ArticleAnalytical chemistry2014
A generalizable, tunable microfluidic platform for delivering fast temporally varying chemical signals to probe single-cell response dynamics.
Article in Analytical chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
13 citing papers in PubMed.
- Self-Regulated Selective Surface Coating Enables Confinement of Adherent Cells in Closed Microfluidic Arrays.Analytical chemistry · 2025Article
- A sharp-edge-based acoustofluidic chemical signal generator.Lab on a chip · 2018Article
- A programmable platform for sub-second multichemical dynamic stimulation and neuronal functional imaging in C. elegans.Lab on a chip · 2018Article
- Oscillatory IL-2 stimulus reveals pertinent signaling timescales of T cell responsiveness.PloS one · 2018Article
- Multimodal microfluidic platform for controlled culture and analysis of unicellular organisms.Biomicrofluidics · 2017Article
- Single-cell resolution of intracellular T cell CaIntegrative biology : quantitative biosciences from nano to macro · 2017Article
- Microfluidic techniques for high throughput single cell analysis.Current opinion in biotechnology · 2016Review
- Three-dimensional models for studying development and disease: moving on from organisms to organs-on-a-chip and organoids.Integrative biology : quantitative biosciences from nano to macro · 2016Review
- Microfluidics in systems biology-hype or truly useful?Current opinion in biotechnology · 2016Review
- An integrated platform for large-scale data collection and precise perturbation of live Drosophila embryos.Scientific reports · 2016Article
- Compartmentalized microchannel array for high-throughput analysis of single cell polarized growth and dynamics.Scientific reports · 2015Article
- Advances in microfluidic platforms for analyzing and regulating human pluripotent stem cells.Current opinion in genetics & development · 2015Review
- An automated programmable platform enabling multiplex dynamic stimuli delivery and cellular response monitoring for high-throughput suspension single-cell signaling studies.Lab on a chip · 2015Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
Understanding how biological systems transduce dynamic, soluble chemical cues into physiological processes requires robust experimental tools for generating diverse temporal chemical patterns. The advent of microfluidics has seen the development of platforms for rapid fluid exchange allowing ease of changes in the cellular microenvironment and precise cell handling. Rapid exchange is important for exposing systems to temporally varying signals. However, direct coupling of macroscale fluid flow with microstructures is potentially problematic due to the high shear stresses that inevitably add confounding mechanical perturbation effects to the biological system of interest. Here, we have devised a method of translating fast and precise macroscale flows to microscale flows using a monolithically integrated perforated membrane. We integrated a high-density cell trap array for nonadherent cells that are challenging to handle under flow conditions with a soluble chemical signal generator module. The platform enables fast and repeatable switching of stimulus and buffer at low shear stresses for quantitative live, single-cell fluorescent studies. This modular design allows facile integration of any cell-handling chip design with any chemical delivery module. We demonstrate the utility of this device by characterizing heterogeneity of oscillatory response for cells exposed to alternating Ca(2+) waveforms at various periodicities. This platform enables the analysis of cell responses to chemical perturbations at a single-cell resolution that is necessary in understanding signal transduction pathways.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.