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Identification of CCR8: a human monocyte and thymus receptor for the CC chemokine I-309.


ABSTRACT: The human CC chemokine I-309 is a potent monocyte chemoattractant and inhibits apoptosis in thymic cell lines. Here, we identify a specific human I-309 receptor, and name it CCR8 according to an accepted nomenclature system. The receptor has seven predicted transmembrane domains, is expressed constitutively in monocytes and thymus, and is encoded by a previously reported gene of previously unknown function named, alternatively, CY6, TER1, and CKR-L1. After transfection with the CY6 open reading frame, a mouse pre-B cell line exhibited calcium flux and chemotaxis in response to I-309 (EC50 = 2 nM for each), whereas 20 other chemokines were inactive. Signaling was sensitive to pertussis toxin, suggesting coupling to a Gi-type G protein. These properties parallel those of endogenous I-309 receptors expressed in an HL-60 clone 15 cell line model. The apparent monogamous relationship between I-309 and CCR8 is unusual among known CC chemokines and known CC chemokine receptors. CCR8 may regulate monocyte chemotaxis and thymic cell line apoptosis.

SUBMITTER: Tiffany HL 

PROVIDER: S-EPMC2198957 | biostudies-literature | 1997 Jul

REPOSITORIES: biostudies-literature

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Identification of CCR8: a human monocyte and thymus receptor for the CC chemokine I-309.

Tiffany H L HL   Lautens L L LL   Gao J L JL   Pease J J   Locati M M   Combadiere C C   Modi W W   Bonner T I TI   Murphy P M PM  

The Journal of experimental medicine 19970701 1


The human CC chemokine I-309 is a potent monocyte chemoattractant and inhibits apoptosis in thymic cell lines. Here, we identify a specific human I-309 receptor, and name it CCR8 according to an accepted nomenclature system. The receptor has seven predicted transmembrane domains, is expressed constitutively in monocytes and thymus, and is encoded by a previously reported gene of previously unknown function named, alternatively, CY6, TER1, and CKR-L1. After transfection with the CY6 open reading  ...[more]

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