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Hair follicle epidermal stem cells define a niche for tactile sensation

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...

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Autores principales: Cheng, Chun-Chun, Tsutsui, Ko, Taguchi, Toru, Sanzen, Noriko, Nakagawa, Asako, Kakiguchi, Kisa, Yonemura, Shigenobu, Tanegashima, Chiharu, Keeley, Sean D, Kiyonari, Hiroshi, Furuta, Yasuhide, Tomono, Yasuko, Watt, Fiona M, Fujiwara, Hironobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226291/
https://www.ncbi.nlm.nih.gov/pubmed/30355452
http://dx.doi.org/10.7554/eLife.38883
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author Cheng, Chun-Chun
Tsutsui, Ko
Taguchi, Toru
Sanzen, Noriko
Nakagawa, Asako
Kakiguchi, Kisa
Yonemura, Shigenobu
Tanegashima, Chiharu
Keeley, Sean D
Kiyonari, Hiroshi
Furuta, Yasuhide
Tomono, Yasuko
Watt, Fiona M
Fujiwara, Hironobu
author_facet Cheng, Chun-Chun
Tsutsui, Ko
Taguchi, Toru
Sanzen, Noriko
Nakagawa, Asako
Kakiguchi, Kisa
Yonemura, Shigenobu
Tanegashima, Chiharu
Keeley, Sean D
Kiyonari, Hiroshi
Furuta, Yasuhide
Tomono, Yasuko
Watt, Fiona M
Fujiwara, Hironobu
author_sort Cheng, Chun-Chun
collection PubMed
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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spelling pubmed-62262912018-11-14 Hair follicle epidermal stem cells define a niche for tactile sensation Cheng, Chun-Chun Tsutsui, Ko Taguchi, Toru Sanzen, Noriko Nakagawa, Asako Kakiguchi, Kisa Yonemura, Shigenobu Tanegashima, Chiharu Keeley, Sean D Kiyonari, Hiroshi Furuta, Yasuhide Tomono, Yasuko Watt, Fiona M Fujiwara, Hironobu eLife Stem Cells and Regenerative Medicine 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. eLife Sciences Publications, Ltd 2018-10-25 /pmc/articles/PMC6226291/ /pubmed/30355452 http://dx.doi.org/10.7554/eLife.38883 Text en © 2018, Cheng et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Stem Cells and Regenerative Medicine
Cheng, Chun-Chun
Tsutsui, Ko
Taguchi, Toru
Sanzen, Noriko
Nakagawa, Asako
Kakiguchi, Kisa
Yonemura, Shigenobu
Tanegashima, Chiharu
Keeley, Sean D
Kiyonari, Hiroshi
Furuta, Yasuhide
Tomono, Yasuko
Watt, Fiona M
Fujiwara, Hironobu
Hair follicle epidermal stem cells define a niche for tactile sensation
title Hair follicle epidermal stem cells define a niche for tactile sensation
title_full Hair follicle epidermal stem cells define a niche for tactile sensation
title_fullStr Hair follicle epidermal stem cells define a niche for tactile sensation
title_full_unstemmed Hair follicle epidermal stem cells define a niche for tactile sensation
title_short Hair follicle epidermal stem cells define a niche for tactile sensation
title_sort hair follicle epidermal stem cells define a niche for tactile sensation
topic Stem Cells and Regenerative Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226291/
https://www.ncbi.nlm.nih.gov/pubmed/30355452
http://dx.doi.org/10.7554/eLife.38883
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