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Hypertonic Salt Solution Enhances Inflammatory Responses in Cultured Splenic T-Cells from Dahl Salt-Sensitive Rats but Not Dahl Salt-Resistant Rats
This study aimed to delineate the effect of sodium chloride on the induction of inflammatory responses and the development of hypertension in Dahl salt-sensitive (SS) and salt-resistant (SR) rats. Splenocytes were isolated from the spleens of SS and SR rats, and cultured on anti-CD3-coated plates fo...
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Published in: | Journal of cardiovascular development and disease 2023-10, Vol.10 (10), p.414 |
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description | This study aimed to delineate the effect of sodium chloride on the induction of inflammatory responses and the development of hypertension in Dahl salt-sensitive (SS) and salt-resistant (SR) rats. Splenocytes were isolated from the spleens of SS and SR rats, and cultured on anti-CD3-coated plates for 5 days. The cultured splenic T-cells were challenged with a hypertonic salt solution (0, 20, or 40 mM) in the absence or presence of IL-6 (0, 20, or 60 ng/mL), TGF-β (0, 5, or 15 ng/mL), or IL-23 (0, 10, or 30 ng/mL), and analyzed via ELISA, flow cytometry, and immunofluorescence. The hypertonic salt solution potentiated IL-17A production, as well as the differentiation of Th17 cells via IL-6/TGF-β/IL-23, exclusively in SS rats. However, it did not affect IL-10 production or the differentiation of Treg cells in any of the groups. Furthermore, it potentiated the signal of RORγt in IL-6-treated splenic T-cells from SS rats. To summarize, cultured splenic T-cells exhibited enhanced inflammatory responses on exposure to a hypertonic salt solution in SS rats only, which indicated that sodium chloride and inflammatory cytokines synergistically drove the induction of pathogenic Th17 cells and the development of hypertension in this group only. |
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Splenocytes were isolated from the spleens of SS and SR rats, and cultured on anti-CD3-coated plates for 5 days. The cultured splenic T-cells were challenged with a hypertonic salt solution (0, 20, or 40 mM) in the absence or presence of IL-6 (0, 20, or 60 ng/mL), TGF-β (0, 5, or 15 ng/mL), or IL-23 (0, 10, or 30 ng/mL), and analyzed via ELISA, flow cytometry, and immunofluorescence. The hypertonic salt solution potentiated IL-17A production, as well as the differentiation of Th17 cells via IL-6/TGF-β/IL-23, exclusively in SS rats. However, it did not affect IL-10 production or the differentiation of Treg cells in any of the groups. Furthermore, it potentiated the signal of RORγt in IL-6-treated splenic T-cells from SS rats. To summarize, cultured splenic T-cells exhibited enhanced inflammatory responses on exposure to a hypertonic salt solution in SS rats only, which indicated that sodium chloride and inflammatory cytokines synergistically drove the induction of pathogenic Th17 cells and the development of hypertension in this group only.</description><identifier>ISSN: 2308-3425</identifier><identifier>EISSN: 2308-3425</identifier><identifier>DOI: 10.3390/jcdd10100414</identifier><identifier>PMID: 37887861</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Antibodies ; Blood pressure ; Cell culture ; Cloning ; Cytokines ; Dahl salt-resistant rats ; Dahl salt-sensitive rats ; Enzyme-linked immunosorbent assay ; Flow cytometry ; Growth factors ; Hypertension ; hypertonic salt solution ; Kinases ; Laboratory animals ; Nitric oxide ; Salt ; salt sensitivity ; Sodium ; Software ; T cells ; Th17 cells ; Transcription factors ; Transforming growth factors ; Treg cells ; Tumor necrosis factor-TNF</subject><ispartof>Journal of cardiovascular development and disease, 2023-10, Vol.10 (10), p.414</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 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 (https://creativecommons.org/licenses/by/4.0/). 