Suppr超能文献

表达与脊椎骨骺发育不良相关的部分展开的R789C/p.R989C II型前胶原突变体的细胞会发生凋亡。

Cells expressing partially unfolded R789C/p.R989C type II procollagen mutant associated with spondyloepiphyseal dysplasia undergo apoptosis.

作者信息

Hintze Vera, Steplewski Andrzej, Ito Hidetoshi, Jensen Deborah A, Rodeck Ulrich, Fertala Andrzej

机构信息

Department of Dermatology and Cutaneous Biology, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

Hum Mutat. 2008 Jun;29(6):841-51. doi: 10.1002/humu.20736.

Abstract

We investigated the effects of the presence of R75C (p.R275C), R519C (p.719C), R789C (p.R989C), and G853E (p.G1053E) type II collagen (COL2A1) mutants, associated with distinct forms of spondyloepiphyseal dysplasia (SED), on the biological processes occurring in chondrocytic cells harboring those mutants. Mutant-specific biological responses of cells were initiated by activating tetracycline (Tet)-dependent expression of type II collagen mutants. Employing microscopic and biochemical assays, we determined that cells expressing the thermolabile R789C (p.R989C) type II collagen mutant undergo apoptosis. In contrast, in cells expressing the thermostable R75C (p.R275C), R519C (p.719C), and G853E (p.G1053E) mutants, apoptotic markers were not apparent. We also demonstrated that the R789C (p.R989C) mutant formed atypical complexes with endoplasmic reticulum (ER)-resident chaperones, thereby indicating an "unfolded protein response" (UPR) of cells harboring this specific mutant. Apoptotic changes were also demonstrated by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) and cleaved caspase 3 assays in the growth plates of mice harboring the R992C (p.R1147C) substitution in type II collagen. Based on these results, we propose that the intracellular presence of structurally altered type II collagen mutants could activate an apoptotic response, thereby limiting cell survival. By analyzing the response of cells to the altered structure of collagen mutants, our study contributes to better understanding the molecular basis of the pathological changes seen in vivo at the tissue level.

摘要

我们研究了与不同形式的脊椎骨骺发育不良(SED)相关的R75C(p.R275C)、R519C(p.719C)、R789C(p.R989C)和G853E(p.G1053E)II型胶原(COL2A1)突变体的存在对携带这些突变体的软骨细胞中发生的生物学过程的影响。通过激活四环素(Tet)依赖性II型胶原突变体的表达来启动细胞的突变体特异性生物学反应。利用显微镜和生化分析,我们确定表达热不稳定的R789C(p.R989C)II型胶原突变体的细胞会发生凋亡。相比之下,在表达热稳定的R75C(p.R275C)、R519C(p.719C)和G853E(p.G1053E)突变体的细胞中,凋亡标志物并不明显。我们还证明,R789C(p.R989C)突变体与内质网(ER)驻留伴侣形成非典型复合物,从而表明携带这种特定突变体的细胞出现了“未折叠蛋白反应”(UPR)。在II型胶原中存在R992C(p.R1147C)替代的小鼠生长板中,通过末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)和裂解的半胱天冬酶3分析也证实了凋亡变化。基于这些结果,我们提出结构改变的II型胶原突变体在细胞内的存在可能激活凋亡反应,从而限制细胞存活。通过分析细胞对胶原突变体结构改变的反应,我们的研究有助于更好地理解在组织水平上体内所见病理变化的分子基础。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验