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Aire Controls Heterogeneity of Medullary Thymic Epithelial Cells for the Expression of Self-Antigens
The deficiency of Aire, a transcriptional regulator whose defect results in the development of autoimmunity, is associated with reduced expression of tissue-restricted self-Ags (TRAs) in medullary thymic epithelial cells (mTECs). Although the mechanisms underlying Aire-dependent expression of TRAs n...
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Published in: | The Journal of immunology (1950) 2022-01, Vol.208 (2), p.303-320 |
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container_title | The Journal of immunology (1950) |
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creator | Nishijima, Hitoshi Matsumoto, Minoru Morimoto, Junko Hosomichi, Kazuyoshi Akiyama, Nobuko Akiyama, Taishin Oya, Takeshi Tsuneyama, Koichi Yoshida, Hideyuki Matsumoto, Mitsuru |
description | The deficiency of Aire, a transcriptional regulator whose defect results in the development of autoimmunity, is associated with reduced expression of tissue-restricted self-Ags (TRAs) in medullary thymic epithelial cells (mTECs). Although the mechanisms underlying Aire-dependent expression of TRAs need to be explored, the physical identification of the target(s) of Aire has been hampered by the low and promiscuous expression of TRAs. We have tackled this issue by engineering mice with augmented Aire expression. Integration of the transcriptomic data from Aire-augmented and Aire-deficient mTECs revealed that a large proportion of so-called Aire-dependent genes, including those of TRAs, may not be direct transcriptional targets downstream of Aire. Rather, Aire induces TRA expression indirectly through controlling the heterogeneity of mTECs, as revealed by single-cell analyses. In contrast, Ccl25 emerged as a canonical target of Aire, and we verified this both in vitro and in vivo. Our approach has illuminated the Aire's primary targets while distinguishing them from the secondary targets. |
doi_str_mv | 10.4049/jimmunol.2100692 |
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Although the mechanisms underlying Aire-dependent expression of TRAs need to be explored, the physical identification of the target(s) of Aire has been hampered by the low and promiscuous expression of TRAs. We have tackled this issue by engineering mice with augmented Aire expression. Integration of the transcriptomic data from Aire-augmented and Aire-deficient mTECs revealed that a large proportion of so-called Aire-dependent genes, including those of TRAs, may not be direct transcriptional targets downstream of Aire. Rather, Aire induces TRA expression indirectly through controlling the heterogeneity of mTECs, as revealed by single-cell analyses. In contrast, Ccl25 emerged as a canonical target of Aire, and we verified this both in vitro and in vivo. Our approach has illuminated the Aire's primary targets while distinguishing them from the secondary targets.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.2100692</identifier><identifier>PMID: 34930780</identifier><language>eng</language><publisher>United States</publisher><subject>AIRE Protein ; Animals ; Autoantigens - immunology ; Autoimmunity - genetics ; Autoimmunity - immunology ; Chemokines, CC - genetics ; Chemokines, CC - metabolism ; Epithelial Cells - immunology ; Gene Expression Regulation ; Gene Knock-In Techniques ; Gene Knockout Techniques ; Mice ; Mice, Inbred C57BL ; Mice, Inbred NOD ; Mice, Transgenic ; Thymus Gland - cytology ; Thymus Gland - immunology ; Transcription Factors - genetics ; Transcription Factors - metabolism ; Transcription, Genetic - genetics</subject><ispartof>The Journal of immunology (1950), 2022-01, Vol.208 (2), p.303-320</ispartof><rights>Copyright © 2022 by The American Association of