归巢(生物学)
趋化因子受体
趋化因子受体
XCL2型
CCL21型
C-C趋化因子受体6型
20立方厘米
CCL25型
CCR1
生物
CCL13型
趋化因子
免疫学
淋巴细胞归巢受体
受体
分子生物学
免疫系统
细胞
生态学
生物化学
细胞粘附
遗传学
作者
Brian A. Zabel,William W. Agace,James J. Campbell,Heidi Heath,David Parent,Arthur I. Roberts,Ellen C. Ebert,Nasim Kassam,Shixin Qin,Maria Zovko,Gregory J. LaRosa,Lili Yang,Dulce Soler,Eugene C. Butcher,Paul Ponath,Christina M. Parker,David P. Andrew
标识
DOI:10.1084/jem.190.9.1241
摘要
TECK (thymus-expressed chemokine), a recently described CC chemokine expressed in thymus and small intestine, was found to mediate chemotaxis of human G protein-coupled receptor GPR-9-6/L1.2 transfectants. This activity was blocked by anti-GPR-9-6 monoclonal antibody (mAb) 3C3. GPR-9-6 is expressed on a subset of memory alpha4beta7(high) intestinal trafficking CD4 and CD8 lymphocytes. In addition, all intestinal lamina propria and intraepithelial lymphocytes express GPR-9-6. In contrast, GPR-9-6 is not displayed on cutaneous lymphocyte antigen-positive (CLA(+)) memory CD4 and CD8 lymphocytes, which traffic to skin inflammatory sites, or on other systemic alpha4beta7(-)CLA(-) memory CD4/CD8 lymphocytes. The majority of thymocytes also express GPR-9-6, but natural killer cells, monocytes, eosinophils, basophils, and neutrophils are GPR-9-6 negative. Transcripts of GPR-9-6 and TECK are present in both small intestine and thymus. Importantly, the expression profile of GPR-9-6 correlates with migration to TECK of blood T lymphocytes and thymocytes. As migration of these cells is blocked by anti-GPR-9-6 mAb 3C3, we conclude that GPR-9-6 is the principal chemokine receptor for TECK. In agreement with the nomenclature rules for chemokine receptors, we propose the designation CCR-9 for GPR-9-6. The selective expression of TECK and GPR-9-6 in thymus and small intestine implies a dual role for GPR-9-6/CCR-9, both in T cell development and the mucosal immune response.
科研通智能强力驱动
Strongly Powered by AbleSci AI