Gap junction connexin43 is a key element in mediating phagocytosis activity in human trabecular meshwork cells.

International journal of physiology, pathophysiology and pharmacology Pub Date : 2020-02-25 eCollection Date: 2020-01-01
Xinbo Li, James I Nagy, Davey Li, Ted S Acott, Mary J Kelley
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引用次数: 0

Abstract

Human trabecular meshwork (TM) cells play pivotal roles in maintaining homeostasis of intraocular pressure via regulation of aqueous humor outflow. These cells are capable of phagocytosis, which is considered to be essential for their regulatory function. In addition, there is a strong expression of the gap junction protein connexin43 (Cx43) in the TM. Here, we investigated functional relationships between phagocytosis activity of TM cells and their expression of Cx43. Phagocytosis was measured by showing the ability of TM cells to engulf inert fluorescent particles consisting of pHrodo. We found that internalized pHrodo was partially co-localized with Cx43 and that the phagocytic activity was dramatically reduced after knockdown of Cx43 using lentiviral Cx43 shRNA. These results suggest that Cx43 is involved in the regulation of phagocytosis by TM cells.

缝隙连接connexin43是介导人类小梁网细胞吞噬活动的关键因素。
人类小梁网(TM)细胞通过调节房水外流,在维持眼压平衡方面发挥着关键作用。这些细胞具有吞噬能力,这被认为是其调节功能的关键。此外,缝隙连接蛋白 connexin43(Cx43)也在 TM 中大量表达。在此,我们研究了 TM 细胞的吞噬活性与 Cx43 表达之间的功能关系。通过显示 TM 细胞吞噬由 pHrodo 组成的惰性荧光颗粒的能力来测量吞噬能力。我们发现,内化的pHrodo部分与Cx43共定位,而且使用慢病毒Cx43 shRNA敲除Cx43后,吞噬活性显著降低。这些结果表明,Cx43 参与调控 TM 细胞的吞噬作用。
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