Desmoglein-2: A novel regulator of apoptosis in the intestinal epithelium

被引:96
作者
Nava, Porfirio
Laukoetter, Mike G.
Hopkins, Ann M.
Laur, Oskar
Gerner-Smidt, Kirsten
Green, Kathleen J.
Parkos, Charles A.
Nusrat, Asma [1 ]
机构
[1] Emory Univ, Epithelial Pathobiol Res Unit, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
[2] Univ Munster, Dept Gen Surg, D-48149 Munster, Germany
[3] Univ Coll Dublin, UCD Sch Med & Med Sci, Dublin 4, Ireland
[4] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
关键词
D O I
10.1091/mbc.E07-05-0426
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Intestinal epithelial intercellular junctions regulate barrier properties, and they have been linked to epithelial differentiation and programmed cell death (apoptosis). However, mechanisms regulating these processes are poorly defined. Desmosomes are critical elements of intercellular junctions; they are punctate structures made up of transmembrane desmosomal cadherins termed desmoglein-2 (Dsg2) and desmocollin-2 (Dsc2) that affiliate with the underlying intermediate filaments via linker proteins to provide mechanical strength to epithelia. In the present study, we generated an antibody, AH12.2, that recognizes Dsg2. We show that Dsg2 but not another desmosomal cadherin, Dsc2, is cleaved by cysteine proteases during the onset of intestinal epithelial cell (IEC) apoptosis. Small interfering RNA-mediated downregulation of Dsg2 protected epithelial cells from apoptosis. Moreover, we report that a C-terminal fragment of Dsg2 regulates apoptosis and Dsg2 protein levels. Our studies highlight a novel mechanism by which Dsg2 regulates IEC apoptosis driven by cysteine proteases during physiological differentiation and inflammation.
引用
收藏
页码:4565 / 4578
页数:14
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