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Regulation of Connexin Gap Junctions and Hemichannels by Calcium and Calcium Binding Protein Calmodulin

Connexins are the structural components of gap junctions and hemichannels that mediate the communication and exchange of small molecules between cells, and between the intracellular and extracellular environment, respectively. Connexin (Cx) 46 is predominately expressed in lens fiber cells, where th...

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Autores principales: Hu, Zhengping, Riquelme, Manuel A., Gu, Sumin, Jiang, Jean X.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663298/
https://www.ncbi.nlm.nih.gov/pubmed/33147690
http://dx.doi.org/10.3390/ijms21218194
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author Hu, Zhengping
Riquelme, Manuel A.
Gu, Sumin
Jiang, Jean X.
author_facet Hu, Zhengping
Riquelme, Manuel A.
Gu, Sumin
Jiang, Jean X.
author_sort Hu, Zhengping
collection PubMed
description Connexins are the structural components of gap junctions and hemichannels that mediate the communication and exchange of small molecules between cells, and between the intracellular and extracellular environment, respectively. Connexin (Cx) 46 is predominately expressed in lens fiber cells, where they function in maintaining the homeostasis and transparency of the lens. Cx46 mutations are associated with impairment of channel function, which results in the development of congenital cataracts. Cx46 gap junctions and hemichannels are closely regulated by multiple mechanisms. Key regulators of Cx46 channel function include Ca(2+) and calmodulin (CaM). Ca(2+) plays an essential role in lens homeostasis, and its dysregulation causes cataracts. Ca(2+) associated CaM is a well-established inhibitor of gap junction coupling. Recent studies suggest that elevated intracellular Ca(2+) activates Cx hemichannels in lens fiber cells and Cx46 directly interacts with CaM. A Cx46 site mutation (Cx46-G143R), which is associated with congenital Coppock cataracts, shows an increased Cx46-CaM interaction and this interaction is insensitive to Ca(2+), given that depletion of Ca(2+) reduces the interaction between CaM and wild-type Cx46. Moreover, inhibition of CaM function greatly reduces the hemichannel activity in the Cx46 G143R mutant. These research findings suggest a new regulatory mechanism by which enhanced association of Cx46 with CaM leads to the increase in hemichannel activity and dysregulation may lead to cataract development. In this review, we will first discuss the involvement of Ca(2+)/CaM in lens homeostasis and pathology, and follow by providing a general overview of Ca(2+)/CaM in the regulation of Cx46 gap junctions. We discuss the most recent studies concerning the molecular mechanism of Ca(2+)/CaM in regulating Cx46 hemichannels. Finally, we will offer perspectives of the impacts of Ca(2+)/CaM and dysregulation on Cx46 channels and vice versa.
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spelling pubmed-76632982020-11-14 Regulation of Connexin Gap Junctions and Hemichannels by Calcium and Calcium Binding Protein Calmodulin Hu, Zhengping Riquelme, Manuel A. Gu, Sumin Jiang, Jean X. Int J Mol Sci Review Connexins are the structural components of gap junctions and hemichannels that mediate the communication and exchange of small molecules between cells, and between the intracellular and extracellular environment, respectively. Connexin (Cx) 46 is predominately expressed in lens fiber cells, where they function in maintaining the homeostasis and transparency of the lens. Cx46 mutations are associated with impairment of channel function, which results in the development of congenital cataracts. Cx46 gap junctions and hemichannels are closely regulated by multiple mechanisms. Key regulators of Cx46 channel function include Ca(2+) and calmodulin (CaM). Ca(2+) plays an essential role in lens homeostasis, and its dysregulation causes cataracts. Ca(2+) associated CaM is a well-established inhibitor of gap junction coupling. Recent studies suggest that elevated intracellular Ca(2+) activates Cx hemichannels in lens fiber cells and Cx46 directly interacts with CaM. A Cx46 site mutation (Cx46-G143R), which is associated with congenital Coppock cataracts, shows an increased Cx46-CaM interaction and this interaction is insensitive to Ca(2+), given that depletion of Ca(2+) reduces the interaction between CaM and wild-type Cx46. Moreover, inhibition of CaM function greatly reduces the hemichannel activity in the Cx46 G143R mutant. These research findings suggest a new regulatory mechanism by which enhanced association of Cx46 with CaM leads to the increase in hemichannel activity and dysregulation may lead to cataract development. In this review, we will first discuss the involvement of Ca(2+)/CaM in lens homeostasis and pathology, and follow by providing a general overview of Ca(2+)/CaM in the regulation of Cx46 gap junctions. We discuss the most recent studies concerning the molecular mechanism of Ca(2+)/CaM in regulating Cx46 hemichannels. Finally, we will offer perspectives of the impacts of Ca(2+)/CaM and dysregulation on Cx46 channels and vice versa. MDPI 2020-11-02 /pmc/articles/PMC7663298/ /pubmed/33147690 http://dx.doi.org/10.3390/ijms21218194 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hu, Zhengping
Riquelme, Manuel A.
Gu, Sumin
Jiang, Jean X.
Regulation of Connexin Gap Junctions and Hemichannels by Calcium and Calcium Binding Protein Calmodulin
title Regulation of Connexin Gap Junctions and Hemichannels by Calcium and Calcium Binding Protein Calmodulin
title_full Regulation of Connexin Gap Junctions and Hemichannels by Calcium and Calcium Binding Protein Calmodulin
title_fullStr Regulation of Connexin Gap Junctions and Hemichannels by Calcium and Calcium Binding Protein Calmodulin
title_full_unstemmed Regulation of Connexin Gap Junctions and Hemichannels by Calcium and Calcium Binding Protein Calmodulin
title_short Regulation of Connexin Gap Junctions and Hemichannels by Calcium and Calcium Binding Protein Calmodulin
title_sort regulation of connexin gap junctions and hemichannels by calcium and calcium binding protein calmodulin
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663298/
https://www.ncbi.nlm.nih.gov/pubmed/33147690
http://dx.doi.org/10.3390/ijms21218194
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