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Splenocytes were isolated from the spleens of SS and SR rats, and cultured on anti-CD3-coated plates for 5 days. The cultured splenic T-cells were challenged with a hypertonic salt solution (0, 20, or 40 mM) in the absence or presence of IL-6 (0, 20, or 60 ng/mL), TGF-β (0, 5, or 15 ng/mL), or IL-23 (0, 10, or 30 ng/mL), and analyzed via ELISA, flow cytometry, and immunofluorescence. The hypertonic salt solution potentiated IL-17A production, as well as the differentiation of Th17 cells via IL-6/TGF-β/IL-23, exclusively in SS rats. However, it did not affect IL-10 production or the differentiation of Treg cells in any of the groups. Furthermore, it potentiated the signal of RORγt in IL-6-treated splenic T-cells from SS rats. To summarize, cultured splenic T-cells exhibited enhanced inflammatory responses on exposure to a hypertonic salt solution in SS rats only, which indicated that sodium chloride and inflammatory cytokines synergistically drove the induction of pathogenic Th17 cells and the development of hypertension in this group only.</description><subject>Antibodies</subject><subject>Blood pressure</subject><subject>Cell culture</subject><subject>Cloning</subject><subject>Cytokines</subject><subject>Dahl salt-resistant rats</subject><subject>Dahl salt-sensitive rats</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Flow cytometry</subject><subject>Growth factors</subject><subject>Hypertension</subject><subject>hypertonic salt solution</subject><subject>Kinases</subject><subject>Laboratory animals</subject><subject>Nitric oxide</subject><subject>Salt</subject><subject>salt sensitivity</subject><subject>Sodium</subject><subject>Software</subject><subject>T cells</subject><subject>Th17 cells</subject><subject>Transcription factors</subject><subject>Transforming growth factors</subject><subject>Treg cells</subject><subject>Tumor necrosis factor-TNF</subject><issn>2308-3425</issn><issn>2308-3425</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptks1uEzEQgFcIRKvSGw9giQsHtvhn1_aeUBUKjVSB1JSz5fVP4shrB9tbKc_BC7ObVJAi5IPt8TefNaOpqrcIXhHSwY9bpTWCCMIGNS-qc0wgr0mD25cn57PqMucthBBNN4jw6-qMMM4Zp-i8-nW735lUYnAKrKQvYBX9WFwM4CZsZFAmg2WwXg6DLDHtwb3JuxjyFHYBLEZfxmQ0WO28mQ0P9cJ4n4FNcQCf5cYfnPXKhOyKezTgXpYM-rGAb7GcAJPV5SJDOQBvqldW-mwun_aL6seXm4fFbX33_etycX1Xq4bDUltIuWkZwRha2hOEW0Q1VRZ2ba8tUQoT2komOba8J42i0tpeQ9pq1nBKLLmolkevjnIrdskNMu1FlE4cAjGthUzFKW-ERcZI1vVMEdgwjDjsOdeosQwRKyWfXJ-Ort3YD0YrE0qS_pn0-UtwG7GOjwJBChlCzWR4_2RI8edochGDy2pqpwwmjllgzklLO8Rn9N0_6DaOKUy9mincMt516C-1llMFLtg4faxmqbhmDEPatM3suvoPNS1tBqdiMNZN8WcJH44JKsWck7F_ikRQzEMpToeS_Abvs9Ld</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Jang, Sungmin</creator><creator>Kim, Jee Young</creator><creator>Kim, Cheong-Wun</creator><creator>Kim, Inkyeom</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-8009-5801</orcidid><orcidid>https://orcid.org/0000-0002-3229-8935</orcidid><orcidid>https://orcid.org/0000-0002-2169-713X</orcidid><orcidid>https://orcid.org/0000-0002-2074-9479</orcidid></search><sort><creationdate>20231001</creationdate><title>Hypertonic Salt Solution Enhances Inflammatory Responses in Cultured Splenic T-Cells from Dahl Salt-Sensitive Rats but Not Dahl Salt-Resistant Rats</title><author>Jang, Sungmin ; Kim, Jee Young ; Kim, Cheong-Wun ; Kim, Inkyeom</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c480t-f068e573220f6b312516d6cf095bdf3cc2365a7a82f8b34c6affbd065d74863f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antibodies</topic><topic>Blood