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预先神经化的组织工程肌肉促进了容积性肌肉损失后的促再生微环境。

Pre-innervated tissue-engineered muscle promotes a pro-regenerative microenvironment following volumetric muscle loss.

机构信息

Center for Brain Injury & Repair, Department of Neurosurgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Center for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.

出版信息

Commun Biol. 2020 Jun 25;3(1):330. doi: 10.1038/s42003-020-1056-4.

Abstract

Volumetric muscle loss (VML) is the traumatic or surgical loss of skeletal muscle beyond the inherent regenerative capacity of the body, generally leading to severe functional deficit. Formation of appropriate somato-motor innervations remains one of the biggest challenges for both autologous grafts as well as tissue-engineered muscle constructs. We aim to address this challenge by developing pre-innervated tissue-engineered muscle comprised of long aligned networks of spinal motor neurons and skeletal myocytes on aligned nanofibrous scaffolds. Motor neurons led to enhanced differentiation and maturation of skeletal myocytes in vitro. These pre-innervated tissue-engineered muscle constructs when implanted in a rat VML model significantly increased satellite cell density, neuromuscular junction maintenance, graft revascularization, and muscle volume over three weeks as compared to myocyte-only constructs and nanofiber scaffolds alone. These pro-regenerative effects may enhance functional neuromuscular regeneration following VML, thereby improving the levels of functional recovery following these devastating injuries.

摘要

体积性肌肉损失(VML)是指骨骼肌肉的创伤性或手术性损失,超出了身体固有的再生能力,通常导致严重的功能缺陷。适当的躯体运动神经支配的形成仍然是自体移植物和组织工程肌肉构建体的最大挑战之一。我们旨在通过开发预先支配的组织工程肌肉来解决这一挑战,该肌肉由脊髓运动神经元和排列在纳米纤维支架上的骨骼肌细胞的长排列网络组成。运动神经元导致体外骨骼肌细胞的分化和成熟增强。与仅肌细胞构建体和纳米纤维支架相比,这些预先支配的组织工程肌肉构建体在大鼠 VML 模型中植入后,在三周内显著增加了卫星细胞密度、神经肌肉接头维持、移植物再血管化和肌肉体积。这些促进再生的作用可能会增强 VML 后的神经肌肉再生功能,从而提高这些毁灭性损伤后的功能恢复水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab89/7316777/6b231fa72fb4/42003_2020_1056_Fig1_HTML.jpg

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