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Title: Omentum-derived stromal cells improve myocardial regeneration in pig post-infarcted heart through a potent paracrine mechanism

Journal Article · · Experimental Cell Research
; ; ; ;  [1];  [2];  [1];  [3]; ;  [1];  [4];  [5];  [6];  [2]; ; ;  [7];  [7]
  1. Medestea Research and Production Laboratories, Consorzio Carso, 70010 Valenzano, Bari (Italy)
  2. Department of Veterinary Medicine, University of Bari, 70010 Valenzano, Bari (Italy)
  3. Department of Surgery, Hospital 'F. Miulli' 70021 AcquaViva delle Fonti, Bari (Italy)
  4. Experimental Cardiovascular Medicine, Bristol Heart Institute, Bristol BS2 8WH (United Kingdom)
  5. Department of Pathology, University of Camerino, 63100 Ascoli Piceno (Italy)
  6. Department of Human Anatomy, University of Bari, 70125 Bari (Italy)
  7. Cellular Neurobiology Laboratory, Department of Cerebrovascular Diseases, Fondazione IRCCS Neurological Institute 'Carlo Besta', 20133 Milan (Italy)

Cell-based therapy could be a valid option to treat myocardial infarct (MI). Adipose-derived stromal cells (ADStCs) have demonstrated tissue regenerative potential including cardiomyogenesis. Omentum is an extremely rich source of visceral fat and its accumulation seems to correlate with cardiovascular diseases. We investigated the capacity of human fat Omentum-derived StCs (FOStCs) to affect heart function upon acute infarct in pigs induced by permanent ligation of the anterior interventricular artery (IVA). We demonstrated for the first time that the local injection of 50 x 10{sup 6} of FOStCs ameliorates the functional parameters of post-infarct heart. Most importantly, histology of FOStCs treated hearts demonstrated a substantial improvement of cardiomyogenesis. In culture, FOStCs produced an impressive number and amount of angiogenic factors and cytokines. Moreover, the conditioned medium of FOStCs (FOStCs-CM) stimulates in vitro cardiac endothelial cells (ECs) proliferation and vascular morphogenesis and inhibits monocytes, EC activation and cardiomyocyte apoptosis. Since FOStCs in vivo did not trans-differentiate into cardiomyocyte-like cells, we conclude that FOStCs efficacy was presumably mediated by a potent paracrine mechanism involving molecules that concomitantly improved angiogenesis, reduced inflammation and prevented cardiomyocytes death. Our results highlight for the first time the important role that human FOStCs may have in cardiac regeneration.

OSTI ID:
22209882
Journal Information:
Experimental Cell Research, Vol. 316, Issue 11; Other Information: Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0014-4827
Country of Publication:
United States
Language:
English