Schwartz G N, Kessler S W, Rothwell S W, Burrell L M, Reid T J, Meltzer M S, Wright D G
Department of Hematology, Walter Reed Army Institute of Research, Washington, DC.
Exp Hematol. 1994 Dec;22(13):1288-96.
This report presents the results of studies using long-term bone marrow cultures (LTBMC) of human bone marrow cells to investigate the effect of HIV-1 on in vitro hematopoiesis. Confluent stromal cell layers established from human bone marrow cells were irradiated to eliminate residual hematopoietic progenitor cells and exposed to HIV-1ADA or to HIV-1IIIB, monocytotropic and lymphocytotropic strains of HIV-1, respectively. A productive infection did not develop in cultures exposed to HIV-1IIIB but did for cultures exposed to HIV-1ADA as there was a progressive increase in HIV-1 p24 antigen. Stromal cell layers infected with HIV-1ADA were also cocultured with autologous CD34+ bone marrow cells. Four days, 1, 2, and 3 weeks later, the number of colony-forming units granulocyte/macrophage (CFU-GM) in non- and HIV-infected LTBMC was determined. The number of CFU-GM increased during the first week in both non- and HIV-infected LTBMC. One week after the coculture of CD34+ cells with stromal cell layers infected with HIV-1ADA, the number of CFU-GM in six out of eight experiments was reduced compared to noninfected control LTBMC. In those six experiments, the number of CFU-GM was 53 +/- 6% standard error of the mean (SEM) of the number in noninfected LTBMC. A reduced number of CFU-GM was observed in the nonadherent fraction of HIV-infected LTBMC for at least 2 weeks. These results demonstrate that some cells in the stromal cell layers of LTBMC were targets for HIV-1 and that HIV-infected stromal cell layers suppressed or delayed the production of CFU-GM.
本报告展示了使用人类骨髓细胞的长期骨髓培养(LTBMC)来研究HIV - 1对体外造血作用的研究结果。从人类骨髓细胞建立的汇合基质细胞层经过辐照以消除残留的造血祖细胞,然后分别暴露于HIV - 1ADA或HIV - 1IIIB,这两种分别是HIV - 1的嗜单核细胞株和嗜淋巴细胞株。暴露于HIV - 1IIIB的培养物中未发生有效感染,但暴露于HIV - 1ADA的培养物中发生了有效感染,因为HIV - 1 p24抗原呈逐渐增加。感染了HIV - 1ADA的基质细胞层也与自体CD34 + 骨髓细胞共培养。4天、1周、2周和3周后,测定未感染和感染HIV的LTBMC中粒细胞/巨噬细胞集落形成单位(CFU - GM)的数量。在未感染和感染HIV的LTBMC中,CFU - GM的数量在第一周均增加。在将CD34 + 细胞与感染HIV - 1ADA的基质细胞层共培养1周后,与未感染的对照LTBMC相比,8个实验中有6个实验的CFU - GM数量减少。在这6个实验中,CFU - GM的数量为未感染LTBMC中数量平均标准误差(SEM)的53±6%。在感染HIV的LTBMC的非贴壁部分中,至少2周观察到CFU - GM数量减少。这些结果表明,LTBMC基质细胞层中的一些细胞是HIV - 1的靶细胞,并且感染HIV的基质细胞层抑制或延迟了CFU - GM的产生。