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使用纳米纤维支架治疗小鼠的容积性肌肉损失可增强血管组织和整合。

Treatment of volumetric muscle loss in mice using nanofibrillar scaffolds enhances vascular organization and integration.

机构信息

1Veterans Affairs Palo Alto Health Care System, Palo Alto, CA 94304 USA.

2The Stanford Cardiovascular Institute, Stanford University, Stanford, CA 94305 USA.

出版信息

Commun Biol. 2019 May 7;2:170. doi: 10.1038/s42003-019-0416-4. eCollection 2019.

Abstract

Traumatic skeletal muscle injuries cause irreversible tissue damage and impaired revascularization. Engineered muscle is promising for enhancing tissue revascularization and regeneration in injured muscle. Here we fabricated engineered skeletal muscle composed of myotubes interspersed with vascular endothelial cells using spatially patterned scaffolds that induce aligned cellular organization, and then assessed their therapeutic benefit for treatment of murine volumetric muscle loss. Murine skeletal myoblasts co-cultured with endothelial cells in aligned nanofibrillar scaffolds form endothelialized and aligned muscle with longer myotubes, more synchronized contractility, and more abundant secretion of angiogenic cytokines, compared to endothelialized engineered muscle formed from randomly-oriented scaffolds. Treatment of traumatically injured muscle with endothelialized and aligned skeletal muscle promotes the formation of highly organized myofibers and microvasculature, along with greater vascular perfusion, compared to treatment of muscle derived from randomly-oriented scaffolds. This work demonstrates the potential of endothelialized and aligned engineered skeletal muscle to promote vascular regeneration following transplantation.

摘要

创伤性骨骼肌损伤会导致不可逆转的组织损伤和血管再灌注受损。工程化肌肉在增强损伤肌肉的组织再血管化和再生方面具有广阔的应用前景。在这里,我们使用空间图案化支架制造了由肌管与血管内皮细胞交织而成的工程化骨骼肌,该支架可诱导细胞排列,然后评估其对治疗小鼠体积性肌肉损失的治疗益处。与由随机定向支架形成的内皮化工程化肌肉相比,在排列的纳米纤维支架中共培养的内皮细胞和骨骼肌细胞形成了内皮化和排列的肌肉,具有更长的肌管、更同步的收缩性和更丰富的血管生成细胞因子分泌。与治疗源自随机定向支架的肌肉相比,用内皮化和排列的骨骼肌治疗创伤性损伤的肌肉可促进高度组织化的肌纤维和微血管的形成,以及更大的血管灌注。这项工作证明了内皮化和排列的工程化骨骼肌在移植后促进血管再生的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab88/6505043/19aec8828f8c/42003_2019_416_Fig1_HTML.jpg

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