4.7 Article

Autoimmune animal models in the analysis of the CD47-SIRPα signaling pathway

期刊

METHODS
卷 65, 期 2, 页码 254-259

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymeth.2013.09.016

关键词

Autoimmunity; CD47; Dendritic cells; EAE; SIRP alpha

资金

  1. Ministry of Education, Culture, Sports, Science, and Technology of Japan
  2. Grants-in-Aid for Scientific Research [24111508, 23370061] Funding Source: KAKEN

向作者/读者索取更多资源

Signal regulatory protein alpha (SIRP alpha), also known as SHPS-1/SIRPA, is an immunoglobulin superfamily protein that binds to the protein tyrosine phosphatases Shp1 and Shp2 through its cytoplasmic region and is predominantly expressed in dendritic cells and macrophages. CD47, a widely expressed transmembrane protein, is a ligand for SIRPa, with the two proteins constituting a cell-cell communication system. It was previously demonstrated that the CD47-SIRP alpha signaling pathway is important for prevention of clearance by splenic macrophages of red blood cells or platelets from the bloodstream. In addition, this signaling pathway is also implicated in homeostatic regulation of dendritic cells and development of autoimmunity. Here we describe the detailed protocols for methods that were used in our recent studies to study the role of the CD47-SIRP alpha signaling pathway in autoimmunity. We also demonstrate that hematopoietic SIRPa as well as nonhematopoietic CD47 are important for development of experimental autoimmune encephalomyelitis. Thus, we here strengthen the importance of experimental animal models as well as other methods for the study of molecular pathogenesis of autoimmunity. (C) 2013 Elsevier Inc. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据