Speculations on the evolution of humoral adaptive immunity

被引:8
|
作者
Horton, Miles B. [1 ,2 ]
Hawkins, Edwin D. [1 ,2 ]
Heinzel, Susanne [1 ,2 ]
Hodgkin, Philip D. [1 ,2 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Div Immunol, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Dept Med Biol, Parkville, Vic 3010, Australia
来源
IMMUNOLOGY AND CELL BIOLOGY | 2020年 / 98卷 / 06期
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
B cells; cell fate; cell signaling; comparative immunology; evolutionary immunology; humoral immunity; proliferation; VARIABLE LYMPHOCYTE RECEPTORS; GERMINAL CENTER; MYC; SELECTION; GENES; PROTOONCOGENE; PROLIFERATION; ACTIVATION; EXPRESSION; DIVISION;
D O I
10.1111/imcb.12323
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The protection of a multicellular organism from infection, at both cell and humoral levels, has been a tremendous driver of gene selection and cellular response strategies. Here we focus on a critical event in the development of humoral immunity: The transition from principally innate responses to a system of adaptive cell selection, with all the attendant mechanical problems that must be solved in order for it to work effectively. Here we review recent advances, but our major goal is to highlight that the development of adaptive immunity resulted from the adoption, reuse and repurposing of an ancient, autonomous cellular program that combines and exploits three titratable cellular fate timers. We illustrate how this common cell machinery recurs and appears throughout biology, and has been essential for the evolution of complex organisms, at many levels of scale.
引用
收藏
页码:439 / 448
页数:10
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