Transplantation of Mesenchymal Stem Cells Improves Cardiac Function in a Rat Model of Dilated Cardiomyopathy

TLDR

Pluripotent mesenchymal stem cells can differentiate into cardiomyocytes and vascular endothelial cells, yet their therapeutic potency in dilated cardiomyopathy remains poorly understood. The study aimed to determine whether transplanted MSCs induce myogenesis and angiogenesis and thereby improve cardiac function in a rat model of DCM. MSCs were isolated from bone‑marrow aspirates of isogenic adult rats, expanded ex vivo, and injected into the myocardium five weeks after immunization. MSC transplantation increased capillary density, reduced myocardial fibrosis, and improved left‑ventricular function, likely through differentiation into cardiomyocytes and vascular cells and secretion of angiogenic, anti‑apoptotic, and mitogenic factors.

Abstract

Background— Pluripotent mesenchymal stem cells (MSCs) differentiate into a variety of cells, including cardiomyocytes and vascular endothelial cells. However, little information is available about the therapeutic potency of MSC transplantation in cases of dilated cardiomyopathy (DCM), an important cause of heart failure. Methods and Results— We investigated whether transplanted MSCs induce myogenesis and angiogenesis and improve cardiac function in a rat model of DCM. MSCs were isolated from bone marrow aspirates of isogenic adult rats and expanded ex vivo. Cultured MSCs secreted large amounts of the angiogenic, antiapoptotic, and mitogenic factors vascular endothelial growth factor, hepatocyte growth factor, adrenomedullin, and insulin-like growth factor-1. Five weeks after immunization, MSCs or vehicle was injected into the myocardium. Some engrafted MSCs were positive for the cardiac markers desmin, cardiac troponin T, and connexin-43, whereas others formed vascular structures and were positive for von Willebrand factor or smooth muscle actin. Compared with vehicle injection, MSC transplantation significantly increased capillary density and decreased the collagen volume fraction in the myocardium, resulting in decreased left ventricular end-diastolic pressure (11±1 versus 16±1 mm Hg, P <0.05) and increased left ventricular maximum dP / dt (6767±323 versus 5138±280 mm Hg/s, P <0.05). Conclusions— MSC transplantation improved cardiac function in a rat model of DCM, possibly through induction of myogenesis and angiogenesis, as well as by inhibition of myocardial fibrosis. The beneficial effects of MSCs might be mediated not only by their differentiation into cardiomyocytes and vascular cells but also by their ability to supply large amounts of angiogenic, antiapoptotic, and mitogenic factors.