4.7 Article

MicroRNA-21 expression in single living cells revealed by fluorescence and SERS dual-response microfluidic droplet platform

Journal

LAB ON A CHIP
Volume 22, Issue 11, Pages 2165-2172

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2lc00096b

Keywords

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Funding

  1. National Natural Science Foundation of China [22004117, 31900986, U2032134]
  2. Natural Science Foundation of Jiangsu Province of China [BK20201443]

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Analysis of single-cell microRNA is essential for revealing genetic heterogeneity at the cell level. In this study, SERS and fluorescence imaging technology were used to achieve direct in situ, nondestructive, and highly sensitive detection of a small number of microRNA-21 (miR-21) in a single intact living cell. A multifunctional plasmonic nanoprobe was designed, allowing for highly sensitive and reliable detection of miR-21 through dual-signal switching. The combination of SERS and microdroplets encapsulation provided a feasible way to determine miR-21 secreted by single cells without cell lysis and time-consuming isolation steps. The research accurately and quantitatively evaluated the cellular heterogeneity in miR-21 expression, providing important reference information for understanding the effects of miRNAs on cancer diseases at the single-cell level.
Analysis of single-cell microRNA is essential to reveal cell heterogeneity at the genetic level. It raises a high demand for single-cell analytical methods because single-cell microRNA sequences are highly similar and small in size and feature low-level expression. Herein, SERS and fluorescence imaging technology were introduced into a microfluidic droplet platform to realize direct in situ, nondestructive, and highly sensitive detection of a small number of microRNA-21 (miR-21) in a single intact living cell. A multifunctional plasmonic nanoprobe was designed by decorating a gold nanoparticle with fluorescent dye (ROX)-labeled probe DNA and capture DNA strands. The dual-signal switching of fluorescence turn-off and SERS turn-on of ROX in response to miR-21 achieves highly sensitive and reliable detection of miR-21 in a single cell. The turn-on of SERS signal with a zero background guarantees the sensitivity of the detection. The fluorescence-SERS simultaneous response strategy was able to mutually corroborate the test results, improving the reliability of determining low-level expression of miR-21. SERS combined with encapsulation of microdroplets provides a feasible way to conduct in situ, nondestructive determination of miR-21 secreted by single cells, avoiding cell lysis and tedious time-consuming steps of miR-21 isolation. As a result, the miR-21 expressed by various types of single cells was investigated by fluorescence imaging and the cellular heterogeneity in miR-21 expression was evaluated accurately and quantitatively by SERS. This research would provide important reference information for understanding the effects of miRNAs on cancer diseases at the single-cell level.

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