Litcius/Paper detail

Matrix stiffness regulates myocardial differentiation of human umbilical cord mesenchymal stem cells

Yingying Sun, Jingwei Liu, Ziran Xu, Xiaoxuan Lin, Xiaoling Zhang, Lisha Li, Yulin Li

2020Aging49 citationsDOIOpen Access PDF

Abstract

Myocardial infarction is a cardiovascular disease with high mortality. Human umbilical cord mesenchymal stem cells (hUC-MSCs) with strong self-renewal capacity and multipotency, provide the possibility of replacing injured cardiomyocytes. hUC-MSCs were cultured on polyacrylamide hydrogels with stiffnesses corresponding to Young's modulus of 13-16kPa and 62-68kPa which mimic the stiffnesses of healthy heart tissue and fibrotic myocardium. The expression of early myocardial markers Nkx2.5, GATA4, Mesp1 and the mature myocardial markers cTnT, cTnI, α-actin were detected by RT-PCR and Western Blot, which showed that soft matrix (13-16 kPa) tended to induce the differentiation of hUC-MSCs into myocardium, compared with stiff matrix (62-68 kPa). Piezos are mechanically sensitive non-selective cation channels. The expression of Piezo1 increased with the stiffness gradient of 1-10kPa, 13-16kPa, 35-38kPa and 62-68kPa on the 1st day, but Piezo2 expression was irregular. The expression of integrin β1 and calcium ions were also higher on stiff substrate than on soft substrate. hUC-MSCs tend to differentiate into myocardium on the matrix stiffness of 13-16 kPa. The relationship among matrix stiffness, Piezo1 and myocardial differentiation needs further validation.

Topics & Concepts

Mesenchymal stem cellUmbilical cordExtracellular matrixMyocardial infarctionMatrix (chemical analysis)Cell biologyTroponin complexStem cellBiomedical engineeringChemistryCardiologyAnatomyMedicineBiologyTroponin IChromatographyCellular Mechanics and InteractionsErythrocyte Function and PathophysiologyElectrospun Nanofibers in Biomedical Applications