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Vitamin A supplementation leads to increases in regulatory CD4+Foxp3+LAP+ T cells in mice
Abstract Dietary compounds, including micronutrients such as vitamin A and its metabolite retinoic acid, directly influence the development and function of the immune system. In this study, we show that either dietary deficiency of or supplementation with vitamin A had immunologic effects in mice th...
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Published in: | Nutrition (Burbank, Los Angeles County, Calif.) Los Angeles County, Calif.), 2015-10, Vol.31 (10), p.1260-1265 |
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creator | Medeiros, Samara R., Ph.D Pinheiro-Rosa, Natalia, B.Sc Lemos, Luisa, M.A Loli, Flavia G., B.Sc Pereira, Alline G., B.Sc Santiago, Andrezza F., Ph.D Pinter, Ester C Alves, Andrea C., Ph.D Oliveira, Jamil S., B.Sc Cara, Denise C., Ph.D Maioli, Tatiani U., Ph.D Faria, Ana Maria C., M.D., Ph.D |
description | Abstract Dietary compounds, including micronutrients such as vitamin A and its metabolite retinoic acid, directly influence the development and function of the immune system. In this study, we show that either dietary deficiency of or supplementation with vitamin A had immunologic effects in mice that were fed these diets during their development (for 8 wk during the postweaning period). Deficient mice presented higher levels of interferon-γ, interleukin (IL)-6, transforming growth factor-β, IL-17, and IL-10 in the gut-associated lymphoid tissues and draining lymph nodes, indicating a proinflammatory shift in the gut mucosa. Serum immunoglobulin G levels also were elevated in these mice. Conversely, supplemented mice showed higher frequencies of CD4+Foxp3+LAP+ regulatory T cells in gut lymphoid tissues and spleen, suggesting that vitamin A supplementation in the diet may be beneficial in pathologic situations such as inflammatory bowel diseases. |
doi_str_mv | 10.1016/j.nut.2015.03.004 |
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In this study, we show that either dietary deficiency of or supplementation with vitamin A had immunologic effects in mice that were fed these diets during their development (for 8 wk during the postweaning period). Deficient mice presented higher levels of interferon-γ, interleukin (IL)-6, transforming growth factor-β, IL-17, and IL-10 in the gut-associated lymphoid tissues and draining lymph nodes, indicating a proinflammatory shift in the gut mucosa. Serum immunoglobulin G levels also were elevated in these mice. Conversely, supplemented mice showed higher frequencies of CD4+Foxp3+LAP+ regulatory T cells in gut lymphoid tissues and spleen, suggesting that vitamin A supplementation in the diet may be beneficial in pathologic situations such as inflammatory bowel diseases.</description><identifier>ISSN: 0899-9007</identifier><identifier>EISSN: 1873-1244</identifier><identifier>DOI: 10.1016/j.nut.2015.03.004</identifier><identifier>PMID: 26004193</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; CD4-Positive T-Lymphocytes - metabolism ; Chromatography ; Colon ; Cytokines ; Dietary Supplements ; Enzymes ; Female ; Forkhead Transcription Factors - metabolism ; Gastroenterology and Hepatology ; Immune system ; Immunoglobulin G - blood ; Immunoglobulins ; Interferon-gamma - metabolism ; Interleukin-10 - metabolism ; Interleukin-17 - metabolism ; Interleukin-6 - metabolism ; Intestines - immunology ; Lymph nodes ; Lymphocytes ; Lymphoid Tissue - metabolism ; Metabolites ; Mice ; Mice, Inbred C57BL ; Micronutrients ; Regulatory T cells ; Retinoic acid ; Software ; T-Lymphocytes, Regulatory - metabolism ; TGF-β ; Transforming Growth Factor beta - metabolism ; Vitamin A ; Vitamin A - pharmacology ; Vitamins - pharmacology</subject><ispartof>Nutrition (Burbank, Los Angeles County, Calif.), 2015-10, Vol.31 (10), p.1260-1265</ispartof><rights>Elsevier Inc.