Connexin hemichannels regulate redox potential via metabolite exchange and protect lens against cellular oxidative damage

Increased oxidative stress contributes to cataract formation during aging. Anterior epithelial cells are a frontline antioxidant defense system with powerful capacities to maintain redox homeostasis and lens transparency. In this study, we report a new molecular mechanism of connexin (Cx) hemichanne...

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Main Authors: Yumeng Quan, Yu Du, Changrui Wu, Sumin Gu, Jean X. Jiang
Format: Article
Language:English
Published: Elsevier 2021-10-01
Series:Redox Biology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213231721002615
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spelling doaj-d3269034b97647e28c8e337a17f5fc8b2021-09-21T04:09:27ZengElsevierRedox Biology2213-23172021-10-0146102102Connexin hemichannels regulate redox potential via metabolite exchange and protect lens against cellular oxidative damageYumeng Quan0Yu Du1Changrui Wu2Sumin Gu3Jean X. Jiang4Department of Ophthalmology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China; Department of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX, USADepartment of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX, USADepartment of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX, USADepartment of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX, USADepartment of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX, USA; Corresponding author. Department of Biochemistry and Structural Biology, University of Texas Health Science Center, 7703 Floyd Curl Drive, San Antonio, TX, 78229-3900, USA.Increased oxidative stress contributes to cataract formation during aging. Anterior epithelial cells are a frontline antioxidant defense system with powerful capacities to maintain redox homeostasis and lens transparency. In this study, we report a new molecular mechanism of connexin (Cx) hemichannels (HCs) in lens epithelial cells to protect lens against oxidative stress. Our results showed haploinsufficiency of Cx43 elevated oxidative stress and susceptibility to cataracts in the mouse lens. Cx43 HCs opened in response to hydrogen peroxide (H2O2) or ultraviolet radiation (UVR) in human lens epithelium HLE-B3 cells, and this activation contributed to a cellular protective mechanism against oxidative stress-induced apoptotic cell death. Furthermore, we found that Cx43 HCs mediated the exchange of oxidants and antioxidants in lens epithelial cells undergoing oxidative stress. These transporting activities facilitated a reduction of intracellular reactive oxygen species (ROS) accumulation and maintained the intracellular glutathione (GSH) level through the exchange of redox metabolites and change of anti-oxidative gene expression. In addition, we show that Cx43 HCs can be regulated by the intracellular redox state and this regulation is mediated by residue Cys260 located at the Cx43 C-terminus. Together, our results demonstrate that Cx43 HCs activated by oxidative stress in the lens epithelial cells play a key role in maintaining redox homeostasis in lens under oxidative stress. Our findings contribute to advancing our understanding of oxidative stress induced lens disorders, such as age-related non-congenital cataracts.http://www.sciencedirect.com/science/article/pii/S2213231721002615ConnexinHemichannelRedox metaboliteRedox potentialOxidative damageLens
collection DOAJ
language English
format Article
sources DOAJ
author Yumeng Quan
Yu Du
Changrui Wu
Sumin Gu
Jean X. Jiang
spellingShingle Yumeng Quan
Yu Du
Changrui Wu
Sumin Gu
Jean X. Jiang
Connexin hemichannels regulate redox potential via metabolite exchange and protect lens against cellular oxidative damage
Redox Biology
Connexin
Hemichannel
Redox metabolite
Redox potential
Oxidative damage
Lens
author_facet Yumeng Quan
Yu Du
Changrui Wu
Sumin Gu
Jean X. Jiang
author_sort Yumeng Quan
title Connexin hemichannels regulate redox potential via metabolite exchange and protect lens against cellular oxidative damage
title_short Connexin hemichannels regulate redox potential via metabolite exchange and protect lens against cellular oxidative damage
title_full Connexin hemichannels regulate redox potential via metabolite exchange and protect lens against cellular oxidative damage
title_fullStr Connexin hemichannels regulate redox potential via metabolite exchange and protect lens against cellular oxidative damage
title_full_unstemmed Connexin hemichannels regulate redox potential via metabolite exchange and protect lens against cellular oxidative damage
title_sort connexin hemichannels regulate redox potential via metabolite exchange and protect lens against cellular oxidative damage
publisher Elsevier
series Redox Biology
issn 2213-2317
publishDate 2021-10-01
description Increased oxidative stress contributes to cataract formation during aging. Anterior epithelial cells are a frontline antioxidant defense system with powerful capacities to maintain redox homeostasis and lens transparency. In this study, we report a new molecular mechanism of connexin (Cx) hemichannels (HCs) in lens epithelial cells to protect lens against oxidative stress. Our results showed haploinsufficiency of Cx43 elevated oxidative stress and susceptibility to cataracts in the mouse lens. Cx43 HCs opened in response to hydrogen peroxide (H2O2) or ultraviolet radiation (UVR) in human lens epithelium HLE-B3 cells, and this activation contributed to a cellular protective mechanism against oxidative stress-induced apoptotic cell death. Furthermore, we found that Cx43 HCs mediated the exchange of oxidants and antioxidants in lens epithelial cells undergoing oxidative stress. These transporting activities facilitated a reduction of intracellular reactive oxygen species (ROS) accumulation and maintained the intracellular glutathione (GSH) level through the exchange of redox metabolites and change of anti-oxidative gene expression. In addition, we show that Cx43 HCs can be regulated by the intracellular redox state and this regulation is mediated by residue Cys260 located at the Cx43 C-terminus. Together, our results demonstrate that Cx43 HCs activated by oxidative stress in the lens epithelial cells play a key role in maintaining redox homeostasis in lens under oxidative stress. Our findings contribute to advancing our understanding of oxidative stress induced lens disorders, such as age-related non-congenital cataracts.
topic Connexin
Hemichannel
Redox metabolite
Redox potential
Oxidative damage
Lens
url http://www.sciencedirect.com/science/article/pii/S2213231721002615
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