Development of novel methods that monitor necroptosis and the release of DAMPs at the single cell resolution.

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作者： Hiroyasu,Nakano ^[1] ; Shin,Murai ^[2] ; Yoshifumi,Yamaguchi ^[1] ; Yoshitaka,Shirasaki ^[3] ; Osamu,Nakabayashi ^[4] ; Soh,Yamazaki ^[5]

作者单位： Department of Biochemistry, Toho University School of Medicine, 5-21-16 Omori-Nishi, Ota-ku, Tokyo 143-8540, Japan. ^[1] Host Defense Research Center, Toho University School of Medicine, 5-21-16 Omori-Nishi, Ota-ku, Tokyo 143-8540, Japan. ^[2] Hibernation metabolism, physiology, and development Group, Environmental Biology Division, Institute of Low Temperature Science, Hokkaido University, Kita 19, Nishi 8, Kita-ku, Sapporo, Hokkaido 060-0819, Japan. ^[3] Precursory Research for Embryonic Science and Technology, Japan Science and Technology Agency, Chiyoda-ku, Tokyo 102-0075, Japan. ^[4] Department of Biological Sciences, Graduate School of Science, The University of Tokyo, 7-3-1 Bunkyo-ku, Tokyo 113-0033, Japan. ^[5]

关键词 Forster resonance energy transfer (FRET)danger-associated molecular pattern (DAMP)s high mobility group (HMGB)1 mixed lineage kinase domain-like protein (MLKL)necroptosis receptor-interacting kinase (RIPK)3 the endosomal sorting complex required for transport (ESCRT) complex total internal reflection fluorescent microscope (TIRF-M)

DOI 10.15698/cst2019.02.177

PMID 31225501

发布时间 2020-10-01

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Cell stress

2019年3卷2期

66-69页

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Development of novel methods that monitor necroptosis and the release of DAMPs at the single cell resolution.

Cell stress

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Development of novel methods that monitor necroptosis and the release of DAMPs at the single cell resolution.

Cell stress

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Cell stress

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