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Intrathymic Selection and Defects in the Thymic Epithelial Cell Development
Intimate interactions between thymic epithelial cells (TECs) and thymocytes (T) have been repeatedly reported as essential for performing intrathymic T-cell education. Nevertheless, it has been described that animals exhibiting defects in these interactions were capable of a proper positive and nega...
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Published in: | Cells (Basel, Switzerland) Switzerland), 2020-10, Vol.9 (10), p.2226 |
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description | Intimate interactions between thymic epithelial cells (TECs) and thymocytes (T) have been repeatedly reported as essential for performing intrathymic T-cell education. Nevertheless, it has been described that animals exhibiting defects in these interactions were capable of a proper positive and negative T-cell selection. In the current review, we first examined distinct types of TECs and their possible role in the immune surveillance. However, EphB-deficient thymi that exhibit profound thymic epithelial (TE) alterations do not exhibit important immunological defects. Eph and their ligands, the ephrins, are implicated in cell attachment/detachment and govern, therefore, TEC–T interactions. On this basis, we hypothesized that a few normal TE areas could be enough for a proper phenotypical and functional maturation of T lymphocytes. Then, we evaluated in vivo how many TECs would be necessary for supporting a normal T-cell differentiation, concluding that a significantly low number of TEC are still capable of supporting normal T lymphocyte maturation, whereas with fewer numbers, T-cell maturation is not possible. |
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Nevertheless, it has been described that animals exhibiting defects in these interactions were capable of a proper positive and negative T-cell selection. In the current review, we first examined distinct types of TECs and their possible role in the immune surveillance. However, EphB-deficient thymi that exhibit profound thymic epithelial (TE) alterations do not exhibit important immunological defects. Eph and their ligands, the ephrins, are implicated in cell attachment/detachment and govern, therefore, TEC–T interactions. On this basis, we hypothesized that a few normal TE areas could be enough for a proper phenotypical and functional maturation of T lymphocytes. Then, we evaluated in vivo how many TECs would be necessary for supporting a normal T-cell differentiation, concluding that a significantly low number of TEC are still capable of supporting normal T lymphocyte maturation, whereas with fewer numbers, T-cell maturation is not possible.</description><identifier>ISSN: 2073-4409</identifier><identifier>EISSN: 2073-4409</identifier><identifier>DOI: 10.3390/cells9102226</identifier><identifier>PMID: 33023072</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Antigens ; Cell adhesion ; Cell development (Biology) ; Cell differentiation ; Eph/ephrins ; Ephrins ; Epithelial cells ; Immunosurveillance ; Ligands ; Lymphocytes T ; Peptides ; Physiological aspects ; Physiological research ; Population ; regulatory T-cells ; Review ; thymic epithelial cells ; thymocyte education ; Thymocytes ; Thymus ; Thymus gland</subject><ispartof>Cells (Basel, Switzerland), 2020-10, Vol.9 (10), p.2226</ispartof><rights>COPYRIGHT 2020 MDPI AG</rights><rights>2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-9ba79271836f54b27487f333290b2ac37f03301f9016314f75739af8c34232673</citedby><cites>FETCH-LOGICAL-c483t-9ba79271836f54b27487f333290b2ac37f03301f9016314f75739af8c34232673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2548343902/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2548343902?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids></links><search><creatorcontrib>García-Ceca, Javier</creatorcontrib><creatorcontrib>Montero-Herradón, Sara</creatorcontrib><creatorcontrib>Zapata, Agustín G.</creatorcontrib><title>Intrathymic Selection and Defects in the Thymic Epithelial Cell Development</title><title>Cells (Basel, Switzerland)</title><description>Intimate interactions between thymic epithelial cells (TECs) and thymocytes (T) have been repeatedly reported as essential for performing intrathymic T-cell education. Nevertheless, it has been described that animals exhibiting defects in these interactions were capable of a proper positive and negative T-cell selection. In the current review, we first examined distinct types of TECs and their possible role in the immune surveillance. However, EphB-deficient thymi that exhibit profound thymic epithelial (TE) alterations do not exhibit important immunological defects. Eph and their ligands, the ephrins, are implicated in cell attachment/detachment and govern, therefore, TEC–T interactions. On this basis, we hypothesized that a few normal TE areas could be enough for a proper phenotypical and functional maturation of T lymphocytes. Then, we evaluated in vivo how many TECs would be necessary for supporting a normal T-cell differentiation, concluding that a significantly low number of TEC are still capable of supporting normal T lymphocyte maturation, whereas with fewer numbers, T-cell maturation is not possible.