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Asymmetric Notch activity by differential inheritance of lysosomes in human neural stem cells
Author(s) -
Bettina Bohl,
Ammar Jabali,
Julia Ladewig,
Philipp Koch
Publication year - 2022
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.abl5792
Subject(s) - notch signaling pathway , microbiology and biotechnology , neural stem cell , mitosis , biology , hes1 , stem cell , cell division , asymmetric cell division , notch proteins , lysosome , cell fate determination , organoid , notch 1 , receptor , signal transduction , cell , genetics , gene , biochemistry , transcription factor , enzyme
Symmetric and asymmetric cell divisions are conserved strategies for stem cell expansion and the generation of more committed progeny, respectively. Here, we demonstrate that in human neural stem cells (NSCs), lysosomes are asymmetrically inherited during mitosis. We show that lysosomes contain Notch receptors and that Notch activation occurs the acidic lysosome environment. The lysosome asymmetry correlates with the expression of the Notch target geneHES1 and the activity of Notch signaling in the daughter cells. Furthermore, an asymmetry of lysosomes and Notch receptors was also observed in a human organoid model of brain development with mitotic figures showing preferential inheritance of lysosomes and Notch receptor in that daughter cell remaining attached to the apical membrane. Thus, this study suggests a previously unknown function of lysosomes as a signaling hub to establish a bias in Notch signaling activity between daughter cells after an asymmetric cell division of human NSCs.

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