The ciliary pocket: an endocytic membrane domain at the base of primary and motile cilia

Archive ouverte

Mollà-Herman, Anahi | Ghossoub, Rania | Blisnick, Thierry | Meunier, Alice | Serres, Catherine | Silbermann, Flora | Emmerson, Chris | Romeo, Kelly | Bourdoncle, Pierre | Schmitt, Alain | Saunier, Sophie | Spassky, Nathalie | Bastin, Philippe | Benmerah, Alexandre, R.

Edité par CCSD ; Company of Biologists -

International audience. Cilia and flagella are eukaryotic organelles involved in multiple cellular functions. The primary cilium is generally non motile and found in numerous vertebrate cell types where it controls key signalling pathways. Despite a common architecture, ultrastructural data suggest some differences in their organisation. Here, we report the first detailed characterisation of the ciliary pocket, a depression of the plasma membrane in which the primary cilium is rooted. This structure is found at low frequency in kidney epithelial cells (IMCD3) but is associated with virtually all primary cilia in retinal pigment epithelial cells (RPE1). Transmission and scanning electron microscopy, immunofluorescence analysis and videomicroscopy revealed that the ciliary pocket establishes closed links with the actin-based cytoskeleton and that it is enriched in active and dynamic clathrin-coated pits. The existence of the ciliary pocket was confirmed in mouse tissues bearing primary cilia (cumulus), as well as motile cilia and flagella (ependymal cells and spermatids). The ciliary pocket shares striking morphological and functional similarities with the flagellar pocket of Trypanosomatids, a trafficking-specialised membrane domain at the base of the flagellum. Our data therefore highlight the conserved role of membrane trafficking in the vicinity of cilia.

Consulter en ligne

Suggestions

Du même auteur

Alteration of nephrocystins and IFT-A proteins causes similar ciliary phenotypes leading to Nephronophthisis

Archive ouverte | Saunier, Sophie | CCSD

International audience. Nephronophtisis (NPH) is a kidney ciliopathy often associated with extra-renal defects and for which 12 genes (NPHP1-12) have been identified. NPHP1 and NPHP4 control the ciliary access at th...

Targeting of β-Arrestin2 to the Centrosome and Primary Cilium: Role in Cell Proliferation Control

Archive ouverte | Mollà-Herman, Anahi | CCSD

International audience. Background: The primary cilium is a sensory organelle generated from the centrosome in quiescent cells and found at the surface of most cell types, from where it controls important physiologi...

Morphological and Functional Characterization of the Ciliary Pocket by Electron and Fluorescence Microscopy

Archive ouverte | Ghossoub, Rania | CCSD

International audience. In many vertebrate cell types, the proximal part of the primary cilium is positioned within an invagination of the plasma membrane known as the ciliary pocket. Recent evidence points to the c...

Chargement des enrichissements...