Secreted protease ADAMTS18 in development and disease

被引:8
作者
Nie, Jiahui [1 ]
Zhang, Wei [1 ]
机构
[1] East China Normal Univ, Minist Educ & Shanghai, Sch Life Sci, Key Lab Brain Funct Genom, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
ADAMTS18; Morphology; Organogenesis; Substrates; Regulators; Clinical practice; EXTRACELLULAR-MATRIX; BRANCHING MORPHOGENESIS; LACRIMAL GLAND; SUPER-ENHANCERS; CELL IDENTITY; FIBRONECTIN; FIBRILLIN-1; EXPRESSION; PROMOTES; DISINTEGRIN;
D O I
10.1016/j.gene.2023.147169
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
ADAMTS18 was identified in 2002 as a member of the ADAMTS family of 19 secreted Zinc-dependent metalloproteinases. Prior to 2016, ADAMTS18 was known as a candidate gene associated with a wide range of pathologies, particularly various malignancies and eye disorders. However, functions and substrates of ADAMTS18 in normal conditions were unknown. Since 2016, with the development of Adamts18 knockout models, many studies had been conducted on the Adamts18 gene in vivo. These studies revealed that ADAMTS18 is essential for the morphology and organogenesis of several epithelial organs (e.g., lung, kidney, breast, salivary glands, and lacrimal glands), vascular and neuronal systems, adipose tissue, and reproductive tracts. In this review, we describe the current understanding of ADAMTS18 and its substrates and regulators. Limitations in translating new findings on ADAMTS18 to clinical practice are also discussed.
引用
收藏
页数:12
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