生物
免疫系统
设定值
免疫学
免疫
传输(电信)
FOXP3型
表观遗传学
人口
遗传学
基因
工程类
社会学
人口学
人工智能
电气工程
计算机科学
作者
Deepshika Ramanan,Esen Sefik,Silvia Galván-Peña,Meng Wu,Liang Yang,Zhen Yang,Aleksandar D. Kostic,Tatyana V. Golovkina,Dennis L. Kasper,Diane Mathis,Christophe Benoist
出处
期刊:Cell
[Elsevier]
日期:2020-05-12
卷期号:181 (6): 1276-1290.e13
被引量:140
标识
DOI:10.1016/j.cell.2020.04.030
摘要
At the species level, immunity depends on the selection and transmission of protective components of the immune system. A microbe-induced population of RORγ-expressing regulatory T cells (Tregs) is essential in controlling gut inflammation. We uncovered a non-genetic, non-epigenetic, non-microbial mode of transmission of their homeostatic setpoint. RORγ+ Treg proportions varied between inbred mouse strains, a trait transmitted by the mother during a tight age window after birth but stable for life, resistant to many microbial or cellular perturbations, then further transferred by females for multiple generations. RORγ+ Treg proportions negatively correlated with IgA production and coating of gut commensals, traits also subject to maternal transmission, in an immunoglobulin- and RORγ+ Treg-dependent manner. We propose a model based on a double-negative feedback loop, vertically transmitted via the entero-mammary axis. This immunologic mode of multi-generational transmission may provide adaptability and modulate the genetic tuning of gut immune responses and inflammatory disease susceptibility.
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