Ntal/Lab/Lat2.
Journal: 2007/August - International Journal of Biochemistry and Cell Biology
ISSN: 1357-2725
Abstract:
Non-T cell activation linker (NTAL)/linker for activation of B cells (LAB), now officially termed LAT2 (linker for activation of T cells 2) is a 25-30kDa transmembrane adaptor protein (TRAP) associated with glycolipid-enriched membrane fractions (GEMs; lipid rafts) in specific cell types of hematopoietic lineage. Tyrosine phosphorylation of NTAL/LAB/LAT2 is induced by FcvarepsilonRI aggregation and Kit dimerization in mast cells, FcgammaRI aggregation in monocytes, and BCR aggregation in B cells. NTAL/LAB/LAT2 is also expressed in resting NK cells but, unlike the related TRAP, LAT, not in resting T cells. As demonstrated in monocytes and B cells, phosphorylated NTAL/LAB/LAT2 recruits signaling molecules such as Grb2, Gab1 and c-Cbl into receptor-signaling complexes. Although gene knock out and knock down studies have indicated that NTAL/LAB/LAT2 may function as both a positive and negative regulator of mast cell activation, its precise role in the activation of these and other hematopoietic cells remains enigmatic.
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Int J Biochem Cell Biol 39(5): 868-873

NTAL/LAB/LAT2

Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Building 10, Room 11C206, 10 Center Drive, MSC 1881, Bethesda, MD 20892-1881, USA
To whom correspondence should be addressed: vog.hin.diain@nallifliga Tel: 301-496-8757 Fax: 301-480-8384
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Abstract

NTAL (non-T cell activation linker)/LAB (linker for activation of B cells), now officially termed LAT2 (linker for activation of T cells 2) is a 25-30 kD transmembrane adaptor protein (TRAP) associated with glycolipid-enriched membrane fractions (GEMs; lipid raft) in specific cell types of hematopoietic lineage. Tyrosine phosphorylation of NTAL/LAB/LAT2 is induced by FcεRI aggregation and Kit dimerization in mast cells, FcγRI aggregation in monocytes, and BCR aggregation in B cells. NTAL/LAB/LAT2 is also expressed in resting NK cells but, unlike the related TRAP, LAT, not in resting T cells. As demonstrated in monocytes and B cells, phosphorylated NTAL/LAB/LAT2 recruits signaling molecules such as Grb2, Gab1 and c-Cbl into receptor-signaling complexes. Although gene knock out and knock down studies have indicated that NTAL/LAB/LAT2 may function as both a positive and negative regulator of mast cell activation, its precise role in the activation of these and other hematopoietic cells remains enigmatic.

Keywords: NTAL, LAB, LAT2, Transmembrane adaptor protein, Mast cells
Abstract

Footnotes

Work in the authors' laboratory is supported by the NIAID Intramural Program within the National Institutes of Health and a Japan Society for the Promotion of Science research fellowship for Japanese Biomedical and Behavioral Research at National Institutes of Health to S. Iwaki.

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