趋化素样因子1在血管再狭窄中的作用及体外迁移实验研究进展

Advances in mechanism and in vitro cell migration experiments of chemokine like factor 1 involved in restenosis

  • 摘要: 血管平滑肌细胞(vascular smooth muscle cell,VSMC)迁移是血管术后内膜增生再狭窄病理进程的关键性阶段。趋化素样因子1(chemokine like factor 1,CKLF1)功能之一为调控VSMC迁移。传统体外迁移实验制约了VSMC的生长微环境,同样也降低了CKLF1调控VSMC迁移研究的可信级别;应用微流控技术可在体外重建VSMC微环境,表征VSMC在CKLF1作用下的迁移并探讨CKLF1调控VSMC的机制,进而在新细胞研究平台上,为再狭窄提供新的研究思路。

     

    Abstract: Vascular smooth muscle cell (VSMC) migration is an essential element in the development of restenosis. Data show that chemokine like factor 1 (CKLF1) has a pivotal role in mediating VSMC migration. This article reviews the mechanism and cell migration in vitro experiments of CKLF1 involved in restenosis. Current studies of VSMC are based on conventional cell culture approaches (e.g. culture dish and flask), which allow no control over the spatial/temporal distribution of the cells and biomolecules in vivo microenvironments. Microfluidics is a technology of manipulating and detecting fluids in the microscale. Due to its dimensionally comparable with biological cells and capabilities of defining local biophysical, biochemical and physiological cues, a microfluidic assay will be used to reconstruct more in vivo like cell culture models. It can also quantify VSMC migration and explore mechanism involved in VSMC migration. All in all, results obtained from this new assay will deepen our understanding of the pathophysiology function of CKLF1 and provide perspective strategies in the prevention of restenosis.

     

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