Modulation of immune cell proliferation and chemotaxis towards CC chemokine ligand (CCL)-21 and CXC chemokine ligand (CXCL)-12 in undenatured whey protein-treated mice
Whey protein concentrates (WPCs) enhance innate mucosal immunity during early life and have a protective role in some immune disorders. To further elucidate the potential benefits of this protein, the present study investigated the effect of dietary supplementation with WPCs on blood parameters, pla...
Gespeichert in:
Veröffentlicht in: | The Journal of nutritional biochemistry 2012-12, Vol.23 (12), p.1640-1646 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1646 |
---|---|
container_issue | 12 |
container_start_page | 1640 |
container_title | The Journal of nutritional biochemistry |
container_volume | 23 |
creator | Badr, Gamal Ebaid, Hossam Mohany, Mohamed Abuelsaad, Abdelaziz Saber |
description | Whey protein concentrates (WPCs) enhance innate mucosal immunity during early life and have a protective role in some immune disorders. To further elucidate the potential benefits of this protein, the present study investigated the effect of dietary supplementation with WPCs on blood parameters, plasma cytokine profiles, and immune cell proliferation and chemotaxis. A total of 45 male mice were equally distributed into three experimental groups and treated daily for 21 days as follows: group I was a control group that was orally supplemented with distilled water, group II was orally supplemented with undenatured WP (100 mg/kg body weight), and group III was orally supplemented with bovine serum albumin (100 mg/kg body weight). We found that the plasma cytokine levels of interleukin (IL)-1α, IL-1β, IL-10 and tumor necrosis factor-α and the levels of reactive oxygen species, cholesterol, triglycerides and the lipid profile were significantly decreased in the WP-treated group compared to the control group. In contrast, the levels of IL-2, IL-4, IL-7, IL-8 and glutathione were significantly elevated, and consequently, the ability of peripheral blood mononuclear cells to proliferate in response to stimulation with different antigens was significantly increased in the WP-treated group. Moreover, the in vitro chemotaxis of B, T and bone-marrow-derived dendritic cells toward CC chemokine ligand-21 and CXC chemokine ligand-12 was significantly increased, by twofold, in WP-treated mice compared to the control group. Taken together, our data reveal the benefits of WP supplementation in enhancing immune cell proliferation and migration to the secondary lymphoid organs. |
doi_str_mv | 10.1016/j.jnutbio.2011.11.006 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1272737931</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0955286311003159</els_id><sourcerecordid>1151701507</sourcerecordid><originalsourceid>FETCH-LOGICAL-c542t-946acdc954649703a350b2b999156daafb3bd07e5ee2ea928f09a04029c9e8823</originalsourceid><addsrcrecordid>eNqNkk2P1SAUhhujca6jP0HtxmRc9AoUaFkZ0_iVXONCJ5kdoXA6w7WFGaCO84v8m1J71Y1xJCQkh-c9H7wUxWOMthhh_mK_3bs59dZvCcJ4mzdC_E6xwW1TV7Slzd1igwRjFWl5fVQ8iHGPECKU8fvFESE0L9Fuiu8fvJlHlax3pR9KO02zg1LDOJaXwY92gLBeKmdKfQGTT-qbjWXy1yqYWHbdGv1is2y05wt20nW75xXBPzXd2V-JswXBpLSunJ0Bp9IcwJTXF3CzFE5gXZUCqJSDk9XwsLg3qDHCo8N5XJy-ef25e1ftPr59373aVZpRkipBudJGC0Y5FQ2qVc1QT3ohBGbcKDX0dW9QAwyAgBKkHZBQiCIitIC2JfVxcbLmzU1czRCTnGxcnkM58HOUmDSkqRtR4_9F25bdjmKGG4QZajLKVlQHH2OAQV4GO6lwIzGSi_NyLw_Oy8X5rJXZ-ax7cigx9xOY36pfVmfg2QFQUatxCMppG_9wnNc8t5y5pys3KC_VecjM6adciebvU4s8-T8JghmjmXi5EpCt-mohyKgtOA3GBtBJGm9vGecHf-ngOw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1151701507</pqid></control><display><type>article</type><title>Modulation of immune cell proliferation and chemotaxis towards CC chemokine ligand (CCL)-21 and CXC chemokine ligand (CXCL)-12 in undenatured whey protein-treated mice</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Badr, Gamal ; Ebaid, Hossam ; Mohany, Mohamed ; Abuelsaad, Abdelaziz Saber</creator><creatorcontrib>Badr, Gamal ; Ebaid, Hossam ; Mohany, Mohamed ; Abuelsaad, Abdelaziz Saber</creatorcontrib><description>Whey protein concentrates (WPCs) enhance innate mucosal immunity during early life and have a protective role in some immune disorders. To further elucidate the potential benefits of this