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赫尔曼斯基-普德拉克综合征发病机制的新见解。

New insights into the pathogenesis of Hermansky-Pudlak syndrome.

作者信息

Li Wei, Hao Chan-Juan, Hao Zhen-Hua, Ma Jing, Wang Qiao-Chu, Yuan Ye-Feng, Gong Juan-Juan, Chen Yuan-Ying, Yu Jia-Ying, Wei Ai-Hua

机构信息

Beijing Key Laboratory for Genetics of Birth Defects, Beijing Pediatric Research Institute, Beijing Children's Hospital, Capital Medical University, Center of Rare Diseases, National Center for Children's Health, Beijing, China.

MOE Key Laboratory of Major Diseases in Children, Capital Medical University, Beijing, China.

出版信息

Pigment Cell Melanoma Res. 2022 May;35(3):290-302. doi: 10.1111/pcmr.13030. Epub 2022 Feb 13.

Abstract

Hermansky-Pudlak syndrome (HPS) is characterized by defects of multiple tissue-specific lysosome-related organelles (LROs), typically manifesting with oculocutaneous albinism or ocular albinism, bleeding tendency, and in some cases with pulmonary fibrosis, inflammatory bowel disease or immunodeficiency, neuropsychological disorders. Eleven HPS subtypes in humans and at least 15 subtypes in mice have been molecularly identified. Current understanding of the underlying mechanisms of HPS is focusing on the defective biogenesis of LROs. Compelling evidences have shown that HPS protein-associated complexes (HPACs) function in cargo transport, cargo recycling, and cargo removal to maintain LRO homeostasis. Further investigation on the molecular and cellular mechanism of LRO biogenesis and secretion will be helpful for better understanding of its pathogenesis and for the precise intervention of HPS.

摘要

赫尔曼斯基-普德拉克综合征(HPS)的特征是多种组织特异性溶酶体相关细胞器(LRO)存在缺陷,通常表现为眼皮肤白化病或眼白化病、出血倾向,在某些情况下还伴有肺纤维化、炎症性肠病或免疫缺陷、神经心理障碍。人类已在分子水平上鉴定出11种HPS亚型,小鼠中至少有15种亚型。目前对HPS潜在机制的理解集中在LRO生物发生缺陷上。有力证据表明,HPS蛋白相关复合物(HPAC)在货物运输、货物回收和货物清除中发挥作用,以维持LRO的稳态。进一步研究LRO生物发生和分泌的分子和细胞机制将有助于更好地理解其发病机制,并对HPS进行精准干预。

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