</rights><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Oct 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-7dac42a9629cde3543d04ee1162207cef6d0e5f483c889a1008bb66d1f04e3a93</citedby><cites>FETCH-LOGICAL-c469t-7dac42a9629cde3543d04ee1162207cef6d0e5f483c889a1008bb66d1f04e3a93</cites></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/26004193$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Medeiros, Samara R., Ph.D</creatorcontrib><creatorcontrib>Pinheiro-Rosa, Natalia, B.Sc</creatorcontrib><creatorcontrib>Lemos, Luisa, M.A</creatorcontrib><creatorcontrib>Loli, Flavia G., B.Sc</creatorcontrib><creatorcontrib>Pereira, Alline G., B.Sc</creatorcontrib><creatorcontrib>Santiago, Andrezza F., Ph.D</creatorcontrib><creatorcontrib>Pinter, Ester C</creatorcontrib><creatorcontrib>Alves, Andrea C., Ph.D</creatorcontrib><creatorcontrib>Oliveira, Jamil S., B.Sc</creatorcontrib><creatorcontrib>Cara, Denise C., Ph.D</creatorcontrib><creatorcontrib>Maioli, Tatiani U., Ph.D</creatorcontrib><creatorcontrib>Faria, Ana Maria C., M.D., Ph.D</creatorcontrib><title>Vitamin A supplementation leads to increases in regulatory CD4+Foxp3+LAP+ T cells in mice</title><title>Nutrition (Burbank, Los Angeles County, Calif.)</title><addtitle>Nutrition</addtitle><description>Abstract Dietary compounds, including micronutrients such as vitamin A and its metabolite retinoic acid, directly influence the development and function of the immune system. In this study, we show that either dietary deficiency of or supplementation with vitamin A had immunologic effects in mice that were fed these diets during their development (for 8 wk during the postweaning period). Deficient mice presented higher levels of interferon-γ, interleukin (IL)-6, transforming growth factor-β, IL-17, and IL-10 in the gut-associated lymphoid tissues and draining lymph nodes, indicating a proinflammatory shift in the gut mucosa. Serum immunoglobulin G levels also were elevated in these mice. Conversely, supplemented mice showed higher frequencies of CD4+Foxp3+LAP+ regulatory T cells in gut lymphoid tissues and spleen, suggesting that vitamin A supplementation in the diet may be beneficial in pathologic situations such as inflammatory bowel diseases.</description><subject>Animals</subject><subject>CD4-Positive T-Lymphocytes - metabolism</subject><subject>Chromatography</subject><subject>Colon</subject><subject>Cytokines</subject><subject>Dietary Supplements</subject><subject>Enzymes</subject><subject>Female</subject><subject>Forkhead Transcription Factors - metabolism</subject><subject>Gastroenterology and Hepatology</subject><subject>Immune system</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulins</subject><subject>Interferon-gamma - metabolism</subject><subject>Interleukin-10 - metabolism</subject><subject>Interleukin-17 - metabolism</subject><subject>Interleukin-6 - metabolism</subject><subject>Intestines - immunology</subject><subject>Lymph nodes</subject><subject>Lymphocytes</subject><subject>Lymphoid Tissue - metabolism</subject><subject>Metabolites</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Micronutrients</subject><subject>Regulatory T cells</subject><subject>Retinoic acid</subject><subject>Software</subject><subject>T-Lymphocytes, Regulatory - metabolism</subject><subject>TGF-β</subject><subject>Transforming Growth Factor beta - metabolism</subject><subject>Vitamin A</subject><subject>Vitamin A - pharmacology</subject><subject>Vitamins - pharmacology</subject><issn>0899-9007</issn><issn>1873-1244</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kV2L1DAUhoMo7rj6A7yRgjcLQ7vnJG3aIAjD6KowoOAqeBUy6alk7JdJKzv_3tRZFfZiIZBcPO_LyXMYe46QIaC8PGT9PGUcsMhAZAD5A7bCqhQp8jx_yFZQKZUqgPKMPQnhAACopHrMzriMMCqxYt--usl0rk82SZjHsaWO-slMbuiTlkwdkmlIXG89mUAhvhJP3-fWTIM_Jts3-fpquBnFerf5tE6uE0tt-wfqnKWn7FFj2kDPbu9z9uXq7fX2fbr7-O7DdrNLbS7VlJa1sTk3SnJlaxJFLmrIiRAl51BaamQNVDR5JWxVKYMA1X4vZY1NxIRR4pxdnHpHP_ycKUy6c2GZxPQ0zEFjCSoegWVEX95BD8Ps-zhdpBBkiRVfCvFEWT-E4KnRo3ed8UeNoBfv-qCjd7141yB0VBkzL26b531H9b_EX9EReHUCKKr45cjrYB31lmrnyU66Hty99a_vpG3remdN-4OOFP7_QgeuQX9eFr_sHYu4co6F-A2TjaWk</recordid><startdate>20151001</startdate><enddate>20151001</enddate><creator>Medeiros, Samara R., Ph.D</creator><creator>Pinheiro-Rosa, Natalia, B.Sc</creator><creator>Lemos, Luisa, M.A</creator><creator>Loli, Flavia G., B.Sc</creator><creator>Pereira, Alline G., B.Sc</creator><creator>Santiago, Andrezza F., Ph.D</creator><creator>Pinter, Ester C</creator><creator>Alves, Andrea C., Ph.D</creator><creator>Oliveira, Jamil S., B.Sc</creator><creator>Cara, Denise C., Ph.D</creator><creator>Maioli, Tatiani U., Ph.D</creator><creator>Faria, Ana Maria C., M.D., Ph.D</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><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>3V.</scope><scope>7RQ</scope><scope>7RV</scope><scope>7TS</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>ASE</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FPQ</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K6X</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20151001</creationdate><title>Vitamin A supplementation leads to increases in regulatory CD4+Foxp3+LAP+ T cells in mice</title><author>Medeiros, Samara R., Ph.D ; Pinheiro-Rosa, Natalia, B.Sc ; Lemos, Luisa, M.A ; Loli, Flavia G., B.Sc ; Pereira, Alline G., B.Sc ; Santiago, Andrezza F., Ph.D ; Pinter, Ester C ; Alves, Andrea C., Ph.D ; Oliveira, Jamil S., B.Sc ; Cara, Denise C., Ph.D ; Maioli, Tatiani U., Ph.D ; Faria, Ana Maria C., M.D., Ph.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c469t-7dac42a9629cde3543d04ee1162207cef6d0e5f483c889a1008bb66d1f04e3a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>CD4-Positive T-Lymphocytes - 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In this study, we show that either dietary deficiency of or supplementation with vitamin A had immunologic effects in mice that were fed these diets during their development (for 8 wk during the postweaning period). Deficient mice presented higher levels of interferon-γ, interleukin (IL)-6, transforming growth factor-β, IL-17, and IL-10 in the gut-associated lymphoid tissues and draining lymph nodes, indicating a proinflammatory shift in the gut mucosa. Serum immunoglobulin G levels also were elevated in these mice. Conversely, supplemented mice showed higher frequencies of CD4+Foxp3+LAP+ regulatory T cells in gut lymphoid tissues and spleen, suggesting that vitamin A supplementation in the diet may be beneficial in pathologic situations such as inflammatory bowel diseases.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26004193</pmid><doi>10.1016/j.nut.2015.03.004</doi><tpages>6</tpages></addata></record> |
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subjects | Animals CD4-Positive T-Lymphocytes - metabolism Chromatography Colon Cytokines Dietary Supplements Enzymes Female Forkhead Transcription Factors - metabolism Gastroenterology and Hepatology Immune system Immunoglobulin G - blood Immunoglobulins Interferon-gamma - metabolism Interleukin-10 - metabolism Interleukin-17 - metabolism Interleukin-6 - metabolism Intestines - immunology Lymph nodes Lymphocytes Lymphoid Tissue - metabolism Metabolites Mice Mice, Inbred C57BL Micronutrients Regulatory T cells Retinoic acid Software T-Lymphocytes, Regulatory - metabolism TGF-β Transforming Growth Factor beta - metabolism Vitamin A Vitamin A - pharmacology Vitamins - pharmacology |
title | Vitamin A supplementation leads to increases in regulatory CD4+Foxp3+LAP+ T cells in mice |
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