Lasbury Mark E, Tang Xing, Durant Pamela J, Lee Chao-Hung
Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
Infect Immun. 2003 Sep;71(9):4943-52. doi: 10.1128/IAI.71.9.4943-4952.2003.
Alveolar macrophages from Pneumocystis carinii-infected hosts are defective in phagocytosis (W. Chen, J. W. Mills, and A. G. Harmsen, Int. J. Exp. Pathol. 73:709-720, 1992; H. Koziel et al., J. Clin. Investig. 102:1332-1344, 1998). Experiments were performed to determine whether this defect is specific for P. carinii organisms. The results showed that these macrophages were unable to phagocytose both P. carinii organisms and fluorescein isothiocyanate (FITC)-conjugated latex beads, indicating that alveolar macrophages from P. carinii-infected hosts have a general defect in phagocytosis. To determine whether this defect correlates with the recently discovered down-regulation of the GATA-2 transcription factor gene during P. carinii infection, alveolar macrophages from dexamethasone-suppressed or healthy rats were treated with anti-GATA-2 oligonucleotides and then assayed for phagocytosis. Aliquots of the alveolar macrophages were also treated with the sense oligonucleotides as the control. Cells treated with the antisense oligonucleotides were found to have a 46% reduction in phagocytosis of P. carinii organisms and a 65% reduction in phagocytosis of FITC-latex beads compared to those treated with the sense oligonucleotides. To determine whether the defect in phagocytosis in alveolar macrophages from P. carinii-infected hosts can be corrected by overexpression of GATA-2, a plasmid containing the rat GATA-2 gene in the sense orientation driven by the cytomegalovirus (CMV) promoter was introduced into alveolar macrophages from P. carinii-infected rats. Aliquots of the same cells transfected with a plasmid containing GATA-2 in the antisense orientation relative to the CMV promoter served as the control. Alveolar macrophages treated with the sense GATA-2 expression construct were found to increase their phagocytic activity by 66% in phagocytosis of P. carinii organisms and by 280% in phagocytosis of FITC-latex beads compared to those that received the antisense GATA-2 construct. The results of this study indicate that GATA-2 plays an important role in the regulation of phagocytosis in alveolar macrophages during P. carinii infection.
来自卡氏肺孢子虫感染宿主的肺泡巨噬细胞在吞噬作用方面存在缺陷(W. 陈、J. W. 米尔斯和A. G. 哈姆斯en,《国际实验病理学杂志》73:709 - 720,1992;H. 科齐尔等人,《临床研究杂志》102:1332 - 1344,1998)。进行了实验以确定这种缺陷是否是卡氏肺孢子虫生物体所特有的。结果表明,这些巨噬细胞无法吞噬卡氏肺孢子虫生物体和异硫氰酸荧光素(FITC)偶联的乳胶珠,这表明来自卡氏肺孢子虫感染宿主的肺泡巨噬细胞在吞噬作用方面存在普遍缺陷。为了确定这种缺陷是否与最近发现的卡氏肺孢子虫感染期间GATA - 2转录因子基因的下调相关,用抗GATA - 2寡核苷酸处理地塞米松抑制或健康大鼠的肺泡巨噬细胞,然后检测其吞噬作用。肺泡巨噬细胞的等分试样也用正义寡核苷酸作为对照进行处理。与用正义寡核苷酸处理的细胞相比,用反义寡核苷酸处理的细胞在吞噬卡氏肺孢子虫生物体方面吞噬作用降低了46%,在吞噬FITC - 乳胶珠方面吞噬作用降低了65%。为了确定来自卡氏肺孢子虫感染宿主的肺泡巨噬细胞吞噬作用的缺陷是否可以通过GATA - 2的过表达来纠正,将一个含有由巨细胞病毒(CMV)启动子驱动的正义方向大鼠GATA - 2基因的质粒导入来自卡氏肺孢子虫感染大鼠的肺泡巨噬细胞。用相对于CMV启动子反义方向含有GATA - 2的质粒转染的相同细胞的等分试样作为对照。与接受反义GATA - 2构建体的细胞相比,用正义GATA - 2表达构建体处理的肺泡巨噬细胞在吞噬卡氏肺孢子虫生物体方面吞噬活性增加了66%,在吞噬FITC - 乳胶珠方面吞噬活性增加了280%。这项研究的结果表明,GATA - 2在卡氏肺孢子虫感染期间肺泡巨噬细胞吞噬作用的调节中起重要作用。