protein, the present study investigated the effect of dietary supplementation with WPCs on blood parameters, plasma cytokine profiles, and immune cell proliferation and chemotaxis. A total of 45 male mice were equally distributed into three experimental groups and treated daily for 21 days as follows: group I was a control group that was orally supplemented with distilled water, group II was orally supplemented with undenatured WP (100 mg/kg body weight), and group III was orally supplemented with bovine serum albumin (100 mg/kg body weight). We found that the plasma cytokine levels of interleukin (IL)-1α, IL-1β, IL-10 and tumor necrosis factor-α and the levels of reactive oxygen species, cholesterol, triglycerides and the lipid profile were significantly decreased in the WP-treated group compared to the control group. In contrast, the levels of IL-2, IL-4, IL-7, IL-8 and glutathione were significantly elevated, and consequently, the ability of peripheral blood mononuclear cells to proliferate in response to stimulation with different antigens was significantly increased in the WP-treated group. Moreover, the in vitro chemotaxis of B, T and bone-marrow-derived dendritic cells toward CC chemokine ligand-21 and CXC chemokine ligand-12 was significantly increased, by twofold, in WP-treated mice compared to the control group. Taken together, our data reveal the benefits of WP supplementation in enhancing immune cell proliferation and migration to the secondary lymphoid organs.</description><identifier>ISSN: 0955-2863</identifier><identifier>EISSN: 1873-4847</identifier><identifier>DOI: 10.1016/j.jnutbio.2011.11.006</identifier><identifier>PMID: 22444498</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; antigens ; B-Lymphocytes - drug effects ; Biological and medical sciences ; Body weight ; Bone Marrow Cells - cytology ; Bovine serum albumin ; CC chemokines ; Cell proliferation ; Cell Proliferation - drug effects ; Chemokine CCL21 - metabolism ; Chemokine CXCL12 - metabolism ; chemokines ; Chemotaxis ; Chemotaxis - drug effects ; Chemotaxis - immunology ; Cholesterol ; CXC chemokines ; Cytokines ; Data processing ; Dendritic cells ; Dendritic Cells - drug effects ; Dendritic Cells - immunology ; Dietary Supplements ; Feeding. Feeding behavior ; Free radicals ; Fundamental and applied biological sciences. Psychology ; Glutathione ; Interleukin 10 ; Interleukin 2 ; Interleukin 4 ; Interleukin 7 ; Interleukin 8 ; interleukin-1 ; Interleukins - blood ; Leukocyte migration ; Lipid profile ; Lipids ; Lymphocytes - cytology ; Lymphocytes - drug effects ; Lymphocytes - immunology ; Male ; Mice ; Milk Proteins - pharmacology ; mononuclear leukocytes ; Mucosal immunity ; Peripheral blood mononuclear cells ; Protein Denaturation ; Reactive oxygen species ; Serum Albumin, Bovine - pharmacology ; T-Lymphocytes - drug effects ; triacylglycerols ; Triglycerides ; tumor necrosis factor-alpha ; Tumor Necrosis Factor-alpha - blood ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Whey ; whey protein ; whey protein concentrate ; Whey Proteins</subject><ispartof>The Journal of nutritional biochemistry, 2012-12, Vol.23 (12), p.1640-1646</ispartof><rights>2012 Elsevier Inc.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c542t-946acdc954649703a350b2b999156daafb3bd07e5ee2ea928f09a04029c9e8823</citedby><cites>FETCH-LOGICAL-c542t-946acdc954649703a350b2b999156daafb3bd07e5ee2ea928f09a04029c9e8823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0955286311003159$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26636127$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22444498$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Badr, Gamal</creatorcontrib><creatorcontrib>Ebaid, Hossam</creatorcontrib><creatorcontrib>Mohany, Mohamed</creatorcontrib><creatorcontrib>Abuelsaad, Abdelaziz Saber</creatorcontrib><title>Modulation of immune cell proliferation and chemotaxis towards CC chemokine ligand (CCL)-21 and CXC chemokine ligand (CXCL)-12 in undenatured whey protein-treated mice</title><title>The Journal of nutritional biochemistry</title><addtitle>J Nutr Biochem</addtitle><description>Whey protein concentrates (WPCs) enhance innate mucosal immunity during early life and have a protective role