4.7 Review

Launching the T-cell-lineage developmental programme

期刊

NATURE REVIEWS IMMUNOLOGY
卷 8, 期 1, 页码 9-21

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nri2232

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资金

  1. NATIONAL CANCER INSTITUTE [R01CA098925, R01CA090233] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [F32AI068366, R01AI064590] Funding Source: NIH RePORTER
  3. NCI NIH HHS [R01 CA098925-04, R01 CA098925, R01 CA090233-06A1, R01 CA98925, R01 CA90233, R01 CA090233] Funding Source: Medline
  4. NIAID NIH HHS [F32 AI068366, F32 AI068366-01, R01 AI064590-02, R01 AI064590] Funding Source: Medline

向作者/读者索取更多资源

Multipotent blood progenitor cells enter the thymus and begin a protracted differentiation process in which they gradually acquire T-cell characteristics while shedding their legacy of developmental plasticity. Notch signalling and basic helix-loop-helix E-protein transcription factors collaborate repeatedly to trigger and sustain this process throughout the period leading up to T-cell lineage commitment. Nevertheless, the process is discontinuous with separately regulated steps that demand roles for additional collaborating factors. This Review discusses new evidence on the coordination of specification and commitment in the early T-cell pathway; effects of microenvironmental signals; the inheritance of stem-cell regulatory factors; and the ensemble of transcription factors that modulate the effects of Notch and E proteins, to distinguish individual stages and to polarize T-cell-lineage fate determination.

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