Secondary biliary cholestasis promotes testicular macrophage infiltration and autophagy in rats

Am J Reprod Immunol. 2015 Apr;73(4):301-12. doi: 10.1111/aji.12292. Epub 2014 Jul 18.

Abstract

Problem: Cholestasis can cause translocation of gut bacteria, and endotoxemia, and systemic inflammation. Now, little is known about the effects of cholestasis on the testicular inflammation and autophagy.

Methods: A rat biliary cholestasis model caused by common bile duct ligation (CBDL), together with biliary decompression (choledochoduodenostomy), was used.

Results: The magnitude of MCP-1 expression and CD68(+) macrophage infiltration within testes was progressively up-regulated in rats along with increasing duration of CBDL and was maintained at relatively high level in rats with biliary decompression. The large up-regulation of testicular ATG-12, LC3II, and autophagic vacuoles was found with the extending duration of CBDL and kept at 5 weeks following biliary decompression. The autophagic contents were a large accumulation of mitophagy in testes in rats with CBDL, and cytosol components in rats with biliary decompression.

Conclusion: Secondary biliary cholestasis can promote inflammatory reaction and the activation of mitophagy and autophagy in testes.

Keywords: Autophagic vacuole; choledochoduodenostomy; cholestasis; macrophage; mitophagy; monocyte chemo-attractant protein-1; rat; testes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Autophagy / physiology*
  • Chemokine CCL2 / metabolism
  • Choledochostomy / methods
  • Cholestasis / metabolism
  • Cholestasis / pathology*
  • Common Bile Duct / metabolism
  • Common Bile Duct / pathology*
  • Common Bile Duct / surgery
  • Cytosol / metabolism
  • Cytosol / pathology
  • Ligation / methods
  • Macrophages / metabolism
  • Macrophages / pathology*
  • Male
  • Microtubule-Associated Proteins / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Testis / metabolism
  • Testis / pathology*
  • Up-Regulation / physiology

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD68 protein, rat
  • Ccl2 protein, rat
  • Chemokine CCL2
  • LC3 protein, rat
  • Microtubule-Associated Proteins