Immunologists, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-a4d7fc362766ecc5c6eff4d3a78fa6e6f7450d7db64f90d2efb0a277784c83dd3</citedby><cites>FETCH-LOGICAL-c451t-a4d7fc362766ecc5c6eff4d3a78fa6e6f7450d7db64f90d2efb0a277784c83dd3</cites><orcidid>0000-0002-0670-9868 ; 0000-0003-2712-1825 ; 0000-0003-3844-8110</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34930780$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nishijima, Hitoshi</creatorcontrib><creatorcontrib>Matsumoto, Minoru</creatorcontrib><creatorcontrib>Morimoto, Junko</creatorcontrib><creatorcontrib>Hosomichi, Kazuyoshi</creatorcontrib><creatorcontrib>Akiyama, Nobuko</creatorcontrib><creatorcontrib>Akiyama, Taishin</creatorcontrib><creatorcontrib>Oya, Takeshi</creatorcontrib><creatorcontrib>Tsuneyama, Koichi</creatorcontrib><creatorcontrib>Yoshida, Hideyuki</creatorcontrib><creatorcontrib>Matsumoto, Mitsuru</creatorcontrib><title>Aire Controls Heterogeneity of Medullary Thymic Epithelial Cells for the Expression of Self-Antigens</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>The deficiency of Aire, a transcriptional regulator whose defect results in the development of autoimmunity, is associated with reduced expression of tissue-restricted self-Ags (TRAs) in medullary thymic epithelial cells (mTECs). Although the mechanisms underlying Aire-dependent expression of TRAs need to be explored, the physical identification of the target(s) of Aire has been hampered by the low and promiscuous expression of TRAs. We have tackled this issue by engineering mice with augmented Aire expression. Integration of the transcriptomic data from Aire-augmented and Aire-deficient mTECs revealed that a large proportion of so-called Aire-dependent genes, including those of TRAs, may not be direct transcriptional targets downstream of Aire. Rather, Aire induces TRA expression indirectly through controlling the heterogeneity of mTECs, as revealed by single-cell analyses. In contrast, Ccl25 emerged as a canonical target of Aire, and we verified this both in vitro and in vivo. Our approach has illuminated the Aire's primary targets while distinguishing them from the secondary targets.</description><subject>AIRE Protein</subject><subject>Animals</subject><subject>Autoantigens - immunology</subject><subject>Autoimmunity - genetics</subject><subject>Autoimmunity - immunology</subject><subject>Chemokines, CC - genetics</subject><subject>Chemokines, CC - metabolism</subject><subject>Epithelial Cells - immunology</subject><subject>Gene Expression Regulation</subject><subject>Gene Knock-In Techniques</subject><subject>Gene Knockout Techniques</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred NOD</subject><subject>Mice, Transgenic</subject><subject>Thymus Gland - cytology</subject><subject>Thymus Gland - immunology</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><subject>Transcription, Genetic - genetics</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNo9kDFPwzAQRi0EoqWwMyGPLIGL49jJWFWFIhUxUOYotc_UlRMXO5HovydVW6aTTt_7dPcIuU_hiQMvn7e2afrWuyeWAoiSXZBxmueQCAHikowBGEtSKeSI3MS4hSEDjF-TUcbLDGQBY6KnNiCd-bYL3kW6wA6D_8YWbben3tB31L1zddjT1WbfWEXnO9tt0Nna0Rm6ATE-0GFD57-7gDFa3x64T3QmmbadHbriLbkytYt4d5oT8vUyX80WyfLj9W02XSaK52mX1FxLozLBpBCoVK4EGsN1VsvC1AKFkTwHLfVacFOCZmjWUDMpZcFVkWmdTcjjsXcX_E-PsasaG9VwZd2i72PFRMqykkGeDlE4RlXwMQY01S7YZvizSqE6uK3ObquT2wF5OLX36wb1P3CWmf0B9hh4yA</recordid><startdate>20220115</startdate><enddate>20220115</enddate><creator>Nishijima, Hitoshi</creator><creator>Matsumoto, Minoru</creator><creator>Morimoto, Junko</creator><creator>Hosomichi, Kazuyoshi</creator><creator>Akiyama, Nobuko</creator><creator>Akiyama, Taishin</creator><creator>Oya, Takeshi</creator><creator>Tsuneyama, Koichi</creator><creator>Yoshida, Hideyuki</creator><creator>Matsumoto, Mitsuru</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0670-9868</orcidid><orcidid>https://orcid.org/0000-0003-2712-1825</orcidid><orcidid>https://orcid.org/0000-0003-3844-8110</orcidid></search><sort><creationdate>20220115</creationdate><title>Aire Controls Heterogeneity of Medullary Thymic