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研究重组 GMCSF 处理的 RAW 264.7 巨噬细胞体外吞噬凋亡癌细胞的情况。

Studying in vitro phagocytosis of apoptotic cancer cells by recombinant GMCSF-treated RAW 264.7 macrophages.

机构信息

Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati 781039, Assam, India.

Centre for Nanotechnology, Indian Institute of Technology Guwahati, Guwahati 781039, Assam, India.

出版信息

Int J Biol Macromol. 2017 Sep;102:1138-1145. doi: 10.1016/j.ijbiomac.2017.05.003. Epub 2017 May 2.

Abstract

Granulocyte macrophage colony stimulating factor (GMCSF), a therapeutically important cytokine that helps in the proliferation of macrophages, was recombinantly expressed in E. coli BL21 and purified as a GST-tagged protein. Cell viability assay demonstrated significant enhancement in proliferation of RAW 264.7 (murine macrophage) in presence of GMCSF. In vitro activation of macrophages was carried out by lipopolysaccharide (LPS) or pyrogallol and probed by the generation of reactive oxygen species (ROS). Following the induction of apoptosis in A549 lung cancer cells with anticancer drug cisplatin (at 25μM), apoptotic cancer cells were effectively phagocytosed by the recombinant GMCSF-treated and exogenously activated RAW 264.7 cells as observed in fluorescence microscopic images. The current findings attribute possible role of GMCSF as adjuvant in scavenging treated cancer cells.

摘要

粒细胞巨噬细胞集落刺激因子(GMCSF)是一种具有治疗意义的细胞因子,有助于巨噬细胞的增殖,它在大肠杆菌 BL21 中被重组表达,并作为 GST 标签蛋白进行纯化。细胞活力测定表明,GMCSF 存在时 RAW 264.7(鼠巨噬细胞)的增殖显著增强。通过脂多糖(LPS)或焦儿茶酚对内源性巨噬细胞进行体外激活,并通过产生活性氧物种(ROS)进行探测。在用抗癌药物顺铂(25μM)诱导肺癌 A549 细胞凋亡后,用重组 GMCSF 处理和外源性激活的 RAW 264.7 细胞有效吞噬凋亡的癌细胞,如荧光显微镜图像所示。目前的研究结果表明 GMCSF 可能作为清除处理后的癌细胞的辅助因子发挥作用。

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