Multipotent blood progenitor cells migrate into the thymus and initiate the T-cell differentiation program. T-cell progenitor cells gradually acquire T-cell characteristics while shedding their multipotentiality for alternative fates. This process is supported by extracellular signaling molecules, including Notch ligands and cytokines, provided by the thymic microenvironment. T-cell development is associated with dynamic change of gene regulatory networks of transcription factors, which interact with these environmental signals. Together with Notch or pre-T-cell-receptor (TCR) signaling, cytokines always control proliferation, survival, and differentiation of early T cells, but little is known regarding their cross talk with transcription factors. However, recent results suggest ways that cytokines expressed in distinct intrathymic niches can specifically modulate key transcription factors. This review discusses how stage-specific roles of cytokines and transcription factors can jointly guide development of early T cells.
机构:
Louisiana State Univ, Sch Vet Med, Dept Vet Microbiol & Parasitol, Baton Rouge, LA 70803 USALouisiana State Univ, Sch Vet Med, Dept Vet Microbiol & Parasitol, Baton Rouge, LA 70803 USA
机构:
Seattle Biomed Res Inst, Seattle, WA 98109 USA
Univ Washington, Dept Immunol, Seattle, WA 98195 USA
Univ Washington, Dept Pediat, Seattle, WA 98195 USASeattle Biomed Res Inst, Seattle, WA 98109 USA
Urdahl, K. B.
Shafiani, S.
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Seattle Biomed Res Inst, Seattle, WA 98109 USASeattle Biomed Res Inst, Seattle, WA 98109 USA
Shafiani, S.
Ernst, J. D.
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NYU, Sch Med, Dept Med, Div Infect Dis, New York, NY USA
NYU, Sch Med, Dept Pathol, New York, NY USA
NYU, Sch Med, Dept Microbiol, New York, NY 10016 USASeattle Biomed Res Inst, Seattle, WA 98109 USA