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一种可注射水凝胶通过促进细胞外基质重塑来增强脊髓损伤后的组织修复。

An injectable hydrogel enhances tissue repair after spinal cord injury by promoting extracellular matrix remodeling.

机构信息

Department of Brain Science, Ajou University School of Medicine, 164 Worldcup-ro, Yeongtong-gu, Suwon, 16499, Republic of Korea.

Neuroscience Graduate Program, Department of Biomedical Sciences, Ajou University Graduate School of Medicine, 164 Worldcup-ro, Yeongtong-gu, Suwon, 16499, Republic of Korea.

出版信息

Nat Commun. 2017 Sep 14;8(1):533. doi: 10.1038/s41467-017-00583-8.

Abstract

The cystic cavity that develops following injuries to brain or spinal cord is a major obstacle for tissue repair in central nervous system (CNS). Here we report that injection of imidazole-poly(organophosphazenes) (I-5), a hydrogel with thermosensitive sol-gel transition behavior, almost completely eliminates cystic cavities in a clinically relevant rat spinal cord injury model. Cystic cavities are bridged by fibronectin-rich extracellular matrix. The fibrotic extracellular matrix remodeling is mediated by matrix metalloproteinase-9 expressed in macrophages within the fibrotic extracellular matrix. A poly(organophosphazenes) hydrogel lacking the imidazole moiety, which physically interacts with macrophages via histamine receptors, exhibits substantially diminished bridging effects. I-5 injection improves coordinated locomotion, and this functional recovery is accompanied by preservation of myelinated white matter and motor neurons and an increase in axonal reinnervation of the lumbar motor neurons. Our study demonstrates that dynamic interactions between inflammatory cells and injectable biomaterials can induce beneficial extracellular matrix remodeling to stimulate tissue repair following CNS injuries.The cystic cavity that develops following injuries to brain or spinal cord is a major obstacle. Here the authors show an injection of imidazole poly(organophosphazenes), a hydrogel with thermosensitive sol-gel transition behavior, almost completely eliminates cystic cavities in a clinically relevant rat spinal cord injury model.

摘要

颅脑或脊髓损伤后形成的囊腔是中枢神经系统(CNS)组织修复的主要障碍。在这里,作者报告称,注射具有温敏溶胶-凝胶转变行为的咪唑聚(磷腈)(I-5),几乎可以完全消除临床相关的大鼠脊髓损伤模型中的囊腔。纤维连接蛋白丰富的细胞外基质桥接囊腔。纤维性细胞外基质的纤维化重塑是由纤维性细胞外基质中的巨噬细胞表达的基质金属蛋白酶-9 介导的。缺乏与通过组氨酸受体与巨噬细胞物理相互作用的咪唑部分的聚(磷腈)水凝胶,表现出明显降低的桥接作用。I-5 注射可改善协调运动,这种功能恢复伴随着有髓白质和运动神经元的保留以及腰运动神经元的轴突再支配增加。我们的研究表明,炎症细胞和可注射生物材料之间的动态相互作用可以诱导有益的细胞外基质重塑,从而刺激 CNS 损伤后的组织修复。颅脑或脊髓损伤后形成的囊腔是一个主要障碍。在这里,作者展示了一种注射具有温敏溶胶-凝胶转变行为的咪唑聚(磷腈)(I-5),几乎可以完全消除临床相关的大鼠脊髓损伤模型中的囊腔。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8405/5599609/89860fc76d7a/41467_2017_583_Fig1_HTML.jpg

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