Serveur d'exploration MERS

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Presence of distinct AP-1 dimers in normal and transformed rat hepatocytes under basal conditions and after epidermal growth factor stimulation

Identifieur interne : 000306 ( France/Analysis ); précédent : 000305; suivant : 000307

Presence of distinct AP-1 dimers in normal and transformed rat hepatocytes under basal conditions and after epidermal growth factor stimulation

Auteurs : F. Nadori [France] ; B. Lardeux [France] ; M. Rahmani [France] ; A. Bringuier [France] ; A. Durand-Schneider [France] ; D. Bernuau [France]

Source :

RBID : ISTEX:96BB568DB61AD9B8F3DA75C918EA2DD1BB6E96A8

English descriptors

Abstract

Abstract: Activation of the transcriptional regulator AP-1, a dimeric complex formed of various combinations of Fos and Jun proteins, is a key step in the cellular response to mitogens. Because different dimers are believed to display different regulatory functions, we hypothesized that transformed cells that lack normal growth constraints might display AP-1 dimers that are different from those of normal cells. We therefore compared in primary and transformed rat hepatocytes (1) the composition of AP-1 dimers under basal conditions and (2) AP-1 induction by epidermal growth factor (EGF). Under basal conditions, AP-1 contained predominantly Jun homodimers in both cell types. However, whereas normal hepatocytes contained only JunD, both JunD and JunB were present in the AP-1 complex of 7777 cells. EGF treatment triggered almost identical programs of fos and jun gene activation at the messenger RNA (mRNA) level in both cell types, with an early accumulation of c-fos, c-jun, and junB mRNAs, but no change in junD mRNA levels. In both cell types, c-Fos and Fra-1 proteins increased after EGF treatment, but differences in the induction of Jun proteins were noted, with an increase of c-Jun in hepatocytes and an increase of JunB in 7777 cells. In both cell types, activation of AP-1 DNA binding activity by EGF was accompanied by the recruitment of Fra-1 into AP-1, detected earlier in 7777 cells than in hepatocytes, and with the transient appearance of c-Fos in 7777 cells only. Finally, EGF activated AP-1-dependent transcription in 7777 cells but not in hepatocytes. These data indicate important differences in the functional activity of AP-1 in transformed hepatocytes. (Hepatology 1997 Dec;26(6):1477-83)

Url:
DOI: 10.1053/jhep.1997.v26.pm0009397987


Affiliations:


Links toward previous steps (curation, corpus...)


