# Inhibition of GSK-3β Restores Differentiation Potential of Late-Passage Mesenchymal Stem Cells

**Authors:** Kavitha Govarthanan, Raja Sundari Meenakshi Sundaram, Arthi Sunil Richard, Siva Chander Chabathula, Secunda Rupert, Jeswanth Sathyanesan, Rama Shanker Verma, Naveen Jeyaraman, Madhan Jeyaraman, Ramya Lakshmi Rajendran, Prakash Gangadaran, Byeong-Cheol Ahn

PMC · DOI: 10.3390/ph18040483 · Pharmaceuticals · 2025-03-28

## TL;DR

This study shows that treating aged mesenchymal stem cells with CHIR99021 can restore their ability to differentiate into multiple cell types.

## Contribution

The study demonstrates that the Wnt agonist CHIR99021 can reverse differentiation loss in late-passage MSCs.

## Key findings

- Late-passage MSCs show reduced differentiation potential and signs of senescence.
- CHIR99021 treatment restores tri-lineage differentiation in aged MSCs.
- Senescence is reversed in late-passage MSCs after CHIR99021 treatment.

## Abstract

Background/Objectives: Mesenchymal stem cells (MSCs) are regarded as a promising cell type with significant therapeutic benefits owing to their ease of isolation, maintenance, and characterisation. However, repeated passages during cultural maintenance frequently result in cellular senescence, limiting their utility in regenerative medicine. Methods: We investigated the differentiation capability between early- (P3) and late-passage MSCs (>P15) and tested the potential of Wnt agonist 99021 to reverse MSCs using standard cell culture protocols that define minimal criteria for MSCs, primarily tri-lineage differentiation assays, biochemical staining gene expression analysis, and senescence assays. Results: We initially noticed distinct signs of morphological aging between early- (P3) and late-passage MSCs (>P15) and further examined the differentiation capability between early- (P3) and late-passage MSCs (>P15). We found a diminished differentiation potential in late-passage MSCs. Our senescence assay also revealed >P15 cells were able to absorb the senescence dye, indicating that >P15 MSCs underwent senescence. We further demonstrated that CHIR 99021 reversed the differentiation inhibitory potential-mediated impasse of late-passage MSCs by employing tri-lineage specific differentiation assays, biochemical labelling, and gene expression analysis. Senescence assays after CHIR 99021 treatment also revealed no senescence dye uptake at all. Conclusions: Our findings demonstrated that CHIR 99021 Wnt agonist maybe aids in the reversal of MSC aging-related differentiation inhibition glitches and offers a proven demonstrated protocol for rejuvenating late-passage MSCs. Thus, CHIR99021 treatment inherently reverts the tri-lineage potency in late-passage MSCs, and this method could be further employed to ensure a plentiful MSC source for clinical purposes.

## Linked entities

- **Proteins:** GSK3B (glycogen synthase kinase 3 beta)
- **Chemicals:** CHIR 99021 (PubChem CID 9956119), CHIR99021 (PubChem CID 9956119)

## Full-text entities

- **Genes:** GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12030495/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12030495/full.md

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Source: https://tomesphere.com/paper/PMC12030495