Runx3 and T-box Proteins Cooperate to Establish the Transcriptional Program of Effector CTLs

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Runx3 and T-box Proteins Cooperate to Establish the Transcriptional Program of Effector CTLs

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Title: Runx3 and T-box Proteins Cooperate to Establish the Transcriptional Program of Effector CTLs
Author: Cruz-Guilloty, Fernando; Pipkin, Matthew E.; Djuretic, Ivana M.; Levanon, Ditsa; Lotem, Joseph; Lichtenheld, Mathias G.; Groner, Yoram; Rao, Anjana

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Citation: Cruz-Guilloty, Fernando, Matthew E. Pipkin, Ivana M. Djuretic, Ditsa Levanon, Joseph Lotem, Mathias G. Lichtenheld, Yoram Groner, and Anjana Rao. 2009. Runx3 and T-box proteins cooperate to establish the transcriptional program of effector CTLs. The Journal of Experimental Medicine 206:51-59.
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Abstract: Activation of naive CD8+ T cells with antigen induces their differentiation into effector cytolytic T lymphocytes (CTLs). CTLs lyse infected or aberrant target cells by exocytosis of lytic granules containing the pore-forming protein perforin and a family of proteases termed granzymes. We show that effector CTL differentiation occurs in two sequential phases in vitro, characterized by early induction of T-bet and late induction of Eomesodermin (Eomes), T-box transcription factors that regulate the early and late phases of interferon (IFN) γ expression, respectively. In addition, we demonstrate a critical role for the transcription factor Runx3 in CTL differentiation. Runx3 regulates Eomes expression as well as expression of three cardinal markers of the effector CTL program: IFN-γ, perforin, and granzyme B. Our data point to the existence of an elaborate transcriptional network in which Runx3 initially induces and then cooperates with T-box transcription factors to regulate gene transcription in differentiating CTLs.
Published Version: doi:10.1084/jem.20081242
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2626671/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:4513850

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  • FAS Scholarly Articles [7362]
    Peer reviewed scholarly articles from the Faculty of Arts and Sciences of Harvard University
 
 

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