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Bioimpacts. 2025;15: 30600.
doi: 10.34172/bi.30600
  Abstract View: 74
  PDF Download: 10

Original Article

Enhanced reno-protective effects of CHIR99021 modified mesenchymal stem cells against rat acute kidney injury model

Rakhshinda Habib 1* ORCID logo, Rabia Farhat 2, Mohsin Wahid 3, Jahanara Ainuddin 4

1 Dow Research Institute of Biotechnology and Biomedical Sciences, Dow University of Health Sciences (Ojha Campus), Karachi, Pakistan
2 School of Postgraduate Studies, Dow University of Health Sciences (Ojha Campus), Karachi, Pakistan
3 Department of Pathology, Dow International Medical College, Dow University of Health Sciences (Ojha Campus), Karachi, Pakistan
4 Department of Gynecology and Obstetrics, Dow University Hospital, Karachi, Pakistan
*Corresponding Author: Rakhshinda Habib, Email: rakhshinda.habib@duhs.edu.pk

Abstract

Introduction: Mesenchymal stem cells of human umbilical cord origin (hucMSCs) appear to be an attractive candidate for cell-based therapies. However, their efficacy requires improvement as poor survival and specific homing to the site of injury are the major barriers to their effective implementation in cell therapy. As Wnt signaling pathway is involved in the development and repair of organs, we adopted a preconditioning strategy of stem cells by using CHIR99021 compound (a Wnt pathway agonist) to potentiate hucMSCs beneficial effects and circumvent their therapeutic limitations.
Methods: We treated hucMSCs with 5 µM of CHIR99021 and evaluated the expression levels of genes involved in different biological processes through qRT-PCR. Subsequently, we examined the effectiveness of preconditioned cells (CHIR99021-hucMSCs) in a cisplatin-induced rat acute kidney injury model. Amelioration in tissue injury was evaluated by histopathology, immunohistochemistry and renal functional assessment.
Results: In treated groups, we observed preserved renal tissue architecture in terms of lesser epithelial cells necrosis (P ≤ 0.001) and cast formation ( ≤ 0.05). Accelerated proliferation of injured tubular cells (P ≤ 0.001) and low serum creatinine values (P ≤ 0.01) were observed in preconditioned hucMSCs group compared to untreated AKI rats. In addition, administration of preconditioned hucMSCs in kidney injury model offered better restoration of tubular cell membrane β-catenin molecules. Our findings showed that CHIR99021-modified hucMSCs may exhibit better capacity for cell migration and proliferation.
Conclusion: The results showed that preconditioning of stem cells with Wnt pathway activators could provide advanced benefits for organ repair, which may contribute to design a more effective therapeutic approach for renal regeneration.
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Submitted: 01 Jul 2024
Revision: 08 Aug 2024
Accepted: 17 Sep 2024
ePublished: 04 Nov 2024
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