Department of Nephrology, Hiroshima University Hospital, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8551, Japan.
Department of Stem Cell Biology and Medicine, Graduate School of Biomedical & Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553, Japan.
Sci Rep. 2024 May 4;14(1):10251. doi: 10.1038/s41598-024-60928-4.
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.
间充质干细胞 (MSCs) 通过分泌各种体液因子发挥其抗炎和抗纤维化作用。干扰素-γ (IFN-γ) 可以增强 MSCs 的这些作用,并且认为增强调节性 T (Treg) 细胞诱导是一种潜在的机制。然而,IFN-γ 预处理的 MSCs (IFN-γ MSC) 诱导 Treg 细胞的程度对肾纤维化的改善程度尚不清楚。在这项研究中,我们使用 siRNA 敲低系统研究了 IFN-γ MSC 诱导 Treg 细胞对肾炎症和纤维化的影响。与未用 IFN-γ 预处理的对照 MSC 相比,IFN-γ MSC 给药更剧烈地诱导 Treg 细胞并抑制缺血再灌注损伤 (IRI) 大鼠中炎症细胞的浸润。此外,与对照 MSC 相比,IFN-γ MSC 给药更显著地减轻了肾纤维化。IFN-γ 预处理增强了 MSC 条件培养基中吲哚胺 2,3-双加氧酶 (IDO) 的表达水平。此外,IFN-γ MSC 中的 IDO1 敲低通过减少 Treg 细胞诱导,降低了其在 IRI 大鼠中的抗炎和抗纤维化作用。我们的研究结果表明,IFN-γ MSC 通过增强 IDO 的分泌诱导的 Treg 细胞的增加在其抗纤维化作用中发挥了关键作用。IFN-γ MSC 的给药可能是预防肾纤维化进展的一种有用疗法。