Schröder J, Turunen O, Lundqvist C, de la Chapelle A
Acta Pathol Microbiol Scand C. 1978 Dec;86C(6):315-9. doi: 10.1111/j.1699-0463.1978.tb02596.x.
T- and B-lymphocyte markers were studied in cord blood cells cultured with lipopolysaccharide B (LPS). Cells cultured with leucoagglutinin (LA) and pokeweed mitogen (PWM) were used as controls. LPS-induced lymphoblasts were negative for surface Ig, positive for intracellular Ig and did not form rosettes with sheep red blood cells (SRBC). LA-activated cells formed rosettes with SRBC, while PWM cultures showed a varying proportion of surface Ig-positive or SRBC rosetting cells, dependent on the time of culture. About 50% of both LA- and LPS-activated lymphoblasts formed EA rosettes (specific for Fc receptors) and EAC rosettes (specific for complement receptors). The response of foetal cells to LPS was reduced when lymphocytes obtained from Isopaque-Ficoll gradients were passed through nylon wool columns, whereas this procedure led to an increased response to LA. Thus LPS-activated foetal leucocytes are B lymphocytes expressing intracellular but not surface Ig.
在用脂多糖B(LPS)培养的脐血细胞中研究了T和B淋巴细胞标志物。用白细胞凝集素(LA)和商陆有丝分裂原(PWM)培养的细胞用作对照。LPS诱导的淋巴母细胞表面Ig呈阴性,细胞内Ig呈阳性,且不与绵羊红细胞(SRBC)形成玫瑰花结。LA激活的细胞与SRBC形成玫瑰花结,而PWM培养物中表面Ig阳性或SRBC玫瑰花结形成细胞的比例因培养时间而异。大约50%的LA和LPS激活的淋巴母细胞形成EA玫瑰花结(对Fc受体特异)和EAC玫瑰花结(对补体受体特异)。当从Isopaque-Ficoll梯度获得的淋巴细胞通过尼龙毛柱时,胎儿细胞对LPS的反应降低,而此程序导致对LA的反应增加。因此,LPS激活的胎儿白细胞是表达细胞内而非表面Ig的B淋巴细胞。