在受体介导的B细胞激活控制期间的Fc受体酸化
W Hunziker1, T Koch, J A Whitney
1Department of Cell Biology, Yale University School of Medicine, New Haven, Connecticut 06510.
对IgG的Fc受体 (FcRII) 调节B细胞激活. 在B细胞上的FcRII-B1异型中的一个独特的插入物,在巨细胞中缺席,可能会调解这种抑制功能.
科学领域:
- 免疫学 免疫学 免疫学
- 细胞生物学 细胞生物学
背景情况:
- 对IgG (FcRII) 的Fc受体对免疫反应至关重要,它们调解细胞内核和巨细胞的信号传递.
- 在B细胞上,FcRII主要通过膜免疫球蛋白调节B细胞激活,经常抑制激活.
研究的目的:
- 研究B细胞和巨细胞上FcRII异型之间的结构和功能差异.
- 阐明特定氨基酸插入在FcRII-B1异型的功能中的作用.
主要方法:
- 对FcRII异型 (FcRII-B1和FcRII-B2) 的比较分析.
- 研究FcRII-B1的细胞质尾部,包括47-氨基酸插入.
- 检查插入内的血清酸化部位.
主要成果:
- 在淋巴细胞上发现的FcRII-B1异型,在其细胞质尾部具有47-氨基酸插入,在FcRII-B2巨异型中不存在.
- 这种插入阻止了FcRII-B1通过涂层坑和囊泡来调解内细胞分裂.
- 插入物中含有血清酸化部位,可能参与调节B细胞激活.
结论:
- 在B细胞和巨细胞上有不同的FcRII异型,有助于它们不同的功能作用.
- 在FcRII-B1中独特的插入导致其无法调节内细胞分裂,并可能在通过抑制信号调节B细胞激活中发挥关键作用.
更多相关视频
07:41A Kinetic Fluorescence-based Ca2+ Mobilization Assay to Identify G Protein-coupled Receptor Agonists, Antagonists, and Allosteric Modulators
Published on: February 20, 2018
06:56A Flow Cytometry-based Assay to Identify Compounds That Disrupt Binding of Fluorescently-labeled CXC Chemokine Ligand 12 to CXC Chemokine Receptor 4
Published on: March 10, 2018
相关概念视频
Receptor Downregulation in MVBs
The EGFR can initiate signaling pathways that lead to cell proliferation, migration, and differentiation. Overexpression of EGFR stimulates cells to proliferate. Excessive EGFR activation may...
Interactions Between Signaling Pathways
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
Amplifying Signals via Second Messengers
Amplifying Signals via Enzymatic Cascade
MAPK Signaling Cascades
GPCRs Regulate Adenylyl Cylase Activity
Two...
