Apolipoprotein D subcellular distribution pattern in neuronal cells during oxidative stress
Apolipoprotein D (Apo D) is a secreted glycoprotein, member of the lipocalin superfamily, with a related beneficial role in metabolism and lipid transport due to the presence of a binding pocket that allows its interaction with several lipids. Nowadays, it has been clearly demonstrated that Apo D ex...
Gespeichert in:
Veröffentlicht in: | Acta histochemica 2015-07, Vol.117 (6), p.536-544 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 544 |
---|---|
container_issue | 6 |
container_start_page | 536 |
container_title | Acta histochemica |
container_volume | 117 |
creator | Martínez-Pinilla, Eva Navarro, Ana Ordóñez, Cristina del Valle, Eva Tolivia, Jorge |
description | Apolipoprotein D (Apo D) is a secreted glycoprotein, member of the lipocalin superfamily, with a related beneficial role in metabolism and lipid transport due to the presence of a binding pocket that allows its interaction with several lipids. Nowadays, it has been clearly demonstrated that Apo D expression is induced and its subcellular location undergoes modifications in stressful and pathological conditions that characterize aging processes and neurodegenerative diseases. The aim of the present work was to study in detail the effect of H2O2 on the subcellular location of Apo D, in the hippocampal cell line HT22, by structural, ultrastructural, immunocytochemical, and molecular techniques in order to characterize the Apo D distribution pattern in neurons during oxidative stress. Our results indicate that Apo D is located in the cytoplasm under physiological conditions but treatment with H2O2 induces apoptosis and causes a displacement of Apo D location to the nucleus, coinciding with DNA fragmentation. In addition, we demonstrated that Apo D tends to accumulate around the nuclear envelope in neurons and glial cells of different brain areas in some neurodegenerative diseases and during human aging, but never inside the nucleus. These data suggest that the presence of Apo D in the nucleus, which some authors related with a specific transport, is a consequence of structural and functional alterations during oxidative stress and not the result of a specific role in the regulation of nuclear processes. |
doi_str_mv | 10.1016/j.acthis.2015.04.003 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1704353721</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0065128115000781</els_id><sourcerecordid>1704353721</sourcerecordid><originalsourceid>FETCH-LOGICAL-c502t-d1454352a659c8481c654bcb0fe39624efeaacff908f1c604a5609a5619202873</originalsourceid><addsrcrecordid>eNp9kD1PwzAQhi0EglL4Bwh5ZEk4O3aaLEiIb6kSC0wMluNcwFUaB9tB8O9xVWBkOQ_3vHe-h5ATBjkDVp6vcm3imw05ByZzEDlAsUNmrGRVBsWC75IZQCkzxit2QA5DWAFADQXfJwdc1rJYCJiRl8vR9XZ0o3cR7UCvaZgag30_9drT1obobTNF6wY66hjRDzRRA07eDbqnGzLQdvJ2eKXu07Y62g-kKYUhHJG9TvcBj3_eOXm-vXm6us-Wj3cPV5fLzEjgMWuZkKKQXJeyNpWomCmlaEwDHRZ1yQV2qLXpuhqqLvVAaFlCnQqrOfBqUczJ2XZuOuJ9whDV2obNz_SAbgqKLSDNT0pYQsUWNd6F4LFTo7dr7b8UA7XRqlZqq1VttCoQKmlNsdOfDVOzxvYv9OsxARdbANOdHxa9CsbiYLC1Hk1UrbP_b_gGNHyL4Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1704353721</pqid></control><display><type>article</type><title>Apolipoprotein D subcellular distribution pattern in neuronal cells during oxidative stress</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Martínez-Pinilla, Eva ; Navarro, Ana ; Ordóñez, Cristina ; del Valle, Eva ; Tolivia, Jorge</creator><creatorcontrib>Martínez-Pinilla, Eva ; Navarro, Ana ; Ordóñez, Cristina ; del Valle, Eva ; Tolivia, Jorge</creatorcontrib><description>Apolipoprotein D (Apo D) is a secreted glycoprotein, member of the lipocalin superfamily, with a related beneficial role in metabolism and lipid transport due to the presence of a binding pocket that allows its interaction with several lipids. Nowadays, it has been clearly demonstrated that Apo D expression is induced and its subcellular location undergoes modifications in stressful and pathological conditions that characterize aging processes and neurodegenerative diseases. The aim of the present work was to study in detail the effect of H2O2 on the subcellular location of Apo D, in the hippocampal cell line HT22, by structural, ultrastructural, immunocytochemical, and molecular techniques in order to characterize the Apo D distribution pattern in neurons during oxidative stress. Our results indicate that Apo D is located in the cytoplasm under physiological conditions but treatment with H2O2 induces apoptosis and causes a displacement of Apo D location to the nucleus, coinciding with DNA fragmentation. In addition, we demonstrated that Apo D tends to accumulate around the nuclear envelope in neurons and glial cells of different brain areas in some neurodegenerative diseases and during human aging, but never inside the nucleus. These data suggest that the presence of Apo D in the nucleus, which some authors related with a specific transport, is a consequence of structural and functional alterations during oxidative stress and not the result of a specific role in the regulation of nuclear processes.