A nasal airway-on-chip model to evaluate airflow pre-conditioning during epithelial cell maturation at the air-liquid interface.

IF 8.2 2区 医学 Q1 ENGINEERING, BIOMEDICAL Biofabrication Pub Date : 2024-08-13 DOI:10.1088/1758-5090/ad663d
Amanda C Walls, Manon van Vegchel, Abigail Lakey, Hemali Gauri, Joshua Dixon, Laís A Ferreira, Ishita Tandon, Kartik Balachandran
{"title":"A nasal airway-on-chip model to evaluate airflow pre-conditioning during epithelial cell maturation at the air-liquid interface.","authors":"Amanda C Walls, Manon van Vegchel, Abigail Lakey, Hemali Gauri, Joshua Dixon, Laís A Ferreira, Ishita Tandon, Kartik Balachandran","doi":"10.1088/1758-5090/ad663d","DOIUrl":null,"url":null,"abstract":"<p><p>The function of a well-differentiated nasal epithelium is largely affected by airflow-induced wall shear stress, yet few<i>in vitro</i>models recapitulate this dynamic condition. Models which do expose cells to airflow exclusively initiate flow after the differentiation process has occurred.<i>In vivo</i>, basal cells are constantly replenishing the epithelium under airflow conditions, indicating that airflow may affect the development and function of the differentiated epithelium. To address this gap in the field, we developed a physiologically relevant microphysiological model of the human nasal epithelium and investigated the effects of exposing cells to airflow during epithelial maturation at the air-liquid interface. The nasal airway-on-chip platform was engineered to mimic bi-directional physiological airflow during normal breathing. Primary human nasal epithelial cells were seeded on chips and subjected to either: (1) no flow, (2) single flow (0.5 dyne cm<sup>-2</sup>flow on Day 21 of ALI only), or (3) pre-conditioning flow (0.05 dyne cm<sup>-2</sup>on Days 14-20 and 0.5 dyne cm<sup>-2</sup>flow on Day 21) treatments. Cells exposed to pre-conditioning showed decreased morphological changes and mucus secretions, as well as decreased inflammation, compared to unconditioned cells. Our results indicate that flow exposure only post-differentiation may impose acute stress on cells, while pre-conditioning may potentiate a properly functioning epithelium<i>in vitro</i>.</p>","PeriodicalId":8964,"journal":{"name":"Biofabrication","volume":" ","pages":""},"PeriodicalIF":8.2000,"publicationDate":"2024-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biofabrication","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1088/1758-5090/ad663d","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0

Abstract

The function of a well-differentiated nasal epithelium is largely affected by airflow-induced wall shear stress, yet fewin vitromodels recapitulate this dynamic condition. Models which do expose cells to airflow exclusively initiate flow after the differentiation process has occurred.In vivo, basal cells are constantly replenishing the epithelium under airflow conditions, indicating that airflow may affect the development and function of the differentiated epithelium. To address this gap in the field, we developed a physiologically relevant microphysiological model of the human nasal epithelium and investigated the effects of exposing cells to airflow during epithelial maturation at the air-liquid interface. The nasal airway-on-chip platform was engineered to mimic bi-directional physiological airflow during normal breathing. Primary human nasal epithelial cells were seeded on chips and subjected to either: (1) no flow, (2) single flow (0.5 dyne cm-2flow on Day 21 of ALI only), or (3) pre-conditioning flow (0.05 dyne cm-2on Days 14-20 and 0.5 dyne cm-2flow on Day 21) treatments. Cells exposed to pre-conditioning showed decreased morphological changes and mucus secretions, as well as decreased inflammation, compared to unconditioned cells. Our results indicate that flow exposure only post-differentiation may impose acute stress on cells, while pre-conditioning may potentiate a properly functioning epitheliumin vitro.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
鼻腔气道芯片模型,用于评估气液界面上皮细胞成熟过程中的气流预调。
分化良好的鼻腔上皮细胞的功能在很大程度上受到气流引起的鼻壁剪切应力的影响,但很少有体外模型能再现这种动态条件。将细胞暴露于气流的模型只能在分化过程发生后启动气流。在体内,基底细胞在气流条件下不断补充上皮细胞,这表明气流可能会影响分化上皮细胞的发育和功能。为了填补这一领域的空白,我们开发了一个与生理相关的人类鼻腔上皮微观生理模型,并研究了在气液界面上皮成熟过程中将细胞暴露于气流的影响。鼻腔气道芯片平台的设计旨在模拟正常呼吸时的双向生理气流。原代人类鼻腔上皮细胞被播种在芯片上,并接受以下两种情况:1)无气流;2)单气流(仅在 ALI 第 21 天为 0.5 达因/平方厘米气流);或 3)预处理气流(第 14-20 天为 0.05 达因/平方厘米气流,第 21 天为 0.5 达因/平方厘米气流)。与未接受预处理的细胞相比,接受预处理的细胞形态变化和粘液分泌减少,炎症也有所减轻。我们的研究结果表明,仅在分化后暴露于气流可能会对细胞造成急性应激,而预处理可能会增强体外上皮细胞的正常功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Biofabrication
Biofabrication ENGINEERING, BIOMEDICAL-MATERIALS SCIENCE, BIOMATERIALS
CiteScore
17.40
自引率
3.30%
发文量
118
审稿时长
2 months
期刊介绍: Biofabrication is dedicated to advancing cutting-edge research on the utilization of cells, proteins, biological materials, and biomaterials as fundamental components for the construction of biological systems and/or therapeutic products. Additionally, it proudly serves as the official journal of the International Society for Biofabrication (ISBF).
期刊最新文献
Synergizing bioprinting and 3D cell culture to enhance tissue formation in printed synthetic constructs. Purified adipose tissue-derived extracellular vesicles facilitate adipose organoid vascularization through coordinating adipogenesis and angiogenesis. Bioinks for engineering gradient-based osteochondral and meniscal tissue substitutes: a review. Current progress ofin vitrovascular models on microfluidic chips. Enhanced osteogenic differentiation in hyaluronic acid methacrylate (HAMA) matrix: a comparative study of hPDC and hBMSC spheroids for bone tissue engineering.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1