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Intervertebral disc development and disease-related genetic polymorphisms

机译:椎间盘发育与疾病相关的遗传多态性

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摘要

Abstract The intervertebral disc (IVD) comprises a gelatinous inner core (nucleus pulposus; NP) and concentric rings (annulus fibrosus; AF). The NP, an important structure for shock absorption in the vertebrate spinal motion segment, can be traced back to the notochord in ontogenetic lineage. In vertebrates, the notochord undergoes mucinoid changes, and had been considered vestigial until recently. However, observed correlations between {IVD} degeneration and back pain in humans have renewed interest in the {IVD} in biomedical fields. Beyond its mechanical contribution to development, the notochord is also an essential signaling center, which coordinates formation of the neural tube and somites. The pertinent signaling molecules, particularly TGF-β and bone morphogenetic proteins (BMPs), continue to play roles in the adult tissues and have been utilized for tissue regeneration. Genetic factors are major determinants of who will develop {IVD} degeneration and related back pain, and seem to correlate better with disc degeneration and back pain than do external forces on the spine. In summary, the spinal column is a landmark development in evolution. Genes directing the development of the {IVD} may also contribute to its maintenance, degeneration, and regeneration. Likewise, structural genes as well as genes responsible for maintenance of the structure are related to {IVD} degeneration. Finally, genes responsible for inflammation may play a dual role in exacerbating degeneration or facilitating repair responses depending on the context.
机译:摘要椎间盘(IVD)由凝胶状内核(髓核; NP)和同心环(纤维环; AF)组成。 NP是脊椎动物脊柱运动节段中一种重要的减震结构,可以追溯到个体遗传​​世系中的脊索。在脊椎动物中,脊索发生粘液样变化,直到最近才被认为是残余的。然而,人类体内{IVD}退化与背部疼痛之间的相关性已引起人们对{IVD}在生物医学领域的关注。除了其对发育的机械作用外,脊索还是一个重要的信号传导中心,它协调神经管和体节的形成。相关的信号分子,尤其是TGF-β和骨形态发生蛋白(BMP),继续在成人组织中发挥作用,并已被用于组织再生。遗传因素是谁会发展{IVD}变性和相关背痛的主要决定因素,并且与椎间盘退变和背痛的相关性似乎比对脊柱的外力更好。总之,脊柱是进化中的标志性发展。指导{IVD}发育的基因也可能有助于其维持,变性和再生。同样,结构基因以及负责维持结构的基因也与{IVD}变性有关。最后,取决于上下文,负责炎症的基因可能在加剧变性或促进修复反应中起双重作用。

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