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Beyond Immune Cell Migration: The Emerging Role of the Sphingosine-1-phosphate Receptor S1PR4 as a Modulator of Innate Immune Cell Activation

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MEDIATORS OF INFLAMMATION
卷 2017, 期 -, 页码 -

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HINDAWI LTD
DOI: 10.1155/2017/6059203

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资金

  1. Deutsche Krebshilfe [70112451]
  2. Deutsche Forschungsgemeinschaft [SFB 1039, TP B04, TP B06]
  3. Else Kroner-Fresenius Foundation (EKFS)
  4. Research Training Groups Translational Research Innovation-Pharma (TRIP)
  5. Else Kroner-Fresenius-Graduate School (EKF-GK)

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The sphingolipid sphingosine-1-phosphate (S1P) emerges as an important regulator of immunity, mainly by signaling through a family of five specific G protein-coupled receptors (S1PR1-5). While S1P signaling generally has the potential to affect not only trafficking but also differentiation, activation, and survival of a diverse range of immune cells, the specific outcome depends on the S1P receptor repertoire expressed on a given cell. Among the S1PRs, S1PR4 is specifically abundant in immune cells, suggesting a major role of the S1P/S1PR4 axis in immunity. Recent studies indeed highlight its role in activation of immune cells, differentiation, and, potentially, trafficking. In this review, we summarize the emerging data that support a major role of S1PR4 in modulating immunity in humans and mice and discuss therapeutic implications.

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