Bone Marrow Mesenchymal Stem Cells Stimulate Cardiac Stem Cell Proliferation and Differentiation

Author:

Hatzistergos Konstantinos E.1,Quevedo Henry1,Oskouei Behzad N.1,Hu Qinghua1,Feigenbaum Gary S.1,Margitich Irene S.1,Mazhari Ramesh1,Boyle Andrew J.1,Zambrano Juan P.1,Rodriguez Jose E.1,Dulce Raul1,Pattany Pradip M.1,Valdes David1,Revilla Concepcion1,Heldman Alan W.1,McNiece Ian1,Hare Joshua M.1

Affiliation:

1. From the Interdisciplinary Stem Cell Institute (K.E.H., H.Q., B.N.O., Q.H., G.S.F., I.S.M., J.P.Z., J.E.R., R.D., P.M.P., D.V., A.W.H., I.M., J.M.H.); and Cardiovascular Division, Department of Medicine (Q.H., J.P.Z., A.W.H., I.M., J.M.H.), Leonard M Miller School of Medicine, Miami, Fla; Division of Cardiology (R.M.), George Washington University, Washington DC; Division of Cardiology (A.J.B.), Department of Medicine, UCSF Heart and Vascular Center, University of California, San Francisco; and Dpto...

Abstract

Rationale: The regenerative potential of the heart is insufficient to fully restore functioning myocardium after injury, motivating the quest for a cell-based replacement strategy. Bone marrow–derived mesenchymal stem cells (MSCs) have the capacity for cardiac repair that appears to exceed their capacity for differentiation into cardiac myocytes. Objective: Here, we test the hypothesis that bone marrow derived MSCs stimulate the proliferation and differentiation of endogenous cardiac stem cells (CSCs) as part of their regenerative repertoire. Methods And Results: Female Yorkshire pigs (n=31) underwent experimental myocardial infarction (MI), and 3 days later, received transendocardial injections of allogeneic male bone marrow–derived MSCs, MSC concentrated conditioned medium (CCM), or placebo (Plasmalyte). A no-injection control group was also studied. MSCs engrafted and differentiated into cardiomyocytes and vascular structures. In addition, endogenous c-kit + CSCs increased 20-fold in MSC-treated animals versus controls ( P <0.001), there was a 6-fold increase in GATA-4 + CSCs in MSC versus control ( P <0.001), and mitotic myocytes increased 4-fold ( P =0.005). Porcine endomyocardial biopsies were harvested and plated as organotypic cultures in the presence or absence of MSC feeder layers. In vitro, MSCs stimulated c-kit + CSCs proliferation into enriched populations of adult cardioblasts that expressed Nkx2–5 and troponin I. Conclusions: MSCs stimulate host CSCs, a new mechanism of action underlying successful cell-based therapeutics.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

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