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アイテム

  1. Public
  2. 研究紀要
  3. 医学雑誌
  4. 16(1)1991

マウス腹腔内マクロファージのザイモサン貪食について

https://kindai.repo.nii.ac.jp/records/2002612
https://kindai.repo.nii.ac.jp/records/2002612
bba8f6e1-3abe-4a71-af6f-83f1655ae844
名前 / ファイル ライセンス アクション
AN00063584-19910325-0097.pdf AN00063584-19910325-0097.pdf (2.8 MB)
アイテムタイプ ☆紀要論文 / Departmental Bulletin Paper(1)
公開日 2025-03-19
タイトル
タイトル マウス腹腔内マクロファージのザイモサン貪食について
言語 ja
タイトル
タイトル Phagocytosis of zymosan by mouse peritoneal macrophages
言語 en
著者 本田, 秀明

× 本田, 秀明

ja 本田, 秀明
近畿大学

en Honda, Hideaki
Kinki University

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言語
言語 jpn
キーワード
主題 macrophages, zymosan, phagocytosis, crater, cytoskeletons, β-glucan receptor
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 AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
出版者 名前
出版者 近畿大学医学会
言語 ja
bibliographic_information ja : 近畿大学医学雑誌
en : Medical Journal of Kinki University

巻 16, 号 1, p. 97-115, 発行日 1991-03-25
ISSN
収録物識別子タイプ PISSN
収録物識別子 03858367
内容記述
内容記述タイプ Abstract
内容記述 The cell membrane and cytoskeletons of mouse peritoneal macrophages at various stages of phagocytosis of zymosan or latex particles were visualized by scanning electron microscopy (SEM). Zymosan particles were phagocytosed through the characteristic "craters" on the cell surface within 15 min of incubation. After further incubation for 15 min, the zymosan particles were engulfed into the cell and accumulated around the perinuclear region. On the other hand, latex particles were phagocytosed in the conventional style. This difference was confirmed by SEM of the cytoskeleton. At the early stage of phagocytosis, the craters appeared, and the cytoskeleton formed a basket-like shape around the zymosan particles from a distance. At the later stage of plagocytosis, zymosan particles were engulfed into the cell, and the cytoskeleton became attached to and redistributed radially around the zymosan particles at the perinuclear region. On the macrophages phagocytosing latex particles, the basket-like shape of cytoskeleton and the distance were not observed during the phagocytosis. To determine what kind of cytoskeleton distributes during the phagocytosis of zymosan, the cytoskeletons were double stained with rhodamine-phalloidin for F-actin and with indirect immunofluorescence for vimentin or actin binding proteins, α-actinin, calmodulin, clathrin, myosin or gelsolin, and observed with a phase contrast microscope equipped with epifluorescence optics. Within 15 min of incubation, F-actin accumulated and formed a ring around the zymosan particles at the peripheral region. Vimentin and actin binding proteins were also distributed in the same pattern as F-actin. After further incubation for 15 min, the ringed accumulation of cytoskeletons and actin binding proteins disappeared. The distribution of these cytoskeletons and actin binding proteins of macrophages phagocytosing latex particles was similar to that observed during zymosan phagocytosis. The effect of the major constituents of zymosan on zymosan binding to the cell membrane of macrophage at 4℃ was investigated. The yeast β-glucan and the algal β-glucan (laminarin) markedly indibited zymosan binding to the cell membrane and the inhibitory effect was does dependent, but mannan and N-acetyl-D-glucosamine did not affect it. These results suggest that, the receptor of macrophage for zymosan is the β-glucan receptor.
言語 en
内容記述
内容記述タイプ Other
内容記述 本文データはCiNiiから複製したものである。
言語 ja
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