WeightNameValue
1000 Titel
  • The ADAP/SKAP55 Signaling Module Regulates T-Cell Receptor-Mediated Integrin Activation through Plasma Membrane Targeting of Rap1
1000 Autor/in
  1. Kliche, Stefanie |
  2. Breitling, Dennis |
  3. Togni, Mauro |
  4. Pusch, Rico |
  5. Heuer, Katja |
  6. Wang, Xiaoqian |
  7. Freund, Christian |
  8. Kasirer-Friede, Ana |
  9. Menasche, Gael |
  10. Koretzky, Gary A. |
  11. Schraven, Burkhart |
1000 Erscheinungsjahr 2006
1000 LeibnizOpen
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2006-10-01
1000 Erschienen in
1000 Quellenangabe
  • 26(19):7130–7144
1000 FRL-Sammlung
1000 Verlagsversion
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1592884/ |
  • https://doi.org/10.1128/MCB.00331-06 |
1000 Ergänzendes Material
  • http://mcb.asm.org/content/26/19/7130/suppl/DC1 |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Adhesion of T cells after stimulation of the T-cell receptor (TCR) is mediated via signaling processes that have collectively been termed inside-out signaling. The molecular basis for inside-out signaling is not yet completely understood. Here, we show that a signaling module comprising the cytosolic adapter proteins ADAP and SKAP55 is involved in TCR-mediated inside-out signaling and, moreover, that the interaction between ADAP and SKAP55 is mandatory for integrin activation. Disruption of the ADAP/SKAP55 module leads to displacement of the small GTPase Rap1 from the plasma membrane without influencing its GTPase activity. These findings suggest that the ADAP/SKAP55 complex serves to recruit activated Rap1 to the plasma membrane. In line with this hypothesis is the finding that membrane targeting of the ADAP/SKAP55 module induces T-cell adhesion in the absence of TCR-mediated stimuli. However, it appears as if the ADAP/SKAP55 module can exert its signaling function outside of the classical raft fraction of the cell membrane.
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/creator/S2xpY2hlLCBTdGVmYW5pZQ==|https://frl.publisso.de/adhoc/creator/QnJlaXRsaW5nLCBEZW5uaXM=|https://frl.publisso.de/adhoc/creator/VG9nbmksIE1hdXJv|https://frl.publisso.de/adhoc/creator/UHVzY2gsIFJpY28=|https://frl.publisso.de/adhoc/creator/SGV1ZXIsIEthdGph|https://frl.publisso.de/adhoc/creator/V2FuZywgWGlhb3FpYW4=|https://frl.publisso.de/adhoc/creator/RnJldW5kLCBDaHJpc3RpYW4=|https://frl.publisso.de/adhoc/creator/S2FzaXJlci1GcmllZGUsIEFuYQ==|https://frl.publisso.de/adhoc/creator/TWVuYXNjaGUsIEdhZWw=|https://frl.publisso.de/adhoc/creator/S29yZXR6a3ksIEdhcnkgQS4=|https://frl.publisso.de/adhoc/creator/U2NocmF2ZW4sIEJ1cmtoYXJ0
1000 Label
1000 Förderer
  1. Deutsche Forschungsgemeinschaft |
  2. U.S. National Institutes of Health |
1000 Fördernummer
  1. KL1292/5-1; GRK1167
  2. -
1000 Förderprogramm
  1. -
  2. -
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Deutsche Forschungsgemeinschaft |
    1000 Förderprogramm -
    1000 Fördernummer KL1292/5-1; GRK1167
  2. 1000 joinedFunding-child
    1000 Förderer U.S. National Institutes of Health |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6406583.rdf
1000 Erstellt am 2018-01-31T14:11:43.684+0100
1000 Erstellt von 22
1000 beschreibt frl:6406583
1000 Bearbeitet von 288
1000 Zuletzt bearbeitet 2022-08-18T07:42:54.558+0200
1000 Objekt bearb. Thu Apr 08 12:10:48 CEST 2021
1000 Vgl. frl:6406583
1000 Oai Id
  1. oai:frl.publisso.de:frl:6406583 |
1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
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