Notch Signaling--constantly on the Move
Overview
Physiology
Affiliations
The Notch pathway is a highly conserved and ubiquitous signaling system that functions in determining a diverse array of cell fates and regulates many cellular processes during embryonic development and throughout adulthood. Links to cancer, stroke and Alzheimer's disease underscore the need to define the molecular basis of Notch activation. Notch signaling is induced through direct cell-cell interactions that promote receptor activation following engagement with a membrane-bound Delta, Serrate, Lag-2 (DSL) ligand on adjacent cells. Cells take on distinct fates because Notch signaling is consistently activated in only one of the two interacting cells, highlighting the importance of establishing and maintaining signaling polarity. Studies in flies and worms have identified positive and negative transcriptional feedback mechanisms that amplify small differences in Notch and DSL ligand expression to bias which cells send or receive signals. However, endocytosis by signal-sending and signal-receiving cells also appears critical for directing and regulating Notch activation. In particular, endocytosis and membrane trafficking of DSL ligands, Notch and modulators can determine the competence of cells to send or receive signals that ensure reproducibility in generating cell types regulated by Notch signaling.
Qian C, Dong G, Yang C, Zheng W, Zhong C, Shen Q Cell Commun Signal. 2025; 23(1):16.
PMID: 39789529 PMC: 11720945. DOI: 10.1186/s12964-025-02028-y.
The Biological Significance of Trogocytosis.
Agbakwuru D, Wetzel S Results Probl Cell Differ. 2024; 73:87-129.
PMID: 39242376 PMC: 11784324. DOI: 10.1007/978-3-031-62036-2_5.
The Intricate Notch Signaling Dynamics in Therapeutic Realms of Cancer.
Sen P, Ghosh S ACS Pharmacol Transl Sci. 2023; 6(5):651-670.
PMID: 37200816 PMC: 10186364. DOI: 10.1021/acsptsci.2c00239.
Germline protein, Cup, non-cell autonomously limits migratory cell fate in Drosophila oogenesis.
Saha B, Acharjee S, Ghosh G, Dasgupta P, Prasad M PLoS Genet. 2023; 19(2):e1010631.
PMID: 36791149 PMC: 9974129. DOI: 10.1371/journal.pgen.1010631.
Distinct and redundant roles for zebrafish genes during mineralization and craniofacial patterning.
Stenzel A, Mumme-Monheit A, Sucharov J, Walker M, Mitchell J, Appel B Front Endocrinol (Lausanne). 2022; 13:1033843.
PMID: 36578958 PMC: 9791542. DOI: 10.3389/fendo.2022.1033843.