Loading…
DNA demethylation fine‐tunes IL‐2 production during thymic regulatory T cell differentiation
Regulatory T (T reg) cells developing in the thymus are essential to maintain tolerance and prevent fatal autoimmunity in mice and humans. Expression of the T reg lineage‐defining transcription factor FoxP3 is critically dependent upon T cell receptor (TCR) and interleukin‐2 (IL‐2) signaling. Here,...
Saved in:
Published in: | EMBO reports 2023-05, Vol.24 (5), p.e55543-n/a |
---|---|
Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c5143-febc1984d79eea11974190ed180a70271f6628aa9909393eb12ed4fe68099c303 |
---|---|
cites | cdi_FETCH-LOGICAL-c5143-febc1984d79eea11974190ed180a70271f6628aa9909393eb12ed4fe68099c303 |
container_end_page | n/a |
container_issue | 5 |
container_start_page | e55543 |
container_title | EMBO reports |
container_volume | 24 |
creator | Teghanemt, Athmane Misel‐Wuchter, Kara Heath, Jace Thurman, Andrew Pulipati, Priyanjali Dixit, Garima Geesala, Ramasatya Meyerholz, David K Maretzky, Thorsten Pezzulo, Alejandro Issuree, Priya D |
description | Regulatory T (T reg) cells developing in the thymus are essential to maintain tolerance and prevent fatal autoimmunity in mice and humans. Expression of the T reg lineage‐defining transcription factor FoxP3 is critically dependent upon T cell receptor (TCR) and interleukin‐2 (IL‐2) signaling. Here, we report that ten‐eleven translocation (Tet) enzymes, which are DNA demethylases, are required early during double‐positive (DP) thymic T cell differentiation and prior to the upregulation of FoxP3 in CD4 single‐positive (SP) thymocytes, to promote Treg differentiation. We show that Tet3 selectively controls the development of CD25
−
FoxP3
lo
CD4SP Treg cell precursors in the thymus and is critical for TCR‐dependent IL‐2 production, which drive chromatin remodeling at the FoxP3 locus as well as other Treg‐effector gene loci in an autocrine/paracrine manner. Together, our results demonstrate a novel role for DNA demethylation in regulating the TCR response and promoting Treg cell differentiation. These findings highlight a novel epigenetic pathway to promote the generation of endogenous Treg cells for mitigation of autoimmune responses.
Synopsis
This study identifies a temporal requirement for DNA demethylation during Treg cell differentiation from thymic CD4
+
T cell and shows a role for Tet3 in modulating IL‐2 production and the development of CD25
−
FoxP3
lo
precursors.
DNA demethylases are required prior to the upregulation of FoxP3 in CD4 single‐positive thymocytes to promote Treg differentiation.
Tet3 selectively controls the development of CD25
‐
FoxP3
lo
CD4 Treg cell precursors in the thymus.
Tet3 is critical for TCR‐dependent IL‐2 production, which drives genome‐wide chromatin remodeling in an autocrine/paracrine manner.