pressure</topic><topic>Cell culture</topic><topic>Cloning</topic><topic>Cytokines</topic><topic>Dahl salt-resistant rats</topic><topic>Dahl salt-sensitive rats</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Flow cytometry</topic><topic>Growth factors</topic><topic>Hypertension</topic><topic>hypertonic salt solution</topic><topic>Kinases</topic><topic>Laboratory animals</topic><topic>Nitric oxide</topic><topic>Salt</topic><topic>salt sensitivity</topic><topic>Sodium</topic><topic>Software</topic><topic>T cells</topic><topic>Th17 cells</topic><topic>Transcription factors</topic><topic>Transforming growth factors</topic><topic>Treg cells</topic><topic>Tumor necrosis factor-TNF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jang, Sungmin</creatorcontrib><creatorcontrib>Kim, Jee Young</creatorcontrib><creatorcontrib>Kim, Cheong-Wun</creatorcontrib><creatorcontrib>Kim, Inkyeom</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of cardiovascular development and disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jang, Sungmin</au><au>Kim, Jee Young</au><au>Kim, Cheong-Wun</au><au>Kim, Inkyeom</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypertonic Salt Solution Enhances Inflammatory Responses in Cultured Splenic T-Cells from Dahl Salt-Sensitive Rats but Not Dahl Salt-Resistant Rats</atitle><jtitle>Journal of cardiovascular development and disease</jtitle><date>2023-10-01</date><risdate>2023</risdate><volume>10</volume><issue>10</issue><spage>414</spage><pages>414-</pages><issn>2308-3425</issn><eissn>2308-3425</eissn><abstract>This study aimed to delineate the effect of sodium chloride on the induction of inflammatory responses and the development of hypertension in Dahl salt-sensitive (SS) and salt-resistant (SR) rats. Splenocytes were isolated from the spleens of SS and SR rats, and cultured on anti-CD3-coated plates for 5 days. The cultured splenic T-cells were challenged with a hypertonic salt solution (0, 20, or 40 mM) in the absence or presence of IL-6 (0, 20, or 60 ng/mL), TGF-β (0, 5, or 15 ng/mL), or IL-23 (0, 10, or 30 ng/mL), and analyzed via ELISA, flow cytometry, and immunofluorescence. The hypertonic salt solution potentiated IL-17A production, as well as the differentiation of Th17 cells via IL-6/TGF-β/IL-23, exclusively in SS rats. However, it did not affect IL-10 production or the differentiation of Treg cells in any of the groups. Furthermore, it potentiated the signal of RORγt in IL-6-treated splenic T-cells from SS rats. To summarize, cultured splenic T-cells exhibited enhanced inflammatory responses on exposure to a hypertonic salt solution in SS rats only, which indicated that sodium chloride and inflammatory cytokines synergistically drove the induction of pathogenic Th17 cells and the development of hypertension in this group only.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>37887861</pmid><doi>10.3390/jcdd10100414</doi><orcidid>https://orcid.org/0000-0001-8009-5801</orcidid><orcidid>https://orcid.org/0000-0002-3229-8935</orcidid><orcidid>https://orcid.org/0000-0002-2169-713X</orcidid><orcidid>https://orcid.org/0000-0002-2074-9479</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies Blood pressure Cell culture Cloning Cytokines Dahl salt-resistant rats Dahl salt-sensitive rats Enzyme-linked immunosorbent assay Flow cytometry Growth factors Hypertension hypertonic salt solution Kinases Laboratory animals Nitric oxide Salt salt sensitivity Sodium Software T cells Th17 cells Transcription factors Transforming growth factors Treg cells Tumor necrosis factor-TNF |
title | Hypertonic Salt Solution Enhances Inflammatory Responses in Cultured Splenic T-Cells from Dahl Salt-Sensitive Rats but Not Dahl Salt-Resistant Rats |
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