Abstract

Primary cilia are antenna-like structures projected from the apical surface of various mammalian cells including renal tubular cells. Functional or structural defects of the cilium lead to systemic disorders comprising polycystic kidneys as a key feature. Here we show that anoctamin 6 (ANO6), a member of the anoctamin chloride channel family, is localized in the primary cilium of renal epithelial cells in vitro and in vivo. ANO6 was not essential for cilia formation and had no effect on in vitro cyst expansion. However, knockdown of ANO6 impaired cyst lumen formation of MDCK cells in three-dimensional culture. In the absence of ANO6, apoptosis was reduced and epithelial cells were incompletely removed from the center of cell aggregates, which form in the early phase of cystogenesis. In line with these data, we show that ANO6 is highly expressed in apoptotic cyst epithelial cells of human polycystic kidneys. These data identify ANO6 as a cilium-associated protein and suggest its functional relevance in cyst formation.

Highlights

  • Anoctamins (ANO1-ANO10, TMEM16A-K) form a family of 10 proteins that are supposed to act as Ca2+-activated chloride channels with no homology to other known ion channels.[4,5] In contrast to the other paralogues, the function of ANO1 and ANO2 as Ca2+-activated chloride channels has been confirmed in vivo and in vitro.[6,7,8] Besides its ability to conduct ions ANO6 has been shown to act as a phospholipid scramblase.[9,10] ANO3, 4, 7, 9 may act as Ca2+-dependent phospholipid scramblases.[11]

  • Anoctamin 6 is localized in the primary cilium of renal tubular cells

  • We analyzed the subcellular localization of endogenous ANO6 in polarized Madin-Darby Canine Kidney (MDCK) cells, which originate from collecting duct cells

Read more

Summary

Introduction

Anoctamins (ANO1-ANO10, TMEM16A-K) form a family of 10 proteins that are supposed to act as Ca2+-activated chloride channels with no homology to other known ion channels.[4,5] In contrast to the other paralogues, the function of ANO1 and ANO2 as Ca2+-activated chloride channels has been confirmed in vivo and in vitro.[6,7,8] Besides its ability to conduct ions ANO6 has been shown to act as a phospholipid scramblase.[9,10] ANO3, 4, 7, 9 may act as Ca2+-dependent phospholipid scramblases.[11] data about their functional roles are very limited so far. ANO6 is the most widely expressed paralogue.[12] Mutations in ANO6 cause the Scott syndrome, which is characterized by a defect in Ca2+-dependent phospholipid scrambling of plasma membrane phospholipids.[10] In addition, ANO6 is involved in bone mineralization, cell volume regulation, cell proliferation and apoptosis.[12] Despite the broad expression and function of ANO6, there is only sparse data about the subcellular localization of ANO6. This study was conducted to determine the subcellular localization of ANO6 in renal tubular cells and a possible role of this protein in cyst formation

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call