Absorption of intact proteins by the intestinal epithelium of trout, Salmo gairdneri. A luminescence enzyme immunoassay and cytochemical study

In the rainbow trout, a carnivorous species with a stomach, orally administered horseradish peroxidase (HRP) crossed the intestinal epithelium into the circulation. The protein first appeared in the blood 7 to 8 h after intubation, and could be assayed up to 24 h after administration. The method use...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cell and tissue research 1988, Vol.251 (1), p.145-152
Hauptverfasser: GEORGOPOULOU, U, DABROWSKI, K, SIRE, M. F, VERNIER, J. M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 152
container_issue 1
container_start_page 145
container_title Cell and tissue research
container_volume 251
creator GEORGOPOULOU, U
DABROWSKI, K
SIRE, M. F
VERNIER, J. M
description In the rainbow trout, a carnivorous species with a stomach, orally administered horseradish peroxidase (HRP) crossed the intestinal epithelium into the circulation. The protein first appeared in the blood 7 to 8 h after intubation, and could be assayed up to 24 h after administration. The method used, which combines ELISA (enzyme-linked immunoabsorbant assay) and chemiluminescence, enabled the transfer to be measured quantitatively. There was a direct correlation between the quantity ingested and the quantity transferred to the plasma within the experimental limits chosen. The clearance was monophasic and exponential (clearance rate: 3% per minute). Up to 6% of the ingested HRP was transferred to the blood. By cytochemistry it was possible to demonstrate that the protein crossed the intestinal cells at the level of the posterior segment, escaping the particularly intense intracellular lysosomal digestion. After entering the intercellular space, HRP was transferred to the interstitial space of the subepithelial lamina propria. During this transfer the HRP was in close contact with infiltrated macrophages and leukocytes resembling lymphoid cells. Thus, the passage of these protein particles could be the first indispensable step in the possible triggering of a local and/or a systemic immune response.
doi_str_mv 10.1007/BF00215459
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_78097094</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>78097094</sourcerecordid><originalsourceid>FETCH-LOGICAL-c270t-b22a2068a483077fd60073db55ba01c40611e1d1a58ccefed03fa5986a5614ca3</originalsourceid><addsrcrecordid>eNpFkEFv1DAQhS0EKtvChTuSD4gDImXsJHZy3Fa0IFXiAEjcookzoUaxvdjOIfwIfjNedVVOI7336WneY-yVgEsBoD9c3QBI0TZt_4TtRFPLCjrdPWU7qEFWWqkfz9l5Sr8ARKNUf8bOaqm1FnLH_u7HFOIh2-B5mLn1GU3mhxgyWZ_4uPF8T0eZUrYeF04HW5TFru7I5xjW_J5_xcUF_hNtnDxFe8n3fFmd9ZQMeUOc_J_NlRjnVh8wJdw4-ombLQdzT86aEpzyOm0v2LMZl0QvT_eCfb_5-O36U3X35fbz9f6uMlJDrkYpUYLqsOlq0HqeVJmhnsa2HRGEaUAJQWIS2HbG0EwT1DO2faewVaIxWF-wtw-5penvtXQbnC2_Lgt6CmsadAe9hr4p4LsH0MSQUqR5OETrMG6DgOE4_vB__AK_PqWuo6PpET2tXfw3Jx9TqTxH9MamR0yrvm9Lo39yPY53</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>78097094</pqid></control><display><type>article</type><title>Absorption of intact proteins by the intestinal epithelium of trout, Salmo gairdneri. A luminescence enzyme immunoassay and cytochemical study</title><source>MEDLINE</source><source>SpringerLink Journals</source><creator>GEORGOPOULOU, U ; DABROWSKI, K ; SIRE, M. F ; VERNIER, J. M</creator><creatorcontrib>GEORGOPOULOU, U ; DABROWSKI, K ; SIRE, M. F ; VERNIER, J. M</creatorcontrib><description>In the rainbow trout, a carnivorous species with a stomach, orally administered horseradish peroxidase (HRP) crossed the intestinal epithelium into the circulation. The protein first appeared in the blood 7 to 8 h after intubation, and could be assayed up to 24 h after administration. The method used, which combines ELISA (enzyme-linked immunoabsorbant assay) and chemiluminescence, enabled the transfer to be measured quantitatively. There was a direct correlation between the quantity ingested and the quantity transferred to the plasma within the experimental limits chosen. The clearance was monophasic and exponential (clearance rate: 3% per minute). Up to 6% of the ingested HRP was transferred to the blood. By cytochemistry it was possible to demonstrate that the protein crossed the intestinal cells at the level of the posterior segment, escaping the particularly intense intracellular lysosomal digestion. After entering the intercellular space, HRP was transferred to the interstitial space of the subepithelial lamina propria. During this transfer the HRP was in close contact with infiltrated macrophages and leukocytes resembling lymphoid cells. Thus, the passage of these protein particles could be the first indispensable step in the possible triggering of a local and/or a systemic immune response.