Huang Qizhao, Wang Haoqiang, Xu Lifan, Hu Jianjun, Wang Pengcheng, Li Yiding, Ye Lilin
Institute of Immunology, Third Military Medical University, Chongqing, 400038, China.
Methods Mol Biol. 2018;1707:95-109. doi: 10.1007/978-1-4939-7474-0_7.
B lymphocytes and their differentiated daughter cells are charged with responding to invading pathogens and producing protective antibodies against these pathogens. The physiology of B cells is intimately connected with the function of the B cell antigen receptor (BCR). Upon activation of BCR, transmembrane signals are generated, and several downstream pathways are activated, which provide a primary directive for the cell's subsequent response. mTOR is a serine/threonine kinase that controls cell proliferation and metabolism in response to a diverse range of extracellular stimuli. The activation of mTOR signaling downstream of PI3K/Akt activity by B cell receptor (BCR) engagement has been generally assumed to be essential for B cell responses. This chapter seeks to present two protocols to evaluate mTOR activity in B cells bearing BCR specific to 4-hydroxy-3-nitrophenylacetyl (NP)-hapten.
B淋巴细胞及其分化的子代细胞负责应对入侵的病原体,并产生针对这些病原体的保护性抗体。B细胞的生理学与B细胞抗原受体(BCR)的功能密切相关。BCR激活后会产生跨膜信号,并激活多个下游通路,这些通路为细胞的后续反应提供主要指令。mTOR是一种丝氨酸/苏氨酸激酶,可响应多种细胞外刺激来控制细胞增殖和代谢。一般认为,B细胞受体(BCR)结合后通过PI3K/Akt活性在下游激活mTOR信号对于B细胞反应至关重要。本章旨在介绍两种方案,用于评估携带对4-羟基-3-硝基苯基乙酰(NP)半抗原具有特异性BCR的B细胞中的mTOR活性。