Links to Exploration step

ISTEX:96BB568DB61AD9B8F3DA75C918EA2DD1BB6E96A8

Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Presence of distinct AP-1 dimers in normal and transformed rat hepatocytes under basal conditions and after epidermal growth factor stimulation</title>
<author>
<name sortKey="Nadori, F" sort="Nadori, F" uniqKey="Nadori F" first="F" last="Nadori">F. Nadori</name>
</author>
<author>
<name sortKey="Lardeux, B" sort="Lardeux, B" uniqKey="Lardeux B" first="B" last="Lardeux">B. Lardeux</name>
</author>
<author>
<name sortKey="Rahmani, M" sort="Rahmani, M" uniqKey="Rahmani M" first="M" last="Rahmani">M. Rahmani</name>
</author>
<author>
<name sortKey="Bringuier, A" sort="Bringuier, A" uniqKey="Bringuier A" first="A" last="Bringuier">A. Bringuier</name>
</author>
<author>
<name sortKey="Durand Schneider, A" sort="Durand Schneider, A" uniqKey="Durand Schneider A" first="A" last="Durand-Schneider">A. Durand-Schneider</name>
</author>
<author>
<name sortKey="Bernuau, D" sort="Bernuau, D" uniqKey="Bernuau D" first="D" last="Bernuau">D. Bernuau</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:96BB568DB61AD9B8F3DA75C918EA2DD1BB6E96A8</idno>
<date when="1997" year="1997">1997</date>
<idno type="doi">10.1053/jhep.1997.v26.pm0009397987</idno>
<idno type="url">https://api.istex.fr/ark:/67375/6H6-KFHGF0MS-H/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001D80</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001D80</idno>
<idno type="wicri:Area/Istex/Curation">001D80</idno>
<idno type="wicri:Area/Istex/Checkpoint">001509</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">001509</idno>
<idno type="wicri:doubleKey">0270-9139:1997:Nadori F:presence:of:distinct</idno>
<idno type="wicri:Area/Main/Merge">003D88</idno>
<idno type="wicri:Area/Main/Curation">003D33</idno>
<idno type="wicri:Area/Main/Exploration">003D33</idno>
<idno type="wicri:Area/France/Extraction">000306</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main" xml:lang="en">Presence of distinct AP-1 dimers in normal and transformed rat hepatocytes under basal conditions and after epidermal growth factor stimulation</title>
<author>
<name sortKey="Nadori, F" sort="Nadori, F" uniqKey="Nadori F" first="F" last="Nadori">F. Nadori</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de Biologie Cellulaire, INSERM Unite 327, Faculte de Medecine Xavier Bichat, Universite Paris</wicri:regionArea>
<wicri:noRegion>Universite Paris</wicri:noRegion>
<wicri:noRegion>Universite Paris</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Lardeux, B" sort="Lardeux, B" uniqKey="Lardeux B" first="B" last="Lardeux">B. Lardeux</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de Biologie Cellulaire, INSERM Unite 327, Faculte de Medecine Xavier Bichat, Universite Paris</wicri:regionArea>
<wicri:noRegion>Universite Paris</wicri:noRegion>
<wicri:noRegion>Universite Paris</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Rahmani, M" sort="Rahmani, M" uniqKey="Rahmani M" first="M" last="Rahmani">M. Rahmani</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de Biologie Cellulaire, INSERM Unite 327, Faculte de Medecine Xavier Bichat, Universite Paris</wicri:regionArea>
<wicri:noRegion>Universite Paris</wicri:noRegion>
<wicri:noRegion>Universite Paris</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Bringuier, A" sort="Bringuier, A" uniqKey="Bringuier A" first="A" last="Bringuier">A. Bringuier</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de Biologie Cellulaire, INSERM Unite 327, Faculte de Medecine Xavier Bichat, Universite Paris</wicri:regionArea>
<wicri:noRegion>Universite Paris</wicri:noRegion>
<wicri:noRegion>Universite Paris</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Durand Schneider, A" sort="Durand Schneider, A" uniqKey="Durand Schneider A" first="A" last="Durand-Schneider">A. Durand-Schneider</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de Biologie Cellulaire, INSERM Unite 327, Faculte de Medecine Xavier Bichat, Universite Paris</wicri:regionArea>
<wicri:noRegion>Universite Paris</wicri:noRegion>
<wicri:noRegion>Universite Paris</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Bernuau, D" sort="Bernuau, D" uniqKey="Bernuau D" first="D" last="Bernuau">D. Bernuau</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de Biologie Cellulaire, INSERM Unite 327, Faculte de Medecine Xavier Bichat, Universite Paris</wicri:regionArea>
<wicri:noRegion>Universite Paris</wicri:noRegion>
<wicri:noRegion>Universite Paris</wicri:noRegion>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Hepatology</title>
<title level="j" type="abbrev">YJHEP</title>
<idno type="ISSN">0270-9139</idno>
<imprint>
<publisher>ELSEVIER</publisher>
<date type="published" when="1997">1997</date>
<biblScope unit="volume">26</biblScope>
<biblScope unit="issue">6</biblScope>
<biblScope unit="page" from="1477">1477</biblScope>
<biblScope unit="page" to="1483">1483</biblScope>
</imprint>
<idno type="ISSN">0270-9139</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0270-9139</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="Teeft" xml:lang="en">
<term>Activator protein</term>
<term>Anal biochem</term>
<term>Assay</term>
<term>Basal</term>
<term>Basal binding activity</term>
<term>Basal conditions</term>
<term>Bernuau</term>
<term>Binding activity</term>
<term>Binding affinities</term>
<term>Biol</term>
<term>Biologie cellulaire</term>
<term>Cell biol</term>
<term>Cell cycle</term>
<term>Cell growth</term>
