Cilium, centrosome and cell cycle regulation in polycystic kidney disease

Kyung Lee, Lorenzo Battini, G. Luca Gusella

Research output: Contribution to journalReview articlepeer-review

34 Scopus citations


Polycystic kidney disease is the defining condition of a group of common life-threatening genetic disorders characterized by the bilateral formation and progressive expansion of renal cysts that lead to end stage kidney disease. Although a large body of information has been acquired in the past years about the cellular functions that characterize the cystic cells, the mechanisms triggering the cystogenic conversion are just starting to emerge. Recent findings link defects in ciliary functions, planar cell polarity pathway, and centrosome integrity in early cystic development. Many of the signals dysregulated during cystogenesis may converge on the centrosome for its central function as a structural support for cilia formation and a coordinator of protein trafficking, polarity, and cell division. Here, we will discuss the contribution of proliferation, cilium and planar cell polarity to the cystic signal and will analyze in particular the possible role that the basal bodies/centrosome may play in the cystogenetic mechanisms.

Original languageEnglish
Pages (from-to)1263-1271
Number of pages9
JournalBiochimica et Biophysica Acta - Molecular Basis of Disease
Issue number10
StatePublished - Oct 2011


  • Cell cycle
  • Centrosome
  • Cilium
  • Cystogenesis
  • Kidney
  • Planar cell polarity


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