Tubular STAT3 Limits Renal Inflammation in Autosomal Dominant Polycystic Kidney Disease

J Am Soc Nephrol. 2020 May;31(5):1035-1049. doi: 10.1681/ASN.2019090959. Epub 2020 Apr 1.

Abstract

Background: The inactivation of the ciliary proteins polycystin 1 or polycystin 2 leads to autosomal dominant polycystic kidney disease (ADPKD). Although signaling by primary cilia and interstitial inflammation both play a critical role in the disease, the reciprocal interactions between immune and tubular cells are not well characterized. The transcription factor STAT3, a component of the cilia proteome that is involved in crosstalk between immune and nonimmune cells in various tissues, has been suggested as a factor fueling ADPKD progression.

Method: To explore how STAT3 intersects with cilia signaling, renal inflammation, and cyst growth, we used conditional murine models involving postdevelopmental ablation of Pkd1, Stat3, and cilia, as well as cultures of cilia-deficient or STAT3-deficient tubular cell lines.

Results: Our findings indicate that, although primary cilia directly modulate STAT3 activation in vitro, the bulk of STAT3 activation in polycystic kidneys occurs through an indirect mechanism in which primary cilia trigger macrophage recruitment to the kidney, which in turn promotes Stat3 activation. Surprisingly, although inactivating Stat3 in Pkd1-deficient tubules slightly reduced cyst burden, it resulted in a massive infiltration of the cystic kidneys by macrophages and T cells, precluding any improvement of kidney function. We also found that Stat3 inactivation led to increased expression of the inflammatory chemokines CCL5 and CXCL10 in polycystic kidneys and cultured tubular cells.

Conclusions: STAT3 appears to repress the expression of proinflammatory cytokines and restrict immune cell infiltration in ADPKD. Our findings suggest that STAT3 is not a critical driver of cyst growth in ADPKD but rather plays a major role in the crosstalk between immune and tubular cells that shapes disease expression.

Keywords: ADPKD; STAT3; cilia; inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged, 80 and over
  • Animals
  • Cells, Cultured
  • Chemokine CCL5 / metabolism
  • Chemokine CXCL10 / metabolism
  • Cilia / metabolism
  • Dogs
  • Humans
  • Inflammation
  • Kidney Tubules / metabolism*
  • Kidney Tubules / pathology
  • Macrophages / physiology
  • Madin Darby Canine Kidney Cells
  • Mice
  • Mice, Inbred C57BL
  • Polycystic Kidney, Autosomal Dominant / genetics
  • Polycystic Kidney, Autosomal Dominant / immunology
  • Polycystic Kidney, Autosomal Dominant / metabolism
  • Polycystic Kidney, Autosomal Dominant / pathology*
  • STAT3 Transcription Factor / physiology*
  • Specific Pathogen-Free Organisms
  • T-Lymphocytes / physiology
  • TRPP Cation Channels / deficiency
  • TRPP Cation Channels / metabolism

Substances

  • Ccl5 protein, mouse
  • Chemokine CCL5
  • Chemokine CXCL10
  • Cxcl10 protein, mouse
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • TRPP Cation Channels
  • polycystic kidney disease 1 protein