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  1. Article ; Online: Soluble and multivalent Jag1 DNA origami nanopatterns activate Notch without pulling force.

    Smyrlaki, Ioanna / Fördős, Ferenc / Rocamonde-Lago, Iris / Wang, Yang / Shen, Boxuan / Lentini, Antonio / Luca, Vincent C / Reinius, Björn / Teixeira, Ana I / Högberg, Björn

    Nature communications

    2024  Volume 15, Issue 1, Page(s) 465

    Abstract: The Notch signaling pathway has fundamental roles in embryonic development and in the nervous system. The current model of receptor activation involves initiation via a force-induced conformational change. Here, we define conditions that reveal pulling ... ...

    Abstract The Notch signaling pathway has fundamental roles in embryonic development and in the nervous system. The current model of receptor activation involves initiation via a force-induced conformational change. Here, we define conditions that reveal pulling force-independent Notch activation using soluble multivalent constructs. We treat neuroepithelial stem-like cells with molecularly precise ligand nanopatterns displayed from solution using DNA origami. Notch signaling follows with clusters of Jag1, and with chimeric structures where most Jag1 proteins are replaced by other binders not targeting Notch. Our data rule out several confounding factors and suggest a model where Jag1 activates Notch upon prolonged binding without appearing to need a pulling force. These findings reveal a distinct mode of activation of Notch and lay the foundation for the development of soluble agonists.
    MeSH term(s) Receptors, Notch/metabolism ; Jagged-1 Protein/genetics ; Jagged-1 Protein/metabolism ; Signal Transduction/physiology ; Calcium-Binding Proteins/metabolism
    Chemical Substances Receptors, Notch ; Jagged-1 Protein ; Calcium-Binding Proteins
    Language English
    Publishing date 2024-01-18
    Publishing country England
    Document type Journal Article
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-023-44059-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Boundary cap neural crest stem cell transplants contribute Mts1/S100A4-expressing cells in the glial scar.

    Trolle, Carl / Ivert, Patrik / Hoeber, Jan / Rocamonde-Lago, Iris / Vasylovska, Svitlana / Lukanidin, Eugen / Kozlova, Elena N

    Regenerative medicine

    2017  Volume 12, Issue 4, Page(s) 339–351

    Abstract: Aim: During development, boundary cap neural crest stem cells (bNCSCs) assist sensory axon growth into the spinal cord. Here we repositioned them to test if they assist regeneration of sensory axons in adult mice after dorsal root avulsion injury.: ... ...

    Abstract Aim: During development, boundary cap neural crest stem cells (bNCSCs) assist sensory axon growth into the spinal cord. Here we repositioned them to test if they assist regeneration of sensory axons in adult mice after dorsal root avulsion injury.
    Materials & methods: Avulsed mice received bNCSC or human neural progenitor (hNP) cell transplants and their contributions to glial scar formation and sensory axon regeneration were analyzed with immunohistochemistry and transganglionic tracing.
    Results: hNPs and bNCSCs form similar gaps in the glial scar, but unlike hNPs, bNCSCs contribute Mts1/S100A4 (calcium-binding protein) expression to the scar and do not assist sensory axon regeneration.
    Conclusion: bNCSC transplants contribute nonpermissive Mts1/S100A4-expressing cells to the glial scar after dorsal root avulsion.
    Language English
    Publishing date 2017-04
    Publishing country England
    Document type Journal Article
    ZDB-ID 2274500-2
    ISSN 1746-076X ; 1746-0751
    ISSN (online) 1746-076X
    ISSN 1746-0751
    DOI 10.2217/rme-2016-0163
    Database MEDical Literature Analysis and Retrieval System OnLINE

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