Chung Hye Jin, Jensen Deborah A, Gawron Katarzyna, Steplewski Andrzej, Fertala Andrzej
Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
J Mol Biol. 2009 Jul 10;390(2):306-18. doi: 10.1016/j.jmb.2009.05.004. Epub 2009 May 8.
We investigated the molecular bases of spondyloepiphyseal dysplasia (SED) associated with the R992C (p.R1192C) substitution in collagen II. At the protein level, we analyzed the structure and integrity of mutant molecules, and at the cellular level, we specifically studied the effects of the presence of the R992C collagen II on the biological processes taking place in host cells. Our studies demonstrated that mutant collagen II molecules were characterized by altered electrophoretic mobility, relatively low thermostability, the presence of atypical disulfide bonds, and slow rates of secretion into the extracellular space. Analyses of cellular responses to the presence of the mutant molecules showed that excessive accumulation of thermolabile collagen II was associated with the activation of an "unfolded protein response" and an increase in apoptosis of host cells. Collectively, these data suggest that molecular mechanisms of SED may be driven not only by structural changes in the architecture of extracellular collagenous matrices, but also by intracellular processes activated by the presence of mutant collagen II molecules.
我们研究了与胶原蛋白II中R992C(p.R1192C)替代相关的脊椎骨骺发育不良(SED)的分子基础。在蛋白质水平上,我们分析了突变分子的结构和完整性,在细胞水平上,我们专门研究了R992C胶原蛋白II的存在对宿主细胞中发生的生物学过程的影响。我们的研究表明,突变的胶原蛋白II分子具有电泳迁移率改变、热稳定性相对较低、存在非典型二硫键以及分泌到细胞外空间的速率较慢等特征。对细胞对突变分子存在的反应分析表明,热不稳定胶原蛋白II的过度积累与“未折叠蛋白反应”的激活以及宿主细胞凋亡的增加有关。总体而言,这些数据表明,SED的分子机制可能不仅由细胞外胶原基质结构的变化驱动,还由突变胶原蛋白II分子的存在激活的细胞内过程驱动。