Macrophage transition to a myofibroblast state drives fibrotic disease in uropathogenic E. coli-induced epididymo-orchitis

J Clin Invest. 2025 Oct 1;135(19):e193793. doi: 10.1172/JCI193793.

Abstract

Bacterial infections, particularly uropathogenic E. coli (UPEC), contribute substantially to male infertility through tissue damage and subsequent fibrosis in the testis and epididymis. The role of testicular macrophages (TMs), a diverse cell population integral to tissue maintenance and immune balance, in fibrosis is not fully understood. Here, we used single-cell RNA sequencing in a murine model of epididymo-orchitis to analyze TM dynamics during UPEC infection. Our study identified a marked increase in S100a4+ macrophages, originating from monocytes, strongly associated with fibrotic changes. This association was validated in human testicular and epididymal samples. We further demonstrated that S100a4+ macrophages transition to a myofibroblast-like phenotype, producing extracellular matrix proteins such as collagen I and fibronectin. S100a4, both extracellular and intracellular, activated collagen synthesis through the TGF-β/STAT3 signaling pathway, highlighting this pathway as a therapeutic target. Inhibition of S100a4 with niclosamide or macrophage-specific S100a4 KO markedly reduced immune infiltration, tissue damage, and fibrosis in infected murine models. Our findings establish the critical role of S100a4+ macrophages in fibrosis during UPEC-induced epididymo-orchitis and propose them as potential targets for antifibrotic therapy development.

Keywords: Bacterial infections; Fibrosis; Infectious disease; Inflammation; Macrophages.

MeSH terms

  • Animals
  • Epididymis / metabolism
  • Epididymis / pathology
  • Epididymitis* / genetics
  • Epididymitis* / metabolism
  • Epididymitis* / microbiology
  • Epididymitis* / pathology
  • Escherichia coli Infections* / genetics
  • Escherichia coli Infections* / metabolism
  • Escherichia coli Infections* / pathology
  • Fibrosis
  • Humans
  • Macrophages* / immunology
  • Macrophages* / metabolism
  • Macrophages* / pathology
  • Male
  • Mice
  • Mice, Knockout
  • Myofibroblasts* / metabolism
  • Myofibroblasts* / pathology
  • Orchitis* / genetics
  • Orchitis* / metabolism
  • Orchitis* / microbiology
  • Orchitis* / pathology
  • S100 Calcium-Binding Protein A4 / genetics
  • S100 Calcium-Binding Protein A4 / metabolism
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction
  • Testis / metabolism
  • Testis / pathology
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / metabolism
  • Uropathogenic Escherichia coli*

Substances

  • S100 Calcium-Binding Protein A4
  • S100a4 protein, mouse
  • STAT3 Transcription Factor
  • S100A4 protein, human
  • Transforming Growth Factor beta