Ex vivo culture of intestinal crypt organoids as a model system for assessing cell death induction in intestinal epithelial cells and enteropathy
Intestinal epithelial cells (IECs) not only have a critical function in the absorption of nutrients, but also act as a physical barrier between our body and the outside world. Damage and death of the epithelial cells lead to the breakdown of this barrier function and inflammation due to access of th...
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creator | Grabinger, T Luks, L Kostadinova, F Zimberlin, C Medema, J P Leist, M Brunner, T |
description | Intestinal epithelial cells (IECs) not only have a critical function in the absorption of nutrients, but also act as a physical barrier between our body and the outside world. Damage and death of the epithelial cells lead to the breakdown of this barrier function and inflammation due to access of the immune system to compounds of the intestinal flora. Intestinal epithelial damage is frequently associated with various inflammatory disorders, chemo- and radiotherapy as well as drug-mediated toxicity. Until recently, intestinal epithelial-damaging activities of drugs and treatments could be tested only
in vivo
in animal models because of the poor survival rate of primary IECs
ex vivo
. The three-dimensional culture and outgrowth of intestinal crypt stem cells into organoids have offered new possibilities to culture and study IECs
ex vivo
. Here we demonstrate that intestinal organoids are a useful and physiologically relevant model system to study cell death and survival in IECs. We further describe a number of microscopy-based as well as colorimetric methods to monitor and score survival and death of intestinal organoids. Finally, the comparison of organoids isolated from gene-deficient mice and wild-type mice allows investigating the role of specific genes in the regulation of IEC death. Owing to their comparable structure and behavior, intestinal organoids may serve as an interesting and physiologically relevant surrogate system for large- and mid-scale
in vitro
testing of intestinal epithelium-damaging drugs and toxins, and for the investigation of cell death pathways. |
doi_str_mv | 10.1038/cddis.2014.183 |
format | Article |
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in vivo
in animal models because of the poor survival rate of primary IECs
ex vivo
. The three-dimensional culture and outgrowth of intestinal crypt stem cells into organoids have offered new possibilities to culture and study IECs
ex vivo
. Here we demonstrate that intestinal organoids are a useful and physiologically relevant model system to study cell death and survival in IECs. We further describe a number of microscopy-based as well as colorimetric methods to monitor and score survival and death of intestinal organoids. Finally, the comparison of organoids isolated from gene-deficient mice and wild-type mice allows investigating the role of specific genes in the regulation of IEC death. Owing to their comparable structure and behavior, intestinal organoids may serve as an interesting and physiologically relevant surrogate system for large- and mid-scale
in vitro
testing of intestinal epithelium-damaging drugs and toxins, and for the investigation of cell death pathways.</description><identifier>ISSN: 2041-4889</identifier><identifier>EISSN: 2041-4889</identifier><identifier>DOI: 10.1038/cddis.2014.183</identifier><identifier>PMID: 24832600</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/154/1435 ; 631/1647/767 ; 631/80/82 ; 692/699/1503/1581 ; Animals ; Antibodies ; Apoptosis - drug effects ; Apoptosis Regulatory Proteins - deficiency ; Apoptosis Regulatory Proteins - genetics ; Bcl-2-Like Protein 11 ; Biochemistry ; Biological Assay ; Biomedical and Life Sciences ; Caco-2 Cells ; Camptothecin - analogs & derivatives ; Camptothecin - toxicity ; Cell Biology ; Cell Culture ; Cisplatin - toxicity ; Dose-Response Relationship, Drug ; Epithelial Cells - drug effects ; Epithelial Cells - metabolism ; Epithelial Cells - pathology ; Humans ; Immunology ; Intestinal Diseases - genetics ; Intestinal Diseases - metabolism ; Intestinal Diseases - pathology ; Intestinal Mucosa - drug effects ; Intestinal Mucosa - metabolism ; Intestinal Mucosa - pathology ; Intestine, Small - drug effects ; Intestine, Small - metabolism ; Intestine, Small - pathology ; Life Sciences ; Membrane Proteins - deficiency ; Membrane Proteins - genetics ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Organoids ; Original ; original-article ; Proto-Oncogene Proteins - deficiency ; Proto-Oncogene Proteins - genetics ; Time Factors ; Tumor Necrosis Factor-alpha - toxicity</subject><ispartof>Cell death & disease, 2014-05, Vol.5 (5), p.e1228-e1228</ispartof><rights>The Author(s) 2014</rights><rights>Copyright Nature Publishing Group May 2014</rights><rights>Copyright © 2014 Macmillan Publishers Limited 2014 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-68622aeafef356cc886f69aa47d9b7e4d5fdb43347e459517290f1fa0887a5e83</citedby><cites>FETCH-LOGICAL-c524t-68622aeafef356cc886f69aa47d9b7e4d5fdb43347e459517290f1fa0887a5e83</cites><orcidid>0000-0002-3778-8693 ; 0000000237788693</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4047863/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4047863/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24832600$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grabinger, T</creatorcontrib><creatorcontrib>Luks, L</creatorcontrib><creatorcontrib>Kostadinova, F</creatorcontrib><creatorcontrib>Zimberlin, C</creatorcontrib><creatorcontrib>Medema, J P</creatorcontrib><creatorcontrib>Leist, M</creatorcontrib><creatorcontrib>Brunner, T</creatorcontrib><title>Ex vivo culture of intestinal crypt organoids as a model system for assessing cell death induction in intestinal epithelial cells and enteropathy</title><title>Cell death & disease</title><addtitle>Cell Death Dis</addtitle><addtitle>Cell Death Dis</addtitle><description>Intestinal epithelial cells (IECs) not only have a critical function in the absorption of nutrients, but also act as a physical barrier between our body and the outside world. Damage and death of the epithelial cells lead to the breakdown of this barrier function and inflammation due to access of the immune system to compounds of the intestinal flora. Intestinal epithelial damage is frequently associated with various inflammatory disorders, chemo- and radiotherapy as well as drug-mediated toxicity. Until recently, intestinal epithelial-damaging activities of drugs and treatments could be tested only
in vivo
in animal models because of the poor survival rate of primary IECs
ex vivo
. The three-dimensional culture and outgrowth of intestinal crypt stem cells into organoids have offered new possibilities to culture and study IECs
ex vivo
. Here we demonstrate that intestinal organoids are a useful and physiologically relevant model system to study cell death and survival in IECs. We further describe a number of microscopy-based as well as colorimetric methods to monitor and score survival and death of intestinal organoids. Finally, the comparison of organoids isolated from gene-deficient mice and wild-type mice allows investigating the role of specific genes in the regulation of IEC death. Owing to their comparable structure and behavior, intestinal organoids may serve as an interesting and physiologically relevant surrogate system for large- and mid-scale
in vitro
testing of intestinal epithelium-damaging drugs and toxins, and for the investigation of cell death pathways.</description><subject>631/154/1435</subject><subject>631/1647/767</subject><subject>631/80/82</subject><subject>692/699/1503/1581</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Apoptosis - drug effects</subject><subject>Apoptosis Regulatory Proteins - deficiency</subject><subject>Apoptosis Regulatory Proteins - genetics</subject><subject>Bcl-2-Like Protein 11</subject><subject>Biochemistry</subject><subject>Biological Assay</subject><subject>Biomedical and Life Sciences</subject><subject>Caco-2 Cells</subject><subject>Camptothecin - analogs & derivatives</subject><subject>Camptothecin - toxicity</subject><subject>Cell Biology</subject><subject>Cell Culture</subject><subject>Cisplatin - toxicity</subject><subject>Dose-Response Relationship, Drug</subject><subject>Epithelial Cells - drug effects</subject><subject>Epithelial Cells - metabolism</subject><subject>Epithelial Cells - pathology</subject><subject>Humans</subject><subject>Immunology</subject><subject>Intestinal Diseases - genetics</subject><subject>Intestinal Diseases - metabolism</subject><subject>Intestinal Diseases - pathology</subject><subject>Intestinal Mucosa - drug effects</subject><subject>Intestinal Mucosa - metabolism</subject><subject>Intestinal Mucosa - pathology</subject><subject>Intestine, Small - drug effects</subject><subject>Intestine, Small - metabolism</subject><subject>Intestine, Small - pathology</subject><subject>Life Sciences</subject><subject>Membrane Proteins - deficiency</subject><subject>Membrane Proteins - genetics</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Organoids</subject><subject>Original</subject><subject>original-article</subject><subject>Proto-Oncogene Proteins - deficiency</subject><subject>Proto-Oncogene Proteins - genetics</subject><subject>Time Factors</subject><subject>Tumor Necrosis Factor-alpha - 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drug effects</topic><topic>Apoptosis Regulatory Proteins - deficiency</topic><topic>Apoptosis Regulatory Proteins - genetics</topic><topic>Bcl-2-Like Protein 11</topic><topic>Biochemistry</topic><topic>Biological Assay</topic><topic>Biomedical and Life Sciences</topic><topic>Caco-2 Cells</topic><topic>Camptothecin - analogs & derivatives</topic><topic>Camptothecin - toxicity</topic><topic>Cell Biology</topic><topic>Cell Culture</topic><topic>Cisplatin - toxicity</topic><topic>Dose-Response Relationship, Drug</topic><topic>Epithelial Cells - drug effects</topic><topic>Epithelial Cells - metabolism</topic><topic>Epithelial Cells - pathology</topic><topic>Humans</topic><topic>Immunology</topic><topic>Intestinal