Academic Journal

Syk facilitates phagosome-lysosome fusion by regulating actin-remodeling in complement-mediated phagocytosis

التفاصيل البيبلوغرافية
العنوان: Syk facilitates phagosome-lysosome fusion by regulating actin-remodeling in complement-mediated phagocytosis
المؤلفون: Tabata, Hiroyuki, Morita, Hiroyuki, Kaji, Hiroaki, Tohyama, Kaoru, Tohyama, Yumi
المساهمون: Grant-in-Aid for Scientific Research (KAKENHI) from Japan Society for the Promotion of Science, Grant program for biomedical engineering research from Nakatani Foundation
المصدر: Scientific Reports ; volume 10, issue 1 ; ISSN 2045-2322
بيانات النشر: Springer Science and Business Media LLC
سنة النشر: 2020
الوصف: Effective phagocytosis is crucial for host defense against pathogens. Macrophages entrap pathogens into a phagosome and subsequently acidic lysosomes fuse to the phagosome. Previous studies showed the pivotal role of actin-remodeling mediated by phosphoinositide-related signaling in phagosome formation, but the mechanisms of phagosome-lysosome fusion remain unexplored. Here we show that in complement-mediated phagocytosis, phagosome-lysosome fusion requires the disappearance of F-actin structure surrounding the phagosome and a tyrosine kinase Syk plays a key role in this process. Using macrophage-like differentiated HL60 and Syk-knockout (Syk-KO) HL60 cells, we found that Syk-KO cells showed insufficient phagosome acidification caused by impaired fusion with lysosomes and permitted the survival of Candida albicans in complement-mediated phagocytosis. Phagosome tracking analysis showed that during phagosome internalization process, F-actin surrounding phagosomes disappeared in both parental and Syk-KO cells but this structure was reconstructed immediately only in Syk-KO cells. In addition, F-actin-stabilizing agent induced a similar impairment of phagosome-lysosome fusion. Collectively, Syk-derived signaling facilitates phagosome-lysosome fusion by regulating actin-remodeling.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1038/s41598-020-79156-7
الاتاحة: http://dx.doi.org/10.1038/s41598-020-79156-7
https://www.nature.com/articles/s41598-020-79156-7.pdf
https://www.nature.com/articles/s41598-020-79156-7
Rights: https://creativecommons.org/licenses/by/4.0 ; https://creativecommons.org/licenses/by/4.0
رقم الانضمام: edsbas.DE1BBEA
قاعدة البيانات: BASE
الوصف
DOI:10.1038/s41598-020-79156-7