Plants have emerged in the past decade as a suitable alternative to the current production systems for recombinant pharmaceutical proteins and, today their potential for low-cost production of high quality, much safer and biologically active mammalian proteins is largely documented.
Among various plant expression systems being explored, genetically modified suspension-cultured plant cells offer a promising system for production of biopharmaceuticals. Indeed, when compared to other plant-based production platforms that have been explored, suspension-cultured plant cells have the advantage of being totally devoid of problems associated with the vagaries of weather, pest, soil and gene flow in the environment. Because of short growth cycles, the timescale needed for the production of recombinant proteins in plant cell culture can be counted in days or weeks after transformation compared to months needed for the production in transgenic plants. Moreover, recovery and purification of recombinant proteins from plant biomass is an expensive and technically challenging business that may amount to 80–94% of the final product cost. One additional advantage of plant cell culture is that the recombinant protein fused with a signal sequence can be expressed and secreted into the culture medium, and therefore recovered and purified in the absence of large quantities of contaminating proteins. Consequently, the downstream processing of proteins extracted from plant cell culture medium is less expensive, which may/does balance the higher costs of fermentation. When needed for clinical use, recombinant proteins are easily produced in suspension-cultured plant cells under certified, controllable and sterile conditions that offer improved safety and provide advantages for good manufacturing practices and regulatory compliance. In this chapter, we present basic protocols for rapid generation of transgenic suspension-cultured cells of Nicotiana tabacum, Oriza sativa and Arabidopis thaliana. These systems are powerful tools for plant-made pharmaceuticals production in highly controlled conditions.
活性氮(RNS)是巨噬细胞在称为氧化爆发的过程中响应病原体而产生的一组杀菌分子。一氧化氮(NO)是由精氨酸通过诱导的一氧化氮合酶(iNOS)产生的RNS的成员。刺激后巨噬细胞产生iNOS的活性和NO是......
粒细胞-巨噬细胞集落刺激因子(granulocyte-macrophagecolony-stimulatingfactor,GM-CSF)主要由T细胞和巨噬细胞产生,能够诱导粒细胞前体和巨噬细胞前体细......
艾美捷牛粒细胞-巨噬细胞集落刺激因子/BovineGM-CSF重组蛋白中文说明书:目录编号(规格):RP0871B-005(5µg)RP0871B-025(25µg)RP0871B-100(100µg......
粒细胞-巨噬细胞集落刺激因子(GM-CSF)是由巨噬细胞、T细胞、肥大细胞、NK细胞、内皮细胞和成纤维细胞分泌的蛋白质。GM-CSF刺激干细胞产生粒细胞(中性粒细胞,嗜酸性粒细胞和嗜碱性粒细胞)和单核......