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本文引用的文献

1
CCN3 (NOV) is a negative regulator of CCN2 (CTGF) and a novel endogenous inhibitor of the fibrotic pathway in an in vitro model of renal disease.CCN3(肾骨蛋白3)是CCN2(结缔组织生长因子)的负调节因子,在肾脏疾病的体外模型中是纤维化途径的一种新型内源性抑制剂。
Am J Pathol. 2009 May;174(5):1725-34. doi: 10.2353/ajpath.2009.080241. Epub 2009 Apr 9.
2
Molecular subsets in the gene expression signatures of scleroderma skin.硬皮病皮肤基因表达特征中的分子亚群。
PLoS One. 2008 Jul 16;3(7):e2696. doi: 10.1371/journal.pone.0002696.
3
The gene expression profile induced by Wnt 3a in NIH 3T3 fibroblasts.Wnt 3a 诱导 NIH 3T3 成纤维细胞的基因表达谱。
J Cell Commun Signal. 2007 Dec;1(3-4):175-83. doi: 10.1007/s12079-007-0015-x. Epub 2008 Jan 20.
4
Increased expression of Wnt2 and SFRP4 in Tsk mouse skin: role of Wnt signaling in altered dermal fibrillin deposition and systemic sclerosis.Wnt2和SFRP4在Tsk小鼠皮肤中的表达增加:Wnt信号在真皮原纤维蛋白沉积改变和系统性硬化症中的作用
J Invest Dermatol. 2008 Apr;128(4):871-81. doi: 10.1038/sj.jid.5701101. Epub 2007 Oct 18.
5
Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis.衰老过程中Wnt信号增加会改变肌肉干细胞命运并增加纤维化。
Science. 2007 Aug 10;317(5839):807-10. doi: 10.1126/science.1144090.
6
Smad4 cooperates with lymphoid enhancer-binding factor 1/T cell-specific factor to increase c-myc expression in the absence of TGF-beta signaling.在缺乏转化生长因子-β信号传导的情况下,Smad4与淋巴样增强子结合因子1/ T细胞特异性因子协同作用,以增加c-myc的表达。
Proc Natl Acad Sci U S A. 2006 Dec 5;103(49):18580-5. doi: 10.1073/pnas.0604773103. Epub 2006 Nov 28.
7
Microfibril-associated MAGP-2 stimulates elastic fiber assembly.微原纤维相关糖蛋白MAGP-2刺激弹性纤维组装。
J Biol Chem. 2007 Jan 5;282(1):800-8. doi: 10.1074/jbc.M609692200. Epub 2006 Nov 10.
8
Wnt and TGF-beta signaling are required for the induction of an in vitro model of primitive streak formation using embryonic stem cells.使用胚胎干细胞诱导原始条纹形成的体外模型需要Wnt和TGF-β信号传导。
Proc Natl Acad Sci U S A. 2006 Nov 7;103(45):16806-11. doi: 10.1073/pnas.0603916103. Epub 2006 Oct 31.
9
Fibrillin in Marfan syndrome and tight skin mice provides new insights into transforming growth factor-beta regulation and systemic sclerosis.马凡综合征和紧皮小鼠中的原纤蛋白为转化生长因子-β调节和系统性硬化症提供了新见解。
Curr Opin Rheumatol. 2006 Nov;18(6):582-7. doi: 10.1097/01.bor.0000245719.64393.57.
10
A critical role for endocytosis in Wnt signaling.内吞作用在Wnt信号传导中的关键作用。
BMC Cell Biol. 2006 Jul 6;7:28. doi: 10.1186/1471-2121-7-28.

细胞基质信号蛋白 CCN3 对系统性硬化症和马凡综合征中 TGF-β 和 Wnt 介导的原纤维蛋白生成的拮抗作用。

Antagonistic effect of the matricellular signaling protein CCN3 on TGF-beta- and Wnt-mediated fibrillinogenesis in systemic sclerosis and Marfan syndrome.

机构信息

Rheumatology Section, The Arthritis Center, Boston University School of Medicine, 72 E Newton Street, Boston, MA 02218, USA.

出版信息

J Invest Dermatol. 2010 Jun;130(6):1514-23. doi: 10.1038/jid.2010.15. Epub 2010 Feb 25.

DOI:10.1038/jid.2010.15
PMID:20182440
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3071475/
Abstract

Abnormal fibrillinogenesis is associated with connective tissue disorders (CTDs), including Marfan syndrome (MFS), systemic sclerosis (SSc) and Tight-skin (Tsk) mice. We have previously shown that TGF-beta and Wnt stimulate fibrillin-1 assembly and that fibrillin-1 and the developmental regulator CCN3 are both highly increased in Tsk skin. We investigated the role of CCN3 in abnormal fibrillinogenesis in Tsk mice, MFS, and SSc. Smad3 deletion in Tsk mice decreased CCN3 overexpression, suggesting that TGF-beta mediates at least part of the effect of Tsk fibrillin on CCN3 which is consistent with a synergistic effect of TGF-beta and Wnt in vitro on CCN3 expression. Disruption of fibrillin-1 assembly by MFS fibrillin decreased CCN3 expression and skin from patients with early diffuse SSc showed a strong correlation between increased CCN3 and fibrillin-1 expression, suggesting that CCN3 regulation by fibrillin-1 extends to these CTDs. Diffuse SSc skin and sera also showed evidence of increased Wnt activity, implicating a Wnt stimulus behind this correlation. CCN3 overexpression markedly repressed fibrillin-1 assembly and also blocked other TGFbeta- and Wnt-regulated profibrotic gene expression. Together, these data indicate that CCN3 counter-regulates positive signals from TGF-beta and Wnt for fibrillin fibrillogenesis and profibrotic gene expression.

摘要

异常原纤维生成与结缔组织疾病(CTD)有关,包括马凡综合征(MFS)、系统性硬化症(SSc)和紧肤(Tsk)小鼠。我们之前已经表明,TGF-β和 Wnt 刺激原纤维蛋白 1 的组装,并且原纤维蛋白 1 和发育调节剂 CCN3 在 Tsk 皮肤中都高度增加。我们研究了 CCN3 在 Tsk 小鼠、MFS 和 SSc 中原纤维蛋白异常生成中的作用。Tsk 小鼠中 Smad3 的缺失减少了 CCN3 的过表达,这表明 TGF-β至少介导了 Tsk 原纤维蛋白对 CCN3 的部分作用,这与 TGF-β和 Wnt 在体外对 CCN3 表达的协同作用一致。MFS 原纤维蛋白破坏原纤维蛋白 1 的组装,降低了 CCN3 的表达,而早期弥漫性 SSc 的皮肤显示出 CCN3 表达与原纤维蛋白 1 表达之间的强烈相关性,表明 CCN3 受原纤维蛋白 1 的调节扩展到这些 CTD。弥漫性 SSc 的皮肤和血清也显示出 Wnt 活性增加的证据,这暗示了这种相关性背后存在 Wnt 刺激。CCN3 的过表达显著抑制原纤维蛋白 1 的组装,并且还阻断了其他 TGFβ 和 Wnt 调节的促纤维化基因表达。总之,这些数据表明 CCN3 拮抗 TGF-β 和 Wnt 对原纤维蛋白原纤维生成和促纤维化基因表达的正信号。