4.4 Article

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

期刊

MOLECULAR BIOLOGY OF THE CELL
卷 18, 期 11, 页码 4565-4578

出版社

AMER SOC CELL BIOLOGY
DOI: 10.1091/mbc.E07-05-0426

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  1. NCI NIH HHS [R01 CA-122151, R01 CA122151] Funding Source: Medline
  2. NIDDK NIH HHS [R01 DK072564, DK-55679, R24 DK064399, DK-61379, DK-59888, R01 DK055679, DK-64399, R01 DK061379, R01 DK059888, DK-72564, R29 DK055679] Funding Source: Medline

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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.

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