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Notch1 expression in early lymphopoiesis influences B versus T lineage determination.

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TLDR
The results suggest that Notch1 provides a key regulatory signal in determining T lymphoid versus B lymphoid lineage decisions, possibly by influencing lineage commitment from a common lymphoid progenitor cell.
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This article is published in Immunity.The article was published on 1999-09-01 and is currently open access. It has received 1021 citations till now. The article focuses on the topics: Lymphopoiesis & Monocyte differentiation.

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Signals from the Sympathetic Nervous System Regulate Hematopoietic Stem Cell Egress from Bone Marrow

TL;DR: It is demonstrated that enforced HSPC egress from BM niches depends critically on the nervous system, and results indicate that the sympathetic nervous system regulates the attraction of stem cells to their niche.
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HES and HERP families: multiple effectors of the Notch signaling pathway.

TL;DR: The identification of the HERP family as a Notch effector that cooperates with HES/E(spl) family has opened a new avenue to the authors' understanding of the Notch signaling pathway.
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Induction of T Cell Development from Hematopoietic Progenitor Cells by Delta-like-1 In Vitro

TL;DR: It is established that expression of Delta-like-1 on stromal cells provides key signals for the induction of T cell lineage commitment, stage-specific progenitor expansion, TCR gene rearrangement, and T cell differentiation in the absence of a thymus.
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Metabolic regulation of T lymphocytes.

TL;DR: The role of cellular metabolism in T cell development, activation, differentiation, and function is discussed to highlight the clinical relevance and opportunities for therapeutic interventions that may be used to disrupt immune pathogenesis.
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Notch signaling is required for arterial-venous differentiation during embryonic vascular development.

TL;DR: The results suggest that notch signaling is required for the proper development of arterial and venous blood vessels, and that a major role of Notch signaling in blood vessels is to repress venous differentiation within developing arteries.
References
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PatentDOI

Production of high titer helper-free retroviruses by transient transfection

TL;DR: In this article, a method for producing high-titer, helper-free infectious retroviruses is disclosed which employs a novel strategy that uses transient transfection of new retroviral producer cell lines, ecotropic line BOSC 23 and amphotropic line CAK 8.
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TAN-1, the human homolog of the Drosophila notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms.

TL;DR: It is shown that the locus on chromosome 9 contains a gene highly homologous to the Drosophila gene Notch, which may be important for normal lymphocyte function and that alteration of TAN-1 may play a role in the pathogenesis of some T cell neoplasms.
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Resolution and characterization of pro-B and pre-pro-B cell stages in normal mouse bone marrow.

TL;DR: Functional analysis demonstrates that the proliferative response to IL-7, an early B lineage growth factor, is restricted to S7+ stages and, furthermore, that an additional, cell contact-mediated signal is essential for survival of Fr.
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Notch-1 signalling requires ligand-induced proteolytic release of intracellular domain.

TL;DR: It is shown that signalling by a constitutively active membrane-bound Notch-1 protein requires the proteolytic release of the Notch intracellular domain (NICD), which interacts preferentially with CSL.
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Deficient T cell fate specification in mice with an induced inactivation of Notch1.

TL;DR: It is suggested that Notch1 plays an obligatory and selective role in T cell lineage induction in mice with a neonatally induced loss of Notch 1 function.
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