Comparison of the transcellular transport of FDG and D-glucose by the kidney epithelial cell line, LLC-PK1

OBJECTIVESAlmost all D-glucose (GLU) filtered through the glomerulus is reabsorbed by the renal proximal tubules, whereas a high portion of 2-[F]fluoro-2-deoxy-D-glucose [(F)FDG] is excreted through the urine. However, [F]FDG is not entirely excreted in the urine suggesting that it may be partially...

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Veröffentlicht in:Nuclear medicine communications 2010-02, Vol.31 (2), p.141-146
Hauptverfasser: Kobayashi, Masato, Shikano, Naoto, Nishii, Ryuichi, Kiyono, Yasushi, Araki, Hiroyo, Nishi, Kodai, Oh, Myungmi, Okudaira, Hiroyuki, Ogura, Masato, Yoshimoto, Mitsuyoshi, Okazawa, Hidehiko, Fujibayashi, Yasuhisa, Kawai, Keiichi
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container_end_page 146
container_issue 2
container_start_page 141
container_title Nuclear medicine communications
container_volume 31
creator Kobayashi, Masato
Shikano, Naoto
Nishii, Ryuichi
Kiyono, Yasushi
Araki, Hiroyo
Nishi, Kodai
Oh, Myungmi
Okudaira, Hiroyuki
Ogura, Masato
Yoshimoto, Mitsuyoshi
Okazawa, Hidehiko
Fujibayashi, Yasuhisa
Kawai, Keiichi
description OBJECTIVESAlmost all D-glucose (GLU) filtered through the glomerulus is reabsorbed by the renal proximal tubules, whereas a high portion of 2-[F]fluoro-2-deoxy-D-glucose [(F)FDG] is excreted through the urine. However, [F]FDG is not entirely excreted in the urine suggesting that it may be partially reabsorbed by the proximal tubules. The purpose of this study was to compare the time course of transcellular transport of administered [C] labeled FDG ([C]FDG) with that of [C] labeled GLU ([C]GLU) using the kidney epithelial cell line, LLC-PK1. METHODSTranscellular transport of [C]FDG and [C]GLU by LLC-PK1 cells was measured in Na-containing or Na-free Dulbeccoʼs phosphate-buffered saline [PBS(+) and PBS(−), respectively] in the presence or absence of phlorizin, phloretin, probenecid, or tetraethylammonium bromide inhibitors that predominantly inhibit sodium-dependent glucose transporters (SGLTs), sodium-independent glucose transporters, organic anion transporters, and organic cation transporters, respectively. RESULTSWhen assayed in PBS(+), less [C]FDG than [C]GLU was reabsorbed by the proximal tubular cells over the entire incubation time. Reabsorption of [C]FDG was mediated mainly by SGLT at early time points in the incubation, whereas high reabsorption of [C]GLU was mediated by both SGLT and glucose transporter over 90 min of incubation. Secretion of [C]FDG also tended to be slightly higher than that of [C]GLU over 90 min of incubation. CONCLUSIONTranscellular transport of [C]FDG over time by LLC-PK1 cells was clarified. The polarized distribution of transcellular transporters of [C]FDG and [C]GLU in LLC-PK1 cells differs.
