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Expression of beta2 integrins (CD11a/CD18) in K562 cells.

机译:beta2整联蛋白(CD11a / CD18)在K562细胞中的表达。

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摘要

Scope and method of study. Mannheimia haemolytica is the etiological agent for an economically important pneumonic disease of cattle. A critically important virulence factor for this organism is leukotoxin (LKT), an exotoxin elaborated by M. haemolytica that destroys bovine immune cells sent to protect the host. The overall goal of this project was to characterize the interaction between LKT and the putative host cell receptor bovine CD18. Toward this goal, the strategy was to establish transfected cell lines that stably express bovine CD11a/CD18, human CD11a/CD18, or interspecies hybrids (human CD11a/bovine CD18 and bovine CD11a/human CD18). Inserts were generated by PCR of either bovine or human cDNA with CD11a or CD18 specific primers that flanked the coding sequence and included restriction sites to facilitate directional cloning and subcloning. Following generation of recombinant vectors, transfections were performed in both Vero (adherent) and K562 (non-adherent) cells. Initially, Vero cells were transfected with bovine and human CD18 recombinant vectors alone. (Abstract shortened by UMI.)
机译:研究范围和方法。溶血曼海姆病是牛的一种经济上重要的肺炎疾病的病原体。对这种生物而言,至关重要的毒力因子是白细胞毒素(LKT),这是溶血莫拉氏菌精心设计的一种外毒素,可破坏为保护宿主而发送的牛免疫细胞。该项目的总体目标是表征LKT与推定的宿主细胞受体牛CD18之间的相互作用。为了实现这个目标,该策略是建立稳定表达牛CD11a / CD18,人CD11a / CD18或种间杂种(人CD11a /牛CD18和牛CD11a /人CD18)的转染细胞系。通过牛或人cDNA的CD11a或CD18特异性引物的PCR产生插入物,该引物位于编码序列的两侧,并包含限制酶切位点以促进定向克隆和亚克隆。生成重组载体后,在Vero(贴壁)和K562(非贴壁)细胞中进行转染。最初,仅用牛和人CD18重组载体转染Vero细胞。 (摘要由UMI缩短。)

著录项

  • 作者

    Dewan, Amit.;

  • 作者单位

    Oklahoma State University.;

  • 授予单位 Oklahoma State University.;
  • 学科 Biology Molecular.
  • 学位 M.S.
  • 年度 2005
  • 页码 131 p.
  • 总页数 131
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子遗传学;
  • 关键词

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