User-friendly microfluidic system reveals native-like morphological and transcriptomic phenotypes induced by shear stress in proximal tubule epithelium.

IF 6.6 3区 医学 Q1 ENGINEERING, BIOMEDICAL
Natalie N Khalil, Andrew P Petersen, Cheng J Song, Yibu Chen, Kaelyn Takamoto, Austin C Kellogg, Elaine Zhelan Chen, Andrew P McMahon, Megan L McCain
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引用次数: 0

Abstract

Drug-induced nephrotoxicity is a leading cause of drug attrition, partly due to the limited relevance of pre-clinical models of the proximal tubule. Culturing proximal tubule epithelial cells (PTECs) under fluid flow to mimic physiological shear stress has been shown to improve select phenotypes, but existing flow systems are expensive and difficult to implement by non-experts in microfluidics. Here, we designed and fabricated an accessible and modular flow system for culturing PTECs under physiological shear stress, which induced native-like cuboidal morphology, downregulated pathways associated with hypoxia, stress, and injury, and upregulated xenobiotic metabolism pathways. We also compared the expression profiles of shear-dependent genes in our in vitro PTEC tissues to that of ex vivo proximal tubules and observed stronger clustering between ex vivo proximal tubules and PTECs under physiological shear stress relative to PTECs under negligible shear stress. Together, these data illustrate the utility of our user-friendly flow system and highlight the role of shear stress in promoting native-like morphological and transcriptomic phenotypes in PTECs in vitro, which is critical for developing more relevant pre-clinical models of the proximal tubule for drug screening or disease modeling.

用户友好的微流控系统揭示了近端小管上皮剪切应力诱导的原生形态和转录组表型。
药物引起的肾毒性是药物损耗的主要原因,部分原因是近端肾小管临床前模型的相关性有限。在流体流动下培养近端小管上皮细胞(PTECs)以模拟生理剪切应力已被证明可以改善选择的表型,但现有的流动系统昂贵且难以由非微流体专家实施。在这里,我们设计并制造了一个可访问的模块化流动系统,用于在生理剪切应力下培养ptec,诱导原生样立方形态,与缺氧,应激和损伤相关的下调通路,以及上调外源代谢途径。我们还将体外PTEC组织中剪切依赖基因的表达谱与离体近端小管的表达谱进行了比较,发现在生理剪切应力下,离体近端小管与PTEC之间的聚类比在可忽略剪切应力下的PTEC更强。总之,这些数据说明了我们的用户友好型流动系统的实用性,并强调了剪切应力在体外促进ptec中原生样形态和转录组表型中的作用,这对于开发更相关的近端小管临床前模型用于药物筛选或疾病建模至关重要。
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来源期刊
APL Bioengineering
APL Bioengineering ENGINEERING, BIOMEDICAL-
CiteScore
9.30
自引率
6.70%
发文量
39
审稿时长
19 weeks
期刊介绍: APL Bioengineering is devoted to research at the intersection of biology, physics, and engineering. The journal publishes high-impact manuscripts specific to the understanding and advancement of physics and engineering of biological systems. APL Bioengineering is the new home for the bioengineering and biomedical research communities. APL Bioengineering publishes original research articles, reviews, and perspectives. Topical coverage includes: -Biofabrication and Bioprinting -Biomedical Materials, Sensors, and Imaging -Engineered Living Systems -Cell and Tissue Engineering -Regenerative Medicine -Molecular, Cell, and Tissue Biomechanics -Systems Biology and Computational Biology
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