Boosani Chandra Shekhar, Sudhakar Akulapalli
Cell Signaling and Tumor Angiogenesis Laboratory, Department of Genetics, Boys Town National Research Hospital, Omaha, Nebraska, U.S.A.
Clin Med Oncol. 2008;2:73-81. doi: 10.4137/cmo.s461. Epub 2008 Feb 9.
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.
IV型胶原的非胶原α3链或α3(IV)NC1,即IV型胶原28 kDa的C末端结构域,是内皮细胞翻译和血管生成的特异性抑制剂。在本研究中,我们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,并对其多种生物学功能进行了测试。我们发现这种重组小鼠α3(IV)NC1能特异性抑制内皮细胞的增殖、翻译和管腔形成。此外,我们表明α3(IV)NC1处理可特异性诱导增殖内皮细胞凋亡。另外,我们首次报道小鼠α3(IV)NC1除了抑制FAK/Akt/mTOR/4E-BP1信号传导外,还能抑制迁移和p38 MAPK磷酸化。在小鼠中,α3(IV)NC1处理可减少肿瘤生长以及肿瘤中CD-31阳性的内皮血管。总体而言,我们的数据证明了小鼠α3(IV)NC1生物活性形式在Sf-9细胞中的表达,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。