Published online before print April 3, 2008, doi: 10.1161/CIRCRESAHA.108.174623
© 2008 American Heart Association, Inc.
Molecular Medicine |
Proteomic and Metabolomic Analysis of Smooth Muscle Cells Derived From the Arterial Media and Adventitial Progenitors of Apolipoprotein E–Deficient Mice
From the Cardiovascular Division (M.M., A.Z., A.S., U.M., X.Y., Y.H., Q.X.), King’s College, London; Department of Cardiac and Vascular Sciences (A.I.D.S.) and Department of Basic Medical Sciences (Y.-L.C.), St. George’s, University of London, United Kingdom; Cancer Research UK Cambridge Research Institute (J.R.G., B.M.), United Kingdom; and Gaubius Laboratory and Leiden University Medical Center (P.H.Q.), The Netherlands.
Correspondence to Dr Manuel Mayr, Cardiovascular Division, The James Black Centre, King’s College, University of London, 125 Coldharbour Ln, London SE5 9NU, United Kingdom. E-mail manuel.mayr{at}kcl.ac.uk
We have recently demonstrated that stem cell antigen 1–positive (Sca-1+) progenitors exist in the vascular adventitia of apolipoprotein E–deficient (apoE–/–) mice and contribute to smooth muscle cell (SMC) accumulation in vein graft atherosclerosis. Using a combined proteomic and metabolomic approach, we now characterize these local progenitors, which participate in the formation of native atherosclerotic lesions in chow-fed apoE–/– mice. Unlike Sca-1+ progenitors from embryonic stem cells, the resident Sca-1+ stem cell population from the vasculature acquired a mature aortic SMC phenotype after platelet-derived growth factor-BB stimulation. It shared proteomic and metabolomic characteristics of apoE–/– SMCs, which were clearly distinct from wild-type SMCs under normoxic and hypoxic conditions. Among the differentially expressed proteins were key enzymes in glucose metabolism, resulting in faster glucose consumption and a compensatory reduction in baseline interleukin-6 secretion. The latter was associated with a marked upregulation of insulin-like growth factor binding proteins (IGFBPs) 3 and 6. Notably, reconstitution of interleukin-6 to levels measured in the conditioned medium of wild-type SMCs attenuated the elevated IGFBP expression in apoE–/– SMCs and their vascular progenitors. This coregulation of apoE, interleukin-6, and IGFBPs was replicated in wild-type SMCs from hypercholesterolemic mice and confirmed by silencing apoE expression in SMCs from normocholesterolemic mice. In summary, we provide evidence that Sca-1+ progenitors contribute to native atherosclerosis in apoE–/– mice, that apoE deficiency and hypercholesterolemia alter progenitor cell behavior, and that inflammatory cytokines such as interleukin-6 act as metabolic regulators in SMCs of hyperlipidemic mice.
Key Words: atherosclerosis • insulin-like growth factor-1 • progenitor cells • proteomics • vascular smooth muscle
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