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PMID: 17349208 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

GATA-3 - not just for Th2 cells anymore.

Cellular & molecular immunology ·Vol. 4 ·No. 1 ·2007-02-00 ·Pages 15-29

Ho IC, Pai SY

Abstract

GATA-3 was first cloned as a T cell specific transcription factor in 1991 and its importance in the transcriptional control of T helper type 2 cell (Th2) differentiation was established in the mid to late 90's. A role for GATA-3 during thymic development has long implied by its continuous and regulated expression through out T lineage development, but the absolute requirement for GATA-3 during early T lymphoid commitment/survival previously precluded definitive answers to this question. Several technical breakthroughs have fueled fruitful investigation in recent years and uncovered unexpected and critical roles for GATA-3 in CD4 thymocyte survival, invariant natural killer T cell generation and function, and also in beta selection. Not only does GATA-3 participate in nearly every stage of T cell development from common lymphoid progenitor to Th2, conditional knockout studies have indicated that the influence of GATA-3 also extends beyond the immune system.

MeSH Terms
Animals Cell Differentiation/genetics GATA3 Transcription Factor/genetics,metabolism,physiology Humans Th2 Cells/cytology,immunology Thymus Gland/cytology,immunology
Chemicals
GATA3 Transcription Factor
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ho I-Cheng
Division of Rheumatology, Immunology, and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA. iho@partners.org
Pai Sung-Yun
Article Info
Journal
Cellular & molecular immunology
Abbr.
Cell Mol Immunol
ISSN
1672-7681
Published
2007-02-00
Pages
15-29
Language
English
Region
China
NLM ID
101242872
Subset
IM
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