Different role of Apaf-1 in positive selection, negative selection and death by 
neglect in foetal thymic organ culture

Matsuki, Y.; Zhang, H. G.; Hsu, H. C.; Yang, P. A.; Zhou, T.; Dodd, C. H.; Cecconi, F.; Gruss, P.; Tadakuma, T.; Mountz, J. D.

Datensatz

DATENSATZ AKTIONENEXPORT

Zur Ablage hinzufügen

Lokale TagsFreigabegeschichteDetailsÜbersicht

Freigegeben

Zeitschriftenartikel

Different role of Apaf-1 in positive selection, negative selection and death by neglect in foetal thymic organ culture

MPG-Autoren

/persons/resource/persons15156

Gruss, P.
Department of Molecular Cell Biology, MPI for biophysical chemistry, Max Planck Society;

Externe Ressourcen

Es sind keine externen Ressourcen hinterlegt

Volltexte (beschränkter Zugriff)

Für Ihren IP-Bereich sind aktuell keine Volltexte freigegeben.

Volltexte (frei zugänglich)

Es sind keine frei zugänglichen Volltexte in PuRe verfügbar

Ergänzendes Material (frei zugänglich)

Es sind keine frei zugänglichen Ergänzenden Materialien verfügbar

Zitation

Matsuki, Y., Zhang, H. G., Hsu, H. C., Yang, P. A., Zhou, T., Dodd, C. H., et al. (2002). Different role of Apaf-1 in positive selection, negative selection and death by neglect in foetal thymic organ culture. Scandinavian Journal of Immunology, 56(2), 174-184. Retrieved from http://onlinelibrary.wiley.com/doi/10.1046/j.1365-3083.2002.01120.x/pdf.

Zitierlink: https://hdl.handle.net/11858/00-001M-0000-0012-F345-3

Zusammenfassung

Apoptotic protease-activating factor 1 (Apaf-1) is a component of the apoptosome which is required for the activation of procaspase-9. As Apaf-1 knockout (KO) (Apaf-1(-/-)) mice die before birth, the role of Apaf-1 during thymic selection was investigated using 5 day foetal thymic organ culture (FTOC) of thymi obtained at gestational day 15. There was a lower ratio of CD4 single-positive (SP) to CD8 SP cells and decreased apoptosis of CD4(+) CD8(+) (DP) thymocytes from Apaf-1 (-/-) mice compared with wild-type. To determine if these defects resulted in increased production of neglected thymocytes, the Apaf-1 (-/-)mice were crossed with the T-cell receptor (TCR)- alpha-chain KO mice. There was no difference in thymocyte development in the thymi of TCR-alpha (-/-) Apaf-1 (-/-) and TCR-alpha (-/-) Apaf-1 (+/+) mice 5 days after FTOC. To determine if Apaf-1 is involved in apoptosis during death by negative or positive selection, FTOC of the thymus of Apaf-1 D- -/-(b)/HY TCR-alphabeta transgenic (Tg) mice was carried out. There was decreased apoptosis of the HY clonal-specific M33(+) thymocytes and an increased percentage of the autoreactive CD8(+) M33(+) thymocytes in male, but not female Apaf-1 (-/-) D-b/HY TCR Tg mice. Our data suggest that Apaf-1 is not involved in positive selection or death by neglect, but may have a partial role in negative selection during early thymic T-cell development.