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The kiwi fruit peptide kissper displays anti‐inflammatory and anti‐oxidant effects in in‐vitro and ex‐vivo human intestinal models
Summary Literature reports describe kiwi fruit as a food with significant effects on human health, including anti‐oxidant and anti‐inflammatory activity. Fresh fruit or raw kiwi fruit extracts have been used so far to investigate these effects, but the molecule(s) responsible for these health‐promot...
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Published in: | Clinical and experimental immunology 2014-03, Vol.175 (3), p.476-484 |
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container_title | Clinical and experimental immunology |
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creator | Ciacci, C. Russo, I. Bucci, C. Iovino, P. Pellegrini, L. Giangrieco, I. Tamburrini, M. Ciardiello, M. A. |
description | Summary
Literature reports describe kiwi fruit as a food with significant effects on human health, including anti‐oxidant and anti‐inflammatory activity. Fresh fruit or raw kiwi fruit extracts have been used so far to investigate these effects, but the molecule(s) responsible for these health‐promoting activities have not yet been identified. Kissper is a kiwi fruit peptide displaying pore‐forming activity in synthetic lipid bilayers, the composition of which is similar to that found in intestinal cells. The objective of this study was to investigate the kissper influence on intestinal inflammation using cultured cells and ex‐vivo tissues from healthy subjects and Crohn's disease (CD) patients. The anti‐oxidant and anti‐inflammatory properties of kissper were tested on Caco‐2 cells and on the colonic mucosa from 23 patients with CD, by challenging with the lipopolysaccharide from Escherichia coli (EC‐LPS) and monitoring the appropriate markers by Western blot and immunofluorescence. EC‐LPS challenge determined an increase in the intracellular concentration of calcium and reactive oxygen species (ROS). The peptide kissper was highly effective in preventing the increase of LPS‐induced ROS levels in both the Caco‐2 cells and CD colonic mucosa. Moreover, it controls the calcium increase, p65‐nuclear factor (NF)‐kB induction and transglutaminase 2 (TG2) activation inflammatory response in Caco‐2 cells and CD colonic mucosa. Kissper efficiently counteracts the oxidative stress and inflammatory response in valuable model systems consisting of intestinal cells and CD colonic mucosa. This study reports the first evidence supporting a possible correlation between some beneficial effects of kiwi fruit and a specific protein molecule rather than generic nutrients. |
doi_str_mv | 10.1111/cei.12229 |
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Literature reports describe kiwi fruit as a food with significant effects on human health, including anti‐oxidant and anti‐inflammatory activity. Fresh fruit or raw kiwi fruit extracts have been used so far to investigate these effects, but the molecule(s) responsible for these health‐promoting activities have not yet been identified. Kissper is a kiwi fruit peptide displaying pore‐forming activity in synthetic lipid bilayers, the composition of which is similar to that found in intestinal cells. The objective of this study was to investigate the kissper influence on intestinal inflammation using cultured cells and ex‐vivo tissues from healthy subjects and Crohn's disease (CD) patients. The anti‐oxidant and anti‐inflammatory properties of kissper were tested on Caco‐2 cells and on the colonic mucosa from 23 patients with CD, by challenging with the lipopolysaccharide from Escherichia coli (EC‐LPS) and monitoring the appropriate markers by Western blot and immunofluorescence. EC‐LPS challenge determined an increase in the intracellular concentration of calcium and reactive oxygen species (ROS). The peptide kissper was highly effective in preventing the increase of LPS‐induced ROS levels in both the Caco‐2 cells and CD colonic mucosa. Moreover, it controls the calcium increase, p65‐nuclear factor (NF)‐kB induction and transglutaminase 2 (TG2) activation inflammatory response in Caco‐2 cells and CD colonic mucosa. Kissper efficiently counteracts the oxidative stress and inflammatory response in valuable model systems consisting of intestinal cells and CD colonic mucosa. This study reports the first evidence supporting a possible correlation between some beneficial effects of kiwi fruit and a specific protein molecule rather than generic nutrients.