Transplantation of SNAP-treated adipose tissue-derived stem cells improves cardiac function and induces neovascularization after myocardium infarct in rats

Stem cell therapy has been considered a promise for damaged myocardial tissue. We have previously shown that S-nitroso-N-acetyl-D,L-penicillamine (SNAP) increases the expression of several muscular markers and VEGF in mesenchymal stem cells, indicating that transplantation of SNAP-treated cells coul...

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Veröffentlicht in:Experimental and molecular pathology 2011-04, Vol.90 (2), p.149-156
Hauptverfasser: Berardi, Gel R.M., Rebelatto, Carmen K., Tavares, Heloísa F., Ingberman, Max, Shigunov, Patrícia, Barchiki, Fabiane, Aguiar, Alessandra M., Miyague, Nelson I., Francisco, Julio C., Correa, Alejandro, Senegaglia, Alexandra C., Suss, Paula Hansen, Moutinho, José A., Sotomaior, Vanessa S., Nakao, Lia S., Brofman, Paulo S.
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Sprache:eng
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Zusammenfassung:Stem cell therapy has been considered a promise for damaged myocardial tissue. We have previously shown that S-nitroso-N-acetyl-D,L-penicillamine (SNAP) increases the expression of several muscular markers and VEGF in mesenchymal stem cells, indicating that transplantation of SNAP-treated cells could provide better functional outcomes. Here, we transplanted SNAP-treated adipose tissue-derived stem cells (ADSCs) in rat infarcted myocardium. After 30days, we observed a significant improvement of the ejection fraction in rats that received SNAP-treated ADSCs, compared with those that received untreated cells (p=0.008). Immunohistochemical reactions showed an increased expression of troponin T–C and von Willebrand factor, and organized vascular units in the infarcted area of tissue transplanted with treated ADSCs. SNAP exposure induced intracellular S-nitrosation, a decreased GSH/GSSG ratio, but did not increase cGMP levels. Collectively, these results indicate that SNAP alters the redox environment of ADSCs, possibly associated with a pre-differentiation state, which may improve cardiac function after transplantation.
ISSN:0014-4800
1096-0945
DOI:10.1016/j.yexmp.2010.11.005