in some immune disorders. To further elucidate the potential benefits of this protein, the present study investigated the effect of dietary supplementation with WPCs on blood parameters, plasma cytokine profiles, and immune cell proliferation and chemotaxis. A total of 45 male mice were equally distributed into three experimental groups and treated daily for 21 days as follows: group I was a control group that was orally supplemented with distilled water, group II was orally supplemented with undenatured WP (100 mg/kg body weight), and group III was orally supplemented with bovine serum albumin (100 mg/kg body weight). We found that the plasma cytokine levels of interleukin (IL)-1α, IL-1β, IL-10 and tumor necrosis factor-α and the levels of reactive oxygen species, cholesterol, triglycerides and the lipid profile were significantly decreased in the WP-treated group compared to the control group. In contrast, the levels of IL-2, IL-4, IL-7, IL-8 and glutathione were significantly elevated, and consequently, the ability of peripheral blood mononuclear cells to proliferate in response to stimulation with different antigens was significantly increased in the WP-treated group. Moreover, the in vitro chemotaxis of B, T and bone-marrow-derived dendritic cells toward CC chemokine ligand-21 and CXC chemokine ligand-12 was significantly increased, by twofold, in WP-treated mice compared to the control group. Taken together, our data reveal the benefits of WP supplementation in enhancing immune cell proliferation and migration to the secondary lymphoid organs.</description><subject>Animals</subject><subject>antigens</subject><subject>B-Lymphocytes - drug effects</subject><subject>Biological and medical sciences</subject><subject>Body weight</subject><subject>Bone Marrow Cells - cytology</subject><subject>Bovine serum albumin</subject><subject>CC chemokines</subject><subject>Cell proliferation</subject><subject>Cell Proliferation - drug effects</subject><subject>Chemokine CCL21 - metabolism</subject><subject>Chemokine CXCL12 - metabolism</subject><subject>chemokines</subject><subject>Chemotaxis</subject><subject>Chemotaxis - drug effects</subject><subject>Chemotaxis - immunology</subject><subject>Cholesterol</subject><subject>CXC chemokines</subject><subject>Cytokines</subject><subject>Data processing</subject><subject>Dendritic cells</subject><subject>Dendritic Cells - drug effects</subject><subject>Dendritic Cells - immunology</subject><subject>Dietary Supplements</subject><subject>Feeding. Feeding behavior</subject><subject>Free radicals</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glutathione</subject><subject>Interleukin 10</subject><subject>Interleukin 2</subject><subject>Interleukin 4</subject><subject>Interleukin 7</subject><subject>Interleukin 8</subject><subject>interleukin-1</subject><subject>Interleukins - blood</subject><subject>Leukocyte migration</subject><subject>Lipid profile</subject><subject>Lipids</subject><subject>Lymphocytes - cytology</subject><subject>Lymphocytes - drug effects</subject><subject>Lymphocytes - immunology</subject><subject>Male</subject><subject>Mice</subject><subject>Milk Proteins - pharmacology</subject><subject>mononuclear leukocytes</subject><subject>Mucosal immunity</subject><subject>Peripheral blood mononuclear cells</subject><subject>Protein Denaturation</subject><subject>Reactive oxygen species</subject><subject>Serum Albumin, Bovine - pharmacology</subject><subject>T-Lymphocytes - drug effects</subject><subject>triacylglycerols</subject><subject>Triglycerides</subject><subject>tumor necrosis factor-alpha</subject><subject>Tumor Necrosis Factor-alpha - blood</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Whey</subject><subject>whey protein</subject><subject>whey protein concentrate</subject><subject>Whey