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Mesenchymal stem cells pretreated with interferon-gamma attenuate renal fibrosis by enhancing regulatory T cell induction. | LitMetric

AI Article Synopsis

  • * In a study with ischemia reperfusion injury (IRI) rats, IFN-γ MSCs were found to significantly increase Treg cells and decrease inflammatory cell infiltration and renal fibrosis compared to regular MSCs.
  • * The study also revealed that the enhanced anti-inflammatory and anti-fibrotic effects of IFN-γ MSCs were linked to increased expression of indoleamine 2,3-dioxygenase (IDO), with IDO1 knockdown reducing

Article Abstract

Mesenchymal stem cells (MSCs) exert their anti-inflammatory and anti-fibrotic effects by secreting various humoral factors. Interferon-gamma (IFN-γ) can enhance these effects of MSCs, and enhancement of regulatory T (Treg) cell induction is thought to be an underlying mechanism. However, the extent to which Treg cell induction by MSCs pretreated with IFN-γ (IFN-γ MSCs) ameliorates renal fibrosis remains unknown. In this study, we investigated the effects of Treg cell induction by IFN-γ MSCs on renal inflammation and fibrosis using an siRNA knockdown system. Administration of IFN-γ MSCs induced Treg cells and inhibited infiltration of inflammatory cells in ischemia reperfusion injury (IRI) rats more drastically than control MSCs without IFN-γ pretreatment. In addition, administration of IFN-γ MSCs more significantly attenuated renal fibrosis compared with control MSCs. Indoleamine 2,3-dioxygenase (IDO) expression levels in conditioned medium from MSCs were enhanced by IFN-γ pretreatment. Moreover, IDO1 knockdown in IFN-γ MSCs reduced their anti-inflammatory and anti-fibrotic effects in IRI rats by reducing Treg cell induction. Our findings suggest that the increase of Treg cells induced by enhanced secretion of IDO by IFN-γ MSCs played a pivotal role in their anti-fibrotic effects. Administration of IFN-γ MSCs may potentially be a useful therapy to prevent renal fibrosis progression.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11069572PMC
http://dx.doi.org/10.1038/s41598-024-60928-4DOI Listing

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