Literature DB >> 33523201

KATP Opener Attenuates Diabetic-Induced Müller Gliosis and Inflammation by Modulating Kir6.1 in Microglia.

Hong Li1,2, Donglong Chen2, Wei Sun3, Jiansu Chen1,2, Chang Luo1,2, Heping Xu1,2,4, Jacey Hongjie Ma1,2, Shibo Tang1,2,5.   

Abstract

Purpose: This study aimed to determine the effect of pinacidil, a nonselective KATP channel opener, on diabetes-induced retinal gliosis and inflammation.
Methods: Primary and immortalized cell lines of retinal microglia and Müller cells were used to set up a coculture model. In the trans-well system, microglia were seeded in the upper chamber and Müller cells in the bottom chamber. Microglia were polarized into proinflammatory (M1, with lipopolysaccharide and INF-γ) with or without different pinacidil concentrations before coculturing with Müller cells. The expression of inflammatory or anti-inflammatory genes and protein in microglia, and the expression of glial fibrillary acidic protein (GFAP), Kir4.1, and AQP4 in Müller cells were examined by real-time polymerase chain reaction and Western blot. Pinacidil was injected intravitreally into streptozotocin-induced diabetic rats. Retinal gliosis and inflammation were examined by immunohistochemistry and Western blot.
Results: Intravitreal injection of pinacidil alleviated diabetes-induced Müller cell gliosis and microglial activation and reduced vascular endothelial growth factor expression. In vitro study demonstrated that pinacidil inhibited tumor necrosis factor and interleukin-1β expression in M1-type microglia and alleviated the M1 microglia-induced GFAP expression in the Müller cells. Furthermore, we found that pinacidil on its own, or in combination with IL-4, can upregulate arginase-1 (Arg-1) and Kir6.1 expression in microglial cells. Conclusions: Our results suggest that potassium channels are critically involved in diabetes-induced gliosis and microglial activation. The KATP opener, pinacidil, can reduce microglial activation by upregulating Kir6.1 expression.

Entities:  

Year:  2021        PMID: 33523201      PMCID: PMC7862730          DOI: 10.1167/iovs.62.2.3

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  29 in total

1.  Isolation and culture of retinal microglia.

Authors:  R S Roque; R B Caldwell
Journal:  Curr Eye Res       Date:  1993-03       Impact factor: 2.424

2.  Expression of aquaporin 4 and Kir4.1 in diabetic rat retina: treatment with minocycline.

Authors:  Y Zhang; G Xu; Q Ling; C Da
Journal:  J Int Med Res       Date:  2011       Impact factor: 1.671

Review 3.  Modulation of microglia in the retina: new insights into diabetic retinopathy.

Authors:  Ana I Arroba; Ángela M Valverde
Journal:  Acta Diabetol       Date:  2017-03-27       Impact factor: 4.280

Review 4.  Mechanisms of macular edema: Beyond the surface.

Authors:  Alejandra Daruich; Alexandre Matet; Alexandre Moulin; Laura Kowalczuk; Michaël Nicolas; Alexandre Sellam; Pierre-Raphaël Rothschild; Samy Omri; Emmanuelle Gélizé; Laurent Jonet; Kimberley Delaunay; Yvonne De Kozak; Marianne Berdugo; Min Zhao; Patricia Crisanti; Francine Behar-Cohen
Journal:  Prog Retin Eye Res       Date:  2017-11-07       Impact factor: 21.198

5.  Functional K(ATP) channels in the rat retinal microvasculature: topographical distribution, redox regulation, spermine modulation and diabetic alteration.

Authors:  Eisuke Ishizaki; Masanori Fukumoto; Donald G Puro
Journal:  J Physiol       Date:  2009-03-16       Impact factor: 5.182

6.  Interaction between microglia and retinal pigment epithelial cells determines the integrity of outer blood-retinal barrier in diabetic retinopathy.

Authors:  Dong Hyun Jo; Jang-Hyuk Yun; Chang Sik Cho; Jin Hyoung Kim; Jeong Hun Kim; Chung-Hyun Cho
Journal:  Glia       Date:  2018-11-16       Impact factor: 7.452

7.  Kir6.1 knockdown aggravates cerebral ischemia/reperfusion-induced neural injury in mice.

Authors:  Yin-Feng Dong; Lin-Xiao Wang; Xu Huang; Wen-Jing Cao; Ming Lu; Jian-Hua Ding; Xiu-Lan Sun; Gang Hu
Journal:  CNS Neurosci Ther       Date:  2013-05-11       Impact factor: 5.243

Review 8.  ATP-sensitive potassium channels: a promising target for protecting neurovascular unit function in stroke.

Authors:  Xiu-Lan Sun; Gang Hu
Journal:  Clin Exp Pharmacol Physiol       Date:  2009-04-27       Impact factor: 2.557

9.  Differential Kv1.3, KCa3.1, and Kir2.1 expression in "classically" and "alternatively" activated microglia.

Authors:  Hai M Nguyen; Eva M Grössinger; Makoto Horiuchi; Kyle W Davis; Lee-Way Jin; Izumi Maezawa; Heike Wulff
Journal:  Glia       Date:  2016-10-03       Impact factor: 7.452

10.  Microglia-derived IL-1β promotes chemokine expression by Müller cells and RPE in focal retinal degeneration.

Authors:  Riccardo Natoli; Nilisha Fernando; Michele Madigan; Joshua A Chu-Tan; Krisztina Valter; Jan Provis; Matt Rutar
Journal:  Mol Neurodegener       Date:  2017-04-24       Impact factor: 14.195

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  2 in total

Review 1.  Contribution of Müller Cells in the Diabetic Retinopathy Development: Focus on Oxidative Stress and Inflammation.

Authors:  Raul Carpi-Santos; Ricardo A de Melo Reis; Flávia Carvalho Alcantara Gomes; Karin C Calaza
Journal:  Antioxidants (Basel)       Date:  2022-03-23

2.  Diabetes-Independent Retinal Phenotypes in an Aldose Reductase Transgenic Mouse Model.

Authors:  Jonathan Mark Petrash; Biehuoy Shieh; David A Ammar; Michelle G Pedler; David J Orlicky
Journal:  Metabolites       Date:  2021-07-10
  2 in total

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