</description><identifier>ISSN: 0009-9104</identifier><identifier>EISSN: 1365-2249</identifier><identifier>DOI: 10.1111/cei.12229</identifier><identifier>PMID: 24168016</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Actinidia - chemistry ; Adolescent ; Adult ; Anti-Inflammatory Agents - isolation & purification ; Anti-Inflammatory Agents - pharmacology ; Antioxidants - isolation & purification ; Antioxidants - pharmacology ; Caco-2 Cells ; Colon ; Enzyme Activation - drug effects ; Escherichia coli ; Fruit - chemistry ; GTP-Binding Proteins ; Humans ; inflammation ; Intestinal Mucosa - drug effects ; Intestinal Mucosa - metabolism ; lipopolysaccharide ; NF-kappa B - metabolism ; Original ; Oxidative Stress - drug effects ; Peptides ; Peptides - isolation & purification ; Peptides - pharmacology ; Plant Extracts - chemistry ; Plant Extracts - isolation & purification ; Plant Extracts - pharmacology ; reactive oxygen species ; Reactive Oxygen Species - metabolism ; Transglutaminases - metabolism ; Young Adult</subject><ispartof>Clinical and experimental immunology, 2014-03, Vol.175 (3), p.476-484</ispartof><rights>2013 British Society for Immunology</rights><rights>2013 British Society for Immunology.</rights><rights>Copyright © 2014 British Society for Immunology</rights><rights>2013 British Society for Immunology, Clinical and Experimental Immunology 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4769-c0254d6480b8fe2610b5cd1edb0f088987f212fd04883ecadebc0a8836ee123d3</citedby><cites>FETCH-LOGICAL-c4769-c0254d6480b8fe2610b5cd1edb0f088987f212fd04883ecadebc0a8836ee123d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927908/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927908/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24168016$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ciacci, C.</creatorcontrib><creatorcontrib>Russo, I.</creatorcontrib><creatorcontrib>Bucci, C.</creatorcontrib><creatorcontrib>Iovino, P.</creatorcontrib><creatorcontrib>Pellegrini, L.</creatorcontrib><creatorcontrib>Giangrieco, I.</creatorcontrib><creatorcontrib>Tamburrini, M.</creatorcontrib><creatorcontrib>Ciardiello, M. A.</creatorcontrib><title>The kiwi fruit peptide kissper displays anti‐inflammatory and anti‐oxidant effects in in‐vitro and ex‐vivo human intestinal models</title><title>Clinical and experimental immunology</title><addtitle>Clin Exp Immunol</addtitle><description>Summary
Literature reports describe kiwi fruit as a food with significant effects on human health, including anti‐oxidant and anti‐inflammatory activity. Fresh fruit or raw kiwi fruit extracts have been used so far to investigate these effects, but the molecule(s) responsible for these health‐promoting activities have not yet been identified. Kissper is a kiwi fruit peptide displaying pore‐forming activity in synthetic lipid bilayers, the composition of which is similar to that found in intestinal cells. The objective of this study was to investigate the kissper influence on intestinal inflammation using cultured cells and ex‐vivo tissues from healthy subjects and Crohn's disease (CD) patients. The anti‐oxidant and anti‐inflammatory properties of kissper were tested on Caco‐2 cells and on the colonic mucosa from 23 patients with CD, by challenging with the lipopolysaccharide from Escherichia coli (EC‐LPS) and monitoring the appropriate markers by Western blot and immunofluorescence. EC‐LPS challenge determined an increase in the intracellular concentration of calcium and reactive oxygen species (ROS). The peptide kissper was highly effective in preventing the increase of LPS‐induced ROS levels in both the Caco‐2 cells and CD colonic mucosa. Moreover, it controls the calcium increase, p65‐nuclear factor (NF)‐kB induction and transglutaminase 2 (TG2) activation inflammatory response in Caco‐2 cells and CD colonic mucosa. Kissper efficiently counteracts the oxidative stress and inflammatory response in valuable model systems consisting of intestinal cells and CD colonic mucosa. This study reports the first evidence supporting a possible correlation between some beneficial effects of kiwi fruit and a specific protein molecule rather than generic nutrients.