利用生物物理线索和生物材料改进遗传模型

IF 4.7 3区 工程技术 Q2 ENGINEERING, BIOMEDICAL
Thomas G. Molley , Adam J. Engler
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引用次数: 0

摘要

随着诱导多能干细胞和现代分化方案的出现,通过体外疾病建模,我们对疾病的理解取得了许多进展;在某些情况下,它们的使用可能已经取代了动物模型。然而,体外模型通常依赖于坚硬的细胞培养基质,这可能会限制我们在培养皿中完全复制人类疾病的能力。然而,早期的研究表明,生物材料和/或先进的微生理系统(可以更好地概括组织特性)与表达疾病模拟遗传学的干细胞相结合,可以大大改善目前仅靠遗传学还不够的疾病建模工作。这篇综述将突出这些最近的进展,以及回顾当前的挑战,该领域必须克服,以创造更多的个性化治疗在未来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Using biophysical cues and biomaterials to improve genetic models

With the advent of induced pluripotent stem cells and modern differentiation protocols, many advances in our understanding of disease have been made possible by in vitro disease modeling; in some cases, their use may have supplanted animal models. Yet in vitro models often rely on rigid cell culture substrates that could limit our ability to completely reproduce human disease in a dish. Nascent work, however, suggests that the combination of biomaterials and/or advanced microphysiological systems–which better recapitulate tissue properties–with stem cells expressing disease mimicking genetics, could substantially improve current disease modeling efforts where genetics alone is insufficient. This review will highlight such recent advances as well as review current challenges that the fields must overcome to create more personalized therapeutics in the future.

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来源期刊
Current Opinion in Biomedical Engineering
Current Opinion in Biomedical Engineering Medicine-Medicine (miscellaneous)
CiteScore
8.60
自引率
2.60%
发文量
59
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