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人类G蛋白偶联受体GPR-9-6/CC趋化因子受体9在肠道归巢性T淋巴细胞、黏膜淋巴细胞和胸腺细胞上选择性表达,是胸腺表达的趋化因子介导的趋化作用所必需的。

Human G protein-coupled receptor GPR-9-6/CC chemokine receptor 9 is selectively expressed on intestinal homing T lymphocytes, mucosal lymphocytes, and thymocytes and is required for thymus-expressed chemokine-mediated chemotaxis.

作者信息

Zabel B A, Agace W W, Campbell J J, Heath H M, Parent D, Roberts A I, Ebert E C, Kassam N, Qin S, Zovko M, LaRosa G J, Yang L L, Soler D, Butcher E C, Ponath P D, Parker C M, Andrew D P

机构信息

LeukoSite, Inc., Cambridge, Massachusetts 02142, USA.

出版信息

J Exp Med. 1999 Nov 1;190(9):1241-56. doi: 10.1084/jem.190.9.1241.

Abstract

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.

摘要

胸腺表达趋化因子(TECK)是一种最近发现的CC趋化因子,在胸腺和小肠中表达,被发现可介导人G蛋白偶联受体GPR-9-6/L1.2转染细胞的趋化作用。该活性被抗GPR-9-6单克隆抗体(mAb)3C3阻断。GPR-9-6在一部分记忆性α4β7(高表达)肠道归巢CD4和CD8淋巴细胞上表达。此外,所有肠固有层和上皮内淋巴细胞均表达GPR-9-6。相比之下,GPR-9-6不在迁移至皮肤炎症部位的皮肤淋巴细胞抗原阳性(CLA(+))记忆性CD4和CD8淋巴细胞上表达,也不在其他系统性α4β7(-)CLA(-)记忆性CD4/CD8淋巴细胞上表达。大多数胸腺细胞也表达GPR-9-6,但自然杀伤细胞、单核细胞、嗜酸性粒细胞、嗜碱性粒细胞和中性粒细胞为GPR-9-6阴性。GPR-9-6和TECK的转录本在小肠和胸腺中均有存在。重要的是,GPR-9-6的表达谱与血液T淋巴细胞和胸腺细胞向TECK的迁移相关。由于这些细胞的迁移被抗GPR-9-6 mAb 3C3阻断,我们得出结论,GPR-9-6是TECK的主要趋化因子受体。根据趋化因子受体的命名规则,我们提议将GPR-9-6命名为CCR-9。TECK和GPR-9-6在胸腺和小肠中的选择性表达意味着GPR-9-6/CCR-9在T细胞发育和黏膜免疫反应中具有双重作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/341d/2195678/ab0a6a822af7/JEM990293.f1.jpg

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