Proteins</subject><issn>0955-2863</issn><issn>1873-4847</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk2P1SAUhhujca6jP0HtxmRc9AoUaFkZ0_iVXONCJ5kdoXA6w7WFGaCO84v8m1J71Y1xJCQkh-c9H7wUxWOMthhh_mK_3bs59dZvCcJ4mzdC_E6xwW1TV7Slzd1igwRjFWl5fVQ8iHGPECKU8fvFESE0L9Fuiu8fvJlHlax3pR9KO02zg1LDOJaXwY92gLBeKmdKfQGTT-qbjWXy1yqYWHbdGv1is2y05wt20nW75xXBPzXd2V-JswXBpLSunJ0Bp9IcwJTXF3CzFE5gXZUCqJSDk9XwsLg3qDHCo8N5XJy-ef25e1ftPr59373aVZpRkipBudJGC0Y5FQ2qVc1QT3ohBGbcKDX0dW9QAwyAgBKkHZBQiCIitIC2JfVxcbLmzU1czRCTnGxcnkM58HOUmDSkqRtR4_9F25bdjmKGG4QZajLKVlQHH2OAQV4GO6lwIzGSi_NyLw_Oy8X5rJXZ-ax7cigx9xOY36pfVmfg2QFQUatxCMppG_9wnNc8t5y5pys3KC_VecjM6adciebvU4s8-T8JghmjmXi5EpCt-mohyKgtOA3GBtBJGm9vGecHf-ngOw</recordid><startdate>20121201</startdate><enddate>20121201</enddate><creator>Badr, Gamal</creator><creator>Ebaid, Hossam</creator><creator>Mohany, Mohamed</creator><creator>Abuelsaad, Abdelaziz Saber</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</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>7X8</scope><scope>7QR</scope><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope></search><sort><creationdate>20121201</creationdate><title>Modulation of immune cell proliferation and chemotaxis towards CC chemokine ligand (CCL)-21 and CXC chemokine ligand (CXCL)-12 in undenatured whey protein-treated mice</title><author>Badr, Gamal ; Ebaid, Hossam ; Mohany, Mohamed ; Abuelsaad, Abdelaziz Saber</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c542t-946acdc954649703a350b2b999156daafb3bd07e5ee2ea928f09a04029c9e8823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>antigens</topic><topic>B-Lymphocytes - drug effects</topic><topic>Biological and medical sciences</topic><topic>Body weight</topic><topic>Bone Marrow Cells - cytology</topic><topic>Bovine serum albumin</topic><topic>CC chemokines</topic><topic>Cell proliferation</topic><topic>Cell Proliferation - drug effects</topic><topic>Chemokine CCL21 - metabolism</topic><topic>Chemokine CXCL12 - metabolism</topic><topic>chemokines</topic><topic>Chemotaxis</topic><topic>Chemotaxis - drug effects</topic><topic>Chemotaxis - immunology</topic><topic>Cholesterol</topic><topic>CXC chemokines</topic><topic>Cytokines</topic><topic>Data processing</topic><topic>Dendritic cells</topic><topic>Dendritic Cells - drug effects</topic><topic>Dendritic Cells - immunology</topic><topic>Dietary Supplements</topic><topic>Feeding. Feeding behavior</topic><topic>Free radicals</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glutathione</topic><topic>Interleukin 10</topic><topic>Interleukin 2</topic><topic>Interleukin 4</topic><topic>Interleukin 7</topic><topic>Interleukin 8</topic><topic>interleukin-1</topic><topic>Interleukins - blood</topic><topic>Leukocyte migration</topic><topic>Lipid profile</topic><topic>Lipids</topic><topic>Lymphocytes - cytology</topic><topic>Lymphocytes - drug effects</topic><topic>Lymphocytes - immunology</topic><topic>Male</topic><topic>Mice</topic><topic>Milk Proteins - pharmacology</topic><topic>mononuclear leukocytes</topic><topic>Mucosal immunity</topic><topic>Peripheral blood mononuclear cells</topic><topic>Protein Denaturation</topic><topic>Reactive oxygen species</topic><topic>Serum Albumin, Bovine - pharmacology</topic><topic>T-Lymphocytes - drug effects</topic><topic>triacylglycerols</topic><topic>Triglycerides</topic><topic>tumor necrosis factor-alpha</topic><topic>Tumor Necrosis Factor-alpha - blood</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Whey</topic><topic>whey protein</topic><topic>whey protein concentrate</topic><topic>Whey Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Badr, Gamal</creatorcontrib><creatorcontrib>Ebaid, Hossam</creatorcontrib><creatorcontrib>Mohany, Mohamed</creatorcontrib><creatorcontrib>Abuelsaad, Abdelaziz Saber</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><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><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>The Journal of nutritional biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Badr, Gamal</au><au>Ebaid, Hossam</au><au>Mohany, Mohamed</au><au>Abuelsaad, Abdelaziz Saber</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modulation of immune cell proliferation and chemotaxis towards CC chemokine ligand (CCL)-21 and CXC chemokine ligand (CXCL)-12 in undenatured whey protein-treated mice</atitle><jtitle>The Journal of nutritional biochemistry</jtitle><addtitle>J Nutr Biochem</addtitle><date>2012-12-01</date><risdate>2012</risdate><volume>23</volume><issue>12</issue><spage>1640</spage><epage>1646</epage><pages>1640-1646</pages><issn>0955-2863</issn><eissn>1873-4847</eissn><abstract>Whey protein concentrates (WPCs) enhance innate