Limited power of dopamine transporter mRNA mapping for predicting dopamine transporter availability
Dopamine transporters (DAT) are transmembrane proteins that translocate dopamine from the extracellular space into presynaptic neurons. We aimed to investigate the predictive power of DAT mRNA for DAT protein expression, measured using positron emission tomography (PET). We performed 18F‐FP‐CIT PET...
Gespeichert in:
Veröffentlicht in: | Synapse (New York, N.Y.) N.Y.), 2022-04, Vol.76 (5-6), p.e22226-n/a |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | n/a |
---|---|
container_issue | 5-6 |
container_start_page | e22226 |
container_title | Synapse (New York, N.Y.) |
container_volume | 76 |
creator | Pak, Kyoungjune Seo, Seongho Lee, Myung Jun Im, Hyung‐Jun Kim, Keunyoung Kim, In Joo |
description | Dopamine transporters (DAT) are transmembrane proteins that translocate dopamine from the extracellular space into presynaptic neurons. We aimed to investigate the predictive power of DAT mRNA for DAT protein expression, measured using positron emission tomography (PET). We performed 18F‐FP‐CIT PET scans in 35 healthy individuals. Binding potentials (BPND) from the ventral striatum, caudate nucleus, putamen, and middle frontal, orbitofrontal, cingulate, parietal, and temporal cortices were measured. DAT gene expression data were obtained from the freely available Allen Human Brain Atlas derived from six healthy donors. The auto‐correlation of PET‐derived BPNDs for DAT was intermediate (mean ρ2 = .66) with ρ2 ranging from .0811 to 1. However, the auto‐correlation of mRNA expression was weak across the probes with a mean ρ2 of .09–.23. Cross‐correlations between PET‐derived BPNDs and mRNA expression were weak with a mean ρ2 ranging from 0 to .22 across the probes. In conclusion, we observed weak associations between DAT mRNA expression and DAT availability in human brains. Therefore, DAT mRNA mapping may have only limited predictive power for DAT availability in humans. However, the difference in distribution of DAT mRNA and DAT protein may influence this limitation.
|
doi_str_mv | 10.1002/syn.22226 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2624950766</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2649452499</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3536-f19fd6383b2ecdc0c607b35d823f384490936cee865153d13b421b6d6f67ebe33</originalsourceid><addsrcrecordid>eNp10E1LwzAYB_AgipvTg19ACl700C1vTdPjGL7BUPDl4KmkSSoZbVOT1tFvb-amB9FcHhJ--fPwB-AUwSmCEM_80ExxOGwPjBHMeIxJxvbBGHKexpSmbASOvF9BCAmC9BCMSBIm4XAM5NLUptMqau1au8iWkbKtqE2jo86JxrfWdeG9fryfR7VoW9O8RaV1Ueu0MrLbXP_8ID6EqURhKtMNx-CgFJXXJ7s5AS_XV8-L23j5cHO3mC9jSRLC4hJlpWKEkwJrqSSUDKYFSRTHpCSc0gxmhEmtOUtQQhQiBcWoYIqVLNWFJmQCLra5rbPvvfZdXhsvdVWJRtve55hhmiUwZSzQ8190ZXvXhO2CohlNgsyCutwq6az3Tpd560wt3JAjmG-az0Pz-VfzwZ7tEvui1upHflcdwGwL1qbSw_9J-dPr_TbyE-PVjc0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2649452499</pqid></control><display><type>article</type><title>Limited power of dopamine transporter mRNA mapping for predicting dopamine transporter availability</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Pak, Kyoungjune ; Seo, Seongho ; Lee, Myung Jun ; Im, Hyung‐Jun ; Kim, Keunyoung ; Kim, In Joo</creator><creatorcontrib>Pak, Kyoungjune ; Seo, Seongho ; Lee, Myung Jun ; Im, Hyung‐Jun ; Kim, Keunyoung ; Kim, In Joo</creatorcontrib><description>Dopamine transporters (DAT) are transmembrane proteins that translocate dopamine from the extracellular space into presynaptic neurons. We aimed to investigate the predictive power of DAT mRNA for DAT protein expression, measured using positron emission tomography (PET). We performed 18F‐FP‐CIT PET scans in 35 healthy individuals. Binding potentials (BPND) from the ventral striatum, caudate nucleus, putamen, and middle frontal, orbitofrontal, cingulate, parietal, and temporal cortices were measured. DAT gene expression data were obtained from the freely available Allen Human Brain Atlas derived from six healthy donors. The auto‐correlation of PET‐derived BPNDs for DAT was intermediate (mean ρ2 = .66) with ρ2 ranging from .0811 to 1. However, the auto‐correlation of mRNA expression was weak across the probes with a mean ρ2 of .09–.23. Cross‐correlations between PET‐derived BPNDs and mRNA expression were weak with a mean ρ2 ranging from 0 to .22 across the probes. In conclusion, we observed weak associations between DAT mRNA expression and DAT availability in human brains. Therefore, DAT mRNA mapping may have only limited predictive power for DAT availability in humans. However, the difference in distribution of DAT mRNA and DAT protein may influence this limitation.
