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Human hair follicles operate an internal Cori cycle and modulate their growth via glycogen phosphorylase

Hair follicles (HFs) are unique, multi-compartment, mini-organs that cycle through phases of active hair growth and pigmentation (anagen), apoptosis-driven regression (catagen) and relative quiescence (telogen). Anagen HFs have high demands for energy and biosynthesis precursors mainly fulfilled by...

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Autores principales: Figlak, Katarzyna, Williams, Greg, Bertolini, Marta, Paus, Ralf, Philpott, Michael P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531296/
https://www.ncbi.nlm.nih.gov/pubmed/34675331
http://dx.doi.org/10.1038/s41598-021-99652-8
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author Figlak, Katarzyna
Williams, Greg
Bertolini, Marta
Paus, Ralf
Philpott, Michael P.
author_facet Figlak, Katarzyna
Williams, Greg
Bertolini, Marta
Paus, Ralf
Philpott, Michael P.
author_sort Figlak, Katarzyna
collection PubMed
description Hair follicles (HFs) are unique, multi-compartment, mini-organs that cycle through phases of active hair growth and pigmentation (anagen), apoptosis-driven regression (catagen) and relative quiescence (telogen). Anagen HFs have high demands for energy and biosynthesis precursors mainly fulfilled by aerobic glycolysis. Histochemistry reports the outer root sheath (ORS) contains high levels of glycogen. To investigate a functional role for glycogen in the HF we quantified glycogen by Periodic-Acid Schiff (PAS) histomorphometry and colorimetric quantitative assay showing ORS of anagen VI HFs contained high levels of glycogen that decreased in catagen. qPCR and immunofluorescence microscopy showed the ORS expressed all enzymes for glycogen synthesis and metabolism. Using human ORS keratinocytes (ORS-KC) and ex vivo human HF organ culture we showed active glycogen metabolism by nutrient starvation and use of a specific glycogen phosphorylase (PYGL) inhibitor. Glycogen in ORS-KC was significantly increased by incubation with lactate demonstrating a functional Cori cycle. Inhibition of PYGL significantly stimulated the ex vivo growth of HFs and delayed onset of catagen. This study defines translationally relevant and therapeutically targetable new features of HF metabolism showing that human scalp HFs operate an internal Cori cycle, synthesize glycogen in the presence of lactate and modulate their growth via PYGL activity.
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spelling pubmed-85312962021-10-22 Human hair follicles operate an internal Cori cycle and modulate their growth via glycogen phosphorylase Figlak, Katarzyna Williams, Greg Bertolini, Marta Paus, Ralf Philpott, Michael P. Sci Rep Article Hair follicles (HFs) are unique, multi-compartment, mini-organs that cycle through phases of active hair growth and pigmentation (anagen), apoptosis-driven regression (catagen) and relative quiescence (telogen). Anagen HFs have high demands for energy and biosynthesis precursors mainly fulfilled by aerobic glycolysis. Histochemistry reports the outer root sheath (ORS) contains high levels of glycogen. To investigate a functional role for glycogen in the HF we quantified glycogen by Periodic-Acid Schiff (PAS) histomorphometry and colorimetric quantitative assay showing ORS of anagen VI HFs contained high levels of glycogen that decreased in catagen. qPCR and immunofluorescence microscopy showed the ORS expressed all enzymes for glycogen synthesis and metabolism. Using human ORS keratinocytes (ORS-KC) and ex vivo human HF organ culture we showed active glycogen metabolism by nutrient starvation and use of a specific glycogen phosphorylase (PYGL) inhibitor. Glycogen in ORS-KC was significantly increased by incubation with lactate demonstrating a functional Cori cycle. Inhibition of PYGL significantly stimulated the ex vivo growth of HFs and delayed onset of catagen. This study defines translationally relevant and therapeutically targetable new features of HF metabolism showing that human scalp HFs operate an internal Cori cycle, synthesize glycogen in the presence of lactate and modulate their growth via PYGL activity. Nature Publishing Group UK 2021-10-21 /pmc/articles/PMC8531296/ /pubmed/34675331 http://dx.doi.org/10.1038/s41598-021-99652-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Figlak, Katarzyna
Williams, Greg
Bertolini, Marta
Paus, Ralf
Philpott, Michael P.
Human hair follicles operate an internal Cori cycle and modulate their growth via glycogen phosphorylase
title Human hair follicles operate an internal Cori cycle and modulate their growth via glycogen phosphorylase
title_full Human hair follicles operate an internal Cori cycle and modulate their growth via glycogen phosphorylase
title_fullStr Human hair follicles operate an internal Cori cycle and modulate their growth via glycogen phosphorylase
title_full_unstemmed Human hair follicles operate an internal Cori cycle and modulate their growth via glycogen phosphorylase
title_short Human hair follicles operate an internal Cori cycle and modulate their growth via glycogen phosphorylase
title_sort human hair follicles operate an internal cori cycle and modulate their growth via glycogen phosphorylase
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531296/
https://www.ncbi.nlm.nih.gov/pubmed/34675331
http://dx.doi.org/10.1038/s41598-021-99652-8
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