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利用纤维蛋白凝胶在体外快速形成功能性肌肉。

Rapid formation of functional muscle in vitro using fibrin gels.

作者信息

Huang Yen-Chih, Dennis Robert G, Larkin Lisa, Baar Keith

机构信息

Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.

出版信息

J Appl Physiol (1985). 2005 Feb;98(2):706-13. doi: 10.1152/japplphysiol.00273.2004. Epub 2004 Oct 8.

DOI:10.1152/japplphysiol.00273.2004
PMID:15475606
Abstract

The transition of a muscle cell from a differentiated myotube into an adult myofiber is largely unstudied. This is primarily due to the difficulty of isolating specific developmental stimuli in vivo and the inability to maintain viable myotubes in culture for sufficient lengths of time. To address these limitations, a novel method for rapidly generating three-dimensional engineered muscles using fibrin gel casting has been developed. Myoblasts were seeded and differentiated on top of a fibrin gel. Cell-mediated contraction of the gel around artificial anchors placed 12 mm apart culminates 10 days after plating in a tubular structure of small myotubes (10-microm diameter) surrounded by a fibrin gel matrix. These tissues can be connected to a force transducer and electrically stimulated between parallel platinum electrodes to monitor physiological function. Three weeks after plating, the three-dimensional engineered muscle generated a maximum twitch force of 329 +/- 26.3 microN and a maximal tetanic force of 805.8 +/- 55 microN. The engineered muscles demonstrated normal physiological function including length-tension and force-frequency relationships. Treatment with IGF-I resulted in a 50% increase in force production, demonstrating that these muscles responded to hormonal interventions. Although the force production was maximal at 3 wk, constructs can be maintained in culture for up to 6 wk with no intervention. We conclude that fibrin-based gels provide a novel method to engineer three-dimensional functional muscle tissue and that these tissues may be used to model the development of skeletal muscle in vitro.

摘要

肌肉细胞从分化的肌管转变为成熟肌纤维的过程在很大程度上尚未得到研究。这主要是由于在体内分离特定发育刺激的困难以及无法在培养中使存活的肌管维持足够长的时间。为了解决这些限制,已开发出一种使用纤维蛋白凝胶浇铸快速生成三维工程化肌肉的新方法。将成肌细胞接种在纤维蛋白凝胶上并使其分化。在相距12毫米放置的人工锚周围,细胞介导的凝胶收缩在接种后10天达到顶点,形成由纤维蛋白凝胶基质包围的小肌管(直径10微米)的管状结构。这些组织可以连接到力传感器,并在平行的铂电极之间进行电刺激以监测生理功能。接种三周后,三维工程化肌肉产生的最大抽搐力为329±26.3微牛顿,最大强直力为805.8±55微牛顿。工程化肌肉表现出正常的生理功能,包括长度 - 张力和力 - 频率关系。用胰岛素样生长因子 - I处理导致力产生增加50%,表明这些肌肉对激素干预有反应。尽管力产生在3周时最大,但构建体在无干预的情况下可在培养中维持长达6周。我们得出结论,基于纤维蛋白的凝胶提供了一种构建三维功能性肌肉组织的新方法,并且这些组织可用于在体外模拟骨骼肌的发育。

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