</description><identifier>ISSN: 0065-1281</identifier><identifier>EISSN: 1618-0372</identifier><identifier>DOI: 10.1016/j.acthis.2015.04.003</identifier><identifier>PMID: 25953740</identifier><language>eng</language><publisher>Germany: Elsevier GmbH</publisher><subject>Apolipoprotein D ; Apolipoproteins D - metabolism ; Apoptosis ; Apoptosis - drug effects ; Cell Line ; Cell Survival - drug effects ; DNA Fragmentation - drug effects ; HT22 ; Humans ; Hydrogen Peroxide - pharmacology ; Immunohistochemistry ; In Vitro Techniques ; Microscopy, Electron, Transmission ; Neurons - drug effects ; Neurons - metabolism ; Nuclear location ; Oxidative stress ; Oxidative Stress - drug effects</subject><ispartof>Acta histochemica, 2015-07, Vol.117 (6), p.536-544</ispartof><rights>2015 Elsevier GmbH</rights><rights>Copyright © 2015 Elsevier GmbH. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c502t-d1454352a659c8481c654bcb0fe39624efeaacff908f1c604a5609a5619202873</citedby><cites>FETCH-LOGICAL-c502t-d1454352a659c8481c654bcb0fe39624efeaacff908f1c604a5609a5619202873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.acthis.2015.04.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25953740$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Martínez-Pinilla, Eva</creatorcontrib><creatorcontrib>Navarro, Ana</creatorcontrib><creatorcontrib>Ordóñez, Cristina</creatorcontrib><creatorcontrib>del Valle, Eva</creatorcontrib><creatorcontrib>Tolivia, Jorge</creatorcontrib><title>Apolipoprotein D subcellular distribution pattern in neuronal cells during oxidative stress</title><title>Acta histochemica</title><addtitle>Acta Histochem</addtitle><description>Apolipoprotein D (Apo D) is a secreted glycoprotein, member of the lipocalin superfamily, with a related beneficial role in metabolism and lipid transport due to the presence of a binding pocket that allows its interaction with several lipids. Nowadays, it has been clearly demonstrated that Apo D expression is induced and its subcellular location undergoes modifications in stressful and pathological conditions that characterize aging processes and neurodegenerative diseases. The aim of the present work was to study in detail the effect of H2O2 on the subcellular location of Apo D, in the hippocampal cell line HT22, by structural, ultrastructural, immunocytochemical, and molecular techniques in order to characterize the Apo D distribution pattern in neurons during oxidative stress. Our results indicate that Apo D is located in the cytoplasm under physiological conditions but treatment with H2O2 induces apoptosis and causes a displacement of Apo D location to the nucleus, coinciding with DNA fragmentation. In addition, we demonstrated that Apo D tends to accumulate around the nuclear envelope in neurons and glial cells of different brain areas in some neurodegenerative diseases and during human aging, but never inside the nucleus. These data suggest that the presence of Apo D in the nucleus, which some authors related with a specific transport, is a consequence of structural and functional alterations during oxidative stress and not the result of a specific role in the regulation of nuclear processes.</description><subject>Apolipoprotein D</subject><subject>Apolipoproteins D - metabolism</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Cell Line</subject><subject>Cell Survival - drug effects</subject><subject>DNA Fragmentation - drug effects</subject><subject>HT22</subject><subject>Humans</subject><subject>Hydrogen Peroxide - pharmacology</subject><subject>Immunohistochemistry</subject><subject>In Vitro Techniques</subject><subject>Microscopy, Electron, Transmission</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>Nuclear location</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><issn>0065-1281</issn><issn>1618-0372</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1PwzAQhi0EglL4Bwh5ZEk4O3aaLEiIb6kSC0wMluNcwFUaB9tB8O9xVWBkOQ_3vHe-h5ATBjkDVp6vcm3imw05ByZzEDlAsUNmrGRVBsWC75IZQCkzxit2QA5DWAFADQXfJwdc1rJYCJiRl8vR9XZ0o3cR7UCvaZgag30_9drT1obobTNF6wY66hjRDzRRA07eDbqnGzLQdvJ2eKXu07Y62g-kKYUhHJG9TvcBj3_eOXm-vXm6us-Wj3cPV5fLzEjgMWuZkKKQXJeyNpWomCmlaEwDHRZ1yQV2qLXpuhqqLvVAaFlCnQqrOfBqUczJ2XZuOuJ9whDV2obNz_SAbgqKLSDNT0pYQsUWNd6F4LFTo7dr7b8UA7XRqlZqq1VttCoQKmlNsdOfDVOzxvYv9OsxARdbANOdHxa9CsbiYLC1Hk1UrbP_b_gGNHyL4Q</recordid><startdate>20150701</startdate><enddate>20150701</enddate><creator>Martínez-Pinilla, Eva</creator><creator>Navarro, Ana</creator><creator>Ordóñez, Cristina</creator><creator>del Valle, Eva</creator><creator>Tolivia, Jorge</creator><general>Elsevier GmbH</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>7X8</scope></search><sort><creationdate>20150701</creationdate><title>Apolipoprotein