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Tight Junction barriers in human hair follicles – role of claudin-1

Barrier function of hair follicles (HFs) is of great interest because they might be an entry port for allergens/pathogens, but could on the other hand be used for drug delivery or vaccination. Therefore we investigated tight junction (TJ) barrier function in human HFs. We show that there is a TJ bar...

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Autores principales: Zorn-Kruppa, Michaela, Vidal-y-Sy, Sabine, Houdek, Pia, Wladykowski, Ewa, Grzybowski, Stephan, Gruber, Robert, Gorzelanny, Christian, Harcup, Jason, Schneider, Stefan W., Majumdar, Amitabha, Brandner, Johanna M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109114/
https://www.ncbi.nlm.nih.gov/pubmed/30143655
http://dx.doi.org/10.1038/s41598-018-30341-9
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author Zorn-Kruppa, Michaela
Vidal-y-Sy, Sabine
Houdek, Pia
Wladykowski, Ewa
Grzybowski, Stephan
Gruber, Robert
Gorzelanny, Christian
Harcup, Jason
Schneider, Stefan W.
Majumdar, Amitabha
Brandner, Johanna M.
author_facet Zorn-Kruppa, Michaela
Vidal-y-Sy, Sabine
Houdek, Pia
Wladykowski, Ewa
Grzybowski, Stephan
Gruber, Robert
Gorzelanny, Christian
Harcup, Jason
Schneider, Stefan W.
Majumdar, Amitabha
Brandner, Johanna M.
author_sort Zorn-Kruppa, Michaela
collection PubMed
description Barrier function of hair follicles (HFs) is of great interest because they might be an entry port for allergens/pathogens, but could on the other hand be used for drug delivery or vaccination. Therefore we investigated tight junction (TJ) barrier function in human HFs. We show that there is a TJ barrier in the outermost living layer bordering to the environment from the infundibulum to the lower central part and between Henle’s and Huxles layer of anagen HFs. In club hair typical for catagen and telogen HFs a TJ barrier is found surrounding the club. This demonstrates that there is a continuous TJ barrier along interfollicular epidermis and HFs in different phases of HF cycle. However, interestingly, in cell culture experiments we can show that barrier is less tight in HF keratinocytes compared to interfollicular keratinocytes. Knock-down of the TJ protein claudin-1, which we demonstrate here to be less expressed in HFs of lesional atopic dermatitis skin, results in impaired barrier function, decreased proliferation and increased apoptosis of hair keratinocytes. This is in line with a hair growth phenotype in claudin-1 deficient patients (NISCH syndrome) and corresponding knock-out mice and indicates an important role of claudin-1 in HF barrier function and growth.
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spelling pubmed-61091142018-08-31 Tight Junction barriers in human hair follicles – role of claudin-1 Zorn-Kruppa, Michaela Vidal-y-Sy, Sabine Houdek, Pia Wladykowski, Ewa Grzybowski, Stephan Gruber, Robert Gorzelanny, Christian Harcup, Jason Schneider, Stefan W. Majumdar, Amitabha Brandner, Johanna M. Sci Rep Article Barrier function of hair follicles (HFs) is of great interest because they might be an entry port for allergens/pathogens, but could on the other hand be used for drug delivery or vaccination. Therefore we investigated tight junction (TJ) barrier function in human HFs. We show that there is a TJ barrier in the outermost living layer bordering to the environment from the infundibulum to the lower central part and between Henle’s and Huxles layer of anagen HFs. In club hair typical for catagen and telogen HFs a TJ barrier is found surrounding the club. This demonstrates that there is a continuous TJ barrier along interfollicular epidermis and HFs in different phases of HF cycle. However, interestingly, in cell culture experiments we can show that barrier is less tight in HF keratinocytes compared to interfollicular keratinocytes. Knock-down of the TJ protein claudin-1, which we demonstrate here to be less expressed in HFs of lesional atopic dermatitis skin, results in impaired barrier function, decreased proliferation and increased apoptosis of hair keratinocytes. This is in line with a hair growth phenotype in claudin-1 deficient patients (NISCH syndrome) and corresponding knock-out mice and indicates an important role of claudin-1 in HF barrier function and growth. Nature Publishing Group UK 2018-08-24 /pmc/articles/PMC6109114/ /pubmed/30143655 http://dx.doi.org/10.1038/s41598-018-30341-9 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zorn-Kruppa, Michaela
Vidal-y-Sy, Sabine
Houdek, Pia
Wladykowski, Ewa
Grzybowski, Stephan
Gruber, Robert
Gorzelanny, Christian
Harcup, Jason
Schneider, Stefan W.
Majumdar, Amitabha
Brandner, Johanna M.
Tight Junction barriers in human hair follicles – role of claudin-1
title Tight Junction barriers in human hair follicles – role of claudin-1
title_full Tight Junction barriers in human hair follicles – role of claudin-1
title_fullStr Tight Junction barriers in human hair follicles – role of claudin-1
title_full_unstemmed Tight Junction barriers in human hair follicles – role of claudin-1
title_short Tight Junction barriers in human hair follicles – role of claudin-1
title_sort tight junction barriers in human hair follicles – role of claudin-1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109114/
https://www.ncbi.nlm.nih.gov/pubmed/30143655
http://dx.doi.org/10.1038/s41598-018-30341-9
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