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MIC-1/GDF15 is a member of the TGF-b superfamily, which is thought to have pleiotropic roles in stress responses, inflammation, tissue injury and repair, energy homeostasis, and malignancy. MIC-1/GDF15 was recently identified as a new biomarker for the development of cardiovascular events and the outcome of atherosclerotic disease therapy. The aim of our study was to determine if MIC-1 also directly exerts pro- or antiatherogenic properties during the development of atherosclerosis. We investigated the effect of transgenic overexpression of MIC-1 in macrophages in the ApoE(-/-) mouse model of atherosclerosis. After 6 months of high-fat diet, MIC-1/GDF15 transgenic ApoE(-/-) mice had smaller atherosclerotic lesions; however, no differences in lesion composition, pro- or anti-inflammatory cytokine production, or serum levels of lipids or cytokines were detected. Our results suggest that MIC-1 has an overall protective effect on the disease process, but further studies will be required to define its mechanism of action. Copyright © 2012 Elsevier Inc. All rights reserved.

Citation

Heiko Johnen, Tamara Kuffner, David A Brown, Ben J Wu, Roland Stocker, Samuel N Breit. Increased expression of the TGF-b superfamily cytokine MIC-1/GDF15 protects ApoE(-/-) mice from the development of atherosclerosis. Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology. 2012 Nov-Dec;21(6):499-505

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PMID: 22386250

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