Evidence map›Paper›PMID 34381966›Full record

ArticleiScience2021

Super-multiplex imaging of cellular dynamics and heterogeneity by integrated stimulated Raman and fluorescence microscopy.

Jingwen Shou, Robert Oda, Fanghao Hu, Keiko Karasawa, Mutsuo Nuriya, Masato Yasui, Bruce Shiramizu, Wei Min, Yasuyuki Ozeki

Abstract read
In one paragraph

Article in iScience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

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  11. Analytical Techniques for Single-Cell Biochemical Assays of Lipids.Annual review of biomedical engineering · 2023
    Review
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  17. Miniaturized Chemical Tags for Optical Imaging.Angewandte Chemie (International ed. in English) · 2022
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Jingwen ShouDepartment of Electrical Engineering and Information Systems, The University of Tokyo, Tokyo 113-8656, Japan.
Robert OdaDepartment of Electrical Engineering and Information Systems, The University of Tokyo, Tokyo 113-8656, Japan.
Fanghao HuDepartment of Chemistry, Columbia University, New York, New York 10027, USA.
Keiko KarasawaDepartment of Pharmacology School of Medicine, Keio University, Tokyo 160-8582, Japan.
Mutsuo NuriyaDepartment of Pharmacology School of Medicine, Keio University, Tokyo 160-8582, Japan.
Masato YasuiDepartment of Pharmacology School of Medicine, Keio University, Tokyo 160-8582, Japan.
Bruce ShiramizuDepartment of Molecular Biosciences and Bioengineering, The University of Hawaii, Manoa, 1955 East West Road, Honolulu, Hawaii 96822, USA.
Wei MinDepartment of Chemistry, Columbia University, New York, New York 10027, USA.
Yasuyuki OzekiDepartment of Electrical Engineering and Information Systems, The University of Tokyo, Tokyo 113-8656, Japan.

Funding

Super-multiplex vibrational imaging in living cellsR01GM128214 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI MIN, WEI · 2018 to 2021
$1.5M
NIGMS NIH HHS R01 GM128214
6 · The paper itself

Abstract

Observing multiple molecular species simultaneously with high spatiotemporal resolution is crucial for comprehensive understanding of complex, dynamic, and heterogeneous biological systems. The recently reported super-multiplex optical imaging breaks the "color barrier" of fluorescence to achieve multiplexing number over six in living systems, while its temporal resolution is limited to several minutes mainly by slow color tuning. Herein, we report integrated stimulated Raman and fluorescence microscopy with simultaneous multimodal color tunability at high speed, enabling super-multiplex imaging covering diverse molecular contrasts with temporal resolution of seconds. We highlight this technique by demonstrating super-multiplex time-lapse imaging and image-based cytometry of live cells to investigate the dynamics and cellular heterogeneity of eight intracellular components simultaneously. Our technique provides a powerful tool to elucidate spatiotemporal organization and interactions in biological systems.

Indexed as

Biological sciences research methodologiesCell biologyOptics

Identifiers

PMID34381966
PMCPMC8333161

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.