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https://hdl.handle.net/20.500.14094/0100483079
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2025-07-22
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0100483079 (fulltext)
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メタデータID
0100483079
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open access
出版タイプ
Version of Record
タイトル
Tfl deletion induces extraordinary Cxcl13 secretion and cachexia in VavP-Bcl2 transgenic mice
著者
Minagawa, Kentaro ; Wakahashi, Kanako ; Fukui, Chie ; Kawano, Yuko ; Kawano, Hiroki ; Suzuki, Tomohide ; Ishii, Shinichi ; Sada, Akiko ; Nishikawa, Shinichiro ; Asada, Noboru ; Katayama, Yoshio ; Matsui, Toshimitsu
著者名
Minagawa, Kentaro
著者名
Wakahashi, Kanako
著者名
Fukui, Chie
著者名
Kawano, Yuko
著者名
Kawano, Hiroki
著者名
Suzuki, Tomohide
著者名
Ishii, Shinichi
著者名
Sada, Akiko
著者名
Nishikawa, Shinichiro
著者名
Asada, Noboru
著者ID
A1381
研究者ID
1000080397885
KUID
https://kuid-rm-web.ofc.kobe-u.ac.jp/search/detail?systemId=6d25cff00fdea105520e17560c007669
著者名
Katayama, Yoshio
片山, 義雄
カタヤマ, ヨシオ
所属機関名
医学部附属病院
著者名
Matsui, Toshimitsu
言語
English (英語)
収録物名
Frontiers in Immunology
巻(号)
14
ページ
1197112
出版者
Frontiers Media
刊行日
2023-05-26
公開日
2023-09-11
抄録
Statement of significance: Loss of TFL, found in several types of lymphoma, induces excessive CXCL13 secretion through RNA dysregulation contributing to body weight loss and early death in lymphoma model mice. Follicular lymphoma (FL) is associated with overexpressed BCL-2 and other genetic aberrations, including 6q-. We identified a novel gene on 6q25, “Transformed follicular lymphoma (TFL),” from a transformed FL. TFL regulates several cytokines via mRNA degradation, which has been suggested to underlie resolving inflammation. Fluorescence in situ hybridization revealed a deletion of TFL occurred in 13.6% of various B-cell lymphoma samples. We developed VavP-bcl2 transgenic, TFL deficit mice (Bcl2-Tg/Tfl<sup>-/-</sup>) to seek how TFL affects disease progression in this lymphoma model. While Bcl2-Tg mice developed lymphadenopathy and died around 50 weeks, Bcl2-Tg/Tfl<sup>-/-</sup> mice lost body weight around 30 weeks and died about 20 weeks earlier than Bcl2-Tg mice. Furthermore, we found a unique B220<sup>-</sup>IgM<sup>+</sup> cell population in the bone marrow of Bcl2-Tg mice. cDNA array in this population revealed that Cxcl13 mRNA in Bcl2-Tg/Tfl<sup>-/-</sup> mice expressed significantly higher than Bcl2-Tg mice. In addition, bone marrow extracellular fluid and serum showed an extremely high Cxcl13 concentration in Bcl2-Tg/Tfl<sup>-/-</sup> mice. Among bone marrow cells, the B220<sup>-</sup>IgM<sup>+</sup> fraction was the main producer of Cxcl13 in culture. A reporter assay demonstrated TFL regulates CXCL-13 via induction of 3’UTR mRNA degradation in B lineage cells. These data suggest Tfl regulates Cxcl13 in B220<sup>-</sup>IgM<sup>+</sup> cells in the bone marrow, and a very high concentration of serum Cxcl13 arising from these cells may contribute to early death in lymphoma-bearing mice. Since several reports have suggested the association of CXCL13 expression with lymphoma, these findings provide new insights into cytokine regulation via TFL in lymphoma.
キーワード
Regnase-4
MCPIP-4
RNA regulation
Bcl-2
cachexia
カテゴリ
医学部附属病院
学術雑誌論文
権利
© 2023 Minagawa, Wakahashi, Fukui, Kawano, Kawano, Suzuki, Ishii, Sada, Nishikawa, Asada, Katayama and Matsui.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
関連情報
DOI
https://doi.org/10.3389/fimmu.2023.1197112
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資源タイプ
journal article
eISSN
1664-3224
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