Isolation of a Family of Organic Anion Transporters from Human Liver and Kidney

Five distinct organic anion transporter cDNAs, hOAT1-5, were isolated from human liver and kidney. hOAT1, 2, and 3 are homologous to their respective rat orthologues OAT1-3, whereas hOAT4 and 5 are novel clones that have not been identified in other species. hOAT1- and hOAT3-transfected cells showed...

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Published inBiochemical and biophysical research communications Vol. 283; no. 2; pp. 417 - 422
Main Authors Sun, William, Wu, Rong Rong, van Poelje, Paul D., Erion, Mark D.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 04.05.2001
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ISSN0006-291X
1090-2104
DOI10.1006/bbrc.2001.4774

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Abstract Five distinct organic anion transporter cDNAs, hOAT1-5, were isolated from human liver and kidney. hOAT1, 2, and 3 are homologous to their respective rat orthologues OAT1-3, whereas hOAT4 and 5 are novel clones that have not been identified in other species. hOAT1- and hOAT3-transfected cells showed uptake of p-aminohippurate and fluorescein. Cells expressing hOAT2 showed uptake of p-aminohippurate, methotrexate, cAMP, and α-ketoglutarate. Northern blot analysis indicated differential tissue distribution for the transporter transcripts. These results indicate the existence of a family of organic anion transporting proteins in humans distinct from the oatp-like family of transporters.
AbstractList Five distinct organic anion transporter cDNAs, hOAT1-5, were isolated from human liver and kidney. hOAT1, 2, and 3 are homologous to their respective rat orthologues OAT1-3, whereas hOAT4 and 5 are novel clones that have not been identified in other species. hOAT1- and hOAT3-transfected cells showed uptake of p-aminohippurate and fluorescein. Cells expressing hOAT2 showed uptake of p-aminohippurate, methotrexate, cAMP, and α-ketoglutarate. Northern blot analysis indicated differential tissue distribution for the transporter transcripts. These results indicate the existence of a family of organic anion transporting proteins in humans distinct from the oatp-like family of transporters.
Five distinct organic anion transporter cDNAs, hOAT1-5, were isolated from human liver and kidney. hOAT1, 2, and 3 are homologous to their respective rat orthologues OAT1-3, whereas hOAT4 and 5 are novel clones that have not been identified in other species. hOAT1- and hOAT3-transfected cells showed uptake of p-aminohippurate and fluorescein. Cells expressing hOAT2 showed uptake of p-aminohippurate, methotrexate, cAMP, and alpha-ketoglutarate. Northern blot analysis indicated differential tissue distribution for the transporter transcripts. These results indicate the existence of a family of organic anion transporting proteins in humans distinct from the oatp-like family of transporters.
Five distinct organic anion transporter cDNAs, hOAT1-5, were isolated from human liver and kidney. hOAT1, 2, and 3 are homologous to their respective rat orthologues OAT1-3, whereas hOAT4 and 5 are novel clones that have not been identified in other species. hOAT1- and hOAT3-transfected cells showed uptake of p-aminohippurate and fluorescein. Cells expressing hOAT2 showed uptake of p-aminohippurate, methotrexate, cAMP, and alpha-ketoglutarate. Northern blot analysis indicated differential tissue distribution for the transporter transcripts. These results indicate the existence of a family of organic anion transporting proteins in humans distinct from the oatp-like family of transporters.Five distinct organic anion transporter cDNAs, hOAT1-5, were isolated from human liver and kidney. hOAT1, 2, and 3 are homologous to their respective rat orthologues OAT1-3, whereas hOAT4 and 5 are novel clones that have not been identified in other species. hOAT1- and hOAT3-transfected cells showed uptake of p-aminohippurate and fluorescein. Cells expressing hOAT2 showed uptake of p-aminohippurate, methotrexate, cAMP, and alpha-ketoglutarate. Northern blot analysis indicated differential tissue distribution for the transporter transcripts. These results indicate the existence of a family of organic anion transporting proteins in humans distinct from the oatp-like family of transporters.
Five distinct organic anion transporter cDNAs, hOAT1-5, were isolated from human liver and kidney. hOAT1, 2, and 3 are homologous to their respective rat orthologues OAT1-3, whereas hOAT4 and 5 are novel clones that have not been identified in other species. hOAT1- and hOAT3-transfected cells showed uptake of p-aminohippurate and fluorescein. Cells expressing hOAT2 showed uptake of p-aminohippurate, methotrexate, cAMP, and alpha -ketoglutarate. Northern blot analysis indicated differential tissue distribution for the transporter transcripts. These results indicate the existence of a family of organic anion transporting proteins in humans distinct from the oatp-like family of transporters. Copyright 2001 Academic Press.
Author Wu, Rong Rong
Erion, Mark D.
Sun, William
van Poelje, Paul D.
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Snippet Five distinct organic anion transporter cDNAs, hOAT1-5, were isolated from human liver and kidney. hOAT1, 2, and 3 are homologous to their respective rat...
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StartPage 417
SubjectTerms a-ketoglutarate
Amino Acid Sequence
Animals
Anion Transport Proteins
Carrier Proteins - genetics
Carrier Proteins - isolation & purification
Carrier Proteins - metabolism
Cell Line
Cloning, Molecular
Cyclic AMP - metabolism
DNA, Complementary - genetics
DNA, Complementary - isolation & purification
Female
fluorescein
hOAT1 gene
hOAT2 gene
hOAT3 gene
hOAT4 gene
hOAT5 gene
Humans
In Vitro Techniques
Ketoglutaric Acids - metabolism
Kidney - metabolism
kidney transport
Liver - metabolism
liver transport
membrane transport
methotrexate
Methotrexate - metabolism
Molecular Sequence Data
Oocytes - metabolism
organic anion
Organic Anion Transporters
Organic Anion Transporters, Sodium-Independent
p-aminohippurate
p-Aminohippuric Acid - metabolism
Rats
RNA, Messenger - genetics
RNA, Messenger - metabolism
Sequence Homology, Amino Acid
Species Specificity
Transfection
Xenopus laevis
Title Isolation of a Family of Organic Anion Transporters from Human Liver and Kidney
URI https://dx.doi.org/10.1006/bbrc.2001.4774
https://www.ncbi.nlm.nih.gov/pubmed/11327718
https://www.proquest.com/docview/17892425
https://www.proquest.com/docview/70816628
Volume 283
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