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合成基质增强了创伤合并的营养不良和衰老骨骼肌中移植卫星细胞的植入。

Synthetic matrix enhances transplanted satellite cell engraftment in dystrophic and aged skeletal muscle with comorbid trauma.

机构信息

Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.

Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA 30332, USA.

出版信息

Sci Adv. 2018 Aug 15;4(8):eaar4008. doi: 10.1126/sciadv.aar4008. eCollection 2018 Aug.

Abstract

Muscle satellite cells (MuSCs) play a central role in muscle regeneration, but their quantity and function decline with comorbidity of trauma, aging, and muscle diseases. Although transplantation of MuSCs in traumatically injured muscle in the comorbid context of aging or pathology is a strategy to boost muscle regeneration, an effective cell delivery strategy in these contexts has not been developed. We engineered a synthetic hydrogel-based matrix with optimal mechanical, cell-adhesive, and protease-degradable properties that promotes MuSC survival, proliferation, and differentiation. Furthermore, we establish a biomaterial-mediated cell delivery strategy for treating muscle trauma, where intramuscular injections may not be applicable. Delivery of MuSCs in the engineered matrix significantly improved in vivo cell survival, proliferation, and engraftment in nonirradiated and immunocompetent muscles of aged and dystrophic mice compared to collagen gels and cell-only controls. This platform may be suitable for treating craniofacial and limb muscle trauma, as well as postoperative wounds of elderly and dystrophic patients.

摘要

肌卫星细胞(MuSCs)在肌肉再生中起着核心作用,但它们的数量和功能随着创伤、衰老和肌肉疾病的合并症而下降。虽然在衰老或病理学的合并创伤性损伤肌肉中移植 MuSCs 是促进肌肉再生的一种策略,但在这些情况下尚未开发出有效的细胞输送策略。我们设计了一种基于合成水凝胶的基质,具有最佳的机械、细胞黏附和蛋白酶可降解性能,可促进 MuSC 的存活、增殖和分化。此外,我们建立了一种基于生物材料的细胞输送策略,用于治疗肌肉创伤,其中肌肉内注射可能不适用于这种情况。与胶原凝胶和仅细胞对照相比,在工程化基质中递送 MuSCs 可显著提高非照射和免疫活性老龄和肌肉萎缩症小鼠肌肉中的细胞存活、增殖和植入。该平台可能适用于治疗颅面和肢体肌肉创伤以及老年和肌肉萎缩症患者的术后伤口。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ede/6093653/8b23f716917f/aar4008-F1.jpg

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