Microfluidic Capture Device for Simple, Cell Surface Marker-Based Quantification of Senescent CD8+ T Cells

IF 6.1 3区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS BioChip Journal Pub Date : 2024-03-08 DOI:10.1007/s13206-024-00142-6
Yo-han Choi, Woo-Joong Kim, Dongwoo Lee, Bum-Joon Jung, Eui-Cheol Shin, Wonhee Lee
{"title":"Microfluidic Capture Device for Simple, Cell Surface Marker-Based Quantification of Senescent CD8+ T Cells","authors":"Yo-han Choi, Woo-Joong Kim, Dongwoo Lee, Bum-Joon Jung, Eui-Cheol Shin, Wonhee Lee","doi":"10.1007/s13206-024-00142-6","DOIUrl":null,"url":null,"abstract":"<p>Among human CD8<sup>+</sup> T cells, senescent cells are marked by the expression of CD57. The frequency of senescent CD57<sup>+</sup>CD8<sup>+</sup> T cells is significantly correlated with aging and age-associated disorders, and it can be measured by multi-color flow cytometry. However, multi-color flow cytometry presents challenges in terms of accessibility and requires significant resource allocation. Therefore, developing a rapid and straightforward method for quantifying CD57<sup>+</sup>CD8<sup>+</sup> T cells remains a key challenge. This study introduces a microfluidic device composed of a PDMS microfluidic channel with a pre-modified glass substrate for anti-CD8 antibody immobilization. This design allows blood samples to flow through, enabling the selective capture of CD8<sup>+</sup> T cells while minimizing the required blood sample volume. This technology enables accurate and reliable quantification of CD57<sup>+</sup> cells among captured CD8<sup>+</sup> T cells through fluorescence image analysis. The ability of the device to easily quantify senescent CD57<sup>+</sup>CD8<sup>+</sup> T cells is anticipated to contribute significantly to both immunological research and clinical applications.</p>","PeriodicalId":8768,"journal":{"name":"BioChip Journal","volume":"82 1","pages":""},"PeriodicalIF":6.1000,"publicationDate":"2024-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BioChip Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1007/s13206-024-00142-6","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Among human CD8+ T cells, senescent cells are marked by the expression of CD57. The frequency of senescent CD57+CD8+ T cells is significantly correlated with aging and age-associated disorders, and it can be measured by multi-color flow cytometry. However, multi-color flow cytometry presents challenges in terms of accessibility and requires significant resource allocation. Therefore, developing a rapid and straightforward method for quantifying CD57+CD8+ T cells remains a key challenge. This study introduces a microfluidic device composed of a PDMS microfluidic channel with a pre-modified glass substrate for anti-CD8 antibody immobilization. This design allows blood samples to flow through, enabling the selective capture of CD8+ T cells while minimizing the required blood sample volume. This technology enables accurate and reliable quantification of CD57+ cells among captured CD8+ T cells through fluorescence image analysis. The ability of the device to easily quantify senescent CD57+CD8+ T cells is anticipated to contribute significantly to both immunological research and clinical applications.

Abstract Image

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
基于细胞表面标记的衰老 CD8+ T 细胞简单定量微流体捕获装置
在人类 CD8+ T 细胞中,衰老细胞以表达 CD57 为标志。衰老的 CD57+CD8+ T 细胞的频率与衰老和年龄相关疾病密切相关,可以通过多色流式细胞术测量。然而,多色流式细胞术在可及性方面存在挑战,并且需要大量的资源分配。因此,开发一种快速、直接的方法来量化 CD57+CD8+ T 细胞仍是一项关键挑战。本研究介绍了一种微流控装置,该装置由一个 PDMS 微流控通道和一个用于固定抗 CD8 抗体的预修饰玻璃基底组成。这种设计可使血液样本流过,从而选择性地捕获 CD8+ T 细胞,同时最大限度地减少所需的血液样本量。这项技术可通过荧光图像分析对捕获的 CD8+ T 细胞中的 CD57+ 细胞进行准确可靠的量化。该设备能够轻松量化衰老的 CD57+CD8+ T 细胞,预计将极大地促进免疫学研究和临床应用。
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
BioChip Journal
BioChip Journal 生物-生化研究方法
CiteScore
7.70
自引率
16.30%
发文量
47
审稿时长
6-12 weeks
期刊介绍: BioChip Journal publishes original research and reviews in all areas of the biochip technology in the following disciplines, including protein chip, DNA chip, cell chip, lab-on-a-chip, bio-MEMS, biosensor, micro/nano mechanics, microfluidics, high-throughput screening technology, medical science, genomics, proteomics, bioinformatics, medical diagnostics, environmental monitoring and micro/nanotechnology. The Journal is committed to rapid peer review to ensure the publication of highest quality original research and timely news and review articles.
期刊最新文献
Multiplex Magnetic Biosensor Microarrays Facilitate Personalized Vaccination Schedules for SARS-CoV-2 Variants. Fabrication of Biomimetic Cell Culture Membranes Using Robust and Reusable Nickel Micropillar Molds. CRISPR/Cas-Based Nanobiosensor Using Plasmonic Nanomaterials to Detect Disease Biomarkers. Advancing Blood–Brain Barrier-on-a-Chip Models Through Numerical Simulations Advanced Microfluidic Platform for Tumor Spheroid Formation and Cultivation Fabricated from OSTE+ Polymer
×
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:604180095
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