國家衛生研究院 NHRI:Item 3990099045/12109
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    题名: Nicastrin deficiency induces tyrosinase-dependent depigmentation and skin inflammation
    作者: Hsu, CH;Liou, GG;Jiang, YJ
    贡献者: Institute of Molecular and Genomic Medicine
    摘要: Skin depigmentation diseases, such as vitiligo, are pigmentation disorders that often destroy melanocytes. However, their pathological mechanisms remain unclear and, therefore, promising treatments or prevention have been lacking. Here we demonstrate that a zebrafish insertional mutant showing a significant reduction of nicastrin transcript possesses melanosome maturation defect, Tyrosinase-dependent mitochondrial swelling and melanophore cell death. The depigmentation phenotypes are proven to be a result of gamma-secretase inactivation. Furthermore, live imaging demonstrates that macrophages are recruited to and can phagocytose melanophore debris. Thus, we characterize a potential zebrafish depigmentation disease model, nicastrin(hi1384) mutants, which can be used for further treatment/drug development of diseases related to skin depigmentation and/or inflammation.
    日期: 2020-02
    關聯: Journal of Investigative Dermatology. 2020 Feb;140(2):404-414.e13.
    Link to: http://dx.doi.org/10.1016/j.jid.2019.07.702
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0022-202X&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000508449700029
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85075398490
    显示于类别:[江運金] 期刊論文

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