</description><identifier>ISSN: 0887-4476</identifier><identifier>EISSN: 1098-2396</identifier><identifier>DOI: 10.1002/syn.22226</identifier><identifier>PMID: 35104380</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Caudate nucleus ; Dopamine ; Dopamine - metabolism ; dopamine plasma membrane transport proteins ; Dopamine Plasma Membrane Transport Proteins - genetics ; Dopamine Plasma Membrane Transport Proteins - metabolism ; Dopamine transporter ; Gene expression ; Humans ; Membrane proteins ; messenger RNA ; Neostriatum ; Peptide mapping ; Positron emission tomography ; Probes ; Putamen ; Putamen - metabolism ; RNA, Messenger - metabolism</subject><ispartof>Synapse (New York, N.Y.), 2022-04, Vol.76 (5-6), p.e22226-n/a</ispartof><rights>2022 Wiley Periodicals LLC</rights><rights>2022 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3536-f19fd6383b2ecdc0c607b35d823f384490936cee865153d13b421b6d6f67ebe33</citedby><cites>FETCH-LOGICAL-c3536-f19fd6383b2ecdc0c607b35d823f384490936cee865153d13b421b6d6f67ebe33</cites><orcidid>0000-0002-0101-6472 ; 0000-0001-7894-0535 ; 0000-0001-5051-1894</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fsyn.22226$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fsyn.22226$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35104380$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pak, Kyoungjune</creatorcontrib><creatorcontrib>Seo, Seongho</creatorcontrib><creatorcontrib>Lee, Myung Jun</creatorcontrib><creatorcontrib>Im, Hyung‐Jun</creatorcontrib><creatorcontrib>Kim, Keunyoung</creatorcontrib><creatorcontrib>Kim, In Joo</creatorcontrib><title>Limited power of dopamine transporter mRNA mapping for predicting dopamine transporter availability</title><title>Synapse (New York, N.Y.)</title><addtitle>Synapse</addtitle><description>Dopamine transporters (DAT) are transmembrane proteins that translocate dopamine from the extracellular space into presynaptic neurons. We aimed to investigate the predictive power of DAT mRNA for DAT protein expression, measured using positron emission tomography (PET). We performed 18F‐FP‐CIT PET scans in 35 healthy individuals. Binding potentials (BPND) from the ventral striatum, caudate nucleus, putamen, and middle frontal, orbitofrontal, cingulate, parietal, and temporal cortices were measured. DAT gene expression data were obtained from the freely available Allen Human Brain Atlas derived from six healthy donors. The auto‐correlation of PET‐derived BPNDs for DAT was intermediate (mean ρ2 = .66) with ρ2 ranging from .0811 to 1. However, the auto‐correlation of mRNA expression was weak across the probes with a mean ρ2 of .09–.23. Cross‐correlations between PET‐derived BPNDs and mRNA expression were weak with a mean ρ2 ranging from 0 to .22 across the probes. In conclusion, we observed weak associations between DAT mRNA expression and DAT availability in human brains. Therefore, DAT mRNA mapping may have only limited predictive power for DAT availability in humans. However, the difference in distribution of DAT mRNA and DAT protein may influence this limitation.