doi_str_mv 10.1097/MNM.0b013e328333bcf5
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However, [F]FDG is not entirely excreted in the urine suggesting that it may be partially reabsorbed by the proximal tubules. The purpose of this study was to compare the time course of transcellular transport of administered [C] labeled FDG ([C]FDG) with that of [C] labeled GLU ([C]GLU) using the kidney epithelial cell line, LLC-PK1. METHODSTranscellular transport of [C]FDG and [C]GLU by LLC-PK1 cells was measured in Na-containing or Na-free Dulbeccoʼs phosphate-buffered saline [PBS(+) and PBS(−), respectively] in the presence or absence of phlorizin, phloretin, probenecid, or tetraethylammonium bromide inhibitors that predominantly inhibit sodium-dependent glucose transporters (SGLTs), sodium-independent glucose transporters, organic anion transporters, and organic cation transporters, respectively. RESULTSWhen assayed in PBS(+), less [C]FDG than [C]GLU was reabsorbed by the proximal tubular cells over the entire incubation time. Reabsorption of [C]FDG was mediated mainly by SGLT at early time points in the incubation, whereas high reabsorption of [C]GLU was mediated by both SGLT and glucose transporter over 90 min of incubation. Secretion of [C]FDG also tended to be slightly higher than that of [C]GLU over 90 min of incubation. CONCLUSIONTranscellular transport of [C]FDG over time by LLC-PK1 cells was clarified. The polarized distribution of transcellular transporters of [C]FDG and [C]GLU in LLC-PK1 cells differs.</description><identifier>ISSN: 0143-3636</identifier><identifier>EISSN: 1473-5628</identifier><identifier>DOI: 10.1097/MNM.0b013e328333bcf5</identifier><identifier>PMID: 19949354</identifier><language>eng</language><publisher>England: Lippincott Williams &amp; Wilkins, Inc</publisher><subject>Biological Transport - drug effects ; Cell Line ; Epithelial Cells - drug effects ; Epithelial Cells - metabolism ; Fluorodeoxyglucose F18 - metabolism ; Glucose - metabolism ; Glucose Transport Proteins, Facilitative - antagonists &amp; inhibitors ; Glucose Transport Proteins, Facilitative - metabolism ; Kidney - cytology ; Kidney Tubules, Proximal - cytology ; Organic Anion Transporters - metabolism ; Organic Cation Transport Proteins - metabolism ; Radioisotopes ; Sodium-Glucose Transport Proteins - antagonists &amp; inhibitors ; Sodium-Glucose Transport Proteins - metabolism ; Time Factors</subject><ispartof>Nuclear medicine communications, 2010-02, Vol.31 (2), p.141-146</ispartof><rights>2010 Lippincott Williams &amp; Wilkins, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4215-2bcfcca6f491cbd2583cfb507162eb3334d0e3d8d8ae1fa33789168779666e6f3</citedby><cites>FETCH-LOGICAL-c4215-2bcfcca6f491cbd2583cfb507162eb3334d0e3d8d8ae1fa33789168779666e6f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19949354$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kobayashi, Masato</creatorcontrib><creatorcontrib>Shikano, Naoto</creatorcontrib><creatorcontrib>Nishii, Ryuichi</creatorcontrib><creatorcontrib>Kiyono, Yasushi</creatorcontrib><creatorcontrib>Araki, Hiroyo</creatorcontrib><creatorcontrib>Nishi, Kodai</creatorcontrib><creatorcontrib>Oh, Myungmi</creatorcontrib><creatorcontrib>Okudaira, Hiroyuki</creatorcontrib><creatorcontrib>Ogura, Masato</creatorcontrib><creatorcontrib>Yoshimoto, Mitsuyoshi</creatorcontrib><creatorcontrib>Okazawa, Hidehiko</creatorcontrib><creatorcontrib>Fujibayashi, Yasuhisa</creatorcontrib><creatorcontrib>Kawai, Keiichi</creatorcontrib><title>Comparison of the transcellular transport of FDG and D-glucose by the kidney epithelial cell line, LLC-PK1</title><title>Nuclear medicine communications</title><addtitle>Nucl Med Commun</addtitle><description>OBJECTIVESAlmost all D-glucose (GLU) filtered through the glomerulus is reabsorbed by the renal proximal tubules, whereas a high portion of 2-[F]fluoro-2-deoxy-D-glucose [(F)FDG] is excreted through the urine. However, [F]FDG is not entirely excreted in the urine