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Endoderm and mesoderm reciprocal signaling mediated by CXCL12 and CXCR4 regulates the migration of angioblasts and establishes the pancreatic fate

http://hdl.handle.net/2298/22845
http://hdl.handle.net/2298/22845
fb3dc090-796d-4d0b-837b-d7f80d0a5b76
名前 / ファイル ライセンス アクション
KKpaper.pdf KKpaper.pdf (1.0 MB)
Item type プレプリント / Preprint(1)
公開日 2012-01-06
タイトル
タイトル Endoderm and mesoderm reciprocal signaling mediated by CXCL12 and CXCR4 regulates the migration of angioblasts and establishes the pancreatic fate
言語
言語 eng
キーワード
主題 angioblasts, pancreatic differentiation, CXCL12, CXCR4, endoderm
資源タイプ
資源タイプ other
著者 Katsumoto, Keiichi

× Katsumoto, Keiichi

WEKO 115952

Katsumoto, Keiichi

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Kume, Shoen

× Kume, Shoen

WEKO 115953

Kume, Shoen

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別言語の著者 勝本, 恵一

× 勝本, 恵一

WEKO 115956

勝本, 恵一

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粂, 昭苑

× 粂, 昭苑

WEKO 115957

粂, 昭苑

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内容記述
内容記述 We have discovered that angioblasts trigger an early inductive event in pancreatic differentiation. This event occurs soon after gastrulation, before the formation of blood vessels. Morphological studies revealed that Lmo2-expressing angioblasts reside in proximity to the somitic mesoderm and the gut endoderm from which pancreatic progenitors arise. The chemokine ligand CXCL12 expressed in the gut endoderm functions to attract the angioblasts that express its receptor CXCR4. Angioblasts then signal back to the gut endoderm to induce Pdx1 expression. Gain-of-function and loss-of-function experiments for CXCL12 and CXCR4 were performed to test their function in blood vessel formation and pancreatic differentiation. The ectopic expression of Cxcl12 in the endoderm attracted the angioblasts and induced ectopic Pdx1 expression, resulting in an expanded pancreatic bud and an increased area of insulin-expressing cells. By contrast, in chick embryos treated with beads soaked in AMD3100, an inhibitor of CXCR4, the migration of angioblasts towards the Cxcl12-expressing gut endoderm was arrested, causing a malformation of blood vessels. This led to the generation of a smaller pancreatic bud and a reduced area of insulin-expressing cells. Taken together, these results indicate that the gut endoderm and angioblasts attract each other through reciprocal CXCL12 and CXCR4 signaling. This has a pivotal role in the fate establishment of the pancreatic progenitor cells and in the potentiation of further differentiation into endocrine β-cells.
書誌情報 Development

巻 138, p. 1947-1955, 発行日 2011-05-15
ISSN
収録物識別子 09501991
書誌レコードID
収録物識別子タイプ NCID
収録物識別子 AA10667805
DOI
関連タイプ isVersionOf
関連識別子 10.1242/dev.058719
フォーマット
内容記述タイプ Other
内容記述 application/pdf
形態
1031654 bytes
著者版フラグ
出版タイプ AO
出版タイプResource http://purl.org/coar/version/c_b1a7d7d4d402bcce
日本十進分類法
主題Scheme NDC
主題 493.47
出版者
出版者 The Company of Biologists
資源タイプ・ローカル
雑誌掲載論文
資源タイプ・NII
Preprint
資源タイプ・DCMI
text
資源タイプ・ローカル表示コード
01
URL
内容記述タイプ Other
内容記述 http://dev.biologists.org/content/138/10/1947
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