Selim Mohamed S, Matani Bayan R, Henry-Ojo Harry O, Narayanan S Priya, Somanath Payaningal R
Clinical and Experimental Therapeutics, College of Pharmacy, University of Georgia, Augusta, GA 30912, USA.
Department of Research, Veterans Affairs Augusta Health Care System, Augusta, GA 30912, USA.
Cells. 2025 Aug 29;14(17):1346. doi: 10.3390/cells14171346.
Claudin 5 (Cldn5) is a critical tight junction protein essential for maintaining paracellular barrier integrity across endothelial and epithelial cells in barrier-forming tissues, including the blood-brain barrier and blood-retinal barrier. Cldn5 plays a central role in regulating vascular permeability, immune responses, and tissue homeostasis. The complex distribution and organ-specific regulation of Cldn5 underscore its potential as a promising therapeutic target. This review comprehensively analyzes the role of Cldn5 in endothelial and epithelial barrier function, its regulation of vascular permeability, and the discrepancies in the literature regarding its expression, regulation, and function in both physiological and pathological conditions across multiple organ systems, including the retina, brain, lung, heart, gut, kidney, liver, skin, and peripheral nerves, while emphasizing its tissue-specific expression patterns. We discuss how both reduced and excessive expressions of Cldn5 can disrupt barrier integrity and contribute to the pathogenesis of ischemic retinopathies, neuroinflammation, cardiovascular injury, and other forms of barrier dysfunction. Furthermore, we explore the dual role of Cldn5 as both a biomarker and a therapeutic target, highlighting emerging strategies such as RNA silencing, pharmacological stabilizers, and transcriptional modulators in controlling barrier leakage in disease conditions.
紧密连接蛋白5(Cldn5)是一种关键的紧密连接蛋白,对于维持包括血脑屏障和血视网膜屏障在内的屏障形成组织中内皮细胞和上皮细胞间旁细胞屏障的完整性至关重要。Cldn5在调节血管通透性、免疫反应和组织稳态中发挥核心作用。Cldn5复杂的分布和器官特异性调节突出了其作为一个有前景的治疗靶点的潜力。本综述全面分析了Cldn5在内皮和上皮屏障功能中的作用、其对血管通透性的调节,以及文献中关于其在包括视网膜、脑、肺、心脏、肠道、肾脏、肝脏、皮肤和周围神经在内的多个器官系统的生理和病理条件下的表达、调节和功能的差异,同时强调了其组织特异性表达模式。我们讨论了Cldn5表达降低和过度如何破坏屏障完整性,并导致缺血性视网膜病变、神经炎症、心血管损伤和其他形式的屏障功能障碍的发病机制。此外,我们探讨了Cldn5作为生物标志物和治疗靶点的双重作用,强调了如RNA沉默、药理学稳定剂和转录调节剂等新兴策略在控制疾病状态下屏障渗漏方面的作用。