Gap junction connexin43 is a key element in mediating phagocytosis activity in human trabecular meshwork cells
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...
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Published in: | International journal of physiology, pathophysiology and pharmacology Vol. 12; no. 1; pp. 25 - 31 |
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2020
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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. |
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AbstractList | 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. |
Author | Kelley, Mary J Li, Davey Li, Xinbo Nagy, James I Acott, Ted S |
Author_xml | – sequence: 1 givenname: Xinbo surname: Li fullname: Li, Xinbo organization: Department of Ophthalmology, Casey Eye Institute, Oregon Health & Science University Portland, Oregon, USA – sequence: 2 givenname: James I surname: Nagy fullname: Nagy, James I organization: Department of Physiology and Pathophysiology, University of Manitoba Winnipeg, MB, Canada – sequence: 3 givenname: Davey surname: Li fullname: Li, Davey organization: University of Waterloo Waterloo, ON, Canada – sequence: 4 givenname: Ted S surname: Acott fullname: Acott, Ted S organization: Department of Chemical Physiology & Biochemistry, Oregon Health & Science University Portland, Oregon, USA – sequence: 5 givenname: Mary J surname: Kelley fullname: Kelley, Mary J organization: Department of Integrative Biosciences, Oregon Health & Science University Portland, Oregon, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32211119$$D View this record in MEDLINE/PubMed |
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Keywords | phagocytosis gap junction Trabecular meshwork connexin43 |
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Title | Gap junction connexin43 is a key element in mediating phagocytosis activity in human trabecular meshwork cells |
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