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CalDAG-GEFI Deficiency Reduces Atherosclerotic Lesion Development in Mice
Author(s) -
Yacine Boulaftali,
A. Phillip Owens,
Ashley Beale,
Raymond Piatt,
Caterina Casari,
Robert H. Lee,
Pamela B. Conley,
David S. Paul,
Nigel Mackman,
Wolfgang Bergmeier
Publication year - 2016
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.115.306347
Subject(s) - lesion , medicine , cardiology , pathology
Platelets are important for the development and progression of atherosclerotic lesions. However, relatively little is known about the contribution of platelet signaling to this pathological process. Our recent work identified 2 independent, yet synergistic, signaling pathways that lead to the activation of the small GTPase Rap1; one mediated by the guanine nucleotide exchange factor, CalDAG-GEFI (CDGI), the other by P2Y12, a platelet receptor for adenosine diphosphate and the target of antiplatelet drugs. In this study, we evaluated lesion formation in atherosclerosis-prone low-density lipoprotein receptor deficient (Ldlr(-/-)) mice lacking CDGI or P2Y12 in hematopoietic cells.

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