Adipogenesis of Sprague Dawely rats mesenchymal stem cells: a morphological, immunophenotyping and gene expression follow-up study.
- Author:
Mohamed A SOBH
1
Author Information
- Publication Type:In Vitro ; Original Article
- Keywords: Rat bone marrow; Mesenchymal stromal cells; Adipocyte differentiation; Immunophenotyping; Gene expression levels
- MeSH: Adipocytes; Adipogenesis*; Adiponectin; Animals; Bone Marrow; Flow Cytometry; Follow-Up Studies*; Gene Expression*; Immunophenotyping*; Leptin; Lipoprotein Lipase; Mesenchymal Stromal Cells*; Polymerase Chain Reaction; Rats*; Reverse Transcription; Tissue Engineering; Transplants
- From:Anatomy & Cell Biology 2014;47(2):83-90
- CountryRepublic of Korea
- Language:English
- Abstract: Mesenchymal stem cells (MSCs) offer significant promise as a multipotent source for cell-based therapies and could form the basis for the differentiation and cultivation of tissue grafts to replace damaged tissue. However, no gene expression follow up analysis has been undertaken to characterize the in vitro adipogenic differentiated MSCs. The main goal of this study was to focus on MSCs and to analyze their differentiation capacity. To achieve this aim, bone marrow MSCs from sprague dawely rats were isolated, expanded in monolayer culture and characterized with respect to their cluster of differentiation (CD) and ability for adipogenic differentiation capacity. The expression of CD44, CD45, CD29, CD34, and CD90 on bone marrow derived MSCs was characterized using flow cytometry. Adipogenesis was determined by staining with oil-red O and reverse transcription polymerase chain reaction assessments of lipoprotein lipase, leptin, adiponectin and adipocyte genes at different time intervals, after 4, 7, 14, and 21 days. Our results revealed that the pattern of CD marker expression was highly positive significant with CD29, CD44, and CD90 when compared with CD34 and CD45. MSCs showed proliferative potential and were capable of adipogenic differentiation characterized by reddish brown-droplets following staining with oil-red O and expression of molecular bands of genes. These results demonstrate, at the morphological, immunophenotyping and gene expression levels, the multipotency of MSCs and thus highlight their potential therapeutic value for cell-based tissue engineering.
