Platelet-specific TGFβ1 deficiency aggravates atherosclerosis, vascular inflammation, and hypercholesterolemia in mice

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Abstract

Atherosclerosis involves inflammatory and thrombotic mechanisms, to which both platelets and transforming growth factor β (TGFβ) contribute. The effect of platelet-derived TGFβ on atherosclerosis is, however, unknown and therefore investigated. Murine platelet-selective TGFβ-deficiency (plt-TGFβ -/- ) was created by a Pf4 -Cre approach, and an atherosclerotic mouse model was established by functional abrogation of Ldlr and 10-15 weeks of a high-fat diet in plt-TGFβ -/- mice and their non-plt-TGFβ -/- littermates. En face Oil Red O staining of the aorta showed more atherosclerotic lesion formation in plt-TGFβ -/- mice, with significant increases in both lesion size and lesion coverage of the total aortic area. Cryosections of the aortic root confirmed the aggravation of atherogenesis. Platelet-derived TGFβ deficiency increased circulating platelets and plasma levels of total cholesterol, LDL-cholesterol, and triglycerides after a 10 or 15 week high-fat diet period. RNA sequencing and proteomic analyses of the aorta showed signs of CD4 + T effector cell and macrophage activation in plt-TGFβ -/- mice. In conclusion, platelet-specific TGFβ deficiency aggravates atherosclerosis, via increasing arterial inflammation and plasma levels of cholesterol. Our findings demonstrate that platelet-derived TGFβ is prominently athero-protective.

Key points

  • Platelet-specific transforming growth factor β (TGFβ) deficiency markedly enhances atherosclerosis in a high-fat diet-fed murine model.

  • Platelet TGFβ deficiency aggravates hyperlipidemia, with further elevations of total cholesterol, LDL-cholesterol, and triglycerides.

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