Epithelial Cells for the Expression of Self-Antigens</title><author>Nishijima, Hitoshi ; Matsumoto, Minoru ; Morimoto, Junko ; Hosomichi, Kazuyoshi ; Akiyama, Nobuko ; Akiyama, Taishin ; Oya, Takeshi ; Tsuneyama, Koichi ; Yoshida, Hideyuki ; Matsumoto, Mitsuru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-a4d7fc362766ecc5c6eff4d3a78fa6e6f7450d7db64f90d2efb0a277784c83dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>AIRE Protein</topic><topic>Animals</topic><topic>Autoantigens - immunology</topic><topic>Autoimmunity - genetics</topic><topic>Autoimmunity - immunology</topic><topic>Chemokines, CC - genetics</topic><topic>Chemokines, CC - metabolism</topic><topic>Epithelial Cells - immunology</topic><topic>Gene Expression Regulation</topic><topic>Gene Knock-In Techniques</topic><topic>Gene Knockout Techniques</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred NOD</topic><topic>Mice, Transgenic</topic><topic>Thymus Gland - cytology</topic><topic>Thymus Gland - immunology</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><topic>Transcription, Genetic - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nishijima, Hitoshi</creatorcontrib><creatorcontrib>Matsumoto, Minoru</creatorcontrib><creatorcontrib>Morimoto, Junko</creatorcontrib><creatorcontrib>Hosomichi, Kazuyoshi</creatorcontrib><creatorcontrib>Akiyama, Nobuko</creatorcontrib><creatorcontrib>Akiyama, Taishin</creatorcontrib><creatorcontrib>Oya, Takeshi</creatorcontrib><creatorcontrib>Tsuneyama, Koichi</creatorcontrib><creatorcontrib>Yoshida, Hideyuki</creatorcontrib><creatorcontrib>Matsumoto, Mitsuru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nishijima, Hitoshi</au><au>Matsumoto, Minoru</au><au>Morimoto, Junko</au><au>Hosomichi, Kazuyoshi</au><au>Akiyama, Nobuko</au><au>Akiyama, Taishin</au><au>Oya, Takeshi</au><au>Tsuneyama, Koichi</au><au>Yoshida, Hideyuki</au><au>Matsumoto, Mitsuru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aire Controls Heterogeneity of Medullary Thymic Epithelial Cells for the Expression of Self-Antigens</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2022-01-15</date><risdate>2022</risdate><volume>208</volume><issue>2</issue><spage>303</spage><epage>320</epage><pages>303-320</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>The deficiency of Aire, a transcriptional regulator whose defect results in the development of autoimmunity, is associated with reduced expression of tissue-restricted self-Ags (TRAs) in medullary thymic epithelial cells (mTECs). Although the mechanisms underlying Aire-dependent expression of TRAs need to be explored, the physical identification of the target(s) of Aire has been hampered by the low and promiscuous expression of TRAs. We have tackled this issue by engineering mice with augmented Aire expression. Integration of the transcriptomic data from Aire-augmented and Aire-deficient mTECs revealed that a large proportion of so-called Aire-dependent genes, including those of TRAs, may not be direct transcriptional targets downstream of Aire. Rather, Aire induces TRA expression indirectly through controlling the heterogeneity of mTECs, as revealed by single-cell analyses. In contrast, Ccl25 emerged as a canonical target of Aire, and we verified this both in vitro and in vivo. 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subjects | AIRE Protein Animals Autoantigens - immunology Autoimmunity - genetics Autoimmunity - immunology Chemokines, CC - genetics Chemokines, CC - metabolism Epithelial Cells - immunology Gene Expression Regulation Gene Knock-In Techniques Gene Knockout Techniques Mice Mice, Inbred C57BL Mice, Inbred NOD Mice, Transgenic Thymus Gland - cytology Thymus Gland - immunology Transcription Factors - genetics Transcription Factors - metabolism Transcription, Genetic - genetics |
title | Aire Controls Heterogeneity of Medullary Thymic Epithelial Cells for the Expression of Self-Antigens |
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