4.6 Article

Chemokine-like receptor 1 expression and Chemerin-directed chemotaxis distinguish plasmacytoid from myeloid dendritic cells in human blood

Journal

JOURNAL OF IMMUNOLOGY
Volume 174, Issue 1, Pages 244-251

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.174.1.244

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Funding

  1. NHLBI NIH HHS [HL 67674, HL 57492] Funding Source: Medline
  2. NIAID NIH HHS [AI 47822, AI 37832, 5T32 AI 07290-15] Funding Source: Medline
  3. NIDDK NIH HHS [DK 56339] Funding Source: Medline
  4. NIGMS NIH HHS [GM 37734] Funding Source: Medline
  5. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [P01HL067674, R01HL057492, P50HL067674] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [T32AI007290, R21AI047822, R37AI047822, R01AI047822, R01AI037832] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P30DK056339] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM037734, R37GM037734] Funding Source: NIH RePORTER

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Plasmacytoid dendritic cells (pDCs) are versatile cells of the immune response, secreting type I IFNs and differentiating into potent immunogenic or tolerogenic AM. pDCs can express adhesion and chemokine receptors for lymphoid tissues, but are also recruited by unknown mechanisms during tissue inflammation. We use a novel mAb specific for serpentine chemokine-like receptor 1 (CMKLR1) to evaluate its expression by circulating leukocytes in humans. We show that CMKLR1 is expressed by circulating pDCs in human blood, whereas myeloid DCs (mDCs) as well as lymphocytes, monocytes, neutrophils, and eosinophils are negative. We identify a major serum agonist activity for CMKLR1 as chemerin, a proteolytically activated attractant and the sole known ligand for CMKLR1, and we show that chemerin is activated during blood coagulation and attracts pDC but not mDC in ex vivo chemotaxis assays. We conclude that CMKLR1 expression and chemerin-mediated chemotaxis distinguish circulating pDCs from mDCs, providing a potential mechanism for their differential contribution to or regulation of immune responses at sites of bleeding or inflammatory protease activity. The

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