Chen Min, Kodali Srikanth, Jang Albert, Kuai Le, Wang Jin
Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX 77030
Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX 77030.
J Immunol. 2015 Mar 15;194(6):2607-15. doi: 10.4049/jimmunol.1403001. Epub 2015 Feb 11.
Autophagy is required for the long-term maintenance of Ag-specific memory B cells. However, whether autophagy is also important for the initial formation of memory B cells remains unclear. In this study, we show that newly generated memory B cells do not display active autophagy but are capable of forming Ab-secreting cells after rechallenge with Ags. Increases in autophagy took place over time after the initial formation of memory B cells. The expression of transcription factors involved in autophagy, but not changes in epigenetic regulation by DNA methylation, was required for autophagy gene expression and the development of active autophagy in memory B cells. This indicates that autophagy is not critical for the initial generation of memory B cells but is required for their long-term persistence. Our results suggest that promoting autophagy to improve Ab-dependent immunological memory is more effective during memory B cell maintenance stage.
自噬是抗原特异性记忆B细胞长期维持所必需的。然而,自噬对于记忆B细胞的初始形成是否也很重要仍不清楚。在本研究中,我们发现新产生的记忆B细胞不显示活跃的自噬,但在再次接触抗原后能够形成抗体分泌细胞。自噬在记忆B细胞初始形成后随时间增加。自噬相关转录因子的表达而非DNA甲基化引起的表观遗传调控变化是记忆B细胞中自噬基因表达和活跃自噬发展所必需的。这表明自噬对于记忆B细胞的初始产生并不关键,但对其长期存活是必需的。我们的结果表明,在记忆B细胞维持阶段促进自噬以改善抗体依赖性免疫记忆更有效。