Secretagogue response of goblet cells and columnar cells in human colonic crypts
Crypts of Lieberkühn were isolated from human colon, and differential interference contrast microscopy distinguished goblet and columnar cells. Activation with carbachol (CCh, 100 microM) or histamine (10 microM) released contents from goblet granules. Stimulation with prostaglandin E(2) (PGE(2), 5...
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Veröffentlicht in: | American Journal of Physiology: Cell Physiology 2000-01, Vol.278 (1), p.C212-C233 |
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creator | Halm, D R Halm, S T |
description | Crypts of Lieberkühn were isolated from human colon, and differential interference contrast microscopy distinguished goblet and columnar cells. Activation with carbachol (CCh, 100 microM) or histamine (10 microM) released contents from goblet granules. Stimulation with prostaglandin E(2) (PGE(2), 5 microM) or adenosine (10 microM) did not release goblet granules but caused the apical margin of columnar cells to recede. Goblet volume was lost during stimulation with CCh or histamine ( approximately 160 fl/cell), but not with PGE(2) or adenosine. Three-quarters of goblet cells were responsive to CCh but released only 30% of goblet volume. Half-time for goblet volume release was 3.7 min. PGE(2) stimulated a prolonged fluid secretion that attained a rate of approximately 350 pl/min. Columnar cells lost approximately 50% of apical volume during maximal PGE(2) stimulation, with a half-time of 3.3 min. In crypts from individuals with ulcerative colitis, goblet cells were hypersensitive to CCh for release of goblet volume. These results support separate regulation for mucus secretions from goblet cells and from columnar cells, with control mechanisms restricting total release of mucus stores. |
doi_str_mv | 10.1152/ajpcell.2000.278.1.C212 |
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Activation with carbachol (CCh, 100 microM) or histamine (10 microM) released contents from goblet granules. Stimulation with prostaglandin E(2) (PGE(2), 5 microM) or adenosine (10 microM) did not release goblet granules but caused the apical margin of columnar cells to recede. Goblet volume was lost during stimulation with CCh or histamine ( approximately 160 fl/cell), but not with PGE(2) or adenosine. Three-quarters of goblet cells were responsive to CCh but released only 30% of goblet volume. Half-time for goblet volume release was 3.7 min. PGE(2) stimulated a prolonged fluid secretion that attained a rate of approximately 350 pl/min. Columnar cells lost approximately 50% of apical volume during maximal PGE(2) stimulation, with a half-time of 3.3 min. In crypts from individuals with ulcerative colitis, goblet cells were hypersensitive to CCh for release of goblet volume. These results support separate regulation for mucus secretions from goblet cells and from columnar cells, with control mechanisms restricting total release of mucus stores.</description><identifier>ISSN: 0363-6143</identifier><identifier>DOI: 10.1152/ajpcell.2000.278.1.C212</identifier><identifier>PMID: 10644530</identifier><language>eng</language><publisher>United States</publisher><subject>Adenosine - pharmacology ; Biological Transport - drug effects ; Body Fluids - metabolism ; Carbachol - pharmacology ; Cell Size ; Cholecystokinin - pharmacology ; Cholinergic Agonists - pharmacology ; Colon - cytology ; Cytoplasmic Granules - metabolism ; Dinoprostone - metabolism ; Goblet Cells - classification ; Goblet Cells - drug effects ; Goblet Cells - secretion ; Histamine - pharmacology ; Humans ; Inflammatory Bowel Diseases - metabolism ; Inflammatory Bowel Diseases - pathology ; Intestinal Mucosa - cytology ; Intestinal Mucosa - metabolism ; Mathematics ; Microscopy, Interference ; Microtomy - methods ; Mucus - secretion</subject><ispartof>American Journal of Physiology: Cell Physiology, 2000-01, Vol.278 (1), p.C212-C233</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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/10644530$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Halm, D R</creatorcontrib><creatorcontrib>Halm, S T</creatorcontrib><title>Secretagogue response of goblet cells and columnar cells in human colonic crypts</title><title>American Journal of Physiology: Cell Physiology</title><addtitle>Am J Physiol Cell Physiol</addtitle><description>Crypts of Lieberkühn were isolated from human colon, and differential interference contrast microscopy distinguished goblet and columnar cells. Activation with carbachol (CCh, 100 microM) or histamine (10 microM) released contents from goblet granules. Stimulation with prostaglandin E(2) (PGE(2), 5 microM) or adenosine (10 microM) did not release goblet granules but caused the apical margin of columnar cells to recede. Goblet volume was lost during stimulation with CCh or histamine ( approximately 160 fl/cell), but not with PGE(2) or adenosine. Three-quarters of goblet cells were responsive to CCh but released only 30% of goblet volume. Half-time for goblet volume release was 3.7 min. PGE(2) stimulated a prolonged fluid secretion that attained a rate of approximately 350 pl/min. Columnar cells lost approximately 50% of apical volume during maximal PGE(2) stimulation, with a half-time of 3.3 min. In crypts from individuals with ulcerative colitis, goblet cells were hypersensitive to CCh for release of goblet volume. These results support separate regulation for mucus secretions from goblet cells and from columnar cells, with control mechanisms restricting total release of mucus stores.