Transport of D-glucose across cultured stratified cell layer of human oral mucosal cells
To evaluate the role of several specialized mechanisms for D‐glucose transport in human oral mucosa, a cultured stratified cell layer derived from human oral mucosa was employed. Although this culture system has been used for reconstructive surgery, we, for the first time, tried to apply this system...
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Veröffentlicht in: | Journal of pharmacy and pharmacology 2002-02, Vol.54 (2), p.213-219 |
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creator | Kimura, Toshikiro Yamano, Hitoshi Tanaka, Akihiro Matsumura, Tomohiro Ueda, Minoru Ogawara, Ken-ichi Higaki, Kazutaka |
description | To evaluate the role of several specialized mechanisms for D‐glucose transport in human oral mucosa, a cultured stratified cell layer derived from human oral mucosa was employed. Although this culture system has been used for reconstructive surgery, we, for the first time, tried to apply this system to the evaluation of nutrients and drug transport. Cell number and transepithelial electrical resistance (TEER) reached steady state 7–8 days after inoculation on the Transwell and TEER values at steady state were 130–140 Ω cm2, which was higher or lower than that of small intestine or Caco‐2 cells, respectively. The transport studies were carried out using the cultured epithelium on the Transwell. The transport of D‐glucose across the cultured stratified layer of oral epithelial cells was much more extensive than L‐glucose, and was inhibited by 2‐deoxy‐D‐glucose, a substrate of facilitative glucose transporters, and α‐methyl‐D‐glucoside, a specific substrate of a Na+/glucose cotransporter (SGLT1). The results indicate that the sugar transporters function not only to take up D‐glucose by the epithelial cells but also to transport the sugar across the stratified epithelial layer. |
doi_str_mv | 10.1211/0022357021778402 |
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Although this culture system has been used for reconstructive surgery, we, for the first time, tried to apply this system to the evaluation of nutrients and drug transport. Cell number and transepithelial electrical resistance (TEER) reached steady state 7–8 days after inoculation on the Transwell and TEER values at steady state were 130–140 Ω cm2, which was higher or lower than that of small intestine or Caco‐2 cells, respectively. The transport studies were carried out using the cultured epithelium on the Transwell. The transport of D‐glucose across the cultured stratified layer of oral epithelial cells was much more extensive than L‐glucose, and was inhibited by 2‐deoxy‐D‐glucose, a substrate of facilitative glucose transporters, and α‐methyl‐D‐glucoside, a specific substrate of a Na+/glucose cotransporter (SGLT1). The results indicate that the sugar transporters function not only to take up D‐glucose by the epithelial cells but also to transport the sugar across the stratified epithelial layer.</description><identifier>ISSN: 0022-3573</identifier><identifier>EISSN: 2042-7158</identifier><identifier>DOI: 10.1211/0022357021778402</identifier><identifier>PMID: 11848285</identifier><identifier>CODEN: JPPMAB</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Biological and medical sciences ; Biological Transport, Active ; Cell physiology ; Cells, Cultured ; Epithelial Cells ; Fundamental and applied biological sciences. Psychology ; General pharmacology ; Gingiva - cytology ; Gingiva - metabolism ; Glucose - pharmacokinetics ; Humans ; Medical sciences ; Membrane and intracellular transports ; Molecular and cellular biology ; Mouth Mucosa - cytology ; Mouth Mucosa - metabolism ; Pharmacokinetics. Pharmacogenetics. Drug-receptor interactions ; Pharmacology. 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Although this culture system has been used for reconstructive surgery, we, for the first time, tried to apply this system to the evaluation of nutrients and drug transport. Cell number and transepithelial electrical resistance (TEER) reached steady state 7–8 days after inoculation on the Transwell and TEER values at steady state were 130–140 Ω cm2, which was higher or lower than that of small intestine or Caco‐2 cells, respectively. The transport studies were carried out using the cultured epithelium on the Transwell. The transport of D‐glucose across the cultured stratified layer of oral epithelial cells was much more extensive than L‐glucose, and was inhibited by 2‐deoxy‐D‐glucose, a substrate of facilitative glucose transporters, and α‐methyl‐D‐glucoside, a specific substrate of a Na+/glucose cotransporter (SGLT1). The results indicate that the sugar transporters function not only to take up D‐glucose by the epithelial cells but also to transport the sugar across the stratified epithelial layer.