Laboratory of Lymphocyte Differentiation, WPI Immunology Frontier Research Center, Osaka, Japan.
Department of Respiratory Medicine and Clinical Immunology, Graduate School of Medicine, Osaka University, Osaka, Japan.
Int Immunol. 2020 Sep 30;32(10):683-690. doi: 10.1093/intimm/dxaa042.
Antibodies produced by plasma cells are critical for protection from infection. It has been demonstrated that global epigenetic modification, such as changes in DNA methylation, occurs during differentiation of plasma cells from B cells. However, the precise mechanisms by which DNA methylation controls plasma cell differentiation are not fully understood. We examined the effect of deficiency of DNA demethylases, Tet2 and Tet3, on B-cell activation and plasma cell differentiation, by generating conditional Tet2/3 double-KO (Tet dKO) B cells. We found that Tet dKO B cells failed to differentiate into plasma cells upon immunization with antigens. Tet dKO B cells proliferated normally and were capable of generating cells with IRF4int, but not with IRF4hi, the majority of which were CD138+ plasma cells. IRF4 overexpression rescued the defect of Tet dKO B cells in plasma cell differentiation, suggesting that Tet2/3-dependent high IRF4 expression is required for plasma cell differentiation. We identified CpG sites in the Irf4 locus that were demethylated specifically in plasma cells and in a Tet2/3-dependent manner. Our results suggest that Tet2/3-dependent demethylation of these CpG sites is dispensable for initial IRF4 expression but is essential for high IRF4 expression which is prerequisite for plasma cell differentiation.
浆细胞产生的抗体对于抗感染至关重要。已经证明,在浆细胞从 B 细胞分化过程中,会发生全球表观遗传修饰,如 DNA 甲基化的改变。然而,DNA 甲基化如何控制浆细胞分化的确切机制尚不完全清楚。我们通过生成条件性 Tet2/3 双敲除(Tet dKO)B 细胞,研究了 DNA 去甲基酶 Tet2 和 Tet3 缺失对 B 细胞激活和浆细胞分化的影响。我们发现,Tet dKO B 细胞在抗原免疫后无法分化为浆细胞。Tet dKO B 细胞正常增殖,并能够产生具有 IRF4int 的细胞,但没有具有 IRF4hi 的细胞,其中大多数是 CD138+浆细胞。IRF4 的过表达挽救了 Tet dKO B 细胞在浆细胞分化中的缺陷,表明 Tet2/3 依赖性高 IRF4 表达是浆细胞分化所必需的。我们确定了 Irf4 基因座中的 CpG 位点,这些位点在浆细胞中特异性地去甲基化,并且依赖于 Tet2/3。我们的结果表明,这些 CpG 位点的 Tet2/3 依赖性去甲基化对于初始 IRF4 表达不是必需的,但对于高 IRF4 表达是必需的,高 IRF4 表达是浆细胞分化的前提。