科研之友
微信
新浪微博
Facebook
分享链接
摘要
-Arrestins are multifunctional scaffolding proteins that modulate G protein-coupled receptor (GPCR)-dependent and -independent cell signaling pathways in various types of cells. We recently demonstrated that -arrestin1 (-arr1) deficiency strikingly attenuates dextran sodium sulfate (DSS)-induced colitis in mice. Since DSS-induced colitis is in part dependent on gut epithelial injury, we examined the role of -arr1 in intestinal epithelial cells (IECs) using a colon epithelial cell line, SW480 cells. Surprisingly, we found that knockdown of -arr1 in SW480 cells enhanced epithelial cell death via a caspase-3-dependent process. To understand the in vivo relevance and potential cell type-specific role of -arr1 in colitis development, we generated bone marrow chimeras with -arr1 deficiency in either the hematopoietic or non-hematopoietic compartment. Reconstituted chimeric mice were then subjected to DSS-induced colitis. Similar to our previous findings, -arr1 deficiency in the hematopoietic compartment protected mice from DSS-induced colitis. However, consistent with the role of -arr1 in epithelial apoptosis in vitro, non-hematopoietic -arr1 deficiency led to an exacerbated colitis phenotype. To further understand signaling mechanisms, we examined the effect of -arr1 on TNF--mediated NFB and MAPK pathways. Our results demonstrate that -arr1 has a critical role in modulating ERK, JNK and p38 MAPK pathways mediated by TNF- in IECs. Together, our results show that -arr1-dependent signaling in hematopoietic and non-hematopoietic cells differentially regulates colitis pathogenesis and further demonstrates that -arr1 in epithelial cells inhibits TNF--induced cell death pathways. J. Cell. Physiol. 231: 992-1000, 2016.
- 出版日期2016-5
