Prominin‐1 controls stem cell activation by orchestrating ciliary dynamics

Donald A. Singer(University of Plymouth), Kristina Thamm(Center for Systems Biology Dresden), Heng Zhuang(Peking University), Jana Karbanová(Center for Systems Biology Dresden), Yan Gao(Capital Medical University), Jemma Victoria Walker(University of Plymouth), Heng Jin(University of Iowa), Xiangnan Wu(University of California, San Francisco), Clarissa Coveney(University of Oxford), Pauline Marangoni(University of California, San Francisco), Dongmei Lu(The University of Texas Southwestern Medical Center), Portia Rebecca Clare Grayson(University of Plymouth), Tülay Gülşen(University of Plymouth), Karen Liu(King's College London), Stefano Ardu(University of Geneva), A.K. Wann(University of Oxford), Shouqing Luo(University of Plymouth), Alexander C. Zambon(Keck Graduate Institute), Anton M. Jetten(National Institutes of Health), Christopher Tredwin(University of Plymouth), Ophir D. Klein(University of California, San Francisco), Massimo Attanasio(University of Iowa), Peter Carmeliet(VIB-KU Leuven Center for Cancer Biology), Wieland Β. Huttner(Max Planck Institute of Molecular Cell Biology and Genetics), Denis Corbeil(Center for Systems Biology Dresden), Bing Hu(Peninsula College of Medicine and Dentistry)
The EMBO Journal
December 6, 2018
Cited by 73Open Access
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Abstract

Proper temporal and spatial activation of stem cells relies on highly coordinated cell signaling. The primary cilium is the sensory organelle that is responsible for transmitting extracellular signals into a cell. Primary cilium size, architecture, and assembly-disassembly dynamics are under rigid cell cycle-dependent control. Using mouse incisor tooth epithelia as a model, we show that ciliary dynamics in stem cells require the proper functions of a cholesterol-binding membrane glycoprotein, Prominin-1 (Prom1/CD133), which controls sequential recruitment of ciliary membrane components, histone deacetylase, and transcription factors. Nuclear translocation of Prom1 and these molecules is particularly evident in transit amplifying cells, the immediate derivatives of stem cells. The absence of Prom1 impairs ciliary dynamics and abolishes the growth stimulation effects of sonic hedgehog (SHH) treatment, resulting in the disruption of stem cell quiescence maintenance and activation. We propose that Prom1 is a key regulator ensuring appropriate response of stem cells to extracellular signals, with important implications for development, regeneration, and diseases.


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