Osteogenic differentiation potential of porcine bone marrow mesenchymal stem cell subpopulations selected in different basal media

被引:42
作者
Kannan, Sangeetha [1 ]
Ghosh, Jyotirmoy [2 ]
Dhara, Sujoy K. [3 ]
机构
[1] Jain Univ, Dept Biotechnol, Bangalore 560011, Karnataka, India
[2] ICAR Natl Inst Anim Nutr & Physiol, Mol Biol Lab, Bangalore 560030, Karnataka, India
[3] ICAR Indian Vet Res Inst, Div Vet Biotechnol, Stem Cell Lab, Izatnagar 243122, Uttar Pradesh, India
来源
BIOLOGY OPEN | 2020年 / 9卷 / 10期
关键词
Bone marrow; Basal media; Mesenchymal stem cells; Osteogenic differentiation; Porcine; STROMAL CELLS; CHONDROGENIC DIFFERENTIATION; ALKALINE-PHOSPHATASE; NUCLEAR TRANSFER; GENE-EXPRESSION; CULTURE; OSTEOPONTIN; EXPANSION; PROLIFERATION; ADIPOGENESIS;
D O I
10.1242/bio.053280
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multipotent porcine mesenchymal stem cells (pMSC) are invaluable for research and therapeutic use in regenerative medicine. Media used for derivation and expansion of pMSC may play an important role for the selection of MSC subpopulation at an early stage and thereby, the specific basal medium may also affect differentiation potential of these cells. The present study was undertaken to evaluate the effects of alpha MEM, aDMEM, M199, alpha MEM/M199, alpha DMEM/M199 and alpha MEM/aDMEM media on (1) porcine bone marrow MSC derivation; (2) expression of number of osteogenic markers (ALP. COL1A1, SPP1 and BGLAP) at 5th and 10th passage in pMSC before differentiation; and (3) differentiation of pMSC (at 5th passage) to osteogenic lineage. Morphological changes and matrix formation in osteogenic cells were evaluated by microscopic examination. Calcium deposits in osteocytes were confirmed by Alizarin Red S staining. Based on expression of different markers, it was evident that selection of bone marrow pMSC subpopulations was independent of basal media used. However, the differentiation of those pMSCs, specifically to osteogenic lineage, was dependent on the medium used for expansion of pMSC at the pre-differentiation stage. We demonstrated here that the pMSC grown in combined alpha MEM/aDMEM (1:1) medium expressed number of osteogenic markers and these pMSC underwent osteogenic differentiation most efficiently, in comparison to porcine mesenchymal stem cells grown in other media. In conclusion, osteogenic differentiation potential of pMSC maintained in alpha MEM/aDMEM medium was observed significantly higher compared to cells cultivated in other media and therefore, the combined medium alpha MEM/aDMEM (1:1) may preferentially be used for expansion of pMSC, if needed for osteogenic differentiation.
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页数:11
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