Talabostat, fibroblast activation protein inhibitor, attenuates inflammation and fibrosis in systemic sclerosis

Inflammopharmacology. 2024 Oct;32(5):3181-3193. doi: 10.1007/s10787-024-01536-6. Epub 2024 Aug 21.

Abstract

Background: Systemic sclerosis (SSc) is a connective tissue disorder characterized by excessive fibrosis, where activated fibroblasts play a pivotal role in disease progression. This study aimed to investigate the potential of Talabostat, a small molecule inhibitor of dipeptidyl peptidases, in alleviating fibrosis and inflammation associated with SSc pathogenesis.

Methods: Dermal fibroblasts were obtained from skin biopsies of ten diffuse cutaneous SSc patients and healthy controls. These fibroblasts were subjected to treatment with either TGF-β alone or in combination with Talabostat. Immunofluorescence staining was conducted to evaluate FAPα and α-SMA protein levels. The expression of activated fibroblast markers (FAPα and ACAT2), pro-fibrotic (COL1A1 and COL1A2), anti-fibrotic (MMP1, MMP2, and MMP9), and inflammatory (IL-6 and TGFβ1) related genes was measured by quantitative real-time PCR. Talabostat-treated fibroblasts were assessed for their migratory capacity using a scratch assay and for their viability through MTT assay and Annexin V staining.

Results: The basal expression of COL1A1 and TGFβ1 was notably higher in healthy subjects, while MMP1 expression showed a significant increase in SSc patients. Furthermore, TGF-β stimulation led to upregulation of activated fibroblast markers, pro-fibrotic, and inflammatory-related genes in SSc-derived fibroblasts, which were attenuated upon Talabostat treatment. Interestingly, Talabostat treatment resulted in an upregulation of MMP9 expression. Moreover, Talabostat exhibited a concentration-dependent inhibition of activated fibroblast viability in both healthy and SSc fibroblasts, and suppressed fibroblast migration specifically in SSc patients.

Conclusion: In summary, Talabostat modulates fibrotic genes in SSc, thereby inhibiting myofibroblast differentiation, activation, and migration. These findings suggest promising therapeutic avenues for targeting fibrosis in SSc.

Keywords: Fibrosis; Systemic sclerosis; Talabostat; Transforming growth factor β.

MeSH terms

  • Adult
  • Cell Movement / drug effects
  • Cells, Cultured
  • Endopeptidases
  • Female
  • Fibroblasts* / drug effects
  • Fibroblasts* / metabolism
  • Fibrosis* / drug therapy
  • Humans
  • Inflammation* / drug therapy
  • Inflammation* / metabolism
  • Male
  • Membrane Proteins
  • Middle Aged
  • Scleroderma, Systemic* / drug therapy
  • Scleroderma, Systemic* / metabolism
  • Scleroderma, Systemic* / pathology
  • Skin / drug effects
  • Skin / metabolism
  • Skin / pathology
  • Transforming Growth Factor beta / metabolism

Substances

  • Transforming Growth Factor beta
  • fibroblast activation protein alpha
  • Membrane Proteins
  • Endopeptidases