4.7 Article

Positive and negative regulation of FcεRI-mediated signaling by the adaptor protein LAB/NTAL

Journal

JOURNAL OF EXPERIMENTAL MEDICINE
Volume 200, Issue 8, Pages 991-1000

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20041223

Keywords

LAT; MAPK; calcium flux; degranulation; mast cells

Funding

  1. NIAID NIH HHS [R56 AI056156, R01 AI048674, R56 AI048674, AI048674, AI056156, R01 AI056156] Funding Source: Medline

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Linker for activation of B cells (LAB, also called NTAL; a product of wbscr5 gene) is a newly identified transmembrane adaptor protein that is expressed in B cells, NK cells, and mast cells. Upon BCR activation, LAB is phosphorylated and interacts with Grb2. LAB is capable of rescuing thymocyte development in LAT-deficient mice. To study the in vivo function of LAB, LAB-deficient mice were generated. Although disruption of the Lab gene did not affect lymphocyte development, it caused mast cells to be hyperresponsive to stimulation via the FcepsilonR1, evidenced by enhanced Erk activation, calcium mobilization, degranulation, and cytokine production. These data suggested that LAB negatively regulates mast cell function. However, mast cells that lacked both linker for activation of T cells (LAT) and LAB proteins had a more severe block in FcepsilonR1-mediated signaling than LAT(-/-) mast cells, demonstrating that LAB also shares a redundant function with LAT to play a positive role in FcepsilonR1-mediated signaling.

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