The Nephroprotective Effects of the Allogeneic Transplantation with Mesenchymal Stromal Cells Were Potentiated by ω3 Stimulating Up-Regulation of the PPAR-γ

Author:

de Oliveira Andreia Silva1,Convento Márcia Bastos2ORCID,Razvickas Clara Versolato2,Castino Bianca3,Leme Ala Moana2,da Silva Luiz Rafael2,da Silva Wesley Henrique2,da Glória Maria Aparecida2,Guirão Tatiana Pinotti2,Bondan Eduardo4ORCID,Schor Nestor2,Borges Fernanda Teixeira23ORCID

Affiliation:

1. Translational Medicine Division, Department of Medicine, Federal University of Sao Paulo, São Paulo 04038-901, Brazil

2. Nephrology Division, Department of Medicine, Federal University of Sao Paulo, São Paulo 04038-901, Brazil

3. Interdisciplinary Postgraduate Program in Health Sciences, Cruzeiro do Sul University, São Paulo 01506-000, Brazil

4. Graduate Program in Environmental and Experimental Pathology, Paulista University, São Paulo 04026-002, Brazil

Abstract

Mesenchymal stromal cells (MSCs) obtained from bone marrow are a promising tool for regenerative medicine, including kidney diseases. A step forward in MSCs studies is cellular conditioning through specific minerals and vitamins. The Omega-3 fatty acids (ω3) are essential in regulating MSCs self-renewal, cell cycle, and survival. The ω3 could act as a ligand for peroxisome proliferator-activated receptor gamma (PPAR-γ). This study aimed to demonstrate that ω3 supplementation in rats could lead to the up-regulation of PPAR-γ in the MSCs. The next step was to compare the effects of these MSCs through allogeneic transplantation in rats subjected to unilateral ureteral obstruction (UUO). Independent of ω3 supplementation in the diet of the rats, the MSCs in vitro conserved differentiation capability and phenotypic characteristics. Nevertheless, MSCs obtained from the rats supplemented with ω3 stimulated an increase in the expression of PPAR-γ. After allogeneic transplantation in rats subjected to UUO, the ω3 supplementation in the rats enhanced some nephroprotective effects of the MSCs through a higher expression of antioxidant enzyme (SOD-1), anti-inflammatory marker (IL-10), and lower expression of the inflammatory marker (IL-6), and proteinuria.

Funder

São Paulo Research Foundation

F.T.B.

Publisher

MDPI AG

Subject

Drug Discovery,Pharmaceutical Science,Molecular Medicine

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