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New insights into bone morphogenetic protein signaling: focus on angiogenesis.骨形态发生蛋白信号传导的新见解:聚焦于血管生成。
Curr Opin Hematol. 2009 May;16(3):195-201. doi: 10.1097/MOH.0b013e32832a07d6.
2
Bone morphogenetic proteins.骨形态发生蛋白
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Endocr Metab Immune Disord Drug Targets. 2008 Sep;8(3):208-19. doi: 10.2174/187153008785700127.
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[Signal transduction of BMP/Smad and its relationship with mammalian folliculogenesis].[骨形态发生蛋白/信号转导分子Smad信号转导及其与哺乳动物卵泡发生的关系]
Yi Chuan. 2009 Mar;31(3):245-54. doi: 10.3724/sp.j.1005.2009.00245.
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BMP/SMAD Pathway Promotes Neurogenesis of Midbrain Dopaminergic Neurons and in Human Induced Pluripotent and Neural Stem Cells.BMP/SMAD 通路促进中脑多巴胺能神经元的神经发生,以及在人诱导多能干细胞和神经干细胞中。
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6
Emerging role of bone morphogenetic proteins in angiogenesis.骨形态发生蛋白在血管生成中的新作用。
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Mechanism for the action of bone morphogenetic proteins and regulation of their activity.骨形态发生蛋白的作用机制及其活性调节
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Sequential roles for myosin-X in BMP6-dependent filopodial extension, migration, and activation of BMP receptors.肌球蛋白-X在骨形态发生蛋白6(BMP6)依赖的丝状伪足延伸、迁移及BMP受体激活过程中的顺序作用
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Biol Reprod. 2006 Jun;74(6):1073-82. doi: 10.1095/biolreprod.105.047969. Epub 2006 Jan 25.

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BMP8B Activates Both SMAD2/3 and NF-κB Signals to Inhibit the Differentiation of 3T3-L1 Preadipocytes into Mature Adipocytes.BMP8B 通过激活 SMAD2/3 和 NF-κB 信号通路抑制 3T3-L1 前脂肪细胞向成熟脂肪细胞分化。
Nutrients. 2023 Dec 25;16(1):64. doi: 10.3390/nu16010064.
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Endothelial cell SMAD6 balances Alk1 function to regulate adherens junctions and hepatic vascular development.内皮细胞 SMAD6 平衡 Alk1 功能以调节黏附连接和肝血管发育。
Development. 2023 Nov 1;150(21). doi: 10.1242/dev.201811. Epub 2023 Nov 3.
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Bmp8a deletion leads to obesity through regulation of lipid metabolism and adipocyte differentiation.Bmp8a 缺失通过调节脂质代谢和脂肪细胞分化导致肥胖。
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BMP Signaling Pathway in Dentin Development and Diseases.BMP 信号通路在牙本质发育和疾病中的作用。
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The versatility and paradox of BMP signaling in endothelial cell behaviors and blood vessel function.BMP 信号在血管内皮细胞行为和血管功能中的多功能性和矛盾性。
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In ovariectomy-induced osteoporotic rat models, BMP-2 substantially reversed an impaired alveolar bone regeneration whereas PDGF-BB failed.在去卵巢诱导骨质疏松症大鼠模型中,BMP-2 显著逆转了受损的牙槽骨再生,而 PDGF-BB 则没有。
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Adipose tissue plasticity and the pleiotropic roles of BMP signaling.脂肪组织的可塑性和 BMP 信号的多效性作用。
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It Takes Two to Tango: Endothelial TGFβ/BMP Signaling Crosstalk with Mechanobiology.二人转:血管内皮 TGFβ/BMP 信号转导与机械生物学。
Cells. 2020 Aug 26;9(9):1965. doi: 10.3390/cells9091965.

