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  From Structure To Disease: Differential CD3 Usage In The Human and Mouse γδ T Cell Antigen Receptor Determines The Impact Of CD3 Deficiencies On T Cell Development

Siegers, G., Fernández-Malavé, E., Fisch, P., Regueiro, J. R., & Schamel, W. W. A. (2008). From Structure To Disease: Differential CD3 Usage In The Human and Mouse γδ T Cell Antigen Receptor Determines The Impact Of CD3 Deficiencies On T Cell Development. International Journal of Medical and Biological Frontiers, 14, 117-137.

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Siegers, Gabrielle1, Autor           
Fernández-Malavé, Edgar, Autor
Fisch, Paul, Autor
Regueiro, Jose R., Autor
Schamel, Wolfgang W. A.1, Autor           
Affiliations:
1Research Group and Chair of Molecular Immunology of the University of Freiburg, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society, ou_2243645              

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Schlagwörter: deficiency; CD3 T cell antigen receptor; gamma delta T cells; humanized mouse models
 Zusammenfassung: T cells are classified as belonging to the αβ or γδ lineage depending on which clonotypic heterodimer is incorporated into their T cell antigen receptor (TCR). Associated with αβ or γδ chains are the ζ homodimer and CD3 heterodimers, which are responsible for transducing signals across the plasma membrane into the cytoplasm, where signaling cascades ensue. The TCR is required for signaling governing such processes as development, differentiation and activation. Loss of any CD3 component leads to a block in αβ T cell development, as the signaling required for successful passage through various checkpoints becomes impaired. In mice, the CD3 subunit requirements for assembly and function of the γδTCR are different from those of the αβTCR. Recently, we have determined that they also differ between mouse and man. In this chapter, we discuss αβ and γδTCR composition and function, the novel assay we developed to determine TCR stoichiometries, and how these discoveries lead to a better understanding of CD3 deficiency phenotypes.

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Sprache(n): eng - English
 Datum: 2008
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: eDoc: 402286
 Art des Abschluß: -

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Titel: International Journal of Medical and Biological Frontiers
  Alternativer Titel : Int. J. Med. Biol. Front.
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 14 Artikelnummer: - Start- / Endseite: 117 - 137 Identifikator: -