Yang Ling, McBurney Denise, Tang Shou-Ching, Carlson Sara G, Horton Walter E
Department of Anatomy, Northeastern Ohio Universities College of Medicine, 4209 State Route 44, Rootstown, Ohio 44272, USA.
J Cell Biochem. 2007 Oct 15;102(3):786-800. doi: 10.1002/jcb.21328.
BAG-1 (Bcl-2 associated athanogene-1) is a multifunctional protein, linking cell proliferation, cell death, protein folding, and cell stress. In vivo, BAG-1 is expressed in growth plate and articular cartilage, and the expression of BAG-1 is decreased with aging. Chondrocytes respond to endoplasmic reticulum (ER) stress with decreased expression of extracellular matrix proteins, and prolonged ER stress leads to chondrocyte apoptosis. Here we demonstrate for the first time that BAG-1 is involved in ER stress-induced apoptosis in chondrocytes. Induction of ER stress through multiple mechanisms all resulted in downregulation of BAG-1 expression. In addition, direct suppression of BAG-1 expression resulted in chondrocyte growth arrest and apoptosis, while stable overexpression of BAG-1 delayed the onset of ER stress-mediated apoptosis. In addition to regulating apoptosis, we also observed decreased expression of collagen type II in BAG-1 deficient chondrocytes. In contrast, overexpression of BAG-1 resulted in increased expression of collagen type II. Moreover, under ER stress conditions, the reduced expression of collagen type II was delayed in chondrocytes overexpressing BAG-1. These results suggest a novel role for BAG-1 in supporting viability and matrix expression of chondrocytes.
BAG-1(Bcl-2相关抗凋亡基因-1)是一种多功能蛋白,与细胞增殖、细胞死亡、蛋白质折叠及细胞应激相关。在体内,BAG-1在生长板和关节软骨中表达,且其表达随衰老而降低。软骨细胞对内质网(ER)应激的反应是细胞外基质蛋白表达减少,而长时间的ER应激会导致软骨细胞凋亡。在此我们首次证明BAG-1参与ER应激诱导的软骨细胞凋亡。通过多种机制诱导ER应激均导致BAG-1表达下调。此外,直接抑制BAG-1表达会导致软骨细胞生长停滞和凋亡,而稳定过表达BAG-1则会延迟ER应激介导的凋亡发生。除了调节凋亡外,我们还观察到BAG-1缺陷的软骨细胞中II型胶原蛋白表达降低。相反,BAG-1过表达导致II型胶原蛋白表达增加。此外,在ER应激条件下,过表达BAG-1的软骨细胞中II型胶原蛋白表达降低的情况有所延迟。这些结果表明BAG-1在维持软骨细胞活力和基质表达方面具有新作用。