Govarthanan, K. and Vidyasekar, P. and Gupta, P.K. and Lenka, N. and Verma, R.S. (2020) Glycogen synthasekinase 3β inhibitor- CHIR 99021 augments the differentiation potential ofmesenchymal stem cells. Cytotherapy, 22 (2). pp. 91-105.

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Abstract

Aim Mesenchymal stem cells (MSCs) are immunomodulatory, non-teratogenic and multipotent alternatives to embryonic or induced pluripotent stem cells (ESCs or iPSCs). However, the potency of MSCs is not equivalent to the pluripotency of ESCs or iPSCs. We used CHIR 99021 to improve current protocols and methods of differentiation for the enhanced ransdifferentiation potency of MSCs. Main Methods We used Flurescence activated cell sorter (FACS) for MSC immunophenotyping and biochemical assay for demonstrating the trilineage potential of MSCs. We used real-time polymerase chain reaction, immunocytochemistry and Western blotting assay for analyzing the expression of lineage-specific markers.Key Findings CHIR 99021 treatment of MSCs resulted in enhanced transdifferentiation into neurological, hepatogenic and cardiomyocyte lineages with standardized protocols of differentiation. CHIR 99021–treated MSCs showed increased nuclear localization of β-catenin. These MSCs showed a significantly increased deposition of active histone marks (H3K4Me3, H3K36Me3), whereas no change was observed in repressive marks (H3K9Me3, H3K27Me3). Differential methylation profiling showed demethylation of the transcription factor OCT4 promoter region with subsequent analysis revealing increased gene expression and protein content. The HLA-DR antigen was absent in CHIR 99021–treated MSCs and their differentiated cell types, indicating their immune-privileged status. Karyotyping analysis showed that CHIR 99021–treated MSCs were genomically stable. Teratoma analysis of nude mice injected with CHIR 99021–treated MSCs showed the increased presence of cell types of mesodermal origin at the site of injection.Significance MSCs pretreated with CHIR 99021 can be potent, abundant alternative sources of stem cells with enhanced differentiation capabilities that are well suited to cell-based regenerative therapy.

Item Type:	Article
Depositing User:	Mr. Rameshwar Nema
Date Deposited:	26 Feb 2020 04:40
Last Modified:	26 Feb 2020 04:40
URI:	http://nccs.sciencecentral.in/id/eprint/790

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