In Situ Analysis of Interactions between Fibroblast and Tumor Cells for Drug Assays with Microfluidic Non-Contact Co-Culture

Fibroblasts have significant involvement in cancer progression and are an important therapeutic target for cancer. Here, we present a microfluidic non-contact co-culture device to analyze interactions between tumor cells and fibroblasts. Further, we investigate myofibroblast behaviors induced by lun...

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Main Authors: Hongmei Chen, Wenting Liu, Bin Wang, Zhifeng Zhang
Format: Article
Language:English
Published: MDPI AG 2018-12-01
Series:Micromachines
Subjects:
Online Access:https://www.mdpi.com/2072-666X/9/12/665
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spelling doaj-7ef5d317e93b4a50b85b7702583ff8072020-11-25T01:49:47ZengMDPI AGMicromachines2072-666X2018-12-0191266510.3390/mi9120665mi9120665In Situ Analysis of Interactions between Fibroblast and Tumor Cells for Drug Assays with Microfluidic Non-Contact Co-CultureHongmei Chen0Wenting Liu1Bin Wang2Zhifeng Zhang3School of Mathematics and Physics of Science and Engineering, Anhui University of Technology, Maanshan 243002, ChinaDivision of Nanobionic Research, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences (CAS), Suzhou 215123, ChinaSchool of Mathematics and Physics of Science and Engineering, Anhui University of Technology, Maanshan 243002, ChinaDepartment of Engineering Science and Mechanics, The Pennsylvania State University, State College, PA 16802, USAFibroblasts have significant involvement in cancer progression and are an important therapeutic target for cancer. Here, we present a microfluidic non-contact co-culture device to analyze interactions between tumor cells and fibroblasts. Further, we investigate myofibroblast behaviors induced by lung tumor cells as responses to gallic acid and baicalein. Human lung fibroblast (HLF) and lung cancer cell line (A549) cells were introduced into neighboring, separated regions by well-controlled laminar flows. The phenotypic behavior and secretion activity of the tumor cells indicate that fibroblasts could become activated through paracrine signaling to create a supportive microenvironment for cancer cells when HLF is co-cultured with A549. Furthermore, both gallic acid (GA) and baicalein (BAE) could inhibit the activation of fibroblasts. In situ analysis of various cell communications via the paracrine pathway could be realizable in this contactless co-culture single device. This device facilitates a better understanding of interactions between heterotypic cells, thus exploring the mechanism of cancer, and performs anti-invasion drug assays in a relatively complex microenvironment.https://www.mdpi.com/2072-666X/9/12/665laminar flowsparacrine signalingco-culture
collection DOAJ
language English
format Article
sources DOAJ
author Hongmei Chen
Wenting Liu
Bin Wang
Zhifeng Zhang
spellingShingle Hongmei Chen
Wenting Liu
Bin Wang
Zhifeng Zhang
In Situ Analysis of Interactions between Fibroblast and Tumor Cells for Drug Assays with Microfluidic Non-Contact Co-Culture
Micromachines
laminar flows
paracrine signaling
co-culture
author_facet Hongmei Chen
Wenting Liu
Bin Wang
Zhifeng Zhang
author_sort Hongmei Chen
title In Situ Analysis of Interactions between Fibroblast and Tumor Cells for Drug Assays with Microfluidic Non-Contact Co-Culture
title_short In Situ Analysis of Interactions between Fibroblast and Tumor Cells for Drug Assays with Microfluidic Non-Contact Co-Culture
title_full In Situ Analysis of Interactions between Fibroblast and Tumor Cells for Drug Assays with Microfluidic Non-Contact Co-Culture
title_fullStr In Situ Analysis of Interactions between Fibroblast and Tumor Cells for Drug Assays with Microfluidic Non-Contact Co-Culture
title_full_unstemmed In Situ Analysis of Interactions between Fibroblast and Tumor Cells for Drug Assays with Microfluidic Non-Contact Co-Culture
title_sort in situ analysis of interactions between fibroblast and tumor cells for drug assays with microfluidic non-contact co-culture
publisher MDPI AG
series Micromachines
issn 2072-666X
publishDate 2018-12-01
description Fibroblasts have significant involvement in cancer progression and are an important therapeutic target for cancer. Here, we present a microfluidic non-contact co-culture device to analyze interactions between tumor cells and fibroblasts. Further, we investigate myofibroblast behaviors induced by lung tumor cells as responses to gallic acid and baicalein. Human lung fibroblast (HLF) and lung cancer cell line (A549) cells were introduced into neighboring, separated regions by well-controlled laminar flows. The phenotypic behavior and secretion activity of the tumor cells indicate that fibroblasts could become activated through paracrine signaling to create a supportive microenvironment for cancer cells when HLF is co-cultured with A549. Furthermore, both gallic acid (GA) and baicalein (BAE) could inhibit the activation of fibroblasts. In situ analysis of various cell communications via the paracrine pathway could be realizable in this contactless co-culture single device. This device facilitates a better understanding of interactions between heterotypic cells, thus exploring the mechanism of cancer, and performs anti-invasion drug assays in a relatively complex microenvironment.
topic laminar flows
paracrine signaling
co-culture
url https://www.mdpi.com/2072-666X/9/12/665
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AT binwang insituanalysisofinteractionsbetweenfibroblastandtumorcellsfordrugassayswithmicrofluidicnoncontactcoculture
AT zhifengzhang insituanalysisofinteractionsbetweenfibroblastandtumorcellsfordrugassayswithmicrofluidicnoncontactcoculture
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