Profiling signaling mediators for cell-cell interactions and communications with microfluidics-based single-cell analysis tools

被引:0
|
作者
Yuan, Shuai [1 ]
Zhang, Peng [2 ]
Zhang, Feng [3 ]
Yan, Shiqiang [4 ]
Dong, Ruihua [1 ]
Wu, Chengjun [1 ]
Deng, Jiu [1 ]
机构
[1] Univ Hlth & Rehabil Sci, Sch Hlth & Life Sci, Qingdao 266113, Peoples R China
[2] King Abdullah Univ Sci & Technol, Biol & Environm Sci & Engn Div, Thuwal 239556900, Saudi Arabia
[3] Nanjing Med Univ, Affiliated Hosp 1, Dept Cardiol, Nanjing 210000, Peoples R China
[4] Chinese Acad Sci, Shenzhen Inst Adv Technol, Ctr Canc Immunol, Shenzhen 518055, Peoples R China
基金
中国博士后科学基金;
关键词
INTERCELLULAR CROSSTALK; EXTRACELLULAR VESICLES; MULTIPLEXED ANALYSIS; TECHNOLOGIES; CYTOKINE; CANCER; FLOW; HETEROGENEITY; PROTEINS; JUNCTION;
D O I
10.1016/j.isci.2024.111663
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cell-cell interactions and communication represent the fundamental cornerstone of cells' collaborative efforts in executing diverse biological processes. A profound understanding of how cells interface through various mediators is pivotal across a spectrum of biological systems. Recent strides in microfluidic technologies have significantly bolstered the precision and prowess in capturing and manipulating cells with exceptional spatial and temporal resolution. These advanced methodologies converge with multi-signal mediator detection systems, furnishing potent, high-throughput platforms for dissecting cell-cell interactions at the single-cell level. This approach empowers researchers to delve into intricate cellular dynamics with unprecedented accuracy and efficiency. Here, we present a critical evaluation of the latest advancements in microfluidics-driven techniques for detecting signal mediators involved in cell-cell interactions and communication at the single-cell level. We underscore notable biological applications that have benefited from these technologies and identify pressing challenges that must be addressed in future endeavors leveraging microfluidic tools for single-cell interaction studies.
引用
收藏
页数:20
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