Interleukin-22 and keratinocytes; pathogenic implications in skin inflammation
Interleukin (IL)-22 is produced from immune cells such as T helper (Th)22 cells, Th17/22 cells, and group 3 innate lymphoid cells. IL-22 signals via the IL-22 receptor 1 (IL-22R1) and the IL-10 receptor 2 (IL-10R2). As the IL-22R1/IL-10R2 heterodimer is preferentially expressed on border tissue betw...
Guardado en:
Autores principales: | , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Open Exploration Publishing Inc.
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/ca334c05404a437f849d4dd89af3cb9a |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:ca334c05404a437f849d4dd89af3cb9a |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:ca334c05404a437f849d4dd89af3cb9a2021-11-24T01:43:11ZInterleukin-22 and keratinocytes; pathogenic implications in skin inflammation10.37349/ei.2021.000052768-6655https://doaj.org/article/ca334c05404a437f849d4dd89af3cb9a2021-04-01T00:00:00Zhttps://www.explorationpub.com/Journals/ei/Article/10035https://doaj.org/toc/2768-6655Interleukin (IL)-22 is produced from immune cells such as T helper (Th)22 cells, Th17/22 cells, and group 3 innate lymphoid cells. IL-22 signals via the IL-22 receptor 1 (IL-22R1) and the IL-10 receptor 2 (IL-10R2). As the IL-22R1/IL-10R2 heterodimer is preferentially expressed on border tissue between the host and the environment, IL-22 is believed to be involved in border defense. Epidermal keratinocytes are the first-line skin barrier and express IL-22R1/IL-10R2. IL-22 increases keratinocyte proliferation but inhibits differentiation. Aryl hydrocarbon receptor (AHR) is a chemical sensor and an essential transcription factor for IL-22 production. In addition, AHR also upregulates the production of barrier-related proteins such as filaggrin in keratinocytes, suggesting a pivotal role for the AHR-IL-22 axis in regulating the physiological skin barrier. Although IL-22 signatures are elevated in atopic dermatitis and psoriasis, their pathogenic and/or protective implications are not fully understood.Masutaka FurueMihoko FurueOpen Exploration Publishing Inc.articleil-22il-22 receptoraryl hydrocarbon receptorskin barrierkeratinocyteatopic dermatitispsoriasisImmunologic diseases. AllergyRC581-607ENExploration of Immunology, Vol 1, Iss 1, Pp 37-47 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
il-22 il-22 receptor aryl hydrocarbon receptor skin barrier keratinocyte atopic dermatitis psoriasis Immunologic diseases. Allergy RC581-607 |
spellingShingle |
il-22 il-22 receptor aryl hydrocarbon receptor skin barrier keratinocyte atopic dermatitis psoriasis Immunologic diseases. Allergy RC581-607 Masutaka Furue Mihoko Furue Interleukin-22 and keratinocytes; pathogenic implications in skin inflammation |
description |
Interleukin (IL)-22 is produced from immune cells such as T helper (Th)22 cells, Th17/22 cells, and group 3 innate lymphoid cells. IL-22 signals via the IL-22 receptor 1 (IL-22R1) and the IL-10 receptor 2 (IL-10R2). As the IL-22R1/IL-10R2 heterodimer is preferentially expressed on border tissue between the host and the environment, IL-22 is believed to be involved in border defense. Epidermal keratinocytes are the first-line skin barrier and express IL-22R1/IL-10R2. IL-22 increases keratinocyte proliferation but inhibits differentiation. Aryl hydrocarbon receptor (AHR) is a chemical sensor and an essential transcription factor for IL-22 production. In addition, AHR also upregulates the production of barrier-related proteins such as filaggrin in keratinocytes, suggesting a pivotal role for the AHR-IL-22 axis in regulating the physiological skin barrier. Although IL-22 signatures are elevated in atopic dermatitis and psoriasis, their pathogenic and/or protective implications are not fully understood. |
format |
article |
author |
Masutaka Furue Mihoko Furue |
author_facet |
Masutaka Furue Mihoko Furue |
author_sort |
Masutaka Furue |
title |
Interleukin-22 and keratinocytes; pathogenic implications in skin inflammation |
title_short |
Interleukin-22 and keratinocytes; pathogenic implications in skin inflammation |
title_full |
Interleukin-22 and keratinocytes; pathogenic implications in skin inflammation |
title_fullStr |
Interleukin-22 and keratinocytes; pathogenic implications in skin inflammation |
title_full_unstemmed |
Interleukin-22 and keratinocytes; pathogenic implications in skin inflammation |
title_sort |
interleukin-22 and keratinocytes; pathogenic implications in skin inflammation |
publisher |
Open Exploration Publishing Inc. |
publishDate |
2021 |
url |
https://doaj.org/article/ca334c05404a437f849d4dd89af3cb9a |
work_keys_str_mv |
AT masutakafurue interleukin22andkeratinocytespathogenicimplicationsinskininflammation AT mihokofurue interleukin22andkeratinocytespathogenicimplicationsinskininflammation |
_version_ |
1718416059414872064 |