</description><subject>Actinidia - chemistry</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Anti-Inflammatory Agents - isolation & purification</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Antioxidants - isolation & purification</subject><subject>Antioxidants - pharmacology</subject><subject>Caco-2 Cells</subject><subject>Colon</subject><subject>Enzyme Activation - drug effects</subject><subject>Escherichia coli</subject><subject>Fruit - chemistry</subject><subject>GTP-Binding Proteins</subject><subject>Humans</subject><subject>inflammation</subject><subject>Intestinal Mucosa - drug effects</subject><subject>Intestinal Mucosa - metabolism</subject><subject>lipopolysaccharide</subject><subject>NF-kappa B - metabolism</subject><subject>Original</subject><subject>Oxidative Stress - drug effects</subject><subject>Peptides</subject><subject>Peptides - isolation & purification</subject><subject>Peptides - pharmacology</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - isolation & purification</subject><subject>Plant Extracts - pharmacology</subject><subject>reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Transglutaminases - metabolism</subject><subject>Young Adult</subject><issn>0009-9104</issn><issn>1365-2249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNksFu1DAQhi0EokvhwAugSFzgkHbsJF77goRWBSpV4lLOltcesy5JHOxk271x5sQz8iQ4u20FSEhYljzz-9OvGXsIeU7hhOZ1atCfUMaYfEAWtOJNyVgtH5IFAMhSUqiPyJOUrnLKOWePyRGrKRdA-YJ8v9xg8cVf-8LFyY_FgMPo7SylNGAsrE9Dq3ep0P3of3774XvX6q7TY4i7rNk7Pdx4m8MCnUMzpsL3eWd968cY9iDe7NNtKDZTp-frEdPoe90WXbDYpqfkkdNtwme35zH59O7scvWhvPj4_nz19qI09ZLL0gBrastrAWvhkHEK68ZYinYNDoSQYukYZc5CLUSFRltcG9A55oiUVbY6Jm8OvsO07tAa7MeoWzVE3-m4U0F79edN7zfqc9iqSrKlBJENXt0axPB1yk2ozieDbat7DFNStIGmqkCK_0BrKXNRAHVGX_6FXoUp5ueZDZlsmrnVTL0-UCaGlCK6-7opqHkYVB4GtR-GzL74vdF78u73M3B6AK59i7t_O6nV2fnB8hfq-8T7</recordid><startdate>201403</startdate><enddate>201403</enddate><creator>Ciacci, C.</creator><creator>Russo, I.</creator><creator>Bucci, C.</creator><creator>Iovino, P.</creator><creator>Pellegrini, L.</creator><creator>Giangrieco, I.</creator><creator>Tamburrini, M.</creator><creator>Ciardiello, M. A.</creator><general>Oxford University Press</general><general>Blackwell Publishing Ltd</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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>M7N</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201403</creationdate><title>The kiwi fruit peptide kissper displays anti‐inflammatory and anti‐oxidant effects in in‐vitro and ex‐vivo human intestinal models</title><author>Ciacci, C. ; Russo, I. ; Bucci, C. ; Iovino, P. ; Pellegrini, L. ; Giangrieco, I. ; Tamburrini, M. ; Ciardiello, M. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4769-c0254d6480b8fe2610b5cd1edb0f088987f212fd04883ecadebc0a8836ee123d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Actinidia - chemistry</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Anti-Inflammatory Agents - isolation & purification</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Antioxidants - isolation & purification</topic><topic>Antioxidants - pharmacology</topic><topic>Caco-2 Cells</topic><topic>Colon</topic><topic>Enzyme Activation - drug effects</topic><topic>Escherichia coli</topic><topic>Fruit - chemistry</topic><topic>GTP-Binding Proteins</topic><topic>Humans</topic><topic>inflammation</topic><topic>Intestinal Mucosa - drug effects</topic><topic>Intestinal Mucosa - metabolism</topic><topic>lipopolysaccharide</topic><topic>NF-kappa B - metabolism</topic><topic>Original</topic><topic>Oxidative Stress - drug effects</topic><topic>Peptides</topic><topic>Peptides - isolation & purification</topic><topic>Peptides - pharmacology</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - isolation & purification</topic><topic>Plant Extracts - pharmacology</topic><topic>reactive oxygen species</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Transglutaminases - metabolism</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ciacci, C.