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蛋白聚糖功能障碍:椎间盘退变与骨骼发育异常之间的共同联系。

Proteoglycan Dysfunction: A Common Link Between Intervertebral Disc Degeneration and Skeletal Dysplasia.

作者信息

Sao Kimheak, Risbud Makarand V

机构信息

Graduate Program in Cell Biology and Regenerative Medicine, Jefferson College of Life Sciences, Thomas Jefferson University, Philadelphia, PA, USA.

Department of Orthopaedic Surgery, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, USA.

出版信息

Neurospine. 2024 Mar;21(1):162-178. doi: 10.14245/ns.2347342.671. Epub 2024 Mar 31.

DOI:10.14245/ns.2347342.671
PMID:38569642
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10992626/
Abstract

Proteoglycans through their sulfated glycosaminoglycans regulate cell-matrix signaling during tissue development, regeneration, and degeneration processes. Large extracellular proteoglycans such as aggrecan, versican, and perlecan are especially important for the structural integrity of the intervertebral disc and cartilage during development. In these tissues, proteoglycans are responsible for hydration, joint flexibility, and the absorption of mechanical loads. Loss or reduction of these molecules can lead to disc degeneration and skeletal dysplasia, evident from loss of disc height or defects in skeletal development respectively. In this review, we discuss the common proteoglycans found in the disc and cartilage and elaborate on various murine models and skeletal dysplasias in humans to highlight how their absence and/or aberrant expression causes accelerated disc degeneration and developmental defects.

摘要

蛋白聚糖通过其硫酸化糖胺聚糖在组织发育、再生和退变过程中调节细胞-基质信号传导。大型细胞外蛋白聚糖,如聚集蛋白聚糖、多功能蛋白聚糖和基底膜聚糖,在发育过程中对椎间盘和软骨的结构完整性尤为重要。在这些组织中,蛋白聚糖负责水合作用、关节灵活性以及机械负荷的吸收。这些分子的缺失或减少可导致椎间盘退变和骨骼发育异常,分别表现为椎间盘高度降低或骨骼发育缺陷。在本综述中,我们讨论了在椎间盘和软骨中发现的常见蛋白聚糖,并详细阐述了各种小鼠模型和人类骨骼发育异常,以突出它们的缺失和/或异常表达如何导致椎间盘退变加速和发育缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef4/10992626/2bae4e9b9729/ns-2347342-671f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef4/10992626/4fcf4b4dcee1/ns-2347342-671f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef4/10992626/2bae4e9b9729/ns-2347342-671f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef4/10992626/4fcf4b4dcee1/ns-2347342-671f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ef4/10992626/2bae4e9b9729/ns-2347342-671f2.jpg

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Molecular mechanism of decision-making in glycosaminoglycan biosynthesis.糖胺聚糖生物合成中决策的分子机制。
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3
Emodin ameliorates matrix degradation and apoptosis in nucleus pulposus cells and attenuates intervertebral disc degeneration through LRP1 in vitro and in vivo.
用于替代蛋白聚糖功能的仿生策略。
Front Cell Dev Biol. 2024 Aug 6;12:1391769. doi: 10.3389/fcell.2024.1391769. eCollection 2024.
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