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PMID: 11520458 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Subversion of the T/B lineage decision in the thymus by lunatic fringe-mediated inhibition of Notch-1.

Immunity ·Vol. 15 ·No. 2 ·2001-08-00 ·Pages 225-36

Koch U, Lacombe TA, Holland D, Bowman JL, Cohen BL, Egan SE, Guidos CJ

Abstract

Notch-1 signaling is essential for lymphoid progenitors to undergo T cell commitment, but the mechanism has not been defined. Here we show that thymocytes ectopically expressing Lunatic Fringe, a modifier of Notch-1 signaling, induce lymphoid progenitors to develop into B cells in the thymus. This cell fate switch resulted from Lunatic Fringe-mediated inhibition of Notch-1 function, as revealed by experiments utilizing lymphoid progenitors in which Notch-1 activity was genetically manipulated. These data identify Lunatic Fringe as a potent regulator of Notch-1 during the T/B lineage decision and show that an important function of Notch-1 in T cell commitment is to suppress B cell development in the thymus.

MeSH Terms
Animals B-Lymphocytes/cytology,immunology Bone Marrow Cells Cell Differentiation Cell Lineage Glycosyltransferases Membrane Proteins/antagonists & inhibitors Mice Mice, Transgenic Models, Immunological Proteins/genetics,metabolism Receptor, Notch1 Receptors, Cell Surface Recombinant Proteins/metabolism T-Lymphocytes/cytology,immunology Thymus Gland/cytology,immunology Transcription Factors
Chemicals
Membrane Proteins Notch1 protein, mouse Proteins Receptor, Notch1 Receptors, Cell Surface Recombinant Proteins Transcription Factors Glycosyltransferases Lfng protein, mouse
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Koch U
Program in Developmental Biology, Hospital for Sick Children Research Institute, Toronto, Canada.
Lacombe T A
Holland D
Bowman J L
Cohen B L
Egan S E
Guidos C J
Article Info
Journal
Immunity
Abbr.
Immunity
ISSN
1074-7613
Published
2001-08-00
Pages
225-36
Language
English
Region
United States
NLM ID
9432918
Subset
IM
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