Human embryonic stem cell-derived microvascular grafts for cardiac tissue preservation after myocardial infarction
We present use of a synthetic, injectable matrix metalloproteinase (MMP)- responsive, bioactive hydrogel as an in situ forming scaffold to deliver thymosin beta 4 (T beta 4), a pro-angiogenic and pro-survival factor, along with vascular cells derived from human embryonic stem cells (hESC) in ischemic injuries to the heart in a rat model. The gel was found to substitute the degrading extracellular matrix in the infarcted myocardium of rats and to promote structural organization of native endothelial cells, while some of the delivered hESC-derived vascular cells formed de novo capillaries in the infarct zone. Magnetic resonance imaging (MRI) revealed that the microvascular grafts effectively preserved contractile performance 3 d and 6 wk after myocardial infarction, attenuated left ventricular dilation, and decreased infarct size as compared to infarcted rats treated with PBS injection as a control (3 d ejection fraction, + similar to 7%, P < 0.001; 6 wk ejection faction, + similar to 12%, P < 0.001). Elevation in vessel density was observed in response to treatment, which may be due in part to elevations in human (donor)-derived cytokines EGF, VEGF and HGF (1 d). Thus, a clinically relevant matrix for dual delivery of vascular cells and drugs may be useful in engineering sustained tissue preservation and potentially regenerating ischemic cardiac tissue. (c) 2010 Elsevier Ltd. All rights reserved.
Keywords: Hydrogel ; Biomimetic material ; Matrix metalloproteinase ; Cardiac tissue engineering ; Vascular grafts ; Stem cell ; Left-Ventricular Function ; Progenitor Cells ; Matrix Metalloproteinases ; Vascular Development ; In-Vivo ; Heart ; Cytokines ; Hydrogel ; Therapy ; Rats
Record created on 2011-12-16, modified on 2016-08-09