Graphical Abstract
This study identifies a temporal requirement for DNA demethylation during Treg cell differentiation from thymic CD4
+
T cell precursors and shows a role for Tet3 in modulating IL‐2 production and the development of CD25
−
FoxP3
lo
precursors. |
doi_str_mv | 10.15252/embr.202255543 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10157375</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2808830038</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5143-febc1984d79eea11974190ed180a70271f6628aa9909393eb12ed4fe68099c303</originalsourceid><addsrcrecordid>eNqFkU9v1DAQxS0EoqVw5oYsceGy7diOY5sLKqVApS1IqEjcjDeZbF0l8WInoL3xEfiM_ST1_mFpkRCnGWl-8_SeHiFPGRwyySU_wm4WDzlwLqUsxD2yz4rSTART-v5255x92SOPUroCAGmUfkj2RKk1SCX3ydc3H45pjR0Ol8vWDT70tPE9Xv_8NYw9Jno2zSunixjqsVqf6zH6fk4z3_mKRpyP-S_EJb2gFbYtrX3TYMR-8Gu5x-RB49qET7bzgHx-e3px8n4y_fju7OR4OqkkK8SkwVnFjC5qZRAdY0YVzADWTINTwBVrypJr54wBI4zAGeNYFw2WGoypBIgD8mqjuxhnHdZVNhBdaxfRdy4ubXDe3r30_tLOw3fLgEkllMwKL7YKMXwbMQ2282kVyfUYxmS50oXQshRlRp__hV6FMfY5n-UatBYAQmfqaENVMaQUsdm5YWDX9dlVfXZXX_54djvEjv_dVwZeboAfvsXl__Ts6fnrT7fVYfOcFqsKMf5x_S9DN2CuucM</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2808830038</pqid></control><display><type>article</type><title>DNA demethylation fine‐tunes IL‐2 production during thymic regulatory T cell differentiation</title><source>PubMed Central</source><creator>Teghanemt, Athmane ; Misel‐Wuchter, Kara ; Heath, Jace ; Thurman, Andrew ; Pulipati, Priyanjali ; Dixit, Garima ; Geesala, Ramasatya ; Meyerholz, David K ; Maretzky, Thorsten ; Pezzulo, Alejandro ; Issuree, Priya D</creator><creatorcontrib>Teghanemt, Athmane ; Misel‐Wuchter, Kara ; Heath, Jace ; Thurman, Andrew ; Pulipati, Priyanjali ; Dixit, Garima ; Geesala, Ramasatya ; Meyerholz, David K ; Maretzky, Thorsten ; Pezzulo, Alejandro ; Issuree, Priya D</creatorcontrib><description>Regulatory T (T reg) cells developing in the thymus are essential to maintain tolerance and prevent fatal autoimmunity in mice and humans. Expression of the T reg lineage‐defining transcription factor FoxP3 is critically dependent upon T cell receptor (TCR) and interleukin‐2 (IL‐2) signaling. Here, we report that ten‐eleven translocation (Tet) enzymes, which are DNA demethylases, are required early during double‐positive (DP) thymic T cell differentiation and prior to the upregulation of FoxP3 in CD4 single‐positive (SP) thymocytes, to promote Treg differentiation. We show that Tet3 selectively controls the development of CD25
−
FoxP3
lo
CD4SP Treg cell precursors in the thymus and is critical for TCR‐dependent IL‐2 production, which drive chromatin remodeling at the FoxP3 locus as well as other Treg‐effector gene loci in an autocrine/paracrine manner. Together, our results demonstrate a novel role for DNA demethylation in regulating the TCR response and promoting Treg cell differentiation. These findings highlight a novel epigenetic pathway to promote the generation of endogenous Treg cells for mitigation of autoimmune responses.
Synopsis
This study identifies a temporal requirement for DNA demethylation during Treg cell differentiation from thymic CD4
+
T cell and shows a role for Tet3 in modulating IL‐2 production and the development of CD25
−
FoxP3
lo
precursors.
DNA demethylases are required prior to the upregulation of FoxP3 in CD4 single‐positive thymocytes to promote Treg differentiation.
Tet3 selectively controls the development of CD25
‐
FoxP3
lo
CD4 Treg cell precursors in the thymus.
Tet3 is critical for TCR‐dependent IL‐2 production, which drives genome‐wide chromatin remodeling in an autocrine/paracrine manner.
