Institutes of Biology and Medical Sciences, Soochow University, Suzhou, China.
Department of Pathophysiology, School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China.
Front Immunol. 2018 Mar 20;9:580. doi: 10.3389/fimmu.2018.00580. eCollection 2018.
The large ZBTB family comprises a diverse group of transcriptional factors. Several ZBTB proteins have emerged as critical factors that regulate the lineage commitment, differentiation, and function of lymphoid cells as well as many other developmental events. For instance, dysfunctions of ZBTB20 or ZBTB24 have been linked to multisystem failures in humans. Within the B-cell lineage, BCL6, ZBTB7A, ZBTB17, and ZBTB1 regulate the development/differentiation of B cells in both bone marrow and peripheral lymphoid organs, while ZBTB20 and ZBTB32 seem to mainly impact the maintenance of terminal plasma cells. Given the importance of B cells in the prevention and treatment of infectious or autoimmune disorders, we herein summarize the roles of seven ZBTB family members (BCL6, ZBTB7A, ZBTB17, ZBTB20, ZBTB32, ZBTB1, and ZBTB24) in the development, differentiation, and function of B cells as well as the underlying molecular mechanisms.
ZBTB 家族是一个庞大的家族,包含多种转录因子。有几种 ZBTB 蛋白已被证明是调节淋巴细胞谱系定向、分化和功能以及许多其他发育事件的关键因素。例如,ZBTB20 或 ZBTB24 的功能障碍与人类的多系统衰竭有关。在 B 细胞谱系中,BCL6、ZBTB7A、ZBTB17 和 ZBTB1 调节骨髓和外周淋巴器官中 B 细胞的发育/分化,而 ZBTB20 和 ZBTB32 似乎主要影响终末浆细胞的维持。鉴于 B 细胞在预防和治疗感染或自身免疫性疾病方面的重要性,我们在此总结了七个 ZBTB 家族成员(BCL6、ZBTB7A、ZBTB17、ZBTB20、ZBTB32、ZBTB1 和 ZBTB24)在 B 细胞发育、分化和功能中的作用以及潜在的分子机制。