小鼠α3(IV)NC1的克隆及功能表征

Clinical medicine. Oncology Pub Date : 2008-01-01 Epub Date: 2008-02-09 DOI:10.4137/cmo.s461
Chandra Shekhar Boosani, Akulapalli Sudhakar
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引用次数: 11

摘要

IV型胶原的非胶原α3链或α3(IV)NC1,是IV型胶原的一个28 kDa的c端结构域,是内皮细胞翻译和血管生成的特异性抑制剂。本研究在杆状病毒系统中克隆并表达了小鼠α3(IV)NC1。重组蛋白以可溶性形式表达,并测试了其几种生物学功能。我们发现重组小鼠α3(IV)NC1特异性抑制内皮细胞的增殖、翻译和管形成。此外,我们发现α3(IV)NC1处理导致增殖内皮细胞特异性凋亡。此外,我们首次报道了小鼠α3(IV)NC1除抑制FAK/Akt/mTOR/4E-BP1信号外,还抑制迁移和p38 MAPK磷酸化。小鼠α3(IV)NC1治疗可抑制肿瘤生长和肿瘤内CD-31阳性内皮血管。总的来说,我们的数据证明了小鼠α3(IV)NC1在Sf-9细胞中的生物活性形式的表达,并为α3(IV)NC1在内皮细胞中的抗血管生成作用提供了重要的机制见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular Cloning and Functional Characterization of Mouse α3(IV)NC1.

Molecular Cloning and Functional Characterization of Mouse α3(IV)NC1.

Molecular Cloning and Functional Characterization of Mouse α3(IV)NC1.

Molecular Cloning and Functional Characterization of Mouse α3(IV)NC1.

Non-collagenous α3 chain of type IV collagen or α3(IV)NC1, a 28 kDa C-terminal domain of collagen type IV is a specific inhibitor of endothelial cell translation and angiogenesis. In the present study we have cloned and expressed mouse α3(IV)NC1 in baculovirus system. The recombinant protein was expressed in soluble form and tested for several of its biological functions. We identified that this recombinant mouse α3(IV)NC1 specifically inhibited proliferation, translation and tube formation of endothelial cells. Also, we show that α3(IV)NC1 treatment results in apoptosis specifically in proliferating endothelial cells. In addition we report for the first time that mouse α3(IV)NC1 inhibits migration and p38 MAPK phosphorylation in addition to inhibition of FAK/Akt/mTOR/4E-BP1 signaling. In mice α3(IV)NC1 treatment reduced tumor growth and CD-31 positive endothelial vasculature in tumors. Collectively, our data demonstrate the expression of biologically active form of mouse α3(IV)NC1 in Sf-9 cells and provide important mechanistic insights on α3(IV)NC1 antiangiogenic actions in endothelial cells.

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