Effect of stem cells seeded onto biomaterial on the progression of experimental chronic kidney disease

Author:

Caldas Heloisa C1,Fernandes Ida M M1,Kawasaki-Oyama Rosa S1,Baptista Maria Alice S F1,Plepis Ana Maria G2,Martins Virginia A2,Coimbra Terezila M3,Goloni-Bertollo Eny M4,Braile Domingo M1,Abbud-Filho Mario1

Affiliation:

1. Department of Medicine – Laboratory of Immunology and Experimental Transplantation (LITEX), Medical School of Sao Jose do Rio Preto (FAMERP/FUNFARME), 15090-000, Sao Jose do Rio Preto

2. Department of Chemistry, Instituto de Química, Universidade de Sao Paulo (USP), 13560-970, Sao Carlos

3. Department of Physiology and Pathology, USP-Medical School Ribeirao Preto, 14049-900, Ribeirao Preto

4. Genetics and Molecular Biology Research Unit (UPGEM), FAMERP/FUNFARME, 15090-000, Sao Jose do Rio Preto, SP, Brazil

Abstract

Different routes for the administration of bone marrow-derived cells (BMDC) have been proposed to treat the progression of chronic renal failure (CRF). We investigated whether (1) the use of bovine pericardium (BP) as a scaffold for cell therapy would retard the progression of CRF and (2) the efficacy of cell therapy differently impacts distinct degrees of CRF. We used 2/3 and 5/6 models of renal mass reduction to simulate different stages of chronicity. Treatments consisted of BP seeded with either mesenchymal or mononuclear cells implanted in the parenchyma of remnant kidney. Renal function and proteinuria were measured at days 45 and 90 after cell implantation. BMDC treatment reduced glomerulosclerosis, interstitial fibrosis and lymphocytic infiltration. Immunohistochemistry showed decreased macrophage accumulation, proliferative activity and the expression of fibronectin and α-smooth muscle-actin. Our results demonstrate: (1) biomaterial combined with BMDC did retard the progression of experimental CRF; (2) cellular therapy stabilized serum creatinine (sCr), improved creatinine clearance and 1/sCr slope when administered during the less severe stages of CRF; (3) treatment with combined therapy decreased glomerulosclerosis, fibrosis and the expression of fibrogenic molecules; and (4) biomaterials seeded with BMDC can be an alternative route of cellular therapy.

Publisher

SAGE Publications

Subject

General Biochemistry, Genetics and Molecular Biology

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