Diseases - genetics</topic><topic>Intestinal Diseases - metabolism</topic><topic>Intestinal Diseases - pathology</topic><topic>Intestinal Mucosa - drug effects</topic><topic>Intestinal Mucosa - metabolism</topic><topic>Intestinal Mucosa - pathology</topic><topic>Intestine, Small - drug effects</topic><topic>Intestine, Small - metabolism</topic><topic>Intestine, Small - pathology</topic><topic>Life Sciences</topic><topic>Membrane Proteins - deficiency</topic><topic>Membrane Proteins - genetics</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Organoids</topic><topic>Original</topic><topic>original-article</topic><topic>Proto-Oncogene Proteins - deficiency</topic><topic>Proto-Oncogene Proteins - genetics</topic><topic>Time Factors</topic><topic>Tumor Necrosis Factor-alpha - toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grabinger, T</creatorcontrib><creatorcontrib>Luks, L</creatorcontrib><creatorcontrib>Kostadinova, F</creatorcontrib><creatorcontrib>Zimberlin, C</creatorcontrib><creatorcontrib>Medema, J P</creatorcontrib><creatorcontrib>Leist, M</creatorcontrib><creatorcontrib>Brunner, T</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</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>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell death & disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grabinger, T</au><au>Luks, L</au><au>Kostadinova, F</au><au>Zimberlin, C</au><au>Medema, J P</au><au>Leist, M</au><au>Brunner, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ex vivo culture of intestinal crypt organoids as a model system for assessing cell death induction in intestinal epithelial cells and enteropathy</atitle><jtitle>Cell death & disease</jtitle><stitle>Cell Death Dis</stitle><addtitle>Cell Death Dis</addtitle><date>2014-05-15</date><risdate>2014</risdate><volume>5</volume><issue>5</issue><spage>e1228</spage><epage>e1228</epage><pages>e1228-e1228</pages><issn>2041-4889</issn><eissn>2041-4889</eissn><abstract>Intestinal epithelial cells (IECs) not only have a critical function in the absorption of nutrients, but also act as a physical barrier between our body and the outside world. Damage and death of the epithelial cells lead to the breakdown of this barrier function and inflammation due to access of the immune system to compounds of the intestinal flora. Intestinal epithelial damage is frequently associated with various inflammatory disorders, chemo- and radiotherapy as well as drug-mediated toxicity. Until recently, intestinal epithelial-damaging activities of drugs and treatments could be tested only
in vivo
in animal models because of the poor survival rate of primary IECs
ex vivo
. The three-dimensional culture and outgrowth of intestinal crypt stem cells into organoids have offered new possibilities to culture and study IECs
ex vivo
. Here we demonstrate that intestinal organoids are a useful and physiologically relevant model system to study cell death and survival in IECs. We further describe a number of microscopy-based as well as colorimetric methods to monitor and score survival and death of intestinal organoids. Finally, the comparison of organoids isolated from gene-deficient mice and wild-type mice allows investigating the role of specific genes in the regulation of IEC death. Owing to their comparable structure and behavior, intestinal organoids may serve as an interesting and physiologically relevant surrogate system for large- and mid-scale
in vitro
testing of intestinal epithelium-damaging drugs and toxins, and for the investigation of cell death pathways.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>24832600</pmid><doi>10.1038/cddis.2014.183</doi><orcidid>https://orcid.org/0000-0002-3778-8693</orcidid><orcidid>https://orcid.org/0000000237788693</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/154/1435 631/1647/767 631/80/82 692/699/1503/1581 Animals Antibodies Apoptosis - drug effects Apoptosis Regulatory Proteins - deficiency Apoptosis Regulatory Proteins - genetics Bcl-2-Like Protein 11 Biochemistry Biological Assay Biomedical and Life Sciences Caco-2 Cells Camptothecin - analogs & derivatives Camptothecin - toxicity Cell Biology Cell Culture Cisplatin - toxicity Dose-Response Relationship, Drug Epithelial Cells - drug effects Epithelial Cells - metabolism Epithelial Cells - pathology Humans Immunology Intestinal Diseases - genetics Intestinal Diseases - metabolism Intestinal Diseases - pathology Intestinal Mucosa - drug effects Intestinal Mucosa - metabolism Intestinal Mucosa - pathology Intestine, Small - drug effects Intestine, Small - metabolism Intestine, Small - pathology Life Sciences Membrane Proteins - deficiency Membrane Proteins - genetics Mice Mice, Inbred C57BL Mice, Knockout Organoids Original original-article Proto-Oncogene Proteins - deficiency Proto-Oncogene Proteins - genetics Time Factors Tumor Necrosis Factor-alpha - toxicity |
title | Ex vivo culture of intestinal crypt organoids as a model system for assessing cell death induction in intestinal epithelial cells and enteropathy |
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