FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Patel, A., Wu, Y., Han, X., Su, Y., Maugel, T., Shroff, H., Roy, S. (2022). Cytonemes coordinate asymmetric signaling and organization in the Drosophila muscle progenitor niche.  Nat. Commun. 13(1): 1185.
FlyBase ID
FBrf0252816
Publication Type
Research paper
Abstract
Asymmetric signaling and organization in the stem-cell niche determine stem-cell fates. Here, we investigate the basis of asymmetric signaling and stem-cell organization using the Drosophila wing-disc that creates an adult muscle progenitor (AMP) niche. We show that AMPs extend polarized cytonemes to contact the disc epithelial junctions and adhere themselves to the disc/niche. Niche-adhering cytonemes localize FGF-receptor to selectively adhere to the FGF-producing disc and receive FGFs in a contact-dependent manner. Activation of FGF signaling in AMPs, in turn, reinforces disc-specific cytoneme polarity/adhesion, which maintains their disc-proximal positions. Loss of cytoneme-mediated adhesion promotes AMPs to lose niche occupancy and FGF signaling, occupy a disc-distal position, and acquire morphological hallmarks of differentiation. Niche-specific AMP organization and diversification patterns are determined by localized expression and presentation patterns of two different FGFs in the wing-disc and their polarized target-specific distribution through niche-adhering cytonemes. Thus, cytonemes are essential for asymmetric signaling and niche-specific AMP organization.
PubMed ID
PubMed Central ID
PMC8897416 (PMC) (EuropePMC)
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Assignment of cell line based on information provided by the author in the Fast Track Your Paper tool.
FlyBase Curators, 2020-, Assignment of cell line based on information provided by the author in the Fast Track Your Paper tool. [FBrf0247694]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nat. Commun.
    Title
    Nature communications
    ISBN/ISSN
    2041-1723
    Data From Reference
    Alleles (31)
    Genes (18)
    Sequence Features (1)
    Cell Lines (1)
    Natural transposons (1)
    Insertions (6)
    Experimental Tools (9)
    Transgenic Constructs (29)
    Transcripts (4)