the secretion and potential physiological function of non-pathological EVs secreted by polarized normal mammary epithelial cells. Using a transwell system to allow formation of epithelial polarity and EV collection from the apical versus basolateral compartments, we found that impaired secretion of EVs by knockdown of RAB27A or RAB27B suppressed the establishment of mammary epithelial polarity, and that addition of apical but not basolateral EVs suppressed epithelial polarity in a dose-dependent manner. This suggests that apical EV secretion contributes to epithelial polarity, and a possible mechanism is through removal of certain intracellular molecules. In contrast, basolateral but not apical EVs promoted migration of mammary epithelial cells in a motility assay. The protein contents of apical and basolateral EVs from MCF10A and primary human mammary epithelial cells were determined by mass spectrometry proteomic analysis, identifying apical-EV-enriched and basolateral-EV-enriched proteins that may contribute to different physiological functions. Most of these proteins differentially secreted by normal mammary epithelial cells through polarized EV release no longer showed polarized secretion in MCF10A-derived transformed epithelial cells. Our results suggest an essential role of EV secretion in normal mammary epithelial polarization and distinct protein contents and functions in apical versus basolateral EVs secreted by polarized mammary epithelia.
细胞外囊泡(EVs)由多种细胞类型分泌,并且人们对其在包括癌症在内的人类疾病中的作用研究越来越多。在这里,我们聚焦于极化的正常乳腺上皮细胞分泌的非病理性EVs的分泌及其潜在生理功能。利用Transwell系统使上皮细胞形成极性,并从顶侧与基底外侧隔室收集EVs,我们发现敲低RAB27A或RAB27B导致EVs分泌受损会抑制乳腺上皮极性的建立,并且添加顶侧而非基底外侧的EVs会以剂量依赖方式抑制上皮极性。这表明顶侧EV分泌有助于上皮极性,一种可能的机制是通过去除某些细胞内分子。相反,在迁移实验中,基底外侧而非顶侧的EVs促进了乳腺上皮细胞的迁移。通过质谱蛋白质组学分析确定了来自MCF10A和原代人乳腺上皮细胞的顶侧和基底外侧EVs的蛋白质含量,鉴定出可能有助于不同生理功能的顶侧EV富集蛋白和基底外侧EV富集蛋白。正常乳腺上皮细胞通过极化的EV释放差异分泌的这些蛋白质中的大多数,在源自MCF10A的转化上皮细胞中不再显示极化分泌。我们的结果表明EV分泌在正常乳腺上皮极化中起重要作用,并且极化乳腺上皮分泌的顶侧与基底外侧EVs具有不同的蛋白质含量和功能。