</description><subject>Adenosine - pharmacology</subject><subject>Biological Transport - drug effects</subject><subject>Body Fluids - metabolism</subject><subject>Carbachol - pharmacology</subject><subject>Cell Size</subject><subject>Cholecystokinin - pharmacology</subject><subject>Cholinergic Agonists - pharmacology</subject><subject>Colon - cytology</subject><subject>Cytoplasmic Granules - metabolism</subject><subject>Dinoprostone - metabolism</subject><subject>Goblet Cells - classification</subject><subject>Goblet Cells - drug effects</subject><subject>Goblet Cells - secretion</subject><subject>Histamine - pharmacology</subject><subject>Humans</subject><subject>Inflammatory Bowel Diseases - metabolism</subject><subject>Inflammatory Bowel Diseases - pathology</subject><subject>Intestinal Mucosa - cytology</subject><subject>Intestinal Mucosa - metabolism</subject><subject>Mathematics</subject><subject>Microscopy, Interference</subject><subject>Microtomy - methods</subject><subject>Mucus - secretion</subject><issn>0363-6143</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kM1OwzAQhH0A0VJ4BfCJW8J67TjuEVX8SZVAAs6RYzslVWIHOzn07UlFOYxW-nY0Gg0htwxyxgq81_vBuK7LEQByLFXO8g0yPCNL4JJnkgm-IJcp7ee_QLm-IAsGUoiCw5K8fzgT3ah3YTc5Gl0agk-OhobuQt25kR6jE9XeUhO6qfc6nlDr6ffUa3_kwbeGmngYxnRFzhvdJXd9uivy9fT4uXnJtm_Pr5uHbTYwvh4zAVoLUxS6ATlLzLBhugZZKpDcIAPnakSF3KJVKAwqa1VjYe4ti0LxFbn7yx1i-JlcGqu-Tcdm2rswpaoEVWIpxGy8ORmnune2GmLb63io_jfgvyaJXqk</recordid><startdate>200001</startdate><enddate>200001</enddate><creator>Halm, D R</creator><creator>Halm, S T</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200001</creationdate><title>Secretagogue response of goblet cells and columnar cells in human colonic crypts</title><author>Halm, D R ; Halm, S T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p139t-40aa4c55af06af04139f1ab0678063c210eeb22823d2d824c28dd8fd044565583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adenosine - pharmacology</topic><topic>Biological Transport - drug effects</topic><topic>Body Fluids - metabolism</topic><topic>Carbachol - pharmacology</topic><topic>Cell Size</topic><topic>Cholecystokinin - pharmacology</topic><topic>Cholinergic Agonists - pharmacology</topic><topic>Colon - cytology</topic><topic>Cytoplasmic Granules - metabolism</topic><topic>Dinoprostone - metabolism</topic><topic>Goblet Cells - classification</topic><topic>Goblet Cells - drug effects</topic><topic>Goblet Cells - secretion</topic><topic>Histamine - pharmacology</topic><topic>Humans</topic><topic>Inflammatory Bowel Diseases - metabolism</topic><topic>Inflammatory Bowel Diseases - pathology</topic><topic>Intestinal Mucosa - cytology</topic><topic>Intestinal Mucosa - metabolism</topic><topic>Mathematics</topic><topic>Microscopy, Interference</topic><topic>Microtomy - methods</topic><topic>Mucus - secretion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Halm, D R</creatorcontrib><creatorcontrib>Halm, S T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>American Journal of Physiology: Cell Physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Halm, D R</au><au>Halm, S T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Secretagogue response of goblet cells and columnar cells in human colonic crypts</atitle><jtitle>American Journal of Physiology: Cell Physiology</jtitle><addtitle>Am J Physiol Cell Physiol</addtitle><date>2000-01</date><risdate>2000</risdate><volume>278</volume><issue>1</issue><spage>C212</spage><epage>C233</epage><pages>C212-C233</pages><issn>0363-6143</issn><abstract>Crypts of Lieberkühn were isolated from human colon, and differential interference contrast microscopy distinguished goblet and columnar cells. Activation with carbachol (CCh, 100 microM) or histamine (10 microM) released contents from goblet granules. Stimulation with prostaglandin E(2) (PGE(2), 5 microM) or adenosine (10 microM) did not release goblet granules but caused the apical margin of columnar cells to recede. Goblet volume was lost during stimulation with CCh or histamine ( approximately 160 fl/cell), but not with PGE(2) or adenosine. Three-quarters of goblet cells were responsive to CCh but released only 30% of goblet volume. Half-time for goblet volume release was 3.7 min. PGE(2) stimulated a prolonged fluid secretion that attained a rate of approximately 350 pl/min. Columnar cells lost approximately 50% of apical volume during maximal PGE(2) stimulation, with a half-time of 3.3 min. In crypts from individuals with ulcerative colitis, goblet cells were hypersensitive to CCh for release of goblet volume. These results support separate regulation for mucus secretions from goblet cells and from columnar cells, with control mechanisms restricting total release of mucus stores.</abstract><cop>United States</cop><pmid>10644530</pmid><doi>10.1152/ajpcell.2000.278.1.C212</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine - pharmacology Biological Transport - drug effects Body Fluids - metabolism Carbachol - pharmacology Cell Size Cholecystokinin - pharmacology Cholinergic Agonists - pharmacology Colon - cytology Cytoplasmic Granules - metabolism Dinoprostone - metabolism Goblet Cells - classification Goblet Cells - drug effects Goblet Cells - secretion Histamine - pharmacology Humans Inflammatory Bowel Diseases - metabolism Inflammatory Bowel Diseases - pathology Intestinal Mucosa - cytology Intestinal Mucosa - metabolism Mathematics Microscopy, Interference Microtomy - methods Mucus - secretion |
title | Secretagogue response of goblet cells and columnar cells in human colonic crypts |
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