MST1/2 in PDGFRα+ cells negatively regulates TGF-β-induced myofibroblast accumulation in renal fibrosis

Am J Physiol Renal Physiol. 2022 May 1;322(5):F512-F526. doi: 10.1152/ajprenal.00367.2021. Epub 2022 Mar 7.

Abstract

Injury-induced fibroblast-to-myofibroblast differentiation is a key event of renal fibrosis. Yes-associated protein (YAP), a transcriptional coactivator, plays an important role in fibroblast activation and Smad transcriptional activity to promote transforming growth factor-β (TGF-β)-induced differentiation from fibroblasts to myofibrolasts. Macrophage stimulating 1/2 (MST1/2), a negative regulator of YAP, also increases in fibroblasts by TGF-β stimulation. Here, we examined whether MST1/2, as a negative regulator, attenuated YAP and TGF-β/Smad signaling in fibroblasts to reduce fibrosis. MST1/2 and YAP expression levels increased in platelet-derived growth factor receptor-α (PDGFRα)+ cells of obstructed kidneys following the increase of TGF-β and renal fibrosis after unilateral ureteral obstruction. PDGFRα+ cell-specific knockout of Mst1/2 in mice increased unilateral ureteral obstruction-induced myofibroblast accumulation and fibrosis. In cultured fibroblasts, TGF-β increased YAP and promoted its nucleus entry, but a high dose and prolonged treatment of TGF-β increased the MST1/2 activation to prevent YAP from entering the nucleus. Our results indicate that MST1/2 is a negative feedback signal of TGF-β-induced fibroblast differentiation.NEW & NOTEWORTHY Using a mouse model with macrophage stimulating 1/2 (Mst1/2) double knockout in PDGFRα+ cells and an MST1/2 inhibitor, we demonstrated that MST1/2 acted as a negative feedback signal of transforming growth factor-β-induced fibroblast differentiation. Furthermore, we demonstrated that Hippo-MST as a negative feedback signal can decrease the renal fibrosis process. This finding contributes to our understanding of the mechanism of coregulated renal remodeling after injury.

Keywords: Hippo signaling; fibroblast; macrophage stimulating 1/2; myofibroblast; renal fibrosis.

MeSH terms

  • Fibroblasts / metabolism
  • Fibrosis
  • Hepatocyte Growth Factor
  • Hippo Signaling Pathway
  • Humans
  • Intracellular Signaling Peptides and Proteins*
  • Kidney* / pathology
  • Macrophages / metabolism
  • Myofibroblasts* / metabolism
  • Protein Serine-Threonine Kinases*
  • Receptor, Platelet-Derived Growth Factor alpha / metabolism
  • Serine-Threonine Kinase 3*
  • Transforming Growth Factor beta / metabolism
  • Transforming Growth Factor beta / pharmacology
  • Transforming Growth Factor beta1 / metabolism

Substances

  • Intracellular Signaling Peptides and Proteins
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • Hepatocyte Growth Factor
  • STK4 protein, human
  • Receptor, Platelet-Derived Growth Factor alpha
  • Protein Serine-Threonine Kinases
  • STK3 protein, human
  • Serine-Threonine Kinase 3

Associated data

  • figshare/10.6084/m9.figshare.19225224.v1