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Cathepsin E Deficiency Impairs Autophagic Proteolysis in Macrophages
http://hdl.handle.net/10069/34179
http://hdl.handle.net/10069/3417937251f86-91f1-431d-b0c6-80d4c29c5ae2
名前 / ファイル | ライセンス | アクション |
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PLoS8_82415.pdf (865.8 kB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2014-03-05 | |||||
タイトル | ||||||
タイトル | Cathepsin E Deficiency Impairs Autophagic Proteolysis in Macrophages | |||||
言語 | ||||||
言語 | eng | |||||
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資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
著者 |
Tsukuba, Takayuki
× Tsukuba, Takayuki× Yanagawa, Michiyo× Kadowaki, Tomoko× Takii, Ryosuke× Okamoto, Yoshiko× Sakai, Eiko× Okamoto, Kuniaki× Yamamoto, Kenji |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Cathepsin E is an endosomal aspartic proteinase that is predominantly expressed in immune-related cells. Recently, we showed that macrophages derived from cathepsin E-deficient (CatE-/-) mice display accumulation of lysosomal membrane proteins and abnormal membrane trafficking. In this study, we demonstrated that CatE-/- macrophages exhibit abnormalities in autophagy, a bulk degradation system for aggregated proteins and damaged organelles. CatE-/- macrophages showed increased accumulation of autophagy marker proteins such as LC3 and p62, and polyubiquitinated proteins. Cathepsin E deficiency also altered autophagy-related signaling pathways such as those mediated by the mammalian target of rapamycin (mTOR), Akt, and extracellular signal-related kinase (ERK). Furthermore, immunofluorescence microscopy analyses showed that LC3-positive vesicles were merged with acidic compartments in wild-type macrophages, but not in CatE-/- macrophages, indicating inhibition of fusion of autophagosome with lysosomes in CatE-/- cells. Delayed degradation of LC3 protein was also observed under starvation-induced conditions. Since the autophagy system is involved in the degradation of damaged mitochondria, we examined the accumulation of damaged mitochondria in CatE-/- macrophages. Several mitochondrial abnormalities such as decreased intracellular ATP levels, depolarized mitochondrial membrane potential, and decreased mitochondrial oxygen consumption were observed. Such mitochondrial dysfunction likely led to the accompanying oxidative stress. In fact, CatE-/- macrophages showed increased reactive oxygen species (ROS) production and up-regulation of oxidized peroxiredoxin-6, but decreased antioxidant glutathione. These results indicate that cathepsin E deficiency causes autophagy impairment concomitantly with increased aberrant mitochondria as well as increased oxidative stress. | |||||
書誌情報 |
PLoS ONE 巻 8, 号 12, p. e82415, 発行日 2013-12-05 |
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出版者 | Public Library of Science | |||||
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収録物識別子タイプ | ISSN | |||||
収録物識別子 | 19326203 | |||||
DOI | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1371/journal.pone.0082415 | |||||
権利 | ||||||
権利情報 | c 2013 Tsukuba et al. | |||||
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出版タイプ | AM | |||||
出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa | |||||
引用 | ||||||
内容記述タイプ | Other | |||||
内容記述 | PLoS ONE, 8(12), e82415; 2013 |