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Contribution of the Runx1 transcription factor to axonal pathfinding and muscle innervation by hypoglossal motoneurons
http://hdl.handle.net/2241/00131945
http://hdl.handle.net/2241/00131945531c44e3-1b35-49b7-92f8-9ac20d437f94
名前 / ファイル | ライセンス | アクション |
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DN_75-11 (7.5 MB)
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Item type | Journal Article(1) | |||||
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公開日 | 2015-12-22 | |||||
タイトル | ||||||
タイトル | Contribution of the Runx1 transcription factor to axonal pathfinding and muscle innervation by hypoglossal motoneurons | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源 | http://purl.org/coar/resource_type/c_6501 | |||||
タイプ | journal article | |||||
著者 |
Yoshikawa, Masaaki
× Yoshikawa, Masaaki× Hirabayashi, Mizuki× Ito, Ryota× Ozaki, Shigeru× Aizawa, Shin× Masuda, Tomoyuki× Senzaki, Kouji× Shiga, Takashi |
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著者別名 |
尾崎, 繁
× 尾崎, 繁× 増田, 知之× 志賀, 隆 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The runt-related transcription factor Runx1 contributes to cell type specification and axonal targeting projections of the nociceptive dorsal root ganglion neurons. Runx1 is also expressed in the central nervous system, but little is known of its functions in brain development. At mouse embryonic day (E) 17.5, Runx1-positive neurons were detected in the ventrocaudal subdivision of the hypoglossal nucleus. Runx1-positive neurons lacked calcitonin gene-related peptide (CGRP) expression, whereas Runx1-negative neurons expressed CGRP. Expression of CGRP was not changed in Runx1-deficient mice at E17.5, suggesting that Runx1 alone does not suppress CGRP expression. Hypoglossal axon projections to the intrinsic vertical (V) and transverse (T) tongue muscles were sparser in Runx1-deficient mice at E17.5 compared to age-matched wild-type littermates. Concomitantly, vesicular acetylcholine transporter-positive axon terminals and acetylcholine receptor clusters were less dense in the V and T tongue muscles of Runx1-deficient mice. These abnormalities in axonal projection were not caused by a reduction in the total number hypoglossal neurons, failed synaptogenesis, or tongue muscles deficits. Our results implicate Runx1 in the targeting of ventrocaudal hypoglossal axons to specific tongue muscles. However, Runx1 deficiency did not alter neuronal survival or the expression of multiple motoneuron markers as in other neuronal populations. Thus, Runx1 appears to have distinct developmental functions in different brain regions. | |||||
書誌情報 |
Developmental neurobiology 巻 75, 号 11, p. 1295-1314, 発行日 2015-11 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 1932-8451 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA12195729 | |||||
PubMed番号 | ||||||
識別子タイプ | PMID | |||||
関連識別子 | 25762373 | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1002/dneu.22285 | |||||
権利 | ||||||
権利情報 | © 2015 Wiley Periodicals, Inc. | |||||
権利 | ||||||
権利情報 | This is the peer reviewed version of the following article: Develop Neurobiol 75: 1295–1314, 2015, which has been published in final form at http://onlinelibrary.wiley.com/doi/10.1002/dneu.22285. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. | |||||
著者版フラグ | ||||||
値 | author | |||||
出版者 | ||||||
出版者 | Wiley |