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Critical Reviews™ in Immunology

年間 6 号発行

ISSN 印刷: 1040-8401

ISSN オンライン: 2162-6472

The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two preceding years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) IF: 1.3 To calculate the five year Impact Factor, citations are counted in 2017 to the previous five years and divided by the source items published in the previous five years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) 5-Year IF: 2.6 The Eigenfactor score, developed by Jevin West and Carl Bergstrom at the University of Washington, is a rating of the total importance of a scientific journal. Journals are rated according to the number of incoming citations, with citations from highly ranked journals weighted to make a larger contribution to the eigenfactor than those from poorly ranked journals. Eigenfactor: 0.00079 The Journal Citation Indicator (JCI) is a single measurement of the field-normalized citation impact of journals in the Web of Science Core Collection across disciplines. The key words here are that the metric is normalized and cross-disciplinary. JCI: 0.24 SJR: 0.429 SNIP: 0.287 CiteScore™:: 2.7 H-Index: 81

Indexed in

G-Protein-Coupled Receptor Signaling, RGS Proteins, and Lymphocyte Function

巻 24, 発行 6, 2004, 16 pages
DOI: 10.1615/CritRevImmunol.v24.i6.20
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要約

The positioning of lymphocytes in immune organs and the migration of lymphocytes that occurs during normal immune surveillance and following immune activation depends on appropriate signaling through receptors that couple to heterotrimeric G-proteins. In addition other mediators that affect lymphocyte function, such as histamine, purine nucleosides, C5A, prostaglandins, leukotrienes, serotonin, epinephrine, opioids, and certain phospholipids, also signal through G-protein-coupled receptors (GPCRs). Downstream of heterotrimeric G-proteins are a limited number of downstream effectors, which, in turn, activate a large number of other signaling molecules, many of which are shared with other signaling pathways, such as those activated by antigen receptors, coreceptors, and adhesion receptors. Crucial to signaling through GPCRs are finely developed regulatory systems, which control the activation of heterotrimeric G-proteins and their interactions with their immediate downstream effectors. This review will focus on the overall importance of GPCR signaling in lymphocyte function and an upstream regulatory system present in lymphocytes, which fine tunes heterotrimeric G-protein signaling.

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