Fundamental insights into autosomal dominant polycystic kidney disease from human-based cell models

Caroline Weydert, Jean-Paul Decuypere, Humbert De Smedt, Peter Janssens, Rudi Vennekens, Djalila Mekahli

Research output: Contribution to journalScientific reviewpeer-review

6 Citations (Scopus)

Abstract

Several animal- and human-derived models are used in autosomal dominant polycystic kidney disease (ADPKD) research to gain insight in the disease mechanism. However, a consistent correlation between animal and human ADPKD models is lacking. Therefore, established human-derived models are relevant to affirm research results and translate findings into a clinical set-up. In this review, we give an extensive overview of the existing human-based cell models. We discuss their source (urine, nephrectomy and stem cell), immortalisation procedures, genetic engineering, kidney segmental origin and characterisation with nephron segment markers. We summarise the most studied pathways and lessons learned from these different ADPKD models. Finally, we issue recommendations for the derivation of human-derived cell lines and for experimental set-ups with these cell lines.
Original languageEnglish
Pages (from-to)1697-1715
Number of pages19
JournalPediatric Nephrology
Volume34
Issue number10
DOIs
Publication statusPublished - Oct 2019

Keywords

  • ADPKD
  • Human cell lines
  • Calcium
  • cAMP
  • mTOR

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