mucosal immunity during early life and have a protective role in some immune disorders. To further elucidate the potential benefits of this protein, the present study investigated the effect of dietary supplementation with WPCs on blood parameters, plasma cytokine profiles, and immune cell proliferation and chemotaxis. A total of 45 male mice were equally distributed into three experimental groups and treated daily for 21 days as follows: group I was a control group that was orally supplemented with distilled water, group II was orally supplemented with undenatured WP (100 mg/kg body weight), and group III was orally supplemented with bovine serum albumin (100 mg/kg body weight). We found that the plasma cytokine levels of interleukin (IL)-1α, IL-1β, IL-10 and tumor necrosis factor-α and the levels of reactive oxygen species, cholesterol, triglycerides and the lipid profile were significantly decreased in the WP-treated group compared to the control group. In contrast, the levels of IL-2, IL-4, IL-7, IL-8 and glutathione were significantly elevated, and consequently, the ability of peripheral blood mononuclear cells to proliferate in response to stimulation with different antigens was significantly increased in the WP-treated group. Moreover, the in vitro chemotaxis of B, T and bone-marrow-derived dendritic cells toward CC chemokine ligand-21 and CXC chemokine ligand-12 was significantly increased, by twofold, in WP-treated mice compared to the control group. Taken together, our data reveal the benefits of WP supplementation in enhancing immune cell proliferation and migration to the secondary lymphoid organs.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>22444498</pmid><doi>10.1016/j.jnutbio.2011.11.006</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0955-2863 |
ispartof | The Journal of nutritional biochemistry, 2012-12, Vol.23 (12), p.1640-1646 |
issn | 0955-2863 1873-4847 |
language | eng |
recordid | cdi_proquest_miscellaneous_1272737931 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Animals antigens B-Lymphocytes - drug effects Biological and medical sciences Body weight Bone Marrow Cells - cytology Bovine serum albumin CC chemokines Cell proliferation Cell Proliferation - drug effects Chemokine CCL21 - metabolism Chemokine CXCL12 - metabolism chemokines Chemotaxis Chemotaxis - drug effects Chemotaxis - immunology Cholesterol CXC chemokines Cytokines Data processing Dendritic cells Dendritic Cells - drug effects Dendritic Cells - immunology Dietary Supplements Feeding. Feeding behavior Free radicals Fundamental and applied biological sciences. Psychology Glutathione Interleukin 10 Interleukin 2 Interleukin 4 Interleukin 7 Interleukin 8 interleukin-1 Interleukins - blood Leukocyte migration Lipid profile Lipids Lymphocytes - cytology Lymphocytes - drug effects Lymphocytes - immunology Male Mice Milk Proteins - pharmacology mononuclear leukocytes Mucosal immunity Peripheral blood mononuclear cells Protein Denaturation Reactive oxygen species Serum Albumin, Bovine - pharmacology T-Lymphocytes - drug effects triacylglycerols Triglycerides tumor necrosis factor-alpha Tumor Necrosis Factor-alpha - blood Vertebrates: anatomy and physiology, studies on body, several organs or systems Whey whey protein whey protein concentrate Whey Proteins |
title | Modulation of immune cell proliferation and chemotaxis towards CC chemokine ligand (CCL)-21 and CXC chemokine ligand (CXCL)-12 in undenatured whey protein-treated mice |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T05%3A51%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Modulation%20of%20immune%20cell%20proliferation%20and%20chemotaxis%20towards%20CC%20chemokine%20ligand%20(CCL)-21%20and%20CXC%20chemokine%20ligand%20(CXCL)-12%20in%20undenatured%20whey%20protein-treated%20mice&rft.jtitle=The%20Journal%20of%20nutritional%20biochemistry&rft.au=Badr,%20Gamal&rft.date=2012-12-01&rft.volume=23&rft.issue=12&rft.spage=1640&rft.epage=1646&rft.pages=1640-1646&rft.issn=0955-2863&rft.eissn=1873-4847&rft_id=info:doi/10.1016/j.jnutbio.2011.11.006&rft_dat=%3Cproquest_cross%3E1151701507%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1151701507&rft_id=info:pmid/22444498&rft_els_id=S0955286311003159&rfr_iscdi=true |