Carbon nanotube-based substrates promote cardiogenesis in brown adipose-derived stem cells via β1-integrin-dependent TGF-β1 signaling pathway

• Published in: International journal of nanomedicine 2016, Vol.11, p.4381-4395
• Main Authors: Sun, Hongyu, Mou, Yongchao, Li, Yi, Li, Xia, Chen, Zi, Duval, Kayla, Huang, Zhu, Dai, Ruiwu, Tang, Lijun, Tian, Fuzhou
• Format: Article
• Language: English
• Subjects: Bone marrow; brown adipose derived stem cells; Carbon; carbon nanotube; Cardiac function; cardiomyocytes; Cell adhesion & migration; Composite materials; Disease; Extracellular matrix; Heart attacks; Hospitals; Microscopy; Morphology; Nanomaterials; Original Research; Stem cells; TGF-β1; β1-integrin
• ISSN: 1178-2013; 1176-9114; 1178-2013
• DOI: 10.2147/IJN.S114357

Stem cell-based therapy remains one of the promising approaches for cardiac repair and regeneration. However, its applications are restricted by the limited efficacy of cardiac differentiation. To address this issue, we examined whether carbon nanotubes (CNTs) would provide an instructive extracellular microenvironment to facilitate cardiogenesis in brown adipose-derived stem cells (BASCs) and to elucidate the underlying signaling pathways. In this study, we systematically investigated a series of cellular responses of BASCs due to the incorporation of CNTs into collagen (CNT-Col) substrates that promoted cell adhesion, spreading, and growth. Moreover, we found that CNT-Col substrates remarkably improved the efficiency of BASCs cardiogenesis by using fluorescence staining and quantitative real-time reverse transcription-polymerase chain reaction. Critically, CNTs in the substrates accelerated the maturation of BASCs-derived cardiomyocytes. Furthermore, the underlying mechanism for promotion of BASCs cardiac differentiation by CNTs was determined by immunostaining, quantitative real-time reverse transcription-polymerase chain reaction, and Western blotting assay. It is notable that β1-integrin-dependent TGF-β1 signaling pathway modulates the facilitative effect of CNTs in cardiac differentiation of BASCs. Therefore, it is an efficient approach to regulate cardiac differentiation of BASCs by the incorporation of CNTs into the native matrix. Importantly, our findings can not only facilitate the mechanistic understanding of molecular events initiating cardiac differentiation in stem cells, but also offer a potentially safer source for cardiac regenerative medicine.