Engineering muscle constructs for the creation of functional engineered musculoskeletal tissue.

Engineering muscle constructs for the creation of functional engineered musculoskeletal tissue.
复制标题

工程肌肉结构,用于创建功能性工程肌肉骨骼组织。

DOI:
10.2217/rme.13.81
复制
发表时间:
2014-01
影响因子:
2.7
通讯作者:
Larkin LM
Larkin LM
中科院分区:
工程技术4区
文献类型:
--
作者:
Mertens JP;Sugg KB;Lee JD;Larkin LM

文献摘要

参考文献

被引文献

相似文献

容积性肌肉损失(VML)是一种致残性疾病,目前的临床程序是次优的。组织工程领域有许多有前途的策略,在体外创造功能性骨骼肌。然而,仍然有两个关键的限制,阻止它成为治疗VML的解决方案。首先,工程肌肉组织必须具有生物相容性,以促进肌肉组织再生,而不会产生免疫反应。其次,工程肌肉结构必须按比例放大,以便于替换临床相关体积的组织(直径为厘米)。目前还没有组织工程策略来产生既生物相容又足够大以促进临床修复的组织构建体。然而,最近的进展,在组织工程中使用合成支架,天然支架,或无支架的方法可能会导致一个解决方案,修复VML损伤。
Volumetric muscle loss (VML) is a disabling condition in which current clinical procedures are suboptimal. The field of tissue engineering has many promising strategies for the creation of functional skeletal muscle in vitro. However, there are still two key limitations that prevent it from becoming a solution for treating VML. First, engineered muscle tissue must be biocompatible to facilitate muscle tissue regrowth without generating an immune response. Second, engineered muscle constructs must be scaled up to facilitate replacement of clinically relevant volumes of tissue (centimeters in diameter). There are currently no tissue engineering strategies to produce tissue constructs that are both biocompatible and large enough to facilitate clinical repair. However, recent advances in tissue engineering using synthetic scaffolds, native scaffolds, or scaffold-free approaches may lead to a solution for repair of VML injuries.
DOI: 10.1097/01.prs.0000101064.62289.2f
发表时间: 2004-02-01
影响因子: 3.6
作者:
Borschel, GH;Dennis, RG;Kuzon, WM
通讯作者: Kuzon, WM
DOI: 10.1016/j.biomaterials.2004.06.047
发表时间: 2005-05-01
期刊: BIOMATERIALS
影响因子: 14
作者:
Almany, L;Seliktar, D
通讯作者: Seliktar, D
DOI: 10.1088/1748-6041/8/1/014106
发表时间: 2013-02-01
影响因子: 4
作者:
Arenas-Herrera, J. E.;Ko, I. K.;Yoo, J. J.
通讯作者: Yoo, J. J.
DOI: 10.1083/jcb.200405004
发表时间: 2004-09-13
期刊: The Journal of cell biology
影响因子: --
作者:
Engler AJ;Griffin MA;Sen S;Bönnemann CG;Sweeney HL;Discher DE
通讯作者: Discher DE
DOI: 10.5435/00124635-201102001-00007
发表时间: 2011-01-01
影响因子: 3.2
作者:
Grogan, Brian F.;Hsu, Joseph R.
通讯作者: Hsu, Joseph R.