Shao Yan, Kim Sang Yong, Shin Daesung, Kim Mi Sun, Suh Hyun-Woo, Piao Zheng-Hao, Jeong Mira, Lee Suk Hyung, Yoon Suk Ran, Lim Byung Ho, Kim Woo-Ho, Ahn Jeong Keun, Choi Inpyo
Cell Therapy Research Center, Korea Research Institute of Bioscience and Biotechnology, Yusong, Taejon 305-333, Republic of Korea.
Immunol Lett. 2010 Apr 8;129(2):78-84. doi: 10.1016/j.imlet.2010.02.002. Epub 2010 Feb 13.
The detailed mechanism driving the germinal center (GC) reaction to B cell lymphomagenesis has not been clarified. Thioredoxin interacting protein (TXNIP), also known as vitamin D3 up-regulated protein 1 which is an important tumor repressor, is involved in stress responses, redox regulation, and cellular proliferation. Here, we report that TXNIP has a potential role in the formation of GC in peripheral lymphoid organs where B lymphocytes divide rapidly. First, we compared changes in GC from wild type mice and Txnip(-/-) mice. After immunization, Txnip(-/-) mice exhibited higher expression level of BCL-6 and larger percentage of GC B cells with the reduction in antibody production and plasma cell numbers. In addition, Txnip(-/-) spleens had a much larger population which expressed Ki-67, a marker of cell proliferation, in the red pulp border than WT spleens. Furthermore, the expression of BCL-6 was decreased in TXNIP overexpressing cells and elevated in TXNIP deficient cells. Taken together, we conclude that TXNIP may contribute to the formation of GCs after immunization. During this process, TXNIP suppresses BCL-6 expression.
驱动生发中心(GC)反应导致B细胞淋巴瘤发生的详细机制尚未阐明。硫氧还蛋白相互作用蛋白(TXNIP),也被称为维生素D3上调蛋白1,是一种重要的肿瘤抑制因子,参与应激反应、氧化还原调节和细胞增殖。在此,我们报告TXNIP在B淋巴细胞快速分裂的外周淋巴器官中GC的形成中具有潜在作用。首先,我们比较了野生型小鼠和Txnip(-/-)小鼠GC的变化。免疫后,Txnip(-/-)小鼠表现出更高的BCL-6表达水平和更大比例的GC B细胞,同时抗体产生和浆细胞数量减少。此外,Txnip(-/-)脾脏在红髓边界处表达细胞增殖标志物Ki-67的细胞群体比野生型脾脏大得多。此外,在TXNIP过表达细胞中BCL-6表达降低,而在TXNIP缺陷细胞中升高。综上所述,我们得出结论,TXNIP可能有助于免疫后GC的形成。在此过程中,TXNIP抑制BCL-6表达。