A virus-induced kidney disease model based on organ-on-a-chip: Pathogenesis exploration of virus-related renal dysfunctions

Biomaterials. 2019 Oct:219:119367. doi: 10.1016/j.biomaterials.2019.119367. Epub 2019 Jul 17.

Abstract

Renal dysfunctions usually happen in viral infections and many viruses specially infect distal renal tubules, however the pathogenesis remains unknown. Here, in order to explore the pathogenesis of virus-related renal dysfunctions, a Pseudorabies Virus (PrV) induced kidney disease model was built on a distal tubule-on-a-chip (DTC), for the first time. The barrier structure and Na reabsorption of distal renal tubules were successfully reconstituted in DTCs. After PrV infection, results showed electrolyte regulation dysfunction in Na reabsorption for the disordered Na transporters, the broken reabsorption barrier, and the transformed microvilli. And it would lead to virus induced serum electrolyte abnormalities. This work brought us a new cognition about the advantages of organ-on-a-chip (OOC) in virus research, for it had given us a better insight into the pathogenesis of virus induced dysfunctions, based on its unique ability in function reproduction.

Keywords: In vitro virus-induced disease model; Organ-on-a-chip; Pathogenesis exploration; Serum electrolyte abnormalities; Virus-related renal dysfunction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Absorption, Physiological / drug effects
  • Angiotensin II / pharmacology
  • Animals
  • Cell Polarity / drug effects
  • Disease Models, Animal
  • Dogs
  • Herpesvirus 1, Suid / drug effects
  • Herpesvirus 1, Suid / physiology*
  • Kidney / drug effects
  • Kidney / pathology
  • Kidney / physiopathology*
  • Kidney / virology*
  • Kidney Diseases / virology*
  • Kidney Tubules, Proximal / drug effects
  • Kidney Tubules, Proximal / pathology
  • Kidney Tubules, Proximal / physiopathology
  • Kidney Tubules, Proximal / virology
  • Lab-On-A-Chip Devices*
  • Madin Darby Canine Kidney Cells
  • Microfluidics
  • Sodium / metabolism

Substances

  • Angiotensin II
  • Sodium