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Expression and Functional Analysis of Storage Protein 2 in the Silkworm Bombyx mori

机译:家蚕中贮藏蛋白2的表达及功能分析

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摘要

Storage protein 2 (SP2) not only is an important source of energy for the growth and development of silkworm but also has inhibitory effects on cell apoptosis. Endothelial cell (EC) apoptosis is an important contributing factor in the development of atherosclerosis; therefore, study of the antiapoptotic activity of SP2 on ECs provides information related to the treatment of atherosclerosis and other cardiovascular diseases. In this study, the sp2 gene was cloned and expressed in Escherichia coli to produce a 6xHis-tagged fusion protein, which was then used to generate a polyclonal antibody. Western blot results revealed that SP2 levels were higher in the pupal stage and hemolymph of fifth-instar larvae but low in the egg and adult stages. Subcellular localization results showed that SP2 is located mainly on the cell membrane. In addition, a Bac-to-Bac system was used to construct a recombinant baculovirus for SP2 expression. The purified SP2 was then added to a culture medium for human umbilical vein ECs (HUVECs), which were exposed to staurosporine. A cell viability assay demonstrated that SP2 could significantly enhance the viability of HUVEC. Furthermore, both ELISA and flow cytometry results indicated that SP2 has anti-apoptotic effects on staurosporine-induced HUVEC apoptosis.
机译:贮藏蛋白2(SP2)不仅是蚕生长发育的重要能量来源,而且对细胞凋亡具有抑制作用。内皮细胞凋亡是动脉粥样硬化发展的重要因素。因此,对SP2对EC的抗凋亡活性的研究提供了与动脉粥样硬化和其他心血管疾病的治疗有关的信息。在这项研究中,将sp2基因克隆并在大肠杆菌中表达,以产生6xHis标记的融合蛋白,然后将其用于产生多克隆抗体。 Western印迹结果表明,SP5水平在五龄幼虫的stage期和血淋巴中较高,而在卵和成年期中较低。亚细胞定位结果表明,SP2主要位于细胞膜上。另外,使用Bac-to-Bac系统构建用于SP2表达的重组杆状病毒。然后将纯化的SP2添加到暴露于星形孢菌素的人脐静脉EC(HUVEC)的培养基中。细胞活力测定表明SP2可以显着增强HUVEC的活力。此外,ELISA和流式细胞术结果均表明SP2对星形孢菌素诱导的HUVEC凋亡具有抗凋亡作用。

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