生物
免疫学
体内
B细胞
分子生物学
细胞因子
Percoll公司
造血
粒细胞
造血生长因子
体外
抗体
干细胞
细胞生物学
生物化学
生物技术
作者
Vito Pistoia,Anna Corcione,Lucia Baldi,Simona Zupo,Mariella Dono,Manlio Ferrarini
出处
期刊:Stem Cells
[Oxford University Press]
日期:1996-01-01
卷期号:11 (S2): 150-155
被引量:5
标识
DOI:10.1002/stem.5530110824
摘要
In this study we have investigated the ability of human B lymphocytes to produce granulocyte-macrophage colony stimulating factor (GM-CSF) and, in preliminary experiments, granulocyte CSF (G-CSF). The sources of human B cells were surgically removed tonsils from normal individuals and peripheral blood from patients with B cell chronic lymphocytic leukemia (B-CLL). Tonsil B lymphocytes were purified by E rosetting and complement-mediated cytotoxicity with selected monoclonal antibodies and subsequently fractionated by a Percoll density gradient into in vivo activated and resting cells. The latter cell fractions were subsequently cultured with or without stimuli. GM-CSF was detected by a bioassay, G-CSF by an enzyme-linked immunoassay. In vivo and in vitro activated B cells produced GM-CSF, whereas in vivo activated, but not in vitro activated, B lymphocytes produced G-CSF. These results were confirmed by Northern blot experiments with cDNA probes specific for GM-CSF and G-CSF genes. Many B cell suspensions from B-CLL patients produced GM-CSF or G-CSF only following Staphylococcus Aureus Cowan I (SAC) stimulation; in some cases, a spontaneous production or no production at all of the two cytokines was detected. The possible implications of these results for B cell physiology and for the pathogenesis of immunologically mediated diseases will be discussed.
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