| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5605448 | International Journal of Cardiology | 2017 | 43 Pages | 
Abstract
												Our findings show that systemic sirolimus treatment effectively prevents SMC and EC proliferation in vivo without directly affecting these cells. Instead, sirolimus prevents neointima formation and re-endothelialization by attenuating the inflammatory response after injury with secondary effects on SMC and EC proliferation. Thus, despite a similar net effect, the mechanisms of systemic sirolimus treatment are largely different from the local effects achieved after application of sirolimus-eluting stents.
											Keywords
												BMPCα-SMAPDGF-BBSca-1Smooth muscle-like cellsstem cell antigen 1SMCCFSEmTORVCAM-1ICAM-1PCIDESDrug-eluting stentsinflammationα-smooth muscle actinNeointima formationSmooth muscle cellsprogenitor cellsEndothelial cellsSirolimusplatelet-derived growth factor-BBVascular endothelial growth factorVascular Endothelial Growth Factor (VEGF)Re-endothelializationpercutaneous coronary interventionIntercellular adhesion molecule 1mammalian target of rapamycinvascular cell adhesion protein 1Bone marrow transplantationcarboxyfluorescein succinimidyl ester
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											Authors
												Jan-Marcus Daniel, Jochen Dutzmann, Hannes Brunsch, Johann Bauersachs, Rüdiger Braun-Dullaeus, Daniel G. Sedding, 
											