Graphical Abstract
This study identifies a temporal requirement for DNA demethylation during Treg cell differentiation from thymic CD4
+
T cell precursors and shows a role for Tet3 in modulating IL‐2 production and the development of CD25
−
FoxP3
lo
precursors.</description><identifier>ISSN: 1469-221X</identifier><identifier>EISSN: 1469-3178</identifier><identifier>DOI: 10.15252/embr.202255543</identifier><identifier>PMID: 36880575</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Animals ; Autocrine signalling ; Autoimmunity ; CD25 antigen ; CD4 antigen ; Cell Differentiation ; Chromatin remodeling ; Demethylation ; Deoxyribonucleic acid ; Differentiation (biology) ; DNA ; DNA Demethylation ; EMBO09 ; EMBO11 ; EMBO19 ; Epigenetics ; Forkhead Transcription Factors - metabolism ; FoxP3 ; Foxp3 protein ; Humans ; IL‐2 ; Immunological tolerance ; Interleukin-2 ; Interleukins ; Life Sciences ; Lymphocytes ; Lymphocytes T ; Mice ; Paracrine signalling ; Precursors ; Receptors, Antigen, T-Cell - metabolism ; T cell receptors ; T-Lymphocytes, Regulatory ; Tet enzymes ; Thymocytes ; Thymus Gland ; Translocation ; Treg development</subject><ispartof>EMBO reports, 2023-05, Vol.24 (5), p.e55543-n/a</ispartof><rights>The Author(s) 2023</rights><rights>2023 The Authors. Published under the terms of the CC BY NC ND 4.0 license</rights><rights>2023 The Authors. Published under the terms of the CC BY NC ND 4.0 license.</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5143-febc1984d79eea11974190ed180a70271f6628aa9909393eb12ed4fe68099c303</citedby><cites>FETCH-LOGICAL-c5143-febc1984d79eea11974190ed180a70271f6628aa9909393eb12ed4fe68099c303</cites><orcidid>0000-0003-1818-9975 ; 0000-0002-8886-6436 ; 0000-0001-8206-1998 ; 0000-0003-1771-749X ; 0000-0001-7544-5109 ; 0000-0003-1282-6080 ; 0000-0003-2167-5894 ; 0000-0002-8046-0626 ; 0000-0003-1552-3253</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157375/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157375/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36880575$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Teghanemt, Athmane</creatorcontrib><creatorcontrib>Misel‐Wuchter, Kara</creatorcontrib><creatorcontrib>Heath, Jace</creatorcontrib><creatorcontrib>Thurman, Andrew</creatorcontrib><creatorcontrib>Pulipati, Priyanjali</creatorcontrib><creatorcontrib>Dixit, Garima</creatorcontrib><creatorcontrib>Geesala, Ramasatya</creatorcontrib><creatorcontrib>Meyerholz, David K</creatorcontrib><creatorcontrib>Maretzky, Thorsten</creatorcontrib><creatorcontrib>Pezzulo, Alejandro</creatorcontrib><creatorcontrib>Issuree, Priya D</creatorcontrib><title>DNA demethylation fine‐tunes IL‐2 production during thymic regulatory T cell differentiation</title><title>EMBO reports</title><addtitle>EMBO Rep</addtitle><addtitle>EMBO Rep</addtitle><description>Regulatory T (T reg) cells developing in the thymus are essential to maintain tolerance and prevent fatal autoimmunity in mice and humans. Expression of the T reg lineage‐defining transcription factor FoxP3 is critically dependent upon T cell receptor (TCR) and interleukin‐2 (IL‐2) signaling. Here, we report that ten‐eleven translocation (Tet) enzymes, which are DNA demethylases, are required early during double‐positive (DP) thymic T cell differentiation and prior to the upregulation of FoxP3 in CD4 single‐positive (SP) thymocytes, to promote Treg differentiation. We show that Tet3 selectively controls the development of CD25
−
FoxP3
lo
CD4SP Treg cell precursors in the thymus and is critical for TCR‐dependent IL‐2 production, which drive chromatin remodeling at the FoxP3 locus as well as other Treg‐effector gene loci in an autocrine/paracrine manner. Together, our results demonstrate a novel role for DNA demethylation in regulating the TCR response and promoting Treg cell differentiation. These findings highlight a novel epigenetic pathway to promote the generation of endogenous Treg cells for mitigation of autoimmune responses.
Synopsis
This study identifies a temporal requirement for DNA demethylation during Treg cell differentiation from thymic CD4
+
T cell and shows a role for Tet3 in modulating IL‐2 production and the development of CD25
−
FoxP3
lo
precursors.
DNA demethylases are required prior to the upregulation of FoxP3 in CD4 single‐positive thymocytes to promote Treg differentiation.
Tet3 selectively controls the development of CD25
‐
FoxP3
lo
CD4 Treg cell precursors in the thymus.
