Endoplasmic Reticulum Dysfunction: An Emerging Mechanism of Vitiligo Pathogenesis

被引:1
作者
Xie, Yongyi [1 ]
Wu, Nanhui [1 ]
Tang, Suwei [1 ]
Zhou, Zhiyu [1 ]
Chen, Jiashe [1 ]
Li, Jie [1 ]
Wu, Fei [1 ]
Xu, Mingyuan [1 ]
Xu, Xiaoxiang [1 ]
Liu, Yeqiang [1 ]
Ma, Xin [1 ,2 ,3 ]
机构
[1] Tongji Univ, Shanghai Skin Dis Hosp, Inst Dermatol, Sch Med, Shanghai, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Yueyang Hosp Integrated Tradit Chinese & Western M, Dept Dermatol, Shanghai, Peoples R China
[3] Shanghai Skin Dis Hosp, Inst Dermatol, Baode Rd 1278 St, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
vitiligo; endoplasmic reticulum; organelles; cellular interactions; oxidative stress; UNFOLDED PROTEIN RESPONSE; H2O2-INDUCED OXIDATIVE STRESS; ER STRESS; MELANOCYTE DEGENERATION; TYROSINASE EXPORT; CA2+ HOMEOSTASIS; UP-REGULATION; TNF-ALPHA; SKIN; MORPHOLOGY;
D O I
10.2147/CCID.S459070
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The endoplasmic reticulum (ER) is the main site of protein synthesis, transport, and modification. Its abnormal status has now emerged as an established cause of many pathological processes, such as tumors and autoimmune diseases. Recent studies also demonstrated that the defective functions of ER may lead to pigmentary diseases. Vitiligo is a depigmenting ailment skin disorder whose pathogenesis is now found to be associated with ER. However, the detailed mechanism is still unclear. In this review, we try to link the association between ER with its inter- and intra-organellar interactions in vitiligo pathogenesis and focus on the function, mechanism, and clinical potential of ER with vitiligo. Expand ER is found in melanocytes of vitiligo and ER stress (ERS) might be a bridge between oxidative stress and innate and adaptive immunity. Meanwhile, the tight association between ER and mitochondria or melanosomes in organelles levels, as well as genes and cytokines, is the new paradigm in the pathogenesis of vitiligo. This undoubtedly adds a new aspect to the understanding of vitiligo, facilitating the design of targeted therapies for vitiligo.
引用
收藏
页码:1133 / 1144
页数:12
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