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

Author:

Molla-Herman Anahi12,Ghossoub Rania12,Blisnick Thierry3,Meunier Alice4,Serres Catherine12,Silbermann Flora56,Emmerson Chris12,Romeo Kelly12,Bourdoncle Pierre12,Schmitt Alain12,Saunier Sophie56,Spassky Nathalie4,Bastin Philippe3,Benmerah Alexandre12

Affiliation:

1. Institut Cochin, Université Paris Descartes, CNRS UMR 8104, Paris 75014, France

2. INSERM, U1016, Paris 75014, France

3. Trypanosome Cell Biology Unit, Institut Pasteur and CNRS, Paris 75015, France

4. Institut de Biologie de l'Ecole Normale Superieure (IBENS), INSERM U1024, CNRS UMR8197, Paris 75005, France

5. INSERM, U983, Hôpital Necker-Enfants Malades, Paris 75015, France

6. Université Paris Descartes, Paris 75006, France

Abstract

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.

Publisher

The Company of Biologists

Subject

Cell Biology

Cited by 254 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3