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未折叠蛋白反应:伤口愈合中的动态机制

Unfolded protein responses: Dynamic machinery in wound healing.

作者信息

Minjares Morgan, Thepsuwan Pattaraporn, Zhang Kezhong, Wang Jie-Mei

机构信息

Department of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, USA.

Centers for Molecular Medicine and Genetics, Wayne State University, USA.

出版信息

Pharmacol Ther. 2025 Mar;267:108798. doi: 10.1016/j.pharmthera.2025.108798. Epub 2025 Jan 17.

Abstract

Skin wound healing is a dynamic process consisting of multiple cellular and molecular events that must be tightly coordinated to repair the injured tissue efficiently. The healing pace is decided by the type of injuries, the depth and size of the wounds, and whether wound infections occur. However, aging, comorbidities, genetic factors, hormones, and nutrition also impact healing outcomes. During wound healing, cells undergo robust processes of synthesizing new proteins and degrading multifunctional proteins. This imposes an increasing burden on the endoplasmic reticulum (ER), causing ER stress. Unfolded protein response (UPR) represents a collection of highly conserved stress signaling pathways originated from the ER to maintain protein homeostasis and modulate cell physiology. UPR is known to be beneficial for tissue healing. However, when excessive ER stress exceeds ER's folding potential, UPR pathways trigger cell apoptosis, interrupting tissue regeneration. Understanding how UPR pathways modulate the skin's response to injuries is critical for new interventions toward the control of acute and chronic wounds. Herein, in this review, we focus on the participation of the canonical and noncanonical UPR pathways during different stages of wound healing, summarize the available evidence demonstrating UPR's unique position in balancing homeostasis and pathophysiology of healing tissues, and highlight the understudied areas where therapeutic opportunities may arise.

摘要

皮肤伤口愈合是一个动态过程,由多个细胞和分子事件组成,这些事件必须紧密协调才能有效地修复受损组织。愈合速度取决于损伤类型、伤口深度和大小,以及是否发生伤口感染。然而,衰老、合并症、遗传因素、激素和营养也会影响愈合结果。在伤口愈合过程中,细胞会经历合成新蛋白质和降解多功能蛋白质的强大过程。这给内质网(ER)带来了越来越大的负担,导致内质网应激。未折叠蛋白反应(UPR)代表了一系列高度保守的应激信号通路,这些通路源自内质网,以维持蛋白质稳态并调节细胞生理。已知UPR对组织愈合有益。然而,当过度的内质网应激超过内质网的折叠潜力时,UPR通路会触发细胞凋亡,中断组织再生。了解UPR通路如何调节皮肤对损伤的反应对于控制急性和慢性伤口的新干预措施至关重要。在此综述中,我们重点关注经典和非经典UPR通路在伤口愈合不同阶段的参与情况,总结现有证据,证明UPR在平衡愈合组织的稳态和病理生理学方面的独特地位,并强调尚未充分研究但可能产生治疗机会的领域。

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