Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway

被引:117
作者
List, Karin [2 ]
Kosa, Peter
Szabo, Roman
Bey, Alexandra L.
Wang, Chao Becky [2 ]
Molinolo, Alfredo
Bugge, Thomas H. [1 ]
机构
[1] Natl Inst Dent & Craniofacial Res, Proteases & Tissue Remodeling Sect, Oral & Pharyngeal Canc Branch, NIH, Bethesda, MD 20892 USA
[2] Wayne State Univ, Sch Med, Dept Pharmacol, Barbara Ann Karmanos Canc Inst, Detroit, MI 48201 USA
关键词
HEPATOCYTE GROWTH-FACTOR; MACROPHAGE-STIMULATING PROTEIN; AUTOSOMAL RECESSIVE ICHTHYOSIS; EPIDERMAL BARRIER FUNCTION; SERINE-PROTEASE; HYPOTRICHOSIS SYNDROME; FACTOR ACTIVATOR; TIGHT JUNCTIONS; SODIUM-CHANNEL; CELL-SURFACE;
D O I
10.2353/ajpath.2009.090240
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
A pericellular proteolytic pathway initiated by the transmembrane serine protease matriptase plays a critical role in the terminal differentiation of epidermal tissues. Matriptase is constitutively expressed in multiple other epithelia, suggesting a putative role of this membrane serine protease in general epithelial homeostasis. Here we generated mice with conditional deletion of the St14 gene, encoding matriptase, and show that matriptase indeed is essential for the maintenance of multiple types of epithelia in the mouse. Thus, embryonic or postnatal ablation of St14 in epithelial tissues of diverse origin and function caused severe organ dysfunction, which was often associated with increased permeability, loss of tight junction function, mislocation of tight junction-associated proteins, and generalized epithelial demise. The study reveals that the homeostasis of multiple simple and stratified epithelia is matriptase-dependent, and provides an important animal model for the exploration of this membrane serine protease in a range of physiological and pathological processes. (Am J Pathol 2009, 175:1453-1463; DOI: 10.2353/ajpath.2009.090240)
引用
收藏
页码:1453 / 1463
页数:11
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