ID | 115091 |
Author |
Cheng, Chun-Chun
RIKEN Center for Biosystems Dynamics Research|UT Southwestern Medical Center
Tsutsui, Ko
RIKEN Center for Biosystems Dynamics Research
Taguchi, Toru
Nagoya University|Niigata University of Health and Welfare
Sanzen, Noriko
RIKEN Center for Biosystems Dynamics Research
Nakagawa, Asako
RIKEN Center for Biosystems Dynamics Research
Kakiguchi, Kisa
RIKEN Center for Biosystems Dynamics Research
Yonemura, Shigenobu
RIKEN Center for Biosystems Dynamics Research|Tokushima University
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Tanegashima, Chiharu
RIKEN Center for Biosystems Dynamics Research
Keeley, Sean D
RIKEN Center for Life Science Technologies|Technische Universität Dresden
Kiyonari, Hiroshi
RIKEN Center for Biosystems Dynamics Research
Furuta, Yasuhide
RIKEN Center for Biosystems Dynamics Research
Tomono, Yasuko
Shigei Medical Research Institute
Watt, Fiona M
King’s College London
Fujiwara, Hironobu
RIKEN Center for Biosystems Dynamics Research
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Content Type |
Journal Article
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Description | The heterogeneity and compartmentalization of stem cells is a common principle in many epithelia, and is known to function in epithelial maintenance, but its other physiological roles remain elusive. Here we show transcriptional and anatomical contributions of compartmentalized epidermal stem cells in tactile sensory unit formation in the mouse hair follicle. Epidermal stem cells in the follicle upper-bulge, where mechanosensory lanceolate complexes innervate, express a unique set of extracellular matrix (ECM) and neurogenesis-related genes. These epidermal stem cells deposit an ECM protein called EGFL6 into the collar matrix, a novel ECM that tightly ensheathes lanceolate complexes. EGFL6 is required for the proper patterning, touch responses, and αv integrin-enrichment of lanceolate complexes. By maintaining a quiescent original epidermal stem cell niche, the old bulge, epidermal stem cells provide anatomically stable follicle–lanceolate complex interfaces, irrespective of the stage of follicle regeneration cycle. Thus, compartmentalized epidermal stem cells provide a niche linking the hair follicle and the nervous system throughout the hair cycle.
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Journal Title |
eLife
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ISSN | 2050084X
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Publisher | eLife Sciences Publications
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Volume | 7
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Start Page | e38883
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Published Date | 2018-10-25
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Rights | This article is distributed under the terms of the Creative Commons Attribution License(https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.
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DOI (Published Version) | |
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language |
eng
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Publisher
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departments |
Medical Sciences
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