</description><subject>Biological and medical sciences</subject><subject>Biological Transport, Active</subject><subject>Cell physiology</subject><subject>Cells, Cultured</subject><subject>Epithelial Cells</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General pharmacology</subject><subject>Gingiva - cytology</subject><subject>Gingiva - metabolism</subject><subject>Glucose - pharmacokinetics</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Membrane and intracellular transports</subject><subject>Molecular and cellular biology</subject><subject>Mouth Mucosa - cytology</subject><subject>Mouth Mucosa - metabolism</subject><subject>Pharmacokinetics. Pharmacogenetics. Drug-receptor interactions</subject><subject>Pharmacology. Drug treatments</subject><issn>0022-3573</issn><issn>2042-7158</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkDtPwzAURi0EgvLYmVAW2AJ-2x1RCy1vhiLYLNe1IeA0xU4E_fc4pAKJhclXvudcX38A7CN4jDBCJxBiTJiAGAkhKcRroIchxblATK6DXtvOU59sge0YXyGEgnO-CbYQklRiyXrgaRL0PC6qUGeVy4b5s29MFW2mTahizEzj6ybYWRbroOvCFak01vvM66UNrfLSlHqeVUH7rGzVdLZA3AUbTvto91bnDng4P5sMxvn13ehicHqdG5aWyK0TMwaFc5BzK7XBmqQacyYohwZPKTFwignVHOH-jPRJH1rDqBVGMmG4IzvgqJu7CNV7Y2OtyiK2G-i5rZqoBKJ9ThhLIOzA758F69QiFKUOS4WgatNUf9NMysFqdjMt7exXWMWXgMMVoKPR3qUsTRF_OUIlIkwmjnfcR-Ht8t-H1eX9-D5d0STmnVjE2n7-iDq8KS6IYOrxdqRuBlwydDVUE_IFgKeaHQ</recordid><startdate>200202</startdate><enddate>200202</enddate><creator>Kimura, Toshikiro</creator><creator>Yamano, Hitoshi</creator><creator>Tanaka, Akihiro</creator><creator>Matsumura, Tomohiro</creator><creator>Ueda, Minoru</creator><creator>Ogawara, Ken-ichi</creator><creator>Higaki, Kazutaka</creator><general>Blackwell Publishing Ltd</general><general>Pharmaceutical Press</general><scope>BSCLL</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></search><sort><creationdate>200202</creationdate><title>Transport of D-glucose across cultured stratified cell layer of human oral mucosal cells</title><author>Kimura, Toshikiro ; Yamano, Hitoshi ; Tanaka, Akihiro ; Matsumura, Tomohiro ; Ueda, Minoru ; Ogawara, Ken-ichi ; Higaki, Kazutaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5184-ef7d507ff066e8ac2a3ff02657460c2b43c0b234a6129d39390ec54e7c857c6f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Biological and medical sciences</topic><topic>Biological Transport, Active</topic><topic>Cell physiology</topic><topic>Cells, Cultured</topic><topic>Epithelial Cells</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General pharmacology</topic><topic>Gingiva - cytology</topic><topic>Gingiva - metabolism</topic><topic>Glucose - pharmacokinetics</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Membrane and intracellular transports</topic><topic>Molecular and cellular biology</topic><topic>Mouth Mucosa - cytology</topic><topic>Mouth Mucosa - metabolism</topic><topic>Pharmacokinetics. Pharmacogenetics. Drug-receptor interactions</topic><topic>Pharmacology. Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kimura, Toshikiro</creatorcontrib><creatorcontrib>Yamano, Hitoshi</creatorcontrib><creatorcontrib>Tanaka, Akihiro</creatorcontrib><creatorcontrib>Matsumura, Tomohiro</creatorcontrib><creatorcontrib>Ueda, Minoru</creatorcontrib><creatorcontrib>Ogawara, Ken-ichi</creatorcontrib><creatorcontrib>Higaki, Kazutaka</creatorcontrib><collection>Istex</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><jtitle>Journal of pharmacy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kimura, Toshikiro</au><au>Yamano, Hitoshi</au><au>Tanaka, Akihiro</au><au>Matsumura, Tomohiro</au><au>Ueda, Minoru</au><au>Ogawara, Ken-ichi</au><au>Higaki, Kazutaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transport of D-glucose across cultured stratified cell layer of human oral mucosal cells</atitle><jtitle>Journal of pharmacy and pharmacology</jtitle><addtitle>J Pharm Pharmacol</addtitle><date>2002-02</date><risdate>2002</risdate><volume>54</volume><issue>2</issue><spage>213</spage><epage>219</epage><pages>213-219</pages><issn>0022-3573</issn><eissn>2042-7158</eissn><coden>JPPMAB</coden><abstract>To evaluate the role of several specialized mechanisms for D‐glucose transport in human oral mucosa, a cultured stratified cell layer derived from human oral mucosa was employed. Although this culture system has been used for reconstructive surgery, we, for the first time, tried to apply this system to the evaluation of nutrients and drug transport. Cell number and transepithelial electrical resistance (TEER) reached steady state 7–8 days after inoculation on the Transwell and TEER values at steady state were 130–140 Ω cm2, which was higher or lower than that of small intestine or Caco‐2 cells, respectively. The transport studies were carried out using the cultured epithelium on the Transwell. The transport of D‐glucose across the cultured stratified layer of oral epithelial cells was much more extensive than L‐glucose, and was inhibited by 2‐deoxy‐D‐glucose, a substrate of facilitative glucose transporters, and α‐methyl‐D‐glucoside, a specific substrate of a Na+/glucose cotransporter (SGLT1). The results indicate that the sugar transporters function not only to take up D‐glucose by the epithelial cells but also to transport the sugar across the stratified epithelial layer.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>11848285</pmid><doi>10.1211/0022357021778402</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); Wiley Online Library All Journals |
subjects | Biological and medical sciences Biological Transport, Active Cell physiology Cells, Cultured Epithelial Cells Fundamental and applied biological sciences. Psychology General pharmacology Gingiva - cytology Gingiva - metabolism Glucose - pharmacokinetics Humans Medical sciences Membrane and intracellular transports Molecular and cellular biology Mouth Mucosa - cytology Mouth Mucosa - metabolism Pharmacokinetics. Pharmacogenetics. Drug-receptor interactions Pharmacology. Drug treatments |
title | Transport of D-glucose across cultured stratified cell layer of human oral mucosal cells |
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