Symons D B, Clarkson C A
Immunology. 1979 Nov;38(3):503-8.
Bacterial lipopolysaccharide (LPS) from Escherichia coli labelled with tritium has been used to follow the binding of LPS to lymphocytes. Binding to cells rose to a maximum 2-7 min after addition of [3H]-LPS, followed by loss of [3H]-LPS from cells, reducing to about 10% of the peak level at 20-30 min. Peripheral blood lymphocytes, mesenteric lymph node and thymus cells of the pig and CBA, C3H/He and C3H/HeJ mouse spleen cells all bound [3H]-LPS transiently at similar levels. It is concluded that this type of LPS binding cannot be solely responsible for the preferential stimulation of B cells by LPS.
用氚标记的来自大肠杆菌的细菌脂多糖(LPS)已被用于追踪LPS与淋巴细胞的结合。加入[3H]-LPS后2 - 7分钟,与细胞的结合达到最大值,随后[3H]-LPS从细胞中丢失,在20 - 30分钟时降至峰值水平的约10%。猪的外周血淋巴细胞、肠系膜淋巴结和胸腺细胞以及CBA、C3H/He和C3H/HeJ小鼠脾细胞均以相似水平短暂结合[3H]-LPS。得出的结论是,这种类型的LPS结合不能单独解释LPS对B细胞的优先刺激作用。