肠道等离子体细胞中IgA分泌的限制是由一个特定于组织的糖解程序驱动的
Victoria Zoccoli-Rodriguez1, John D Iwaniec1, Joel R Wilmore1
1Department of Microbiology and Immunology, State University of New York Upstate Medical University, Syracuse, NY, United States.
Journal of immunology (Baltimore, Md. : 1950)
|December 3, 2025
概括
肠道IgA+血细胞 (PCs) 使用糖解,限制抗体分泌. 抑制糖解会增加抗体的产生,揭示组织特异性的代谢调节,以改善粘膜免疫和疫苗.
科学领域:
- 免疫学 免疫学 免疫学
- 细胞的新陈代谢
- 粘膜免疫力 粘膜免疫力
背景情况:
- 分泌IgA的血细胞 (PCs) 对于粘膜和全身部位的幽默免疫至关重要.
- 肠道和骨髓 (BM) PCs在抗体分泌方面有所不同,肠道PCs每细胞分泌的较少.
- 代谢严重影响PC功能,但肠道PC代谢研究不足.
研究的目的:
- 为了研究组织寄存IgA+PCs所使用的代谢途径.
- 确定细胞代谢如何影响肠道PC中的抗体分泌.
- 了解PC功能的特定组织代谢调节.
主要方法:
- 利用SCENITH试验分析肠道和BM IgA+ PC中的代谢途径.
- 在PC中评估葡萄糖摄取量,mTORC1活性和活性氧物种 (ROS).
- 采用代谢抑制剂以准生物能途径并评估对抗体分泌的影响.
主要成果:
- 肠道IgA+PCs表现出增加的糖分分解能力,高葡萄糖吸收,高mTORC1活性和低ROS.
- BM IgA+ PCs 显示线粒体依赖性增加.
- 抑制糖解增强了抗体分泌,而抑制氧化酸化则限制了它.
结论:
- 组织特定的代谢程序调节PC功能.
- 糖溶解限制了肠道IgA+PC中的抗体分泌.
- 准代谢途径可以优化对肠道平衡,粘膜病原体和疫苗的抗体反应.
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