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生物物理线索对重编程为心肌细胞的影响。

Effect of biophysical cues on reprogramming to cardiomyocytes.

机构信息

Department of Bioengineering, University of California, Berkeley, USA; UC Berkeley & UCSF Joint Graduate Program in Bioengineering, Berkeley, San Francisco, USA.

Gladstone Institute of Cardiovascular Disease, University of California, San Francisco, USA.

出版信息

Biomaterials. 2016 Oct;103:1-11. doi: 10.1016/j.biomaterials.2016.06.034. Epub 2016 Jun 23.

Abstract

Reprogramming of fibroblasts to cardiomyocytes offers exciting potential in cell therapy and regenerative medicine, but has low efficiency. We hypothesize that physical cues may positively affect the reprogramming process, and studied the effects of periodic mechanical stretch, substrate stiffness and microgrooved substrate on reprogramming yield. Subjecting reprogramming fibroblasts to periodic mechanical stretch and different substrate stiffness did not improve reprogramming yield. On the other hand, culturing the cells on microgrooved substrate enhanced the expression of cardiomyocyte genes by day 2 and improved the yield of partially reprogrammed cells at day 10. By combining microgrooved substrate with an existing optimized culture protocol, yield of reprogrammed cardiomyocytes with striated cardiac troponin T staining and spontaneous contractile activity was increased. We identified the regulation of Mkl1 activity as a new mechanism by which microgroove can affect reprogramming. Biochemical approach could only partially recapitulate the effect of microgroove. Microgroove demonstrated an additional effect of enhancing organization of sarcomeric structure, which could not be recapitulated by biochemical approach. This study provides insights into new mechanisms by which topographical cues can affect cellular reprogramming.

摘要

将成纤维细胞重编程为心肌细胞在细胞治疗和再生医学中具有令人兴奋的潜力,但效率很低。我们假设物理线索可能会对重编程过程产生积极影响,并研究了周期性机械拉伸、基质硬度和微槽基底对重编程效率的影响。将重编程的成纤维细胞暴露于周期性机械拉伸和不同的基质硬度下并没有提高重编程的效率。另一方面,在微槽基底上培养细胞可以在第 2 天增强心肌细胞基因的表达,并在第 10 天提高部分重编程细胞的产量。通过将微槽基底与现有的优化培养方案相结合,可以增加具有横纹肌钙蛋白 T 染色和自发收缩活性的重编程心肌细胞的产量。我们确定了 Mkl1 活性的调节是微槽可以影响重编程的新机制。生化方法只能部分再现微槽的效果。微槽还显示出增强肌节结构组织的额外作用,这是生化方法无法再现的。这项研究为地形线索影响细胞重编程的新机制提供了深入了解。

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