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机械激活的连接蛋白半通道介导细胞间谷胱甘肽转运并维持晶状体氧化还原稳态。

Mechano-activated connexin hemichannels mediate intercellular glutathione transport and support lens redox homeostasis.

作者信息

Wang Guangyan, Quan Yumeng, Ma Bo, Gu Sumin, Jiang Jean X

机构信息

Department of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX, 78229-3900, United States; Department of Ophthalmology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

Department of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX, 78229-3900, United States.

出版信息

Redox Biol. 2025 Jul 14;85:103767. doi: 10.1016/j.redox.2025.103767.

Abstract

Redox homeostasis and transparency in the ocular lens are closely associated with the distribution of the antioxidant reduced glutathione (GSH). While the synthesis and recycling of GSH have been well characterized, the mechanisms governing its intercellular transport within the lens remain largely elusive. Here, we identified a GSH transport pathway mediated by connexin (Cx) hemichannels in both lens epithelial and fiber cells that has not been fully characterized previously. Through a combination of fluid flow shear stress (FFSS) stimulation, in vitro and ex vivo models, and gene knockout mouse models, we demonstrate that Cx43 and Cx50 hemichannels in lens epithelial cells facilitate GSH efflux in response to mechanical stimuli. Notably, Cx43 hemichannels exhibited higher opening efficiency and greater GSH transport capacity than Cx50 hemichannels under FFSS. The extracellular GSH released from epithelial cells was then taken up by activated Cx50 hemichannels in fiber cells under FFSS, effectively reducing oxidative stress and promoting cell survival. This intercellular relay of GSH between epithelial and fiber cells via mechanosensitive Cx hemichannels suggests a novel mechanism for regulating redox balance within the lens. This pathway may be essential for preserving lens homeostasis and offers new insight into lens physiology and potential therapeutic strategies for preventing or delaying cataract formation.

摘要

眼晶状体中的氧化还原稳态和透明度与抗氧化剂还原型谷胱甘肽(GSH)的分布密切相关。虽然GSH的合成和循环已经得到了很好的表征,但其在晶状体细胞间运输的机制仍 largely难以捉摸。在这里,我们在晶状体上皮细胞和纤维细胞中鉴定了一种由连接蛋白(Cx)半通道介导的GSH运输途径,该途径以前尚未得到充分表征。通过流体流动剪切应力(FFSS)刺激、体外和离体模型以及基因敲除小鼠模型的组合,我们证明晶状体上皮细胞中的Cx43和Cx50半通道响应机械刺激促进GSH外流。值得注意的是,在FFSS下,Cx43半通道比Cx50半通道表现出更高的开放效率和更大的GSH运输能力。然后,上皮细胞释放的细胞外GSH在FFSS下被纤维细胞中活化的Cx50半通道摄取,有效降低氧化应激并促进细胞存活。这种通过机械敏感的Cx半通道在上皮细胞和纤维细胞之间进行的GSH细胞间传递提示了一种调节晶状体氧化还原平衡的新机制。该途径可能对维持晶状体稳态至关重要,并为晶状体生理学以及预防或延缓白内障形成的潜在治疗策略提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9d5/12283899/cc4e11c3da65/gr1.jpg

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