Evidence map›Paper›PMID 34876684›Full record

ArticleNature cell biology2021

Label-free multiplexed microtomography of endogenous subcellular dynamics using generalizable deep learning.

YoungJu Jo, Hyungjoo Cho, Wei Sun Park, Geon Kim, DongHun Ryu, Young Seo Kim, Moosung Lee, Sangwoo Park, Mahn Jae Lee, Hosung Joo and 6 more

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Article in Nature cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

54 citing papers in PubMed.

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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

16 authors.

YoungJu Jo *Department of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.ORCID http://orcid.org/0000-0002-2364-7160
Hyungjoo Cho *Tomocube, Daejeon, Republic of Korea.
Wei Sun Park *Department of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
Geon KimDepartment of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
DongHun RyuDepartment of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
Young Seo KimDepartment of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
Moosung LeeDepartment of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
Sangwoo ParkGwangju Center, Korea Basic Science Institute (KBSI), Gwangju, Republic of Korea.
Mahn Jae LeeKAIST Institute for Health Science and Technology, KAIST, Daejeon, Republic of Korea.
Hosung JooTomocube, Daejeon, Republic of Korea.
HangHun JoTomocube, Daejeon, Republic of Korea.
Seongsoo LeeGwangju Center, Korea Basic Science Institute (KBSI), Gwangju, Republic of Korea.
Sumin LeeTomocube, Daejeon, Republic of Korea.ORCID http://orcid.org/0000-0002-2264-2747
Hyun-Seok MinTomocube, Daejeon, Republic of Korea. hsmin@tomocube.com.ORCID http://orcid.org/0000-0002-7435-7884
Won Do HeoDepartment of Biological Sciences, KAIST, Daejeon, Republic of Korea. wdheo@kaist.ac.kr.ORCID http://orcid.org/0000-0001-7541-7319
YongKeun ParkDepartment of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea. yk.park@kaist.ac.kr.ORCID http://orcid.org/0000-0003-0528-6661

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Simultaneous imaging of various facets of intact biological systems across multiple spatiotemporal scales is a long-standing goal in biology and medicine, for which progress is hindered by limits of conventional imaging modalities. Here we propose using the refractive index (RI), an intrinsic quantity governing light-matter interaction, as a means for such measurement. We show that major endogenous subcellular structures, which are conventionally accessed via exogenous fluorescence labelling, are encoded in three-dimensional (3D) RI tomograms. We decode this information in a data-driven manner, with a deep learning-based model that infers multiple 3D fluorescence tomograms from RI measurements of the corresponding subcellular targets, thereby achieving multiplexed microtomography. This approach, called RI2FL for refractive