Suppr超能文献

衰老是影响椎间盘的硫酸软骨素及其合成酶。

Ageing affects chondroitin sulfates and their synthetic enzymes in the intervertebral disc.

机构信息

Centre for Research in Medical Devices (CÚRAM), National University of Ireland, Galway, Ireland.

Department of Microbiology, School of Natural Sciences, National University of Ireland, Galway, Ireland.

出版信息

Signal Transduct Target Ther. 2017 Sep 22;2:17049. doi: 10.1038/sigtrans.2017.49. eCollection 2017.

Abstract

The depletion of chondroitin sulfates (CSs) within the intervertebral disc (IVD) during degenerative disc disease (DDD) results in a decrease in tissue hydration, a loss of fluid movement, cell apoptosis, a loss of nerve growth inhibition and ultimately, the loss of disc function. To date, little is known with regards to the structure and content of chondroitin sulfates (CSs) during IVD ageing. The behavior of glycosaminoglycans (GAGs), specifically CSs, as well as xylosyltransferase I (XT-I) and glucuronyltransferase I (GT-I), two key enzymes involved in CS synthesis as a primer of glycosaminoglycan (GAG) chain elongation and GAG synthesis in the nucleus pulposus (NP), respectively, were evaluated in a bovine ageing IVD model. Here, we showed significant changes in the composition of GAGs during the disc ageing process (6-month-old, 2-year-old and 8-year-old IVDs representing the immature to mature skeleton). The CS quantity and composition of annulus fibrosus (AF) and NP were determined. The expression of both XT-I and GT-I was detected using immunohistochemistry. A significant decrease in GAGs was observed during the ageing process. CSs are affected at both the structural and quantitative levels with important changes in sulfation observed upon maturity, which correlated with a decrease in the expression of both XT-I and GT-I. A progressive switch of the sulfation profile was noted in both NP and AF tissues from 6 months to 8 years. These changes give an appreciation of the potential impact of CSs on the disc biology and the development of therapeutic approaches for disc regeneration and repair.

摘要

在退行性椎间盘疾病(DDD)过程中,软骨素硫酸盐(CSs)在椎间盘(IVD)内的耗竭导致组织水合作用降低、液体流动减少、细胞凋亡、神经生长抑制丧失,最终导致椎间盘功能丧失。迄今为止,关于椎间盘老化过程中软骨素硫酸盐(CSs)的结构和含量知之甚少。糖胺聚糖(GAGs),特别是 CSs,以及木糖基转移酶 I(XT-I)和葡萄糖醛酸基转移酶 I(GT-I)的行为,这两种酶分别作为 GAG 链延伸和核心蛋白聚糖(NP)中 GAG 合成的引物参与 CS 合成,在牛老化 IVD 模型中进行了评估。在这里,我们展示了 GAG 组成在椎间盘老化过程中的显著变化(6 个月、2 岁和 8 岁的 IVD 分别代表不成熟到成熟的骨骼)。测定了纤维环(AF)和 NP 中 GAG 的含量和组成。用免疫组织化学法检测了 XT-I 和 GT-I 的表达。在老化过程中观察到 GAG 显著减少。CSs 在结构和数量水平上都受到影响,成熟时观察到重要的硫酸化变化,这与 XT-I 和 GT-I 的表达减少相关。NP 和 AF 组织中的硫酸化谱从 6 个月到 8 年逐渐发生变化。这些变化使人们对 CSs 对椎间盘生物学的潜在影响以及用于椎间盘再生和修复的治疗方法的发展有了更好的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a776/5661628/ed7cc3e63680/sigtrans201749-f1.jpg

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