<term>Cell systems</term>
<term>Cell types</term>
<term>Cellular transformation</term>
<term>Control cells</term>
<term>Different dimers</term>
<term>Dimer</term>
<term>Dimethyl sulfoxide</term>
<term>Electrophoretic mobility shift assay</term>
<term>Epidermal growth factor</term>
<term>Ethylenediaminetetraacetic acid</term>
<term>Family members</term>
<term>Family proteins</term>
<term>Form heterodimers</term>
<term>Functional activity</term>
<term>Gapdh crna probe</term>
<term>Gapdh mrna</term>
<term>Gene</term>
<term>Gene activation</term>
<term>Gene expression</term>
<term>Growth factor</term>
<term>Growth factors</term>
<term>Hepa</term>
<term>Hepas</term>
<term>Hepatocytes</term>
<term>Hepatology</term>
<term>Hepatology december</term>
<term>Hepatology hepatology</term>
<term>Identical programs</term>
<term>Intracellular mrna</term>
<term>Junb</term>
<term>Junb mrnas</term>
<term>Junb protein</term>
<term>Jund</term>
<term>Jund mrna</term>
<term>Mrna</term>
<term>Mrna level</term>
<term>Mrna levels</term>
<term>Mrna quantification</term>
<term>Nadori</term>
<term>Nitrocellulose membranes</term>
<term>Normal cells</term>
<term>Normal hepatocytes</term>
<term>Nuclear extracts</term>
<term>Nucleic acids</term>
<term>Okadaic acid</term>
<term>Oncogene</term>
<term>Other hand</term>
<term>Phenylmethylsulfonyl fluoride</term>
<term>Phorbol element</term>
<term>Posttranslational modifications</term>
<term>Present study</term>
<term>Primary cultures</term>
<term>Proc natl acad</term>
<term>Protein assay reagent</term>
<term>Protein levels</term>
<term>Quantitative analysis</term>
<term>Quiescent liver</term>
<term>Reaction mixture</term>
<term>Reporter plasmid</term>
<term>Retarded band</term>
<term>Room temperature</term>
<term>Santa cruz biotechnology</term>
<term>Sense mrna</term>
<term>Significant effect</term>
<term>Sodium dodecyl sulfate</term>
<term>Specific complexes</term>
<term>Supershift</term>
<term>Supershift analyses</term>
<term>Supershifted bands</term>
<term>Transcription</term>
<term>Transcription factors</term>
<term>Transfected</term>
<term>Transiently transfected</term>
<term>Unpublished observations</term>
<term>Western blot analysis</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Abstract: Activation of the transcriptional regulator AP-1, a dimeric complex formed of various combinations of Fos and Jun proteins, is a key step in the cellular response to mitogens. Because different dimers are believed to display different regulatory functions, we hypothesized that transformed cells that lack normal growth constraints might display AP-1 dimers that are different from those of normal cells. We therefore compared in primary and transformed rat hepatocytes (1) the composition of AP-1 dimers under basal conditions and (2) AP-1 induction by epidermal growth factor (EGF). Under basal conditions, AP-1 contained predominantly Jun homodimers in both cell types. However, whereas normal hepatocytes contained only JunD, both JunD and JunB were present in the AP-1 complex of 7777 cells. EGF treatment triggered almost identical programs of fos and jun gene activation at the messenger RNA (mRNA) level in both cell types, with an early accumulation of c-fos, c-jun, and junB mRNAs, but no change in junD mRNA levels. In both cell types, c-Fos and Fra-1 proteins increased after EGF treatment, but differences in the induction of Jun proteins were noted, with an increase of c-Jun in hepatocytes and an increase of JunB in 7777 cells. In both cell types, activation of AP-1 DNA binding activity by EGF was accompanied by the recruitment of Fra-1 into AP-1, detected earlier in 7777 cells than in hepatocytes, and with the transient appearance of c-Fos in 7777 cells only. Finally, EGF activated AP-1-dependent transcription in 7777 cells but not in hepatocytes. These data indicate important differences in the functional activity of AP-1 in transformed hepatocytes. (Hepatology 1997 Dec;26(6):1477-83)</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>France</li>
</country>
</list>
<tree>
<country name="France">
<noRegion>
<name sortKey="Nadori, F" sort="Nadori, F" uniqKey="Nadori F" first="F" last="Nadori">F. Nadori</name>
</noRegion>
<name sortKey="Bernuau, D" sort="Bernuau, D" uniqKey="Bernuau D" first="D" last="Bernuau">D. Bernuau</name>
<name sortKey="Bringuier, A" sort="Bringuier, A" uniqKey="Bringuier A" first="A" last="Bringuier">A. Bringuier</name>
<name sortKey="Durand Schneider, A" sort="Durand Schneider, A" uniqKey="Durand Schneider A" first="A" last="Durand-Schneider">A. Durand-Schneider</name>
<name sortKey="Lardeux, B" sort="Lardeux, B" uniqKey="Lardeux B" first="B" last="Lardeux">B. Lardeux</name>
<name sortKey="Rahmani, M" sort="Rahmani, M" uniqKey="Rahmani M" first="M" last="Rahmani">M. Rahmani</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/MersV1/Data/France/Analysis
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000306 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/France/Analysis/biblio.hfd -nk 000306 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    MersV1
   |flux=    France
   |étape=   Analysis
   |type=    RBID
   |clé=     ISTEX:96BB568DB61AD9B8F3DA75C918EA2DD1BB6E96A8
   |texte=   Presence of distinct AP-1 dimers in normal and transformed rat hepatocytes under basal conditions and after epidermal growth factor stimulation
}}

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Mon Apr 20 23:26:43 2020. Site generation: Sat Mar 27 09:06:09 2021