诱导多能干细胞
材料科学
细胞生物学
细胞分化
生物物理学
细胞
生物
纳米技术
胚胎干细胞
生物化学
基因
作者
Parisa Pour Shahid Saeed Abadi,Jessica C. Garbern,Shahed Behzadi,Michael J. Hill,Jason S. Tresback,Tiam Heydari,Mohammad Reza Ejtehadi,Nafis Ahmed,Elizabeth Copley,Haniyeh Aghaverdi,Richard Lee,Omid C. Farokhzad,Morteza Mahmoudi
标识
DOI:10.1002/adfm.201707378
摘要
Abstract Producing mature and functional cardiomyocytes (CMs) by in vitro differentiation of induced pluripotent stem cells (iPSCs) using only biochemical cues is challenging. To mimic the biophysical and biomechanical complexity of the native in vivo environment during the differentiation and maturation process, polydimethylsiloxane substrates with 3D topography at the micrometer and sub‐micrometer levels are developed and used as cell‐culture substrates. The results show that while cylindrical patterns on the substrates resembling mature CMs enhance the maturation of iPSC‐derived CMs, sub‐micrometer‐level topographical features derived by imprinting primary human CMs further accelerate both the differentiation and maturation processes. The resulting CMs exhibit a more‐mature phenotype than control groups—as confirmed by quantitative polymerase chain reaction, flow cytometry, and the magnitude of beating signals—and possess the shape and orientation of mature CMs in human myocardium—as revealed by fluorescence microscopy, Ca 2+ flow direction, and mitochondrial distribution. The experiments, combined with a virtual cell model, show that the physico‐mechanical cues generated by these 3D‐patterned substrates improve the phenotype of the CMs via the reorganization of the cytoskeletal network and the regulation of chromatin conformation.
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