</description><subject>Antigens</subject><subject>Cell adhesion</subject><subject>Cell development (Biology)</subject><subject>Cell differentiation</subject><subject>Eph/ephrins</subject><subject>Ephrins</subject><subject>Epithelial cells</subject><subject>Immunosurveillance</subject><subject>Ligands</subject><subject>Lymphocytes T</subject><subject>Peptides</subject><subject>Physiological aspects</subject><subject>Physiological research</subject><subject>Population</subject><subject>regulatory T-cells</subject><subject>Review</subject><subject>thymic epithelial cells</subject><subject>thymocyte education</subject><subject>Thymocytes</subject><subject>Thymus</subject><subject>Thymus gland</subject><issn>2073-4409</issn><issn>2073-4409</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdks9vFCEUx4nR2Kb25h8wiRcPrgKP4cfFpFmrbmziwXomDAO7bBhYYbZJ_3sZt9FWLvDgm897fN9D6DXB7wEU_mBdjFURTCnlz9A5xQJWjGH1_NH5DF3WusdtScIJ7l-iMwBMAQt6jr5t0lzMvLufgu1-uOjsHHLqTBq7T863qHYhdfPOdbcnzfUhtCgGE7t1S95Udy7mw-TS_Aq98CZWd_mwX6Cfn69v119XN9-_bNZXNyvLJMwrNRihqCASuO_ZQAWTwgMAVXigxoLwuNVHvMKEA2Fe9AKU8dICo0C5gAu0OXHHbPb6UMJkyr3OJug_F7lstSlzsNFp5ZkcewtSMs4ImEHA6DgwRyhw7PvG-nhiHY7D5EbrFjviE-jTlxR2epvvtOCYEIIb4O0DoORfR1dnPYW6tMUkl49VU8YUkZiLRfrmP-k-H0tqVmnaN2tY6yj9p9qa9oGQfG557QLVV7w5wCnpF9W7k8qWXGtx_m_JBOtlNPTj0YDf0m2mlQ</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>García-Ceca, Javier</creator><creator>Montero-Herradón, Sara</creator><creator>Zapata, Agustín G.</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20201001</creationdate><title>Intrathymic Selection and Defects in the Thymic Epithelial Cell Development</title><author>García-Ceca, Javier ; Montero-Herradón, Sara ; Zapata, Agustín G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-9ba79271836f54b27487f333290b2ac37f03301f9016314f75739af8c34232673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antigens</topic><topic>Cell adhesion</topic><topic>Cell development (Biology)</topic><topic>Cell differentiation</topic><topic>Eph/ephrins</topic><topic>Ephrins</topic><topic>Epithelial cells</topic><topic>Immunosurveillance</topic><topic>Ligands</topic><topic>Lymphocytes T</topic><topic>Peptides</topic><topic>Physiological aspects</topic><topic>Physiological research</topic><topic>Population</topic><topic>regulatory T-cells</topic><topic>Review</topic><topic>thymic epithelial cells</topic><topic>thymocyte education</topic><topic>Thymocytes</topic><topic>Thymus</topic><topic>Thymus gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>García-Ceca, Javier</creatorcontrib><creatorcontrib>Montero-Herradón, Sara</creatorcontrib><creatorcontrib>Zapata, Agustín G.</creatorcontrib><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Cells (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>García-Ceca, Javier</au><au>Montero-Herradón, Sara</au><au>Zapata, Agustín G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intrathymic Selection and Defects in the Thymic Epithelial Cell Development</atitle><jtitle>Cells (Basel, Switzerland)</jtitle><date>2020-10-01</date><risdate>2020</risdate><volume>9</volume><issue>10</issue><spage>2226</spage><pages>2226-</pages><issn>2073-4409</issn><eissn>2073-4409</eissn><abstract>Intimate interactions between thymic epithelial cells (TECs) and thymocytes (T) have been repeatedly reported as essential for performing intrathymic T-cell education. Nevertheless, it has been described that animals exhibiting defects in these interactions were capable of a proper positive and negative T-cell selection. In the current review, we first examined distinct types of TECs and their possible role in the immune surveillance. However, EphB-deficient thymi that exhibit profound thymic epithelial (TE) alterations do not exhibit important immunological defects. Eph and their ligands, the ephrins, are implicated in cell attachment/detachment and govern, therefore, TEC–T interactions. On this basis, we hypothesized that a few normal TE areas could be enough for a proper phenotypical and functional maturation of T lymphocytes. 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subjects | Antigens Cell adhesion Cell development (Biology) Cell differentiation Eph/ephrins Ephrins Epithelial cells Immunosurveillance Ligands Lymphocytes T Peptides Physiological aspects Physiological research Population regulatory T-cells Review thymic epithelial cells thymocyte education Thymocytes Thymus Thymus gland |
title | Intrathymic Selection and Defects in the Thymic Epithelial Cell Development |
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