</creatorcontrib><creatorcontrib>Russo, I.</creatorcontrib><creatorcontrib>Bucci, C.</creatorcontrib><creatorcontrib>Iovino, P.</creatorcontrib><creatorcontrib>Pellegrini, L.</creatorcontrib><creatorcontrib>Giangrieco, I.</creatorcontrib><creatorcontrib>Tamburrini, M.</creatorcontrib><creatorcontrib>Ciardiello, M. A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical and experimental immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ciacci, C.</au><au>Russo, I.</au><au>Bucci, C.</au><au>Iovino, P.</au><au>Pellegrini, L.</au><au>Giangrieco, I.</au><au>Tamburrini, M.</au><au>Ciardiello, M. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The kiwi fruit peptide kissper displays anti‐inflammatory and anti‐oxidant effects in in‐vitro and ex‐vivo human intestinal models</atitle><jtitle>Clinical and experimental immunology</jtitle><addtitle>Clin Exp Immunol</addtitle><date>2014-03</date><risdate>2014</risdate><volume>175</volume><issue>3</issue><spage>476</spage><epage>484</epage><pages>476-484</pages><issn>0009-9104</issn><eissn>1365-2249</eissn><abstract>Summary
Literature reports describe kiwi fruit as a food with significant effects on human health, including anti‐oxidant and anti‐inflammatory activity. Fresh fruit or raw kiwi fruit extracts have been used so far to investigate these effects, but the molecule(s) responsible for these health‐promoting activities have not yet been identified. Kissper is a kiwi fruit peptide displaying pore‐forming activity in synthetic lipid bilayers, the composition of which is similar to that found in intestinal cells. The objective of this study was to investigate the kissper influence on intestinal inflammation using cultured cells and ex‐vivo tissues from healthy subjects and Crohn's disease (CD) patients. The anti‐oxidant and anti‐inflammatory properties of kissper were tested on Caco‐2 cells and on the colonic mucosa from 23 patients with CD, by challenging with the lipopolysaccharide from Escherichia coli (EC‐LPS) and monitoring the appropriate markers by Western blot and immunofluorescence. EC‐LPS challenge determined an increase in the intracellular concentration of calcium and reactive oxygen species (ROS). The peptide kissper was highly effective in preventing the increase of LPS‐induced ROS levels in both the Caco‐2 cells and CD colonic mucosa. Moreover, it controls the calcium increase, p65‐nuclear factor (NF)‐kB induction and transglutaminase 2 (TG2) activation inflammatory response in Caco‐2 cells and CD colonic mucosa. Kissper efficiently counteracts the oxidative stress and inflammatory response in valuable model systems consisting of intestinal cells and CD colonic mucosa. This study reports the first evidence supporting a possible correlation between some beneficial effects of kiwi fruit and a specific protein molecule rather than generic nutrients.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>24168016</pmid><doi>10.1111/cei.12229</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actinidia - chemistry Adolescent Adult Anti-Inflammatory Agents - isolation & purification Anti-Inflammatory Agents - pharmacology Antioxidants - isolation & purification Antioxidants - pharmacology Caco-2 Cells Colon Enzyme Activation - drug effects Escherichia coli Fruit - chemistry GTP-Binding Proteins Humans inflammation Intestinal Mucosa - drug effects Intestinal Mucosa - metabolism lipopolysaccharide NF-kappa B - metabolism Original Oxidative Stress - drug effects Peptides Peptides - isolation & purification Peptides - pharmacology Plant Extracts - chemistry Plant Extracts - isolation & purification Plant Extracts - pharmacology reactive oxygen species Reactive Oxygen Species - metabolism Transglutaminases - metabolism Young Adult |
title | The kiwi fruit peptide kissper displays anti‐inflammatory and anti‐oxidant effects in in‐vitro and ex‐vivo human intestinal models |
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