Genomics Research Center, Academia Sinica, 128 Academia Road, Sec. 2, Nankang Dist, Taipei, 115, Taiwan.
Graduate Institute of Immunology, College of Medicine, National Taiwan University, Taipei, 110, Taiwan.
J Biomed Sci. 2019 Sep 1;26(1):64. doi: 10.1186/s12929-019-0558-1.
Terminally differentiated B cell, the plasma cell, is the sole cell type capable of producing antibodies in our body. Over the past 30 years, the identification of many key molecules controlling B cell activation and differentiation has elucidated the molecular pathways for generating antibody-producing plasma cells. Several types of regulation modulating the functions of the important key molecules in B cell activation and differentiation add other layers of complexity in shaping B cell responses following antigen exposure in the absence or presence of T cell help. Further understanding of the mechanisms contributing to the proper activation and differentiation of B cells into antibody-secreting plasma cells may enable us to develop new strategies for managing antibody humoral responses during health and disease. Herein, we reviewed the effect of different types of regulation, including transcriptional regulation, post-transcriptional regulation and epigenetic regulation, on B cell activation, and on mounting memory B cell and antibody responses. We also discussed the link between the dysregulation of the abovementioned regulatory mechanisms and B cell-related disorders.
终末分化的 B 细胞,即浆细胞,是体内唯一能够产生抗体的细胞类型。在过去的 30 年中,许多控制 B 细胞激活和分化的关键分子的鉴定阐明了产生产生抗体的浆细胞的分子途径。几种类型的调节可以调节 B 细胞激活和分化过程中重要关键分子的功能,从而在缺乏或存在 T 细胞帮助的情况下,在抗原暴露后进一步增加 B 细胞反应的复杂性。进一步了解有助于 B 细胞正确激活和分化为抗体分泌浆细胞的机制,可能使我们能够在健康和疾病期间开发出管理抗体体液反应的新策略。在此,我们综述了包括转录调节、转录后调节和表观遗传调节在内的不同类型的调节对 B 细胞激活以及记忆 B 细胞和抗体反应的影响。我们还讨论了上述调节机制失调与 B 细胞相关疾病之间的联系。