</description><subject>Caudate nucleus</subject><subject>Dopamine</subject><subject>Dopamine - metabolism</subject><subject>dopamine plasma membrane transport proteins</subject><subject>Dopamine Plasma Membrane Transport Proteins - genetics</subject><subject>Dopamine Plasma Membrane Transport Proteins - metabolism</subject><subject>Dopamine transporter</subject><subject>Gene expression</subject><subject>Humans</subject><subject>Membrane proteins</subject><subject>messenger RNA</subject><subject>Neostriatum</subject><subject>Peptide mapping</subject><subject>Positron emission tomography</subject><subject>Probes</subject><subject>Putamen</subject><subject>Putamen - metabolism</subject><subject>RNA, Messenger - metabolism</subject><issn>0887-4476</issn><issn>1098-2396</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10E1LwzAYB_AgipvTg19ACl700C1vTdPjGL7BUPDl4KmkSSoZbVOT1tFvb-amB9FcHhJ--fPwB-AUwSmCEM_80ExxOGwPjBHMeIxJxvbBGHKexpSmbASOvF9BCAmC9BCMSBIm4XAM5NLUptMqau1au8iWkbKtqE2jo86JxrfWdeG9fryfR7VoW9O8RaV1Ueu0MrLbXP_8ID6EqURhKtMNx-CgFJXXJ7s5AS_XV8-L23j5cHO3mC9jSRLC4hJlpWKEkwJrqSSUDKYFSRTHpCSc0gxmhEmtOUtQQhQiBcWoYIqVLNWFJmQCLra5rbPvvfZdXhsvdVWJRtve55hhmiUwZSzQ8190ZXvXhO2CohlNgsyCutwq6az3Tpd560wt3JAjmG-az0Pz-VfzwZ7tEvui1upHflcdwGwL1qbSw_9J-dPr_TbyE-PVjc0</recordid><startdate>202204</startdate><enddate>202204</enddate><creator>Pak, Kyoungjune</creator><creator>Seo, Seongho</creator><creator>Lee, Myung Jun</creator><creator>Im, Hyung‐Jun</creator><creator>Kim, Keunyoung</creator><creator>Kim, In Joo</creator><general>Wiley Subscription Services, Inc</general><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>7QP</scope><scope>7TK</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0101-6472</orcidid><orcidid>https://orcid.org/0000-0001-7894-0535</orcidid><orcidid>https://orcid.org/0000-0001-5051-1894</orcidid></search><sort><creationdate>202204</creationdate><title>Limited power of dopamine transporter mRNA mapping for predicting dopamine transporter availability</title><author>Pak, Kyoungjune ; Seo, Seongho ; Lee, Myung Jun ; Im, Hyung‐Jun ; Kim, Keunyoung ; Kim, In Joo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3536-f19fd6383b2ecdc0c607b35d823f384490936cee865153d13b421b6d6f67ebe33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Caudate nucleus</topic><topic>Dopamine</topic><topic>Dopamine - metabolism</topic><topic>dopamine plasma membrane transport proteins</topic><topic>Dopamine Plasma Membrane Transport Proteins - genetics</topic><topic>Dopamine Plasma Membrane Transport Proteins - metabolism</topic><topic>Dopamine transporter</topic><topic>Gene expression</topic><topic>Humans</topic><topic>Membrane proteins</topic><topic>messenger RNA</topic><topic>Neostriatum</topic><topic>Peptide mapping</topic><topic>Positron emission tomography</topic><topic>Probes</topic><topic>Putamen</topic><topic>Putamen - metabolism</topic><topic>RNA, Messenger - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pak, Kyoungjune</creatorcontrib><creatorcontrib>Seo, Seongho</creatorcontrib><creatorcontrib>Lee, Myung Jun</creatorcontrib><creatorcontrib>Im, Hyung‐Jun</creatorcontrib><creatorcontrib>Kim, Keunyoung</creatorcontrib><creatorcontrib>Kim, In Joo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Synapse (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pak, Kyoungjune</au><au>Seo, Seongho</au><au>Lee, Myung Jun</au><au>Im, Hyung‐Jun</au><au>Kim, Keunyoung</au><au>Kim, In Joo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Limited power of dopamine transporter mRNA mapping for predicting dopamine transporter availability</atitle><jtitle>Synapse (New York, N.Y.)