{"title":"利用微流体设备在共培养过程中,生理性缺氧可促进癌细胞迁移并抑制血管生成","authors":"Satoshi Aratake, Kenichi Funamoto","doi":"10.1007/s10404-024-02768-2","DOIUrl":null,"url":null,"abstract":"<div><p>In the tumor microenvironment (TME), the interaction between cancer cells and the microvascular network plays a crucial role in cancer progression. It is also well known that an extremely low oxygen concentration is generated in the TME. However, the effects of oxygen concentration on the interaction between cancer cells and the microvascular network remain poorly understood. In the present study, we developed a microfluidic device with three gel channels and used this device to co-culture cancer cells and a microvascular network. We then investigated the cellular dynamics at different oxygen concentrations. Cancer cells and cells forming a microvascular network (endothelial cells and fibroblasts) were separately mixed with fibrin gels and placed in separate gel channels that flanked a middle gel channel lacking cells. During a seven-day co-culture, the dynamics of cancer cells and formation of a three-dimensional microvascular structure were observed. Cell culture was conducted at three different oxygen concentrations: atmospheric oxygen (21% O<sub>2</sub>), physiological normoxia (5% O<sub>2</sub>), and physiological hypoxia (1% O<sub>2</sub>, resembling the TME). Inspection revealed that cancer cells migrated toward the microvascular network under the co-culture conditions, a property that was potentiated at lower oxygen levels. Under physiological normoxia, endothelial cells formed a thick, dense microvascular network rather than migrating towards the cancer cells. In contrast, under physiological hypoxia, endothelial cells did not exhibit angiogenesis toward cancer cells. These results suggest that the microfluidic device described here will be useful for investigating the interactions between cancer cells and microvascular network under various oxygen conditions.</p></div>","PeriodicalId":706,"journal":{"name":"Microfluidics and Nanofluidics","volume":null,"pages":null},"PeriodicalIF":2.3000,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Physiological hypoxia promotes cancer cell migration and attenuates angiogenesis in co-culture using a microfluidic device\",\"authors\":\"Satoshi Aratake, Kenichi Funamoto\",\"doi\":\"10.1007/s10404-024-02768-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In the tumor microenvironment (TME), the interaction between cancer cells and the microvascular network plays a crucial role in cancer progression. It is also well known that an extremely low oxygen concentration is generated in the TME. However, the effects of oxygen concentration on the interaction between cancer cells and the microvascular network remain poorly understood. In the present study, we developed a microfluidic device with three gel channels and used this device to co-culture cancer cells and a microvascular network. We then investigated the cellular dynamics at different oxygen concentrations. Cancer cells and cells forming a microvascular network (endothelial cells and fibroblasts) were separately mixed with fibrin gels and placed in separate gel channels that flanked a middle gel channel lacking cells. During a seven-day co-culture, the dynamics of cancer cells and formation of a three-dimensional microvascular structure were observed. Cell culture was conducted at three different oxygen concentrations: atmospheric oxygen (21% O<sub>2</sub>), physiological normoxia (5% O<sub>2</sub>), and physiological hypoxia (1% O<sub>2</sub>, resembling the TME). Inspection revealed that cancer cells migrated toward the microvascular network under the co-culture conditions, a property that was potentiated at lower oxygen levels. Under physiological normoxia, endothelial cells formed a thick, dense microvascular network rather than migrating towards the cancer cells. In contrast, under physiological hypoxia, endothelial cells did not exhibit angiogenesis toward cancer cells. These results suggest that the microfluidic device described here will be useful for investigating the interactions between cancer cells and microvascular network under various oxygen conditions.</p></div>\",\"PeriodicalId\":706,\"journal\":{\"name\":\"Microfluidics and Nanofluidics\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2024-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microfluidics and Nanofluidics\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10404-024-02768-2\",\"RegionNum\":4,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"INSTRUMENTS & INSTRUMENTATION\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microfluidics and Nanofluidics","FirstCategoryId":"5","ListUrlMain":"https://link.springer.com/article/10.1007/s10404-024-02768-2","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"INSTRUMENTS & INSTRUMENTATION","Score":null,"Total":0}
Physiological hypoxia promotes cancer cell migration and attenuates angiogenesis in co-culture using a microfluidic device
In the tumor microenvironment (TME), the interaction between cancer cells and the microvascular network plays a crucial role in cancer progression. It is also well known that an extremely low oxygen concentration is generated in the TME. However, the effects of oxygen concentration on the interaction between cancer cells and the microvascular network remain poorly understood. In the present study, we developed a microfluidic device with three gel channels and used this device to co-culture cancer cells and a microvascular network. We then investigated the cellular dynamics at different oxygen concentrations. Cancer cells and cells forming a microvascular network (endothelial cells and fibroblasts) were separately mixed with fibrin gels and placed in separate gel channels that flanked a middle gel channel lacking cells. During a seven-day co-culture, the dynamics of cancer cells and formation of a three-dimensional microvascular structure were observed. Cell culture was conducted at three different oxygen concentrations: atmospheric oxygen (21% O2), physiological normoxia (5% O2), and physiological hypoxia (1% O2, resembling the TME). Inspection revealed that cancer cells migrated toward the microvascular network under the co-culture conditions, a property that was potentiated at lower oxygen levels. Under physiological normoxia, endothelial cells formed a thick, dense microvascular network rather than migrating towards the cancer cells. In contrast, under physiological hypoxia, endothelial cells did not exhibit angiogenesis toward cancer cells. These results suggest that the microfluidic device described here will be useful for investigating the interactions between cancer cells and microvascular network under various oxygen conditions.
期刊介绍:
Microfluidics and Nanofluidics is an international peer-reviewed journal that aims to publish papers in all aspects of microfluidics, nanofluidics and lab-on-a-chip science and technology. The objectives of the journal are to (1) provide an overview of the current state of the research and development in microfluidics, nanofluidics and lab-on-a-chip devices, (2) improve the fundamental understanding of microfluidic and nanofluidic phenomena, and (3) discuss applications of microfluidics, nanofluidics and lab-on-a-chip devices. Topics covered in this journal include:
1.000 Fundamental principles of micro- and nanoscale phenomena like,
flow, mass transport and reactions
3.000 Theoretical models and numerical simulation with experimental and/or analytical proof
4.000 Novel measurement & characterization technologies
5.000 Devices (actuators and sensors)
6.000 New unit-operations for dedicated microfluidic platforms
7.000 Lab-on-a-Chip applications
8.000 Microfabrication technologies and materials
Please note, Microfluidics and Nanofluidics does not publish manuscripts studying pure microscale heat transfer since there are many journals that cover this field of research (Journal of Heat Transfer, Journal of Heat and Mass Transfer, Journal of Heat and Fluid Flow, etc.).