Metabolic Regulation of the Immune Humoral Response

被引:204
作者
Boothby, Mark [1 ,2 ,3 ,4 ,5 ]
Rickert, Robert C. [6 ,7 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Pathol Microbiol & Immunol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Med Ctr, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Dept Canc Biol, Nashville, TN 37232 USA
[5] Vanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37232 USA
[6] Sanford Burnham Prebys Med Discovery Inst SBP, Tumor Microenvironm & Canc Immunol Program, La Jolla, CA 92037 USA
[7] Sanford Burnham Prebys Med Discovery Inst, NCI Designated Canc Ctr, La Jolla, CA 92037 USA
关键词
GERMINAL CENTER B; CLASS-SWITCH RECOMBINATION; T-CELL DIFFERENTIATION; EMBRYONIC STEM-CELLS; ATP-CITRATE LYASE; KINASE C-BETA; NF-KAPPA-B; MEMORY B; TRANSCRIPTION FACTORS; PLASMA-CELLS;
D O I
10.1016/j.immuni.2017.04.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Productive humoral responses require that naive B cells and their differentiated progeny move among distinct micro-environments. In this review, we discuss how studies are beginning to address the nature of these niches as well as the interplay between cellular signaling, metabolic programming, and adaptation to the locale. Recent work adds evidence to the expectation that B cells at distinct stages of development or functional subsets are influenced by the altered profiles of nutrients and metabolic by-products that distinguish these sites. Moreover, emerging findings reveal a cross-talk among the external milieu, signal transduction pathways, and transcription factors that direct B cell fate in the periphery.
引用
收藏
页码:743 / 755
页数:13
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