C(6)-Ceramide-Coated Catheters Promote Re-Endothelialization of Stretch-Injured Arteries.

Sean M O'Neill, Dina K Olympia, Todd E Fox, J Tony Brown, Thomas C Stover, Kristy L Houck, Ronald Wilson, Peter Waybill, Mark Kozak, Steven W Levison, Norbert Weber, Linda M Karavodin, Mark Kester
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引用次数: 9

Abstract

OBJECTIVE: Drug eluting stents have recently been associated with the increased risk of adverse thrombogenic events and/or late luminal loss, which is highly associated with incomplete re-endothelialization. The increased risks behoove the design of alternative delivery modalities and/or drugs that do not compromise the re-endotheliaization process. The objective of the present study is to elucidate the biological mechanism(s) by which non-stent-based delivery modalities for the anti-proliferative lipid metabolite, C(6)-ceramide, could lead to a reduction in arterial injury after angioplasty. RESULTS: Immunohistochemical studies in rabbit and porcine models suggest that C(6)-ceramide-coated balloon catheters limit arterial stenosis without inhibiting endothelial wound healing responses. Specifically, C(6)-ceramide-coated balloon catheters reduce internal elastica injury with a corresponding reduction in medial fracture length in a 28-day porcine coronary artery stretch model. In addition, C(6)-ceramide decreases the formation of the fibrin matrix to possibly augment the subsequent wound healing response. We hypothesized that differential metabolism of exogenous ceramide by coronary endothelial and smooth muscle cells could explain the apparent discrepancy between the anti-proliferative actions of ceramide and the pro-wound healing responses of ceramide. Human coronary artery endothelial cells (HCAEC), in contrast to human coronary artery smooth muscle cells (HCASMC), preferentially express ceramide kinase and form ceramide-1-phosphate, which promotes endothelial cell survival. CONCLUSION: Differential metabolism of ceramide between HCASMC and HCAEC offers a mechanism by which ceramide preferentially limits smooth muscle cell growth, in the presence of active wound healing. The combinatorial ability of ceramide to limit vascular smooth muscle proliferation and promote re-endothelialization, offers the potential for C(6)-ceramide-coated catheters to serve as adjuncts to stent-based modalities or as a stand-alone treatment.

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C(6)-神经酰胺涂层导管促进拉伸损伤动脉的再内皮化。
目的:药物洗脱支架最近与不良血栓形成事件和/或晚期腔内损失的风险增加相关,这与不完全再内皮化高度相关。增加的风险需要设计不危及再内皮化过程的替代给药方式和/或药物。本研究的目的是阐明抗增生性脂质代谢物C(6)-神经酰胺的非支架递送方式可能导致血管成形术后动脉损伤减少的生物学机制。结果:兔和猪模型的免疫组织化学研究表明,C(6)-神经酰胺包被球囊导管限制动脉狭窄,而不抑制内皮伤口愈合反应。具体来说,在28天的猪冠状动脉拉伸模型中,C(6)-神经酰胺涂层球囊导管减少了内部弹性损伤,相应减少了内侧骨折长度。此外,C(6)-神经酰胺减少纤维蛋白基质的形成,可能增强随后的伤口愈合反应。我们假设,冠状动脉内皮细胞和平滑肌细胞对外源性神经酰胺的代谢差异可以解释神经酰胺的抗增殖作用和促进伤口愈合反应之间的明显差异。人冠状动脉内皮细胞(HCAEC)与人冠状动脉平滑肌细胞(HCASMC)相比,优先表达神经酰胺激酶,形成神经酰胺-1-磷酸,促进内皮细胞存活。结论:神经酰胺在HCASMC和HCAEC之间的代谢差异提供了神经酰胺优先限制平滑肌细胞生长的机制,在主动伤口愈合的情况下。神经酰胺限制血管平滑肌增殖和促进再内皮化的组合能力,为C(6)-神经酰胺涂层导管作为支架治疗的辅助手段或作为独立治疗提供了潜力。
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