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椎间盘退变与再生中的炎症

Inflammation in intervertebral disc degeneration and regeneration.

作者信息

Molinos Maria, Almeida Catarina R, Caldeira Joana, Cunha Carla, Gonçalves Raquel M, Barbosa Mário A

机构信息

Instituto de Engenharia Biomédica-INEB, Universidade do Porto, Porto, Portugal Instituto de Ciências Biomédicas Abel Salazar-ICBAS, Universidade do Porto, Porto, Portugal.

Instituto de Engenharia Biomédica-INEB, Universidade do Porto, Porto, Portugal.

出版信息

J R Soc Interface. 2015 Mar 6;12(104):20141191. doi: 10.1098/rsif.2014.1191.

Abstract

Intervertebral disc (IVD) degeneration is one of the major causes of low back pain, a problem with a heavy economic burden, which has been increasing in prevalence as populations age. Deeper knowledge of the complex spatial and temporal orchestration of cellular interactions and extracellular matrix remodelling is critical to improve current IVD therapies, which have so far proved unsatisfactory. Inflammation has been correlated with degenerative disc disease but its role in discogenic pain and hernia regression remains controversial. The inflammatory response may be involved in the onset of disease, but it is also crucial in maintaining tissue homeostasis. Furthermore, if properly balanced it may contribute to tissue repair/regeneration as has already been demonstrated in other tissues. In this review, we focus on how inflammation has been associated with IVD degeneration by describing observational and in vitro studies as well as in vivo animal models. Finally, we provide an overview of IVD regenerative therapies that target key inflammatory players.

摘要

椎间盘(IVD)退变是腰痛的主要原因之一,这一问题带来沉重的经济负担,且随着人口老龄化患病率不断上升。深入了解细胞相互作用和细胞外基质重塑复杂的时空调控对于改进目前的IVD治疗至关重要,而目前的治疗方法迄今已证明并不令人满意。炎症与椎间盘退变疾病相关,但其在椎间盘源性疼痛和疝消退中的作用仍存在争议。炎症反应可能参与疾病的发生,但在维持组织稳态方面也至关重要。此外,如果炎症反应得到适当平衡,它可能有助于组织修复/再生,这在其他组织中已得到证实。在本综述中,我们通过描述观察性研究、体外研究以及体内动物模型,重点关注炎症与IVD退变的关联。最后,我们概述了针对关键炎症因子的IVD再生疗法。

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Inflammation in intervertebral disc degeneration and regeneration.椎间盘退变与再生中的炎症
J R Soc Interface. 2015 Mar 6;12(104):20141191. doi: 10.1098/rsif.2014.1191.

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