Cargando…

The SKINT1-Like Gene Is Inactivated in Hominoids But Not in All Primate Species: Implications for the Origin of Dendritic Epidermal T Cells

Dendritic epidermal T cells, which express an invariant Vγ5Vδ1 T-cell receptor and account for 95% of all resident T cells in the mouse epidermis, play a critical role in skin immune surveillance. These γδ T cells are generated by positive selection in the fetal thymus, after which they migrate to t...

Descripción completa

Detalles Bibliográficos
Autores principales: Mohamed, Rania Hassan, Sutoh, Yoichi, Itoh, Yasushi, Otsuka, Noriyuki, Miyatake, Yukiko, Ogasawara, Kazumasa, Kasahara, Masanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382165/
https://www.ncbi.nlm.nih.gov/pubmed/25830554
http://dx.doi.org/10.1371/journal.pone.0123258
_version_ 1782364562805227520
author Mohamed, Rania Hassan
Sutoh, Yoichi
Itoh, Yasushi
Otsuka, Noriyuki
Miyatake, Yukiko
Ogasawara, Kazumasa
Kasahara, Masanori
author_facet Mohamed, Rania Hassan
Sutoh, Yoichi
Itoh, Yasushi
Otsuka, Noriyuki
Miyatake, Yukiko
Ogasawara, Kazumasa
Kasahara, Masanori
author_sort Mohamed, Rania Hassan
collection PubMed
description Dendritic epidermal T cells, which express an invariant Vγ5Vδ1 T-cell receptor and account for 95% of all resident T cells in the mouse epidermis, play a critical role in skin immune surveillance. These γδ T cells are generated by positive selection in the fetal thymus, after which they migrate to the skin. The development of dendritic epidermal T cells is critically dependent on the Skint1 gene expressed specifically in keratinocytes and thymic epithelial cells, suggesting an indispensable role for Skint1 in the selection machinery for specific intraepithelial lymphocytes. Phylogenetically, rodents have functional SKINT1 molecules, but humans and chimpanzees have a SKINT1-like (SKINT1L) gene with multiple inactivating mutations. In the present study, we analyzed SKINT1L sequences in representative primate species and found that all hominoid species have a common inactivating mutation, but that Old World monkeys such as olive baboons, green monkeys, cynomolgus macaques and rhesus macaques have apparently functional SKINT1L sequences, indicating that SKINT1L was inactivated in a common ancestor of hominoids. Interestingly, the epidermis of cynomolgus macaques contained a population of dendritic-shaped γδ T cells expressing a semi-invariant Vγ10/Vδ1 T-cell receptor. However, this population of macaque T cells differed from rodent dendritic epidermal T cells in that their Vγ10/Vδ1 T-cell receptors displayed junctional diversity and expression of Vγ10 was not epidermis-specific. Therefore, macaques do not appear to have rodent-type dendritic epidermal T cells despite having apparently functional SKINT1L. Comprehensive bioinformatics analysis indicates that SKINT1L emerged in an ancestor of placental mammals but was inactivated or lost multiple times in mammalian evolution and that Skint1 arose by gene duplication in a rodent lineage, suggesting that authentic dendritic epidermal T cells are presumably unique to rodents.
format Online
Article
Text
id pubmed-4382165
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-43821652015-04-09 The SKINT1-Like Gene Is Inactivated in Hominoids But Not in All Primate Species: Implications for the Origin of Dendritic Epidermal T Cells Mohamed, Rania Hassan Sutoh, Yoichi Itoh, Yasushi Otsuka, Noriyuki Miyatake, Yukiko Ogasawara, Kazumasa Kasahara, Masanori PLoS One Research Article Dendritic epidermal T cells, which express an invariant Vγ5Vδ1 T-cell receptor and account for 95% of all resident T cells in the mouse epidermis, play a critical role in skin immune surveillance. These γδ T cells are generated by positive selection in the fetal thymus, after which they migrate to the skin. The development of dendritic epidermal T cells is critically dependent on the Skint1 gene expressed specifically in keratinocytes and thymic epithelial cells, suggesting an indispensable role for Skint1 in the selection machinery for specific intraepithelial lymphocytes. Phylogenetically, rodents have functional SKINT1 molecules, but humans and chimpanzees have a SKINT1-like (SKINT1L) gene with multiple inactivating mutations. In the present study, we analyzed SKINT1L sequences in representative primate species and found that all hominoid species have a common inactivating mutation, but that Old World monkeys such as olive baboons, green monkeys, cynomolgus macaques and rhesus macaques have apparently functional SKINT1L sequences, indicating that SKINT1L was inactivated in a common ancestor of hominoids. Interestingly, the epidermis of cynomolgus macaques contained a population of dendritic-shaped γδ T cells expressing a semi-invariant Vγ10/Vδ1 T-cell receptor. However, this population of macaque T cells differed from rodent dendritic epidermal T cells in that their Vγ10/Vδ1 T-cell receptors displayed junctional diversity and expression of Vγ10 was not epidermis-specific. Therefore, macaques do not appear to have rodent-type dendritic epidermal T cells despite having apparently functional SKINT1L. Comprehensive bioinformatics analysis indicates that SKINT1L emerged in an ancestor of placental mammals but was inactivated or lost multiple times in mammalian evolution and that Skint1 arose by gene duplication in a rodent lineage, suggesting that authentic dendritic epidermal T cells are presumably unique to rodents. Public Library of Science 2015-04-01 /pmc/articles/PMC4382165/ /pubmed/25830554 http://dx.doi.org/10.1371/journal.pone.0123258 Text en © 2015 Mohamed et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mohamed, Rania Hassan
Sutoh, Yoichi
Itoh, Yasushi
Otsuka, Noriyuki
Miyatake, Yukiko
Ogasawara, Kazumasa
Kasahara, Masanori
The SKINT1-Like Gene Is Inactivated in Hominoids But Not in All Primate Species: Implications for the Origin of Dendritic Epidermal T Cells
title The SKINT1-Like Gene Is Inactivated in Hominoids But Not in All Primate Species: Implications for the Origin of Dendritic Epidermal T Cells
title_full The SKINT1-Like Gene Is Inactivated in Hominoids But Not in All Primate Species: Implications for the Origin of Dendritic Epidermal T Cells
title_fullStr The SKINT1-Like Gene Is Inactivated in Hominoids But Not in All Primate Species: Implications for the Origin of Dendritic Epidermal T Cells
title_full_unstemmed The SKINT1-Like Gene Is Inactivated in Hominoids But Not in All Primate Species: Implications for the Origin of Dendritic Epidermal T Cells
title_short The SKINT1-Like Gene Is Inactivated in Hominoids But Not in All Primate Species: Implications for the Origin of Dendritic Epidermal T Cells
title_sort skint1-like gene is inactivated in hominoids but not in all primate species: implications for the origin of dendritic epidermal t cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382165/
https://www.ncbi.nlm.nih.gov/pubmed/25830554
http://dx.doi.org/10.1371/journal.pone.0123258
work_keys_str_mv AT mohamedraniahassan theskint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT sutohyoichi theskint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT itohyasushi theskint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT otsukanoriyuki theskint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT miyatakeyukiko theskint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT ogasawarakazumasa theskint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT kasaharamasanori theskint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT mohamedraniahassan skint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT sutohyoichi skint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT itohyasushi skint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT otsukanoriyuki skint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT miyatakeyukiko skint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT ogasawarakazumasa skint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells
AT kasaharamasanori skint1likegeneisinactivatedinhominoidsbutnotinallprimatespeciesimplicationsfortheoriginofdendriticepidermaltcells