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确定免疫细胞迁移的模式。

Specifying the patterns of immune cell migration.

作者信息

Cyster Jason G

机构信息

Howard Hughes Medical Institute and Department of Microbiology and Immunology, University of California, San Francisco, CA 94143, USA.

出版信息

Novartis Found Symp. 2007;281:54-61; discussion 61-4, 208-9. doi: 10.1002/9780470062128.ch6.

Abstract

Immune system function depends on getting the right cells to the right place at the right time. Inadequate or inappropriate migration of immune cells is involved in many and perhaps all types of immunological disease. Chemokines have been identified as critical guidance factors that help recruit and position cells at each stage of the immune response. Two-photon imaging of intact lymphoid organs has provided evidence of chemotactic migration of lymphocytes in lymphoid organs. Our work on the role of chemokines as organizers of lymphoid tissues will be briefly summarized. Lymphocyte egress from lymphoid organs is necessary for immune surveillance and for effector cell trafficking to sites of inflammation. Sphingosine-1-phosphate (SIP) receptor 1 and the circulatory lipid, S1P, are required for lymphocyte egress from lymphoid organs. We have recently identified CD69 as a regulator of SIP1 and controller of lymphocyte egress. Current molecular understanding of the lymphocyte egress process will be discussed.

摘要

免疫系统的功能依赖于在正确的时间将合适的细胞输送到正确的位置。免疫细胞迁移不足或不恰当与许多甚至可能所有类型的免疫疾病都有关。趋化因子已被确定为关键的导向因子,有助于在免疫反应的每个阶段招募细胞并使其定位。对完整淋巴器官的双光子成像已提供了淋巴细胞在淋巴器官中趋化迁移的证据。我们关于趋化因子作为淋巴组织组织者作用的研究工作将作简要总结。淋巴细胞从淋巴器官逸出对于免疫监视以及效应细胞向炎症部位的运输是必要的。鞘氨醇-1-磷酸(SIP)受体1和循环脂质S1P是淋巴细胞从淋巴器官逸出所必需的。我们最近已确定CD69是SIP1的调节因子以及淋巴细胞逸出的控制器。将讨论目前对淋巴细胞逸出过程的分子理解。

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