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
Main Authors: Li, Xinbo, Nagy, James I, Li, Davey, Acott, Ted S, Kelley, Mary J
Format: Journal Article
Language:English
Published: United States e-Century Publishing Corporation 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.
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
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  givenname: James I
  surname: Nagy
  fullname: Nagy, James I
  organization: Department of Physiology and Pathophysiology, University of Manitoba Winnipeg, MB, Canada
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  givenname: Davey
  surname: Li
  fullname: Li, Davey
  organization: University of Waterloo Waterloo, ON, Canada
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  givenname: Ted S
  surname: Acott
  fullname: Acott, Ted S
  organization: Department of Chemical Physiology & Biochemistry, Oregon Health & Science University Portland, Oregon, USA
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  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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Snippet Human trabecular meshwork (TM) cells play pivotal roles in maintaining homeostasis of intraocular pressure via regulation of aqueous humor outflow. These cells...
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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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