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Autophagic activity rises only after senescence is established in cells exposed to radiation

https://repo.qst.go.jp/records/83431
https://repo.qst.go.jp/records/83431
9eac297e-b2ac-4afd-9e2d-d60290c9cfac
Item type 会議発表用資料 / Presentation(1)
公開日 2021-09-14
タイトル
タイトル Autophagic activity rises only after senescence is established in cells exposed to radiation
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Miho, Noguchi

× Miho, Noguchi

WEKO 1003560

Miho, Noguchi

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Tomokazu, Ihara

× Tomokazu, Ihara

WEKO 1003561

Tomokazu, Ihara

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Keiji, Suzuki

× Keiji, Suzuki

WEKO 1003562

Keiji, Suzuki

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Akinari, Yokoya

× Akinari, Yokoya

WEKO 1003563

Akinari, Yokoya

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Miho, Noguchi

× Miho, Noguchi

WEKO 1003564

en Miho, Noguchi

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Akinari, Yokoya

× Akinari, Yokoya

WEKO 1003565

en Akinari, Yokoya

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内容記述タイプ Abstract
内容記述 Recent studies reported that, in oncogene induced senescence, autophagy is activated during senescence initiation period to ensure rapid protein synthesis. However, senescent cells undergo metabolic and epigenetic changes during their long survival period, and autophagic activity might fluctuate with these changes. To elucidate whether autophagy fluctuates through the progress of senescence, we investigated temporal activity of autophagy over 30 days in normal human diploid cells, hTERT BJ-5ta, exposed to 20 Gy X-rays. Based on the expression levels of p21 and p16, we confirmed that the senescence-like growth arrest was surely induced after irradiation, and senescence was completely established by 7 days post-irradiation. We measured autophagic activity using quantification of LC3-II which is localized in autophagosomes. Autophagosomes are degraded by fusing with lysosomes. Autophagic activity consequently needs to be evaluated including the amount of degraded autophagosomes. We used chloroquine (CQ) as an inhibitor of lysosomal degradation and determined net LC3-II levels including those in the degraded autophagosomes. We found that LC3-II level increased to the same level as control under CQ treatment condition at 1 day after irradiation. At 3 and 7 days, the LC3-II levels with CQ were significantly lower compared to that of control with CQ. At 30 days, it turned to elevate. These results indicate that, in X-ray irradiated cells, autophagy is not significantly activated during senescence initiation, but activated after senescence is established. This delayed activation of autophagy is not seen in oncogene induced senescence, thus it might be due to radiation damage to organelles in cytoplasm.
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内容記述タイプ Other
内容記述 日本放射線影響学会第64回大会
発表年月日
日付 2021-09-22
日付タイプ Issued
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