</jtitle><addtitle>Synapse</addtitle><date>2022-04</date><risdate>2022</risdate><volume>76</volume><issue>5-6</issue><spage>e22226</spage><epage>n/a</epage><pages>e22226-n/a</pages><issn>0887-4476</issn><eissn>1098-2396</eissn><abstract>Dopamine transporters (DAT) are transmembrane proteins that translocate dopamine from the extracellular space into presynaptic neurons. We aimed to investigate the predictive power of DAT mRNA for DAT protein expression, measured using positron emission tomography (PET). We performed 18F‐FP‐CIT PET scans in 35 healthy individuals. Binding potentials (BPND) from the ventral striatum, caudate nucleus, putamen, and middle frontal, orbitofrontal, cingulate, parietal, and temporal cortices were measured. DAT gene expression data were obtained from the freely available Allen Human Brain Atlas derived from six healthy donors. The auto‐correlation of PET‐derived BPNDs for DAT was intermediate (mean ρ2 = .66) with ρ2 ranging from .0811 to 1. However, the auto‐correlation of mRNA expression was weak across the probes with a mean ρ2 of .09–.23. Cross‐correlations between PET‐derived BPNDs and mRNA expression were weak with a mean ρ2 ranging from 0 to .22 across the probes. In conclusion, we observed weak associations between DAT mRNA expression and DAT availability in human brains. Therefore, DAT mRNA mapping may have only limited predictive power for DAT availability in humans. However, the difference in distribution of DAT mRNA and DAT protein may influence this limitation.
</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>35104380</pmid><doi>10.1002/syn.22226</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0101-6472</orcidid><orcidid>https://orcid.org/0000-0001-7894-0535</orcidid><orcidid>https://orcid.org/0000-0001-5051-1894</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0887-4476 |
ispartof | Synapse (New York, N.Y.), 2022-04, Vol.76 (5-6), p.e22226-n/a |
issn | 0887-4476 1098-2396 |
language | eng |
recordid | cdi_proquest_miscellaneous_2624950766 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Caudate nucleus Dopamine Dopamine - metabolism dopamine plasma membrane transport proteins Dopamine Plasma Membrane Transport Proteins - genetics Dopamine Plasma Membrane Transport Proteins - metabolism Dopamine transporter Gene expression Humans Membrane proteins messenger RNA Neostriatum Peptide mapping Positron emission tomography Probes Putamen Putamen - metabolism RNA, Messenger - metabolism |
title | Limited power of dopamine transporter mRNA mapping for predicting dopamine transporter availability |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T21%3A17%3A52IST&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=Limited%20power%20of%20dopamine%20transporter%20mRNA%20mapping%20for%20predicting%20dopamine%20transporter%20availability&rft.jtitle=Synapse%20(New%20York,%20N.Y.)&rft.au=Pak,%20Kyoungjune&rft.date=2022-04&rft.volume=76&rft.issue=5-6&rft.spage=e22226&rft.epage=n/a&rft.pages=e22226-n/a&rft.issn=0887-4476&rft.eissn=1098-2396&rft_id=info:doi/10.1002/syn.22226&rft_dat=%3Cproquest_cross%3E2649452499%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=2649452499&rft_id=info:pmid/35104380&rfr_iscdi=true |