suggesting that it may be partially reabsorbed by the proximal tubules. The purpose of this study was to compare the time course of transcellular transport of administered [C] labeled FDG ([C]FDG) with that of [C] labeled GLU ([C]GLU) using the kidney epithelial cell line, LLC-PK1. METHODSTranscellular transport of [C]FDG and [C]GLU by LLC-PK1 cells was measured in Na-containing or Na-free Dulbeccoʼs phosphate-buffered saline [PBS(+) and PBS(−), respectively] in the presence or absence of phlorizin, phloretin, probenecid, or tetraethylammonium bromide inhibitors that predominantly inhibit sodium-dependent glucose transporters (SGLTs), sodium-independent glucose transporters, organic anion transporters, and organic cation transporters, respectively. RESULTSWhen assayed in PBS(+), less [C]FDG than [C]GLU was reabsorbed by the proximal tubular cells over the entire incubation time. Reabsorption of [C]FDG was mediated mainly by SGLT at early time points in the incubation, whereas high reabsorption of [C]GLU was mediated by both SGLT and glucose transporter over 90 min of incubation. Secretion of [C]FDG also tended to be slightly higher than that of [C]GLU over 90 min of incubation. CONCLUSIONTranscellular transport of [C]FDG over time by LLC-PK1 cells was clarified. The polarized distribution of transcellular transporters of [C]FDG and [C]GLU in LLC-PK1 cells differs.</description><subject>Biological Transport - drug effects</subject><subject>Cell Line</subject><subject>Epithelial Cells - drug effects</subject><subject>Epithelial Cells - metabolism</subject><subject>Fluorodeoxyglucose F18 - metabolism</subject><subject>Glucose - metabolism</subject><subject>Glucose Transport Proteins, Facilitative - antagonists &amp; inhibitors</subject><subject>Glucose Transport Proteins, Facilitative - metabolism</subject><subject>Kidney - cytology</subject><subject>Kidney Tubules, Proximal - cytology</subject><subject>Organic Anion Transporters - metabolism</subject><subject>Organic Cation Transport Proteins - metabolism</subject><subject>Radioisotopes</subject><subject>Sodium-Glucose Transport Proteins - antagonists &amp; inhibitors</subject><subject>Sodium-Glucose Transport Proteins - metabolism</subject><subject>Time Factors</subject><issn>0143-3636</issn><issn>1473-5628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtPwzAQhC0EgvL4Bwj5xoWAnXUc54haXqIFDnCOHGdDA24c7ERV_z0prYTEgdNqtTOzmo-QU84uOcvSq9nT7JIVjANCrACgMFWyQ0ZcpBAlMla7ZMS4gAgkyANyGMIHY0yBTPfJAc8ykUEiRuRj7Bat9nVwDXUV7eZIO6-bYNDa3mq_2Vrnu_X5dnJHdVPSSfRue-MC0mL14_msywZXFNt62GytLV0HUFs3eEGn03H08siPyV6lbcCT7Twib7c3r-P7aPp89zC-nkZGxDyJ4qGIMVpWIuOmKONEgamKhKVcxlgMRUXJEEpVKo280gCpyrhUaZpJKVFWcETON7mtd189hi5f1D99dIOuD3kKIDOhYj4oxUZpvAvBY5W3vl5ov8o5y9eQ8wFy_hfyYDvbPuiLBZa_pi3VQaA2gqWzHfrwafsl-nyO2nbz_7O_AR86iy4</recordid><startdate>201002</startdate><enddate>201002</enddate><creator>Kobayashi, Masato</creator><creator>Shikano, Naoto</creator><creator>Nishii, Ryuichi</creator><creator>Kiyono, Yasushi</creator><creator>Araki, Hiroyo</creator><creator>Nishi, Kodai</creator><creator>Oh, Myungmi</creator><creator>Okudaira, Hiroyuki</creator><creator>Ogura, Masato</creator><creator>Yoshimoto, Mitsuyoshi</creator><creator>Okazawa, Hidehiko</creator><creator>Fujibayashi, Yasuhisa</creator><creator>Kawai, Keiichi</creator><general>Lippincott Williams &amp; 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inhibitors</topic><topic>Glucose Transport Proteins, Facilitative - metabolism</topic><topic>Kidney - cytology</topic><topic>Kidney Tubules, Proximal - cytology</topic><topic>Organic Anion Transporters - metabolism</topic><topic>Organic Cation Transport Proteins - metabolism</topic><topic>Radioisotopes</topic><topic>Sodium-Glucose Transport Proteins - antagonists &amp; inhibitors</topic><topic>Sodium-Glucose Transport Proteins - metabolism</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kobayashi, Masato</creatorcontrib><creatorcontrib>Shikano, Naoto</creatorcontrib><creatorcontrib>Nishii, Ryuichi</creatorcontrib><creatorcontrib>Kiyono, Yasushi</creatorcontrib><creatorcontrib>Araki, Hiroyo</creatorcontrib><creatorcontrib>Nishi, Kodai</creatorcontrib><creatorcontrib>Oh, Myungmi</creatorcontrib><creatorcontrib>Okudaira, Hiroyuki</creatorcontrib><creatorcontrib>Ogura, Masato</creatorcontrib><creatorcontrib>Yoshimoto, Mitsuyoshi</creatorcontrib><creatorcontrib>Okazawa, Hidehiko</creatorcontrib><creatorcontrib>Fujibayashi, Yasuhisa</creatorcontrib><creatorcontrib>Kawai, Keiichi</creatorcontrib><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>Nuclear medicine communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kobayashi, Masato</au><au>Shikano, Naoto</au><au>Nishii, Ryuichi</au><au>Kiyono, Yasushi</au><au>Araki, Hiroyo</au><au>Nishi, Kodai</au><au>Oh, Myungmi</au><au>Okudaira, Hiroyuki</au><au>Ogura, Masato</au><au>Yoshimoto, Mitsuyoshi</au><au>Okazawa, Hidehiko</au><au>Fujibayashi, Yasuhisa</au><au>Kawai, Keiichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of the transcellular transport of FDG and D-glucose by the kidney epithelial cell line, LLC-PK1</atitle><jtitle>Nuclear medicine communications</jtitle><addtitle>Nucl Med Commun</addtitle><date>2010-02</date><risdate>2010</risdate><volume>31</volume><issue>2</issue><spage>141</spage><epage>146</epage><pages>141-146</pages><issn>0143-3636</issn><eissn>1473-5628</eissn><abstract>OBJECTIVESAlmost all D-glucose (GLU) filtered through the glomerulus is reabsorbed by the renal proximal tubules, whereas a high portion of 2-[F]fluoro-2-deoxy-D-glucose [(F)FDG] is excreted through the urine. However, [F]FDG is not entirely excreted in the urine suggesting that it may be partially reabsorbed by the proximal tubules. The purpose of this study was to compare the time course of transcellular transport of administered [C] labeled FDG ([C]FDG) with that of [C] labeled GLU ([C]GLU) using the kidney epithelial cell line, LLC-PK1. METHODSTranscellular transport of [C]FDG and [C]GLU by LLC-PK1 cells was measured in Na-containing or Na-free Dulbeccoʼs phosphate-buffered saline [PBS(+) and PBS(−), respectively] in the presence or absence of phlorizin, phloretin, probenecid, or tetraethylammonium bromide inhibitors that predominantly inhibit sodium-dependent glucose transporters (SGLTs), sodium-independent glucose transporters, organic anion transporters, and organic cation transporters, respectively. RESULTSWhen assayed in PBS(+), less [C]FDG than [C]GLU was reabsorbed by the proximal tubular cells over the entire incubation time. Reabsorption of [C]FDG was mediated mainly by SGLT at early time points in the incubation, whereas high reabsorption of [C]GLU was mediated by both SGLT and glucose transporter over 90 min of incubation. Secretion of [C]FDG also tended to be slightly higher than that of [C]GLU over 90 min of incubation. CONCLUSIONTranscellular transport of [C]FDG over time by LLC-PK1 cells was clarified. The polarized distribution of transcellular transporters of [C]FDG and [C]GLU in LLC-PK1 cells differs.</abstract><cop>England</cop><pub>Lippincott Williams &amp; Wilkins, Inc</pub><pmid>19949354</pmid><doi>10.1097/MNM.0b013e328333bcf5</doi><tpages>6</tpages></addata></record>
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subjects Biological Transport - drug effects
Cell Line
Epithelial Cells - drug effects
Epithelial Cells - metabolism
Fluorodeoxyglucose F18 - metabolism
Glucose - metabolism
Glucose Transport Proteins, Facilitative - antagonists & inhibitors
Glucose Transport Proteins, Facilitative - metabolism
Kidney - cytology
Kidney Tubules, Proximal - cytology
Organic Anion Transporters - metabolism
Organic Cation Transport Proteins - metabolism
Radioisotopes
Sodium-Glucose Transport Proteins - antagonists & inhibitors
Sodium-Glucose Transport Proteins - metabolism
Time Factors
title Comparison of the transcellular transport of FDG and D-glucose by the kidney epithelial cell line, LLC-PK1
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