D subcellular distribution pattern in neuronal cells during oxidative stress</title><author>Martínez-Pinilla, Eva ; Navarro, Ana ; Ordóñez, Cristina ; del Valle, Eva ; Tolivia, Jorge</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c502t-d1454352a659c8481c654bcb0fe39624efeaacff908f1c604a5609a5619202873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Apolipoprotein D</topic><topic>Apolipoproteins D - metabolism</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Cell Line</topic><topic>Cell Survival - drug effects</topic><topic>DNA Fragmentation - drug effects</topic><topic>HT22</topic><topic>Humans</topic><topic>Hydrogen Peroxide - pharmacology</topic><topic>Immunohistochemistry</topic><topic>In Vitro Techniques</topic><topic>Microscopy, Electron, Transmission</topic><topic>Neurons - drug effects</topic><topic>Neurons - metabolism</topic><topic>Nuclear location</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Martínez-Pinilla, Eva</creatorcontrib><creatorcontrib>Navarro, Ana</creatorcontrib><creatorcontrib>Ordóñez, Cristina</creatorcontrib><creatorcontrib>del Valle, Eva</creatorcontrib><creatorcontrib>Tolivia, Jorge</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>Acta histochemica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Martínez-Pinilla, Eva</au><au>Navarro, Ana</au><au>Ordóñez, Cristina</au><au>del Valle, Eva</au><au>Tolivia, Jorge</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Apolipoprotein D subcellular distribution pattern in neuronal cells during oxidative stress</atitle><jtitle>Acta histochemica</jtitle><addtitle>Acta Histochem</addtitle><date>2015-07-01</date><risdate>2015</risdate><volume>117</volume><issue>6</issue><spage>536</spage><epage>544</epage><pages>536-544</pages><issn>0065-1281</issn><eissn>1618-0372</eissn><abstract>Apolipoprotein D (Apo D) is a secreted glycoprotein, member of the lipocalin superfamily, with a related beneficial role in metabolism and lipid transport due to the presence of a binding pocket that allows its interaction with several lipids. Nowadays, it has been clearly demonstrated that Apo D expression is induced and its subcellular location undergoes modifications in stressful and pathological conditions that characterize aging processes and neurodegenerative diseases. The aim of the present work was to study in detail the effect of H2O2 on the subcellular location of Apo D, in the hippocampal cell line HT22, by structural, ultrastructural, immunocytochemical, and molecular techniques in order to characterize the Apo D distribution pattern in neurons during oxidative stress. Our results indicate that Apo D is located in the cytoplasm under physiological conditions but treatment with H2O2 induces apoptosis and causes a displacement of Apo D location to the nucleus, coinciding with DNA fragmentation. In addition, we demonstrated that Apo D tends to accumulate around the nuclear envelope in neurons and glial cells of different brain areas in some neurodegenerative diseases and during human aging, but never inside the nucleus. These data suggest that the presence of Apo D in the nucleus, which some authors related with a specific transport, is a consequence of structural and functional alterations during oxidative stress and not the result of a specific role in the regulation of nuclear processes.</abstract><cop>Germany</cop><pub>Elsevier GmbH</pub><pmid>25953740</pmid><doi>10.1016/j.acthis.2015.04.003</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0065-1281 |
ispartof | Acta histochemica, 2015-07, Vol.117 (6), p.536-544 |
issn | 0065-1281 1618-0372 |
language | eng |
recordid | cdi_proquest_miscellaneous_1704353721 |
source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Apolipoprotein D Apolipoproteins D - metabolism Apoptosis Apoptosis - drug effects Cell Line Cell Survival - drug effects DNA Fragmentation - drug effects HT22 Humans Hydrogen Peroxide - pharmacology Immunohistochemistry In Vitro Techniques Microscopy, Electron, Transmission Neurons - drug effects Neurons - metabolism Nuclear location Oxidative stress Oxidative Stress - drug effects |
title | Apolipoprotein D subcellular distribution pattern in neuronal cells during oxidative stress |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T18%3A58%3A32IST&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=Apolipoprotein%20D%20subcellular%20distribution%20pattern%20in%20neuronal%20cells%20during%20oxidative%20stress&rft.jtitle=Acta%20histochemica&rft.au=Mart%C3%ADnez-Pinilla,%20Eva&rft.date=2015-07-01&rft.volume=117&rft.issue=6&rft.spage=536&rft.epage=544&rft.pages=536-544&rft.issn=0065-1281&rft.eissn=1618-0372&rft_id=info:doi/10.1016/j.acthis.2015.04.003&rft_dat=%3Cproquest_cross%3E1704353721%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=1704353721&rft_id=info:pmid/25953740&rft_els_id=S0065128115000781&rfr_iscdi=true |