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Updated: Aug 6, 2026

Microfluidic Co-Culture Models for Dissecting the Immune Response in in vitro Tumor Microenvironments
Published on: April 30, 2021
Metabolic coupling between a single tumor cell and fibroblasts on microdroplet array chips
Jian Zhao1, Xinxing Miao1, Xiang Xiao1
1Institute of Functional Nano and Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou, Jiangsu Province 215123, P. R. China. jliu@suda.edu.cn.
Abstract:
Metabolic coupling between tumor cells and fibroblasts critically regulates tumor aggressiveness including matrix metalloproteinase-9 (MMP-9) activities via nitric oxide (NO)-mediated pathways. It remains a fundamental challenge to reveal the interactions between tumor cells and fibroblasts at the single cell level. Here we report a microdroplet array platform that enables co-encapsulating a single tumor cell and fibroblasts for the studies of cell-to-cell interactions. We have investigated an inducible nitric oxide synthase (iNOS)-dependent metabolic coupling between tumor cells (HeLa and MCF-7) and fibroblasts (3T3-L1), in which fibroblasts markedly enhance tumor-cell MMP-9 activities via NO signaling. Inhibition with L-NAME effectively disrupts this coupling and markedly reduces MMP-9 activities. Our results obtained using microchips reveal phenotype-dependent correlations between fibroblast lipid droplet accumulation and tumor-cell aggressiveness, highlighting how metabolic competition and enzymatic regulation jointly shape tumor-stroma crosstalk at the single-cell level.
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