本文引用的文献

1
BMPER is an endothelial cell regulator and controls bone morphogenetic protein-4-dependent angiogenesis.BMPER是一种内皮细胞调节剂,可控制骨形态发生蛋白-4依赖性血管生成。
Circ Res. 2008 Oct 10;103(8):804-12. doi: 10.1161/CIRCRESAHA.108.178434. Epub 2008 Sep 11.
2
Crossveinless-2 Is a BMP feedback inhibitor that binds Chordin/BMP to regulate Xenopus embryonic patterning.无横脉-2是一种骨形态发生蛋白(BMP)反馈抑制剂,它与脊索蛋白/骨形态发生蛋白结合以调节非洲爪蟾胚胎模式形成。
Dev Cell. 2008 Aug;15(2):248-60. doi: 10.1016/j.devcel.2008.06.013.
3
Chordin-like 1, a bone morphogenetic protein-4 antagonist, is upregulated by hypoxia in human retinal pericytes and plays a role in regulating angiogenesis.类脊索蛋白1,一种骨形态发生蛋白-4拮抗剂,在人视网膜周细胞中因缺氧而上调,并在调节血管生成中起作用。
Mol Vis. 2008 Jun 20;14:1138-48.
4
SMAD proteins control DROSHA-mediated microRNA maturation.SMAD蛋白控制DROSHA介导的微小RNA成熟。
Nature. 2008 Jul 3;454(7200):56-61. doi: 10.1038/nature07086. Epub 2008 Jun 11.
5
The BMP-binding protein Crossveinless 2 is a short-range, concentration-dependent, biphasic modulator of BMP signaling in Drosophila.骨形态发生蛋白结合蛋白Crossveinless 2是果蝇中骨形态发生蛋白信号传导的一种短程、浓度依赖性双相调节剂。
Dev Cell. 2008 Jun;14(6):940-53. doi: 10.1016/j.devcel.2008.03.023.
6
Angiopoietin-1 mediates the proangiogenic activity of the bone morphogenic protein antagonist Drm.血管生成素-1介导骨形态发生蛋白拮抗剂Drm的促血管生成活性。
Blood. 2008 Aug 15;112(4):1154-7. doi: 10.1182/blood-2007-09-111450. Epub 2008 May 27.
7
Crystal structure analysis reveals how the Chordin family member crossveinless 2 blocks BMP-2 receptor binding.晶体结构分析揭示了脊索蛋白家族成员交叉无翅 2 如何阻断骨形态发生蛋白-2 受体结合。
Dev Cell. 2008 May;14(5):739-50. doi: 10.1016/j.devcel.2008.02.017.
8
Bone morphogenetic protein-9 is a circulating vascular quiescence factor.骨形态发生蛋白-9是一种循环血管静止因子。
Circ Res. 2008 Apr 25;102(8):914-22. doi: 10.1161/CIRCRESAHA.107.165530. Epub 2008 Feb 28.
9
Implication of microRNAs in the cardiovascular system.微小RNA在心血管系统中的作用
Curr Opin Pharmacol. 2008 Apr;8(2):181-8. doi: 10.1016/j.coph.2007.12.013. Epub 2008 Feb 19.
10
Sequential roles for myosin-X in BMP6-dependent filopodial extension, migration, and activation of BMP receptors.肌球蛋白-X在骨形态发生蛋白6(BMP6)依赖的丝状伪足延伸、迁移及BMP受体激活过程中的顺序作用
J Cell Biol. 2007 Dec 31;179(7):1569-82. doi: 10.1083/jcb.200704010. Epub 2007 Dec 24.

骨形态发生蛋白信号传导的新见解:聚焦于血管生成。

New insights into bone morphogenetic protein signaling: focus on angiogenesis.

作者信息

Moreno-Miralles Isabel, Schisler Jonathan C, Patterson Cam

机构信息

Carolina Cardiovascular Biology Center, USA.

出版信息

Curr Opin Hematol. 2009 May;16(3):195-201. doi: 10.1097/MOH.0b013e32832a07d6.

DOI:10.1097/MOH.0b013e32832a07d6
PMID:19346940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3432307/
Abstract

PURPOSE OF REVIEW

The role of bone morphogenetic proteins (BMPs) in vasculogenesis is still not well understood, despite many recent developments in this area of research. In this review, we discuss the most recent studies that identify new critical mechanisms through which BMP signaling acts with a focus on angiogenesis.

RECENT FINDINGS

New evidence brought to light over the last few years suggests that BMP-binding proteins, formerly thought of as antagonists, can also increase BMP activity under certain conditions. It has also recently been determined that components of the extracellular matrix are involved in the BMP signaling pathways that regulate angiogenesis. Through the BMP pathway, myosin-X and cyclooxygenase 2 serve as target genes that have been determined to play a role in blood vessel formation. BMPs also conduct Smad-independent signaling and crosstalk with other pathways. Finally, BMPs have been shown to play an antiangiogenic role in specific settings.

SUMMARY

Better understanding of the BMP signaling pathway and its regulators can have potentially great effects on therapeutic strategies from cardiovascular disease to cancer.

摘要

综述目的

尽管骨形态发生蛋白(BMPs)在血管生成方面的研究最近有许多进展,但人们对其在血管发生中的作用仍未完全了解。在本综述中,我们讨论了最新研究,这些研究确定了BMP信号传导发挥作用的新关键机制,重点是血管生成。

最新发现

过去几年中发现的新证据表明,以前被认为是拮抗剂的BMP结合蛋白在某些条件下也可以增加BMP活性。最近还确定,细胞外基质的成分参与调节血管生成的BMP信号通路。通过BMP途径,肌球蛋白-X和环氧化酶2作为已确定在血管形成中起作用的靶基因。BMP还进行不依赖Smad的信号传导并与其他途径发生串扰。最后,已证明BMP在特定环境中发挥抗血管生成作用。

总结

更好地了解BMP信号通路及其调节剂可能对从心血管疾病到癌症的治疗策略产生潜在的重大影响。