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  1. 広島大学の刊行物
  2. Hiroshima Journal of Medical Sciences
  3. 41巻4号

Cellular Aging and Expression of Fibronectin

https://hiroshima.repo.nii.ac.jp/records/2013311
https://hiroshima.repo.nii.ac.jp/records/2013311
1b7cf88f-4f00-44c5-8167-df26a6b3bce7
名前 / ファイル ライセンス アクション
HiroshimaJMedSci_41_101.pdf HiroshimaJMedSci_41_101.pdf (454.0 KB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル Cellular Aging and Expression of Fibronectin
言語 en
作成者 Kumazaki, Tsutomu

× Kumazaki, Tsutomu

en Kumazaki, Tsutomu

Search repository
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
主題
主題Scheme Other
主題 Cellular aging
主題
主題Scheme Other
主題 Fibroblast
主題
主題Scheme Other
主題 Fibronectin
主題
主題Scheme Other
主題 In situ hybridization
主題
主題Scheme NDC
主題 490
内容記述
内容記述 Several changes in the functional characteristics of fibronectin (FN) have been noted as cells become senescent in culture. In a previous report we showed that the steady state level of FN mRNA increases significantly during the process of in vitro cellular aging in a fibroblast strain. Because a phenomenon observed in one cell strain may not be the case in other cell strains, we extended the previous study and confirmed that this is a common phenomenon in at least two fibroblast strains of different origin. The greatest change in the proportion of cells expressing high levels of FN occurs near the end of a culture's proliferative potential. The proportion of cells unable to synthesize DNA follows a similar pattern. We also found that increasing cell size correlates closely with higher levels of FN expression. Thus, there is a clear correlation between increased FN mRNA content and in vitro cellular senescence. In order to see if this phenomenon could also be observed in cells aged in vivo, we analyzed cells aged in vivo. We found that fibroblasts from donors of higher age show lower labeling index, express a higher level of FN and come to have a larger cell area, similar to cells aged in vitro. This strongly suggests that a fibroblast in vivo ages with aging of the individual in like manner to that observed in in vitro aging cells, that is, by exhausting division potential. This supports studies using in vitro aging cells as a model for cellular aging in vivo.
言語 en
内容記述
内容記述タイプ Other
内容記述 This work was supported in part by grants-in-aid from Ministry of Education, Science and Culture of Japan ( # 02771747 and # 04836018).
出版者
出版者 Hiroshima University Medical Press
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_6501
資源タイプ departmental bulletin paper
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連情報
識別子タイプ PMID
関連識別子 1293071
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0018-2052
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AA00664312
開始ページ
開始ページ 101
書誌情報 Hiroshima Journal of Medical Sciences
Hiroshima Journal of Medical Sciences

巻 41, 号 4, p. 101-104, 発行日 1992-12
旧ID 37950
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