</description><identifier>ISSN: 0302-766X</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/BF00215459</identifier><identifier>PMID: 3277712</identifier><identifier>CODEN: CTSRCS</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Animals ; Biological and medical sciences ; Epithelial Cells ; Epithelium - metabolism ; Epithelium - ultrastructure ; Exocytosis ; Fundamental and applied biological sciences. Psychology ; Horseradish Peroxidase - metabolism ; Immunoenzyme Techniques ; Intestinal Absorption ; Intestinal Mucosa - cytology ; Intestinal Mucosa - metabolism ; Intestinal Mucosa - ultrastructure ; Intestine. Mesentery ; Luminescent Measurements ; Microscopy, Electron ; Peroxidases - metabolism ; Proteins - metabolism ; Trout ; Vertebrates: digestive system</subject><ispartof>Cell and tissue research, 1988, Vol.251 (1), p.145-152</ispartof><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c270t-b22a2068a483077fd60073db55ba01c40611e1d1a58ccefed03fa5986a5614ca3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4009,27902,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=7699548$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3277712$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GEORGOPOULOU, U</creatorcontrib><creatorcontrib>DABROWSKI, K</creatorcontrib><creatorcontrib>SIRE, M. F</creatorcontrib><creatorcontrib>VERNIER, J. M</creatorcontrib><title>Absorption of intact proteins by the intestinal epithelium of trout, Salmo gairdneri. A luminescence enzyme immunoassay and cytochemical study</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><description>In the rainbow trout, a carnivorous species with a stomach, orally administered horseradish peroxidase (HRP) crossed the intestinal epithelium into the circulation. The protein first appeared in the blood 7 to 8 h after intubation, and could be assayed up to 24 h after administration. The method used, which combines ELISA (enzyme-linked immunoabsorbant assay) and chemiluminescence, enabled the transfer to be measured quantitatively. There was a direct correlation between the quantity ingested and the quantity transferred to the plasma within the experimental limits chosen. The clearance was monophasic and exponential (clearance rate: 3% per minute). Up to 6% of the ingested HRP was transferred to the blood. By cytochemistry it was possible to demonstrate that the protein crossed the intestinal cells at the level of the posterior segment, escaping the particularly intense intracellular lysosomal digestion. After entering the intercellular space, HRP was transferred to the interstitial space of the subepithelial lamina propria. During this transfer the HRP was in close contact with infiltrated macrophages and leukocytes resembling lymphoid cells. Thus, the passage of these protein particles could be the first indispensable step in the possible triggering of a local and/or a systemic immune response.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Epithelial Cells</subject><subject>Epithelium - metabolism</subject><subject>Epithelium - ultrastructure</subject><subject>Exocytosis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Horseradish Peroxidase - metabolism</subject><subject>Immunoenzyme Techniques</subject><subject>Intestinal Absorption</subject><subject>Intestinal Mucosa - cytology</subject><subject>Intestinal Mucosa - metabolism</subject><subject>Intestinal Mucosa - ultrastructure</subject><subject>Intestine. Mesentery</subject><subject>Luminescent Measurements</subject><subject>Microscopy, Electron</subject><subject>Peroxidases - metabolism</subject><subject>Proteins - metabolism</subject><subject>Trout</subject><subject>Vertebrates: digestive system</subject><issn>0302-766X</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEFv1DAQhS0EKtvChTuSD4gDImXsJHZy3Fa0IFXiAEjcookzoUaxvdjOIfwIfjNedVVOI7336WneY-yVgEsBoD9c3QBI0TZt_4TtRFPLCjrdPWU7qEFWWqkfz9l5Sr8ARKNUf8bOaqm1FnLH_u7HFOIh2-B5mLn1GU3mhxgyWZ_4uPF8T0eZUrYeF04HW5TFru7I5xjW_J5_xcUF_hNtnDxFe8n3fFmd9ZQMeUOc_J_NlRjnVh8wJdw4-ombLQdzT86aEpzyOm0v2LMZl0QvT_eCfb_5-O36U3X35fbz9f6uMlJDrkYpUYLqsOlq0HqeVJmhnsa2HRGEaUAJQWIS2HbG0EwT1DO2faewVaIxWF-wtw-5penvtXQbnC2_Lgt6CmsadAe9hr4p4LsH0MSQUqR5OETrMG6DgOE4_vB__AK_PqWuo6PpET2tXfw3Jx9TqTxH9MamR0yrvm9Lo39yPY53</recordid><startdate>1988</startdate><enddate>1988</enddate><creator>GEORGOPOULOU, U</creator><creator>DABROWSKI, K</creator><creator>SIRE, M. F</creator><creator>VERNIER, J. M</creator><general>Springer</general><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></search><sort><creationdate>1988</creationdate><title>Absorption of intact proteins by the intestinal epithelium of trout, Salmo gairdneri. A luminescence enzyme immunoassay and cytochemical study</title><author>GEORGOPOULOU, U ; DABROWSKI, K ; SIRE, M. F ; VERNIER, J. M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c270t-b22a2068a483077fd60073db55ba01c40611e1d1a58ccefed03fa5986a5614ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Epithelial Cells</topic><topic>Epithelium - metabolism</topic><topic>Epithelium - ultrastructure</topic><topic>Exocytosis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Horseradish Peroxidase - metabolism</topic><topic>Immunoenzyme Techniques</topic><topic>Intestinal Absorption</topic><topic>Intestinal Mucosa - cytology</topic><topic>Intestinal Mucosa - metabolism</topic><topic>Intestinal Mucosa - ultrastructure</topic><topic>Intestine. Mesentery</topic><topic>Luminescent Measurements</topic><topic>Microscopy, Electron</topic><topic>Peroxidases - metabolism</topic><topic>Proteins - metabolism</topic><topic>Trout</topic><topic>Vertebrates: digestive system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GEORGOPOULOU, U</creatorcontrib><creatorcontrib>DABROWSKI, K</creatorcontrib><creatorcontrib>SIRE, M. F</creatorcontrib><creatorcontrib>VERNIER, J. M</creatorcontrib><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><jtitle>Cell and tissue research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GEORGOPOULOU, U</au><au>DABROWSKI, K</au><au>SIRE, M. F</au><au>VERNIER, J. M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Absorption of intact proteins by the intestinal epithelium of trout, Salmo gairdneri. A luminescence enzyme immunoassay and cytochemical study</atitle><jtitle>Cell and tissue research</jtitle><addtitle>Cell Tissue Res</addtitle><date>1988</date><risdate>1988</risdate><volume>251</volume><issue>1</issue><spage>145</spage><epage>152</epage><pages>145-152</pages><issn>0302-766X</issn><eissn>1432-0878</eissn><coden>CTSRCS</coden><abstract>In the rainbow trout, a carnivorous species with a stomach, orally administered horseradish peroxidase (HRP) crossed the intestinal epithelium into the circulation. The protein first appeared in the blood 7 to 8 h after intubation, and could be assayed up to 24 h after administration. The method used, which combines ELISA (enzyme-linked immunoabsorbant assay) and chemiluminescence, enabled the transfer to be measured quantitatively. There was a direct correlation between the quantity ingested and the quantity transferred to the plasma within the experimental limits chosen. The clearance was monophasic and exponential (clearance rate: 3% per minute). Up to 6% of the ingested HRP was transferred to the blood. By cytochemistry it was possible to demonstrate that the protein crossed the intestinal cells at the level of the posterior segment, escaping the particularly intense intracellular lysosomal digestion. After entering the intercellular space, HRP was transferred to the interstitial space of the subepithelial lamina propria. During this transfer the HRP was in close contact with infiltrated macrophages and leukocytes resembling lymphoid cells. Thus, the passage of these protein particles could be the first indispensable step in the possible triggering of a local and/or a systemic immune response.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>3277712</pmid><doi>10.1007/BF00215459</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0302-766X
ispartof Cell and tissue research, 1988, Vol.251 (1), p.145-152
issn 0302-766X
1432-0878
language eng
recordid cdi_proquest_miscellaneous_78097094
source MEDLINE; SpringerLink Journals
subjects Animals
Biological and medical sciences
Epithelial Cells
Epithelium - metabolism
Epithelium - ultrastructure
Exocytosis
Fundamental and applied biological sciences. Psychology
Horseradish Peroxidase - metabolism
Immunoenzyme Techniques
Intestinal Absorption
Intestinal Mucosa - cytology
Intestinal Mucosa - metabolism
Intestinal Mucosa - ultrastructure
Intestine. Mesentery
Luminescent Measurements
Microscopy, Electron
Peroxidases - metabolism
Proteins - metabolism
Trout
Vertebrates: digestive system
title Absorption of intact proteins by the intestinal epithelium of trout, Salmo gairdneri. A luminescence enzyme immunoassay and cytochemical study
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T13%3A26%3A49IST&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=Absorption%20of%20intact%20proteins%20by%20the%20intestinal%20epithelium%20of%20trout,%20Salmo%20gairdneri.%20A%20luminescence%20enzyme%20immunoassay%20and%20cytochemical%20study&rft.jtitle=Cell%20and%20tissue%20research&rft.au=GEORGOPOULOU,%20U&rft.date=1988&rft.volume=251&rft.issue=1&rft.spage=145&rft.epage=152&rft.pages=145-152&rft.issn=0302-766X&rft.eissn=1432-0878&rft.coden=CTSRCS&rft_id=info:doi/10.1007/BF00215459&rft_dat=%3Cproquest_cross%3E78097094%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=78097094&rft_id=info:pmid/3277712&rfr_iscdi=true