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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

Notch activation stimulates migration of breast cancer cells and promotes tumor growth

TL;DR: These results confirm NOTCH1 as a signal triggering epithelial-mesenchymal transition in epithelial cancer cells, which may have implications in tumor dissemination, metastasis and proliferation in vivo.
Journal ArticleDOI

Isolation and characterization of functional mammary gland stem cells.

TL;DR: Recent data on mammary epithelial stem/progenitor cells in genetically engineered mouse models suggest that the heterogeneity of mouse models of breast cancer may partially reflect the selection or expansion of different progenitors.
Journal Article

Mesenchymal progenitor cells in adult human articular cartilage.

TL;DR: It is demonstrated that normal articular cartilage contains Notch-1+ cells and that the frequency is increased in OA, and the possibility that these progenitor cells might be involved in the pathogenesis of arthritis is raised.
Journal ArticleDOI

Jagged1 protein enhances the differentiation of mesenchymal stem cells into cardiomyocytes

TL;DR: It is shown that MSC differentiation into cardiomyocytes is dependent on the Notch signal, and Jagged1 protein can activate NotCh signal and enhance the differentiation of MSC intoCardiomyocyte, while the effect can be inhibited by DAPT.
Journal ArticleDOI

Intrinsic and Extrinsic Mechanisms of Dendritic Morphogenesis

TL;DR: This review summarizes the major experimental systems that have contributed to the understandings of dendritic development as well as the intrinsic and extrinsic mechanisms that instruct the neurons to form cell type-specific dendrite arbors.
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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