Tet3 is critical for TCR‐dependent IL‐2 production, which drives genome‐wide chromatin remodeling in an autocrine/paracrine manner.
Graphical Abstract
This study identifies a temporal requirement for DNA demethylation during Treg cell differentiation from thymic CD4
+
T cell precursors and shows a role for Tet3 in modulating IL‐2 production and the development of CD25
−
FoxP3
lo
precursors.</description><subject>Animals</subject><subject>Autocrine signalling</subject><subject>Autoimmunity</subject><subject>CD25 antigen</subject><subject>CD4 antigen</subject><subject>Cell Differentiation</subject><subject>Chromatin remodeling</subject><subject>Demethylation</subject><subject>Deoxyribonucleic acid</subject><subject>Differentiation (biology)</subject><subject>DNA</subject><subject>DNA Demethylation</subject><subject>EMBO09</subject><subject>EMBO11</subject><subject>EMBO19</subject><subject>Epigenetics</subject><subject>Forkhead Transcription Factors - metabolism</subject><subject>FoxP3</subject><subject>Foxp3 protein</subject><subject>Humans</subject><subject>IL‐2</subject><subject>Immunological tolerance</subject><subject>Interleukin-2</subject><subject>Interleukins</subject><subject>Life Sciences</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Mice</subject><subject>Paracrine signalling</subject><subject>Precursors</subject><subject>Receptors, Antigen, T-Cell - metabolism</subject><subject>T cell receptors</subject><subject>T-Lymphocytes, Regulatory</subject><subject>Tet enzymes</subject><subject>Thymocytes</subject><subject>Thymus Gland</subject><subject>Translocation</subject><subject>Treg development</subject><issn>1469-221X</issn><issn>1469-3178</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkU9v1DAQxS0EoqVw5oYsceGy7diOY5sLKqVApS1IqEjcjDeZbF0l8WInoL3xEfiM_ST1_mFpkRCnGWl-8_SeHiFPGRwyySU_wm4WDzlwLqUsxD2yz4rSTART-v5255x92SOPUroCAGmUfkj2RKk1SCX3ydc3H45pjR0Ol8vWDT70tPE9Xv_8NYw9Jno2zSunixjqsVqf6zH6fk4z3_mKRpyP-S_EJb2gFbYtrX3TYMR-8Gu5x-RB49qET7bzgHx-e3px8n4y_fju7OR4OqkkK8SkwVnFjC5qZRAdY0YVzADWTINTwBVrypJr54wBI4zAGeNYFw2WGoypBIgD8mqjuxhnHdZVNhBdaxfRdy4ubXDe3r30_tLOw3fLgEkllMwKL7YKMXwbMQ2282kVyfUYxmS50oXQshRlRp__hV6FMfY5n-UatBYAQmfqaENVMaQUsdm5YWDX9dlVfXZXX_54djvEjv_dVwZeboAfvsXl__Ts6fnrT7fVYfOcFqsKMf5x_S9DN2CuucM</recordid><startdate>20230504</startdate><enddate>20230504</enddate><creator>Teghanemt, Athmane</creator><creator>Misel‐Wuchter, Kara</creator><creator>Heath, Jace</creator><creator>Thurman, Andrew</creator><creator>Pulipati, Priyanjali</creator><creator>Dixit, Garima</creator><creator>Geesala, Ramasatya</creator><creator>Meyerholz, David K</creator><creator>Maretzky, Thorsten</creator><creator>Pezzulo, Alejandro</creator><creator>Issuree, Priya D</creator><general>Nature Publishing Group UK</general><general>Springer Nature B.V</general><general>John Wiley and Sons Inc</general><scope>C6C</scope><scope>24P</scope><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>7QL</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1818-9975</orcidid><orcidid>https://orcid.org/0000-0002-8886-6436</orcidid><orcidid>https://orcid.org/0000-0001-8206-1998</orcidid><orcidid>https://orcid.org/0000-0003-1771-749X</orcidid><orcidid>https://orcid.org/0000-0001-7544-5109</orcidid><orcidid>https://orcid.org/0000-0003-1282-6080</orcidid><orcidid>https://orcid.org/0000-0003-2167-5894</orcidid><orcidid>https://orcid.org/0000-0002-8046-0626</orcidid><orcidid>https://orcid.org/0000-0003-1552-3253</orcidid></search><sort><creationdate>20230504</creationdate><title>DNA demethylation fine‐tunes IL‐2 production during thymic regulatory T cell differentiation</title><author>Teghanemt, Athmane ; Misel‐Wuchter, Kara ; Heath, Jace ; Thurman, Andrew ; Pulipati, Priyanjali ; Dixit, Garima ; Geesala, Ramasatya ; Meyerholz, David K ; Maretzky, Thorsten ; Pezzulo, Alejandro ; Issuree, Priya D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5143-febc1984d79eea11974190ed180a70271f6628aa9909393eb12ed4fe68099c303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Autocrine signalling</topic><topic>Autoimmunity</topic><topic>CD25 antigen</topic><topic>CD4 antigen</topic><topic>Cell Differentiation</topic><topic>Chromatin remodeling</topic><topic>Demethylation</topic><topic>Deoxyribonucleic acid</topic><topic>Differentiation (biology)</topic><topic>DNA</topic><topic>DNA Demethylation</topic><topic>EMBO09</topic><topic>EMBO11</topic><topic>EMBO19</topic><topic>Epigenetics</topic><topic>Forkhead Transcription Factors - metabolism</topic><topic>FoxP3</topic><topic>Foxp3 protein</topic><topic>Humans</topic><topic>IL‐2</topic><topic>Immunological tolerance</topic><topic>Interleukin-2</topic><topic>Interleukins</topic><topic>Life Sciences</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Mice</topic><topic>Paracrine signalling</topic><topic>Precursors</topic><topic>Receptors, Antigen, T-Cell - metabolism</topic><topic>T cell receptors</topic><topic>T-Lymphocytes, Regulatory</topic><topic>Tet enzymes</topic><topic>Thymocytes</topic><topic>Thymus Gland</topic><topic>Translocation</topic><topic>Treg development</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Teghanemt, Athmane</creatorcontrib><creatorcontrib>Misel‐Wuchter, Kara</creatorcontrib><creatorcontrib>Heath, Jace</creatorcontrib><creatorcontrib>Thurman, Andrew</creatorcontrib><creatorcontrib>Pulipati, Priyanjali</creatorcontrib><creatorcontrib>Dixit, Garima</creatorcontrib><creatorcontrib>Geesala, Ramasatya</creatorcontrib><creatorcontrib>Meyerholz, David K</creatorcontrib><creatorcontrib>Maretzky, Thorsten</creatorcontrib><creatorcontrib>Pezzulo, Alejandro</creatorcontrib><creatorcontrib>Issuree, Priya D</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>EMBO reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Teghanemt, Athmane</au><au>Misel‐Wuchter, Kara</au><au>Heath, Jace</au><au>Thurman, Andrew</au><au>Pulipati, Priyanjali</au><au>Dixit, Garima</au><au>Geesala, Ramasatya</au><au>Meyerholz, David K</au><au>Maretzky, Thorsten</au><au>Pezzulo, Alejandro</au><au>Issuree, Priya D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DNA demethylation fine‐tunes IL‐2 production during thymic regulatory T cell differentiation</atitle><jtitle>EMBO reports</jtitle><stitle>EMBO Rep</stitle><addtitle>EMBO Rep</addtitle><date>2023-05-04</date><risdate>2023</risdate><volume>24</volume><issue>5</issue><spage>e55543</spage><epage>n/a</epage><pages>e55543-n/a</pages><issn>1469-221X</issn><eissn>1469-3178</eissn><abstract>Regulatory T (T reg) cells developing in the thymus are essential to maintain tolerance and prevent fatal autoimmunity in mice and humans. Expression of the T reg lineage‐defining transcription factor FoxP3 is critically dependent upon T cell receptor (TCR) and interleukin‐2 (IL‐2) signaling. Here, we report that ten‐eleven translocation (Tet) enzymes, which are DNA demethylases, are required early during double‐positive (DP) thymic T cell differentiation and prior to the upregulation of FoxP3 in CD4 single‐positive (SP) thymocytes, to promote Treg differentiation. We show that Tet3 selectively controls the development of CD25
−
FoxP3
lo
CD4SP Treg cell precursors in the thymus and is critical for TCR‐dependent IL‐2 production, which drive chromatin remodeling at the FoxP3 locus as well as other Treg‐effector gene loci in an autocrine/paracrine manner. Together, our results demonstrate a novel role for DNA demethylation in regulating the TCR response and promoting Treg cell differentiation. These findings highlight a novel epigenetic pathway to promote the generation of endogenous Treg cells for mitigation of autoimmune responses.
Synopsis
This study identifies a temporal requirement for DNA demethylation during Treg cell differentiation from thymic CD4
+
T cell and shows a role for Tet3 in modulating IL‐2 production and the development of CD25
−
FoxP3
lo
precursors.
DNA demethylases are required prior to the upregulation of FoxP3 in CD4 single‐positive thymocytes to promote Treg differentiation.
Tet3 selectively controls the development of CD25
‐
FoxP3
lo
CD4 Treg cell precursors in the thymus.
Tet3 is critical for TCR‐dependent IL‐2 production, which drives genome‐wide chromatin remodeling in an autocrine/paracrine manner.
Graphical Abstract
This study identifies a temporal requirement for DNA demethylation during Treg cell differentiation from thymic CD4
+
T cell precursors and shows a role for Tet3 in modulating IL‐2 production and the development of CD25
−
FoxP3
lo
precursors.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>36880575</pmid><doi>10.15252/embr.202255543</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0003-1818-9975</orcidid><orcidid>https://orcid.org/0000-0002-8886-6436</orcidid><orcidid>https://orcid.org/0000-0001-8206-1998</orcidid><orcidid>https://orcid.org/0000-0003-1771-749X</orcidid><orcidid>https://orcid.org/0000-0001-7544-5109</orcidid><orcidid>https://orcid.org/0000-0003-1282-6080</orcidid><orcidid>https://orcid.org/0000-0003-2167-5894</orcidid><orcidid>https://orcid.org/0000-0002-8046-0626</orcidid><orcidid>https://orcid.org/0000-0003-1552-3253</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1469-221X |
ispartof | EMBO reports, 2023-05, Vol.24 (5), p.e55543-n/a |
issn | 1469-221X 1469-3178 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10157375 |
source | PubMed Central |
subjects | Animals Autocrine signalling Autoimmunity CD25 antigen CD4 antigen Cell Differentiation Chromatin remodeling Demethylation Deoxyribonucleic acid Differentiation (biology) DNA DNA Demethylation EMBO09 EMBO11 EMBO19 Epigenetics Forkhead Transcription Factors - metabolism FoxP3 Foxp3 protein Humans IL‐2 Immunological tolerance Interleukin-2 Interleukins Life Sciences Lymphocytes Lymphocytes T Mice Paracrine signalling Precursors Receptors, Antigen, T-Cell - metabolism T cell receptors T-Lymphocytes, Regulatory Tet enzymes Thymocytes Thymus Gland Translocation Treg development |
title | DNA demethylation fine‐tunes IL‐2 production during thymic regulatory T cell differentiation |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T20%3A07%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=DNA%20demethylation%20fine%E2%80%90tunes%20IL%E2%80%902%20production%20during%20thymic%20regulatory%20T%20cell%20differentiation&rft.jtitle=EMBO%20reports&rft.au=Teghanemt,%20Athmane&rft.date=2023-05-04&rft.volume=24&rft.issue=5&rft.spage=e55543&rft.epage=n/a&rft.pages=e55543-n/a&rft.issn=1469-221X&rft.eissn=1469-3178&rft_id=info:doi/10.15252/embr.202255543&rft_dat=%3Cproquest_pubme%3E2808830038%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5143-febc1984d79eea11974190ed180a70271f6628aa9909393eb12ed4fe68099c303%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2808830038&rft_id=info:pmid/36880575&rfr_iscdi=true |