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盘旋:CCM3 与不同的血管生成伴侣共舞。

Gyrate: CCM3 dances with a different angiogenic partner.

机构信息

Division of Cardiology and UNC McAllister Heart Institute, 8200 Medical Biomolecular Research Building, University of North Carolina, Chapel Hill, NC 27599-7126, USA.

出版信息

Sci Signal. 2010 May 18;3(122):pe17. doi: 10.1126/scisignal.3122pe17.

DOI:10.1126/scisignal.3122pe17
PMID:20484115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3328216/
Abstract

A healthy vasculature is an essential component of development and is regulated by different signaling pathways. One of the most critical pathways involved is the vascular endothelial growth factor (VEGF) pathway. Components of this pathway serve as the first marker of primitive endothelial cells and are instrumental in inducing the initial differentiation of endothelial cells and later refining them into either arteries or veins. However, the regulation of VEGF signaling remains a mystery, with most studies focusing on the downstream components of this signaling cascade. New evidence shows that the protein cerebral cavernous malformation 3 (CCM3) is a key regulator of the VEGF pathway, bringing to light a previously unknown component of the VEGF signaling axis and opening the door to an exciting new era of vasculogenic research.

摘要

健康的脉管系统是发育的重要组成部分,受不同信号通路的调节。其中一个最重要的途径是血管内皮生长因子(VEGF)途径。该途径的组成部分是原始内皮细胞的第一个标志物,有助于诱导内皮细胞的初始分化,并随后将其细化为动脉或静脉。然而,VEGF 信号的调节仍然是一个谜,大多数研究都集中在该信号级联的下游成分上。新的证据表明,蛋白脑海绵状血管畸形 3(CCM3)是 VEGF 途径的关键调节剂,揭示了 VEGF 信号轴的一个以前未知的成分,并为血管生成研究的一个令人兴奋的新时代打开了大门。

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本文引用的文献

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Stabilization of VEGFR2 signaling by cerebral cavernous malformation 3 is critical for vascular development.脑动静脉畸形 3 稳定 VEGFR2 信号对血管发育至关重要。
Sci Signal. 2010 Apr 6;3(116):ra26. doi: 10.1126/scisignal.2000722.
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Recent insights into cerebral cavernous malformations: the molecular genetics of CCM.
近期对颅内海绵状血管畸形的认识:CCM 的分子遗传学。
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Apoptotic functions of PDCD10/CCM3, the gene mutated in cerebral cavernous malformation 3.PDCD10/CCM3的凋亡功能,该基因在脑海绵状血管畸形3中发生突变
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A PP2A phosphatase high density interaction network identifies a novel striatin-interacting phosphatase and kinase complex linked to the cerebral cavernous malformation 3 (CCM3) protein.一个PP2A磷酸酶高密度相互作用网络鉴定出一种与大脑海绵状血管瘤3(CCM3)蛋白相关的新型与striatin相互作用的磷酸酶和激酶复合物。
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HOXA13 Is essential for placental vascular patterning and labyrinth endothelial specification.HOXA13对于胎盘血管模式形成和迷路内皮细胞特化至关重要。
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9
The stepwise specification of embryonic stem cells to hematopoietic fate is driven by sequential exposure to Bmp4, activin A, bFGF and VEGF.胚胎干细胞向造血命运的逐步特化是由依次暴露于Bmp4、激活素A、碱性成纤维细胞生长因子(bFGF)和血管内皮生长因子(VEGF)所驱动的。
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PDCD10 interacts with Ste20-related kinase MST4 to promote cell growth and transformation via modulation of the ERK pathway.程序性细胞死亡蛋白10(PDCD10)与Ste20相关激酶MST4相互作用,通过调节细胞外信号调节激酶(ERK)通路来促进细胞生长和转化。
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