ArticleSmall science2025
Integrative Biosensing Nanoplasmonic Array for Real-Time Spatiotemporal Imaging of Protein Secretion in Cell-to-Cell Communication.
Article in Small science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Nano-Enabled Microfluidic Platforms for Functional Immunomonitoring in Pediatric Sepsis.International journal of nanomedicine · 2026Review
- Integrative Biosensing Nanoplasmonic Array for Real-Time Spatiotemporal Imaging of Protein Secretion in Cell-to-Cell Communication.Small science · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
Protein secretion plays a crucial role in cell-to-cell communication, tissue homeostasis, and disease progression. Mapping secretomes from paired cells provides valuable insights into their interactions; however, existing approaches yield only semi-quantitative, endpoint data, lacking real-time and quantitative resolution. Herein, real-time spatiotemporal imaging of extracellular secretions from individual cells using a high-throughput integrative biosensing nanoplasmonic array (iBNA) within microfluidics is presented. The self-assembled iBNA, composed of precisely arranged gold nanostructures functionalized with aptamer receptors, enhances plasmonic resonance and significantly improves the spatiotemporal resolution and specificity of interleukin-6 (IL-6) imaging, surpassing conventional techniques. The iBNA's molecular recognition mechanism exploits biomolecular surface binding-induced localized plasmonic resonance shifts, correlating with cytokine concentration and enabling optoelectronic detection of transmitted light. Using iBNA, spatiotemporal resolution images of polarized cytokine-mediated cell-to-cell communication between Jurkat T cells and CD4+ T cells, which are essential to immune responses, are achieved. This transformative platform provides unprecedented insights into the spatiotemporal dynamics of protein secretion, offering significant potential for immunological research, cellular biology, and diagnostic applications in infectious diseases.
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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.