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  1. J-7. 医薬保健研究域附属AIホスピタル・マクロシグナルダイナミクス研究開発センター
  2. j-7 10. 学術雑誌掲載論文
  3. 1. 査読済論文

Reciprocal changes in factor XIII and retinal transglutaminase expressions in the fish retina during optic nerve regeneration.

https://doi.org/10.24517/00014066
https://doi.org/10.24517/00014066
253f0af1-b4ba-4f98-97ef-de6caed2cfa9
名前 / ファイル ライセンス アクション
ME-PR-SUGITANI-K-759.pdf ME-PR-SUGITANI-K-759.pdf (178.4 kB)
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Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-03
タイトル
タイトル Reciprocal changes in factor XIII and retinal transglutaminase expressions in the fish retina during optic nerve regeneration.
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 journal article
ID登録
ID登録 10.24517/00014066
ID登録タイプ JaLC
著者 Sugitani, Kayo

× Sugitani, Kayo

WEKO 371
金沢大学研究者情報 20162258
研究者番号 20162258

Sugitani, Kayo

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Ogai, Kazuhiro

× Ogai, Kazuhiro

WEKO 23291
e-Rad 40706983

Ogai, Kazuhiro

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Koriyama, Yoshiki

× Koriyama, Yoshiki

WEKO 332
e-Rad 70397199
研究者番号 70397199

Koriyama, Yoshiki

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Kato, Satoru

× Kato, Satoru

WEKO 72
e-Rad 10019614
研究者番号 10019614

Kato, Satoru

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著者別表示 杉谷, 加代

× 杉谷, 加代

杉谷, 加代

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大貝, 和裕

× 大貝, 和裕

大貝, 和裕

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郡山, 恵樹

× 郡山, 恵樹

郡山, 恵樹

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加藤, 聖

× 加藤, 聖

加藤, 聖

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提供者所属
内容記述タイプ Other
内容記述 金沢大学医薬保健研究域医学系
書誌情報 Advances in experimental medicine and biology

巻 801, p. 759-764, 発行日 2014-01-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0065-2598
NCID
収録物識別子タイプ NCID
収録物識別子 AA00512642
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 10.1007/978-1-4614-3209-8_95
出版者
出版者 Kluwer
抄録
内容記述タイプ Abstract
内容記述 Unlike mammals, fish retinal ganglion cells have the capacity to repair their axons even after optic nerve transection. In the process of fish optic nerve regeneration, a large number of genes have been described as regeneration-associated molecules. Using molecular cloning techniques, we identified two types of cDNA clones belonging to the transglutaminase (TG) family which were upregulation genes; one is cellular factor XIII (cFXIII) and the other is a tissue type TG named retinal transglutaminase (TGR). cFXIII mRNA started to increase in the retinal ganglion cells at 1-2 days, peaked at 5-7 days, and returned to the control level by 20 days post optic nerve injury. In contrast, TGR mRNA started to increase at day 5-10, peaked at day 20, and then gradually decreased by day 40 after nerve injury. To elucidate the molecular involvement of these TGs in optic nerve regeneration, we studied the effects of recombinant TGR protein or overexpression of cFXIII using a retinal explant culture system. cFXIII effectively induced neurite outgrowth only from naïve (intact) retinas. In contrast, the TGR protein significantly enhanced neurite outgrowth only from primed retinas, in which the optic nerve had been crushed 5-7 days previously. These reciprocal expressions of cFXIII and TGR suggest that these two types of TGs are important for the neurite sprouting and axonal elongation processes, respectively, during optic nerve regeneration processes.
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
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