Institute of Biochemistry and Molecular Biology, College of Life and Health Sciences, Northeastern University, Shenyang 110819, China.
Int J Mol Sci. 2024 May 2;25(9):4962. doi: 10.3390/ijms25094962.
B cell receptor-associated protein 31 (BAP31) is a transmembrane protein that is widely expressed and primarily located in the endoplasmic reticulum (ER). B cells play a crucial role in the immune system, and BAP31 significantly contributes to the functions of various immune cells. However, the specific role of BAP31 in B lymphocytes development remains unknown. In this study, we utilized a mouse model with BAP31 deleted from B cells to investigate its effects. Our findings reveal a block in early B cell development in the bone marrow and a significant decrease in the number of B cells in peripheral lymphoid organs taken from BAP31 B cell conditional knockout (BAP31-BCKO) mice. B cell receptor (BCR) signaling is crucial for the normal development and differentiation of B lymphocytes. BAP31, an endoplasmic reticulum membrane protein, directly regulates the BCR signaling pathway and was shown to be significantly positively correlated with B cell activation and proliferation. These findings establish BAP31 as a crucial regulator of early B cell development.
B 细胞受体相关蛋白 31(BAP31)是一种广泛表达的跨膜蛋白,主要位于内质网(ER)中。B 细胞在免疫系统中起着至关重要的作用,BAP31 显著促进各种免疫细胞的功能。然而,BAP31 在 B 淋巴细胞发育中的具体作用尚不清楚。在这项研究中,我们利用 B 细胞中缺失 BAP31 的小鼠模型来研究其影响。我们的研究结果表明,BAP31 缺失会导致骨髓中早期 B 细胞发育受阻,以及外周淋巴器官中 B 细胞数量显著减少。B 细胞受体(BCR)信号对于 B 淋巴细胞的正常发育和分化至关重要。BAP31 是一种内质网膜蛋白,直接调节 BCR 信号通路,并且与 B 细胞的激活和增殖呈显著正相关。这些发现确立了 BAP31 作为早期 B 细胞发育的关键调节因子。