Kasukonis Benjamin M, Kim John T, Washington Tyrone A, Wolchok Jeffrey C
Dept. of Biomedical Engineering, College of Engineering, University of Arkansas, Fayetteville, Arkansas.
Dept. of Health, Human Performance, and Health Professionals, College of Education and Health Professionals, University of Arkansas, Fayetteville, Arkansas.
Biotechnol Prog. 2016 May;32(3):745-55. doi: 10.1002/btpr.2257. Epub 2016 May 17.
The implantation of decellularized tissue has shown effectiveness as a strategy for the treatment of volumetric muscle loss (VML) injuries. The preparation of decellularized tissue typically relies on the diffusion driven removal of cellular debris. For bulky tissues like muscle, the process can be lengthy, which introduces opportunities for both tissue contamination and degradation of key ECM molecules. In this study we report on the accelerated preparation of decellularized skeletal muscle (DSM) scaffolds using a infusion system and examine scaffold performance for the repair of VML injuries. The preparation of DSM scaffolds using infusion was dramatically accelerated. As the infusion rate (1% SDS) was increased from 0.1 to 1 and 10ml/hr, the time needed to remove intracellular myoglobin and actin decreased from a maximum of 140 ± 3hrs to 45 ± 3hrs and 10 ± 2hrs respectively. Although infusion appeared to remove cellular debris more aggressively, it did not significantly decrease the collagen or glycosaminoglycan composition of DSM samples when compared to un-infused controls. Infusion prepared DSM samples retained the aligned network structure and mechanical integrity of control samples. Infusion prepared DSM samples supported the attachment and in-vitro proliferation of myoblast cells and was well tolerated by the host when examined in-vivo. © 2016 American Institute of Chemical Engineers Biotechnol. Prog., 32:745-755, 2016.
去细胞组织的植入已被证明是治疗大面积肌肉缺损(VML)损伤的一种有效策略。去细胞组织的制备通常依赖于扩散驱动的细胞碎片清除。对于像肌肉这样的大块组织,这个过程可能会很长,这就带来了组织污染和关键细胞外基质(ECM)分子降解的机会。在本研究中,我们报告了使用灌注系统加速制备去细胞骨骼肌(DSM)支架,并研究了该支架修复VML损伤的性能。使用灌注法制备DSM支架的过程显著加速。随着灌注速率(1%十二烷基硫酸钠)从0.1增加到1和10毫升/小时,去除细胞内肌红蛋白和肌动蛋白所需的时间分别从最长140±3小时减少到45±3小时和10±2小时。虽然灌注似乎更积极地去除了细胞碎片,但与未灌注的对照相比,它并没有显著降低DSM样品的胶原蛋白或糖胺聚糖成分。灌注制备的DSM样品保留了对照样品的排列网络结构和机械完整性。灌注制备的DSM样品支持成肌细胞的附着和体外增殖,并且在体内检测时能被宿主很好地耐受。©2016美国化学工程师学会生物技术进展,32:745 - 755,2016。