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Investigation of Glypican-4 and -6 by Infrared Spectral Imaging during the Hair Growth Cycle

The expression of glypicans in different hair follicle (HF) compartments is still poorly understood. Heparan sulfate proteoglycans (HSPGs) distribution in HF is classically investigated by conventional histology, biochemical analysis, and immunohistochemistry. Our previous study proposed a novel app...

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Autores principales: Colin-Pierre, Charlie, Untereiner, Valérie, Sockalingum, Ganesh D., Ramont, Laurent, Brézillon, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002317/
https://www.ncbi.nlm.nih.gov/pubmed/36901723
http://dx.doi.org/10.3390/ijms24054291
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author Colin-Pierre, Charlie
Untereiner, Valérie
Sockalingum, Ganesh D.
Ramont, Laurent
Brézillon, Stéphane
author_facet Colin-Pierre, Charlie
Untereiner, Valérie
Sockalingum, Ganesh D.
Ramont, Laurent
Brézillon, Stéphane
author_sort Colin-Pierre, Charlie
collection PubMed
description The expression of glypicans in different hair follicle (HF) compartments is still poorly understood. Heparan sulfate proteoglycans (HSPGs) distribution in HF is classically investigated by conventional histology, biochemical analysis, and immunohistochemistry. Our previous study proposed a novel approach to assess hair histology and glypican-1 (GPC1) distribution changes in the HF at different phases of the hair growth cycle using infrared spectral imaging (IRSI). We show in the present manuscript for the first time complementary data on the distribution of glypican-4 (GPC4) and glypican-6 (GPC6) in HF at different phases of the hair growth cycle using IR imaging. Findings were supported by Western blot assays focusing on the GPC4 and GPC6 expression in HFs. Like all proteoglycan features, the glypicans are characterized by a core protein to which sulfated and/or unsulfated glycosaminoglycan (GAG) chains are covalently linked. Our study demonstrates the capacity of IRSI to identify the different HF tissue structures and to highlight protein, proteoglycan (PG), GAG, and sulfated GAG distribution in these structures. The comparison between anagen, catagen, and telogen phases shows the qualitative and/or quantitative evolution of GAGs, as supported by Western blot. Thus, in one analysis, IRSI can simultaneously reveal the location of proteins, PGs, GAGs and sulfated GAGs in HFs in a chemical and label-free manner. From a dermatological point of view, IRSI may constitute a promising technique to study alopecia.
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spelling pubmed-100023172023-03-11 Investigation of Glypican-4 and -6 by Infrared Spectral Imaging during the Hair Growth Cycle Colin-Pierre, Charlie Untereiner, Valérie Sockalingum, Ganesh D. Ramont, Laurent Brézillon, Stéphane Int J Mol Sci Communication The expression of glypicans in different hair follicle (HF) compartments is still poorly understood. Heparan sulfate proteoglycans (HSPGs) distribution in HF is classically investigated by conventional histology, biochemical analysis, and immunohistochemistry. Our previous study proposed a novel approach to assess hair histology and glypican-1 (GPC1) distribution changes in the HF at different phases of the hair growth cycle using infrared spectral imaging (IRSI). We show in the present manuscript for the first time complementary data on the distribution of glypican-4 (GPC4) and glypican-6 (GPC6) in HF at different phases of the hair growth cycle using IR imaging. Findings were supported by Western blot assays focusing on the GPC4 and GPC6 expression in HFs. Like all proteoglycan features, the glypicans are characterized by a core protein to which sulfated and/or unsulfated glycosaminoglycan (GAG) chains are covalently linked. Our study demonstrates the capacity of IRSI to identify the different HF tissue structures and to highlight protein, proteoglycan (PG), GAG, and sulfated GAG distribution in these structures. The comparison between anagen, catagen, and telogen phases shows the qualitative and/or quantitative evolution of GAGs, as supported by Western blot. Thus, in one analysis, IRSI can simultaneously reveal the location of proteins, PGs, GAGs and sulfated GAGs in HFs in a chemical and label-free manner. From a dermatological point of view, IRSI may constitute a promising technique to study alopecia. MDPI 2023-02-21 /pmc/articles/PMC10002317/ /pubmed/36901723 http://dx.doi.org/10.3390/ijms24054291 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Colin-Pierre, Charlie
Untereiner, Valérie
Sockalingum, Ganesh D.
Ramont, Laurent
Brézillon, Stéphane
Investigation of Glypican-4 and -6 by Infrared Spectral Imaging during the Hair Growth Cycle
title Investigation of Glypican-4 and -6 by Infrared Spectral Imaging during the Hair Growth Cycle
title_full Investigation of Glypican-4 and -6 by Infrared Spectral Imaging during the Hair Growth Cycle
title_fullStr Investigation of Glypican-4 and -6 by Infrared Spectral Imaging during the Hair Growth Cycle
title_full_unstemmed Investigation of Glypican-4 and -6 by Infrared Spectral Imaging during the Hair Growth Cycle
title_short Investigation of Glypican-4 and -6 by Infrared Spectral Imaging during the Hair Growth Cycle
title_sort investigation of glypican-4 and -6 by infrared spectral imaging during the hair growth cycle
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002317/
https://www.ncbi.nlm.nih.gov/pubmed/36901723
http://dx.doi.org/10.3390/ijms24054291
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