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Journal ArticleDOI

Notch Signaling: Cell Fate Control and Signal Integration in Development

Spyros Artavanis-Tsakonas, +2 more
- 30 Apr 1999 - 
- Vol. 284, Iss: 5415, pp 770-776
TLDR
Notch signaling defines an evolutionarily ancient cell interaction mechanism, which plays a fundamental role in metazoan development, providing a general developmental tool to influence organ formation and morphogenesis.
Abstract
Notch signaling defines an evolutionarily ancient cell interaction mechanism, which plays a fundamental role in metazoan development. Signals exchanged between neighboring cells through the Notch receptor can amplify and consolidate molecular differences, which eventually dictate cell fates. Thus, Notch signals control how cells respond to intrinsic or extrinsic developmental cues that are necessary to unfold specific developmental programs. Notch activity affects the implementation of differentiation, proliferation, and apoptotic programs, providing a general developmental tool to influence organ formation and morphogenesis.

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Citations
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Journal ArticleDOI

Fringe Modifies O-Fucose on Mouse Notch1 at Epidermal Growth Factor-like Repeats within the Ligand-binding Site and the Abruptex Region

TL;DR: The results reveal that Manic fringe modifies O-fucose both at the ligand-binding site (EGF 12) and in the Abruptex region, and provide insight into potential mechanisms by which Fringe action on Notch receptors may influence both the affinity of notch-ligand binding and cell-autonomous inhibition of Notch signaling by ligand.
Journal ArticleDOI

Evidence for self-renewing lung cancer stem cells and their implications in tumor initiation, progression, and targeted therapy

TL;DR: A critical summary of what is known about the role of normal and malignant lung stem cells in tumor development, the progress in characterizing lung cancer stem cells and the potential for therapeutically targeting pathways of Lung cancer stem cell self-renewal is provided.
Journal ArticleDOI

Role of epithelial cells in the pathogenesis and treatment of inflammatory bowel disease.

TL;DR: The role of epithelial cells in the pathophysiology of IBD is focused on, and a perspective to the upcoming development of regenerative therapies that may become one of the therapeutic choices to achieve mucosal healing in refractory patients of I BD is given.
Journal ArticleDOI

Transcriptional mechanisms of WNT5A based on NF-κB, Hedgehog, TGFβ, and Notch signaling cascades

TL;DR: Together these facts indicate that WNT5A is transcribed based on multiple mechanisms, such as NF-kappaB, Hedgehog, TGFbeta, and Notch signaling cascades.
Journal ArticleDOI

A soluble form of human Delta-like-1 inhibits differentiation of hematopoietic progenitor cells.

TL;DR: It is observed that hDll1(NDSL) delayed the acquisition of differentiation markers by murine hematopoietic progenitor cells (Lin-) cultured in vitro with cytokines, and promoted greater expansion of the primitive hematopolietic precursor cell population than GST controls.
References
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Journal ArticleDOI

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.
Journal ArticleDOI

Signalling downstream of activated mammalian Notch.

TL;DR: It is shown that activated forms of mNotch associate with the human analogue of Su(H), KBF2/RBP-JK and act as transcriptional activators through theKBF2-binding sites of the HES-1 promoter and block MyoD-induced myogenesis5-7.
Journal Article

Notch signaling : Signal transduction

TL;DR: The Notch/Lin-12/Glp-1 receptor family mediates the specification of numerous cell fates during development in Drosophila and Caenorhabditis elegans and putative components of the signaling cascade are identified, including a conserved family of extracellular ligands and two cellular factors that may associate with the Notch Intracellular domain.
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