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Ninjurin 1 mediates peripheral nerve regeneration through Schwann cell maturation of NG2-positive cells.

https://asahikawa-med.repo.nii.ac.jp/records/6174
https://asahikawa-med.repo.nii.ac.jp/records/6174
c3b4eb85-9910-48ba-93a2-2a2f2621d1ec
名前 / ファイル ライセンス アクション
7369.pdf 7369.pdf (2.8 MB)
Item type 学位論文 / Thesis or Dissertation_02(1)
公開日 2020-01-07
タイトル
タイトル Ninjurin 1 mediates peripheral nerve regeneration through Schwann cell maturation of NG2-positive cells.
言語 en
言語
言語 eng
キーワード
主題 Angiogenesis
キーワード
主題 NG2
キーワード
主題 Neurogenesis
キーワード
主題 Ninjurin1
キーワード
主題 Peripheral nerve
キーワード
主題 Schwann cells
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_db06
資源タイプ doctoral thesis
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
著者 富田, 唯

× 富田, 唯

ja 富田, 唯

ja-Kana トミタ, ユイ

en Tomita, Yui

Search repository
書誌情報 Biochemical and biophysical research communications.

巻 519, 号 3, p. 462-468, 発行日 2019-11-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0006-291X
DOI
識別子タイプ DOI
関連識別子 10.1016/j.bbrc.2019.09.007
識別番号 その他
内容記述タイプ Other
内容記述 PMID:31526566
学位授与番号
学位授与番号 甲537
学位授与年月日
学位授与年月日 2019-12-25
学位名
学位名 博士(医学)
学位授与機関
学位授与機関名 旭川医科大学
抄録
内容記述タイプ Abstract
内容記述 Ninjurin 1 (Ninj1) is identified as a peripheral nerve injury-induced protein. However, the role of Ninj1 in nerve regeneration is unclear. Schwann cells (SCs) and microvasculature are critical for peripheral nerve regeneration. SCs precursors and microvascular pericytes (PCs), which are nerve/glial antigen 2 (NG2)-positive cells are observed in peripheral nervous system. In this study, we investigated the role of Ninj1 in peripheral nerve regeneration using NG2+cell-specific inducible deletion of Ninj1 mouse model. The number of NG2+cells, which were associated with and without microvessels was increased after sciatic nerve crush injury. There was a significant increase in the expression of Ninj1 and EphA7 in the injured nerve tissue. This increase was mostly observed in NG2+cells. Genetic tracing of NG2+cells was performed using tamoxifen (Tam) treatment on NG2CreERT:R26R-tdTomato mice. The sciatic nerve was injured following the Tam-treatment, then tdTomato-expressing SCs were mostly observed in regenerated SCs at 21 days after nerve injury. Ninj1 gene knockout (Ninj1 KO) in NG2+cells was induced using NG2CreERT:Ninj1loxp mice. Tam-treated-NG2CreERT or Tam-nontreated NG2CreERT:Ninj1loxp mice were used as controls. Following Tam-treatment, the sciatic nerve in each group was injured. Ninj1KO significantly attenuated the expression of the myelin binding protein (MBP) as well as the number of myelinated axons. The expression of MBP in cultured SCs was significantly reduced by SiRNA-mediated Ninj1 knockdown (KD). Ninj1KD also attenuated the differentiation of SCs by isolated EphA7+multipotent PCs. The current data indicate that Ninj1 plays a vital role in peripheral nerve regeneration. This is observed particularly in the myelination process of NG2+cells including SCs precursors and multipotent PCs.
資源タイプ
内容記述タイプ Other
内容記述 application/pdf
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
フォーマット
内容記述タイプ Other
内容記述 application/pdf
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