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Hypoxic preconditioning effect on stromal cells derived factor-1 and C-X-C chemokine receptor type 4 expression in Wistar rat’s (Rattus norvegicus) bone marrow mesenchymal stem cells (in vitro study)

AIM: To examine the effect of hypoxic preconditions on the ability of bone marrow stem cells culture mediated expression C-X-C chemokine receptor type 4 (CXCR4) and stromal cells derived factor-1 (SDF-1) in vitro. MATERIALS AND METHODS: Bone marrow mesenchymal stem cells (BMSCs) were derived from 12...

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Detalles Bibliográficos
Autores principales: Mulyani, Sri Wigati Mardi, Ernawati, Diah Savitri, Astuti, Eha Renwi, Rantam, Fedik Abdul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Veterinary World 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097555/
https://www.ncbi.nlm.nih.gov/pubmed/30147267
http://dx.doi.org/10.14202/vetworld.2018.965-970
Descripción
Sumario:AIM: To examine the effect of hypoxic preconditions on the ability of bone marrow stem cells culture mediated expression C-X-C chemokine receptor type 4 (CXCR4) and stromal cells derived factor-1 (SDF-1) in vitro. MATERIALS AND METHODS: Bone marrow mesenchymal stem cells (BMSCs) were derived from 12 femurs of 200 g Wistar male rats. The animals were euthanized before BMSCs isolation. BMSCs were divided into two groups, control group: Normoxic condition 21% O(2) and treatment group: Hypoxic condition 1% O(2). The characterization of BMSCs was analyzed using flow cytometry by cluster differentiation 34 and cluster differentiation 105. The expression of CXCR4 and SDF-1 measured using immunocytochemistry immunofluorescence label after 48-h incubation in a low-tension oxygen chamber with an internal atmosphere consisting of 95% N(2,) 5% CO(2), and 1% O(2). All data were subjected to a normality test and then analyzed using t-test statistic (p<0.05). RESULTS: The characterization of bone marrow stem cells showed positive cluster differentiation 34 and cluster differentiation 105. A hypoxic precondition (1% O(2)) in culture increases CXCR4 (p=0.000) and SDF-1 expression than normoxic conditions (p=0.000) (p<0.05). CONCLUSION: Hypoxic preconditioning with 1% O(2) increase CXCR4 and SDF1 expression.