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相聚是开始:椎间盘的形成。

Coming together is a beginning: the making of an intervertebral disc.

作者信息

Chan Wilson C W, Au Tiffany Y K, Tam Vivian, Cheah Kathryn S E, Chan Danny

机构信息

Department of Biochemistry, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong, China.

出版信息

Birth Defects Res C Embryo Today. 2014 Mar;102(1):83-100. doi: 10.1002/bdrc.21061.

Abstract

The intervertebral disc (IVD) is a complex fibrocartilaginous structure located between the vertebral bodies that allows for movement and acts as a shock absorber in our spine for daily activities. It is composed of three components: the nucleus pulposus (NP), annulus fibrosus, and cartilaginous endplate. The characteristics of these cells are different, as they produce specific extracellular matrix (ECM) for tissue function and the niche in supporting the differentiation status of the cells in the IVD. Furthermore, cell heterogeneities exist in each compartment. The cells and the supporting ECM change as we age, leading to degenerative outcomes that often lead to pathological symptoms such as back pain and sciatica. There are speculations as to the potential of cell therapy or the use of tissue engineering as treatments. However, the nature of the cells present in the IVD that support tissue function is not clear. This review looks at the origin of cells in the making of an IVD, from the earliest stages of embryogenesis in the formation of the notochord, and its role as a signaling center, guiding the formation of spine, and in its journey to become the NP at the center of the IVD. While our current understanding of the molecular signatures of IVD cells is still limited, the field is moving fast and the potential is enormous as we begin to understand the progenitor and differentiated cells present, their molecular signatures, and signals that we could harness in directing the appropriate in vitro and in vivo cellular responses in our quest to regain or maintain a healthy IVD as we age.

摘要

椎间盘(IVD)是一种复杂的纤维软骨结构,位于椎体之间,在日常活动中可使脊柱运动并起到减震作用。它由三部分组成:髓核(NP)、纤维环和软骨终板。这些细胞的特征各不相同,因为它们产生特定的细胞外基质(ECM)以实现组织功能,并为椎间盘内细胞的分化状态提供支持环境。此外,每个部分都存在细胞异质性。随着年龄增长,细胞和支持性ECM会发生变化,导致退行性结果,常常引发背痛和坐骨神经痛等病理症状。对于细胞治疗或组织工程治疗的潜力存在诸多猜测。然而,椎间盘内支持组织功能的细胞的本质尚不清楚。本综述探讨了椎间盘形成过程中细胞的起源,从胚胎发育早期脊索形成阶段开始,以及其作为信号中心在引导脊柱形成过程中的作用,以及它如何演变成椎间盘中心的髓核。虽然我们目前对椎间盘细胞分子特征的了解仍然有限,但随着我们开始了解存在的祖细胞和分化细胞、它们的分子特征以及在我们努力随着年龄增长恢复或维持健康椎间盘的过程中可利用的信号,从而指导适当的体外和体内细胞反应,该领域发展迅速且潜力巨大。

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