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Uremic Serum Impairs Osteogenic Differentiation of Human Bone Marrow Mesenchymal Stromal Cells.
Della Bella, Elena; Pagani, Stefania; Giavaresi, Gianluca; Capelli, Irene; Comai, Giorgia; Donadei, Chiara; Cappuccilli, Maria; La Manna, Gaetano; Fini, Milena.
Afiliação
  • Della Bella E; Laboratory of Preclinical and Surgical Studies, Rizzoli Orthopedic Institute, Bologna, Italy.
  • Pagani S; Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
  • Giavaresi G; Laboratory of Preclinical and Surgical Studies, Rizzoli Orthopedic Institute, Bologna, Italy.
  • Capelli I; Laboratory of Biocompatibility, Innovative Technologies and Advanced Therapies, Department Rizzoli RIT, Bologna, Italy.
  • Comai G; Laboratory of Preclinical and Surgical Studies, Rizzoli Orthopedic Institute, Bologna, Italy.
  • Donadei C; Laboratory of Biocompatibility, Innovative Technologies and Advanced Therapies, Department Rizzoli RIT, Bologna, Italy.
  • Cappuccilli M; Nephrology Dialysis and Transplantation Unit, Department of Experimental, Diagnostic and Specialty Medicine, S. Orsola Hospital, University of Bologna, Bologna, Italy.
  • La Manna G; Nephrology Dialysis and Transplantation Unit, Department of Experimental, Diagnostic and Specialty Medicine, S. Orsola Hospital, University of Bologna, Bologna, Italy.
  • Fini M; Nephrology Dialysis and Transplantation Unit, Department of Experimental, Diagnostic and Specialty Medicine, S. Orsola Hospital, University of Bologna, Bologna, Italy.
J Cell Physiol ; 232(8): 2201-2209, 2017 Aug.
Article em En | MEDLINE | ID: mdl-27976811
ABSTRACT
Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD) is characterized by an increased fracture risk. Bone marrow mesenchymal stromal cells (BMSCs) may be involved in the pathogenesis of bone disease and, in view of their promising potential applications in bone tissue engineering, the effect of uremia on BMSCs regenerative potential represents a central issue. The present study evaluated in vitro the effect of a serum pool from hemodialysis patients on BMSCs to observe its influence on osteogenic differentiation. Besides alterations in spatial organization and cytotoxicity along with hyperproliferation, gene expression analysis suggested an impairment in the osteogenic differentiation. More importantly, Receptor activator of nuclear factor kappa-B ligand (RANKL) was upregulated with a mild reduction in osteoprotegerin levels. In summary, uremic environment seems to impair BMSCs osteogenic differentiation. Moreover BMSCs themselves may enhance osteoclastogenesis, feasibly contributing to the altered bone remodeling in CKD-MBD patients. J. Cell. Physiol. 232 2201-2209, 2017. © 2016 Wiley Periodicals, Inc.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteogênese / Uremia / Células da Medula Óssea / Diferenciação Celular / Células-Tronco Mesenquimais / Falência Renal Crônica Limite: Aged80 Idioma: En Revista: J Cell Physiol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteogênese / Uremia / Células da Medula Óssea / Diferenciação Celular / Células-Tronco Mesenquimais / Falência Renal Crônica Limite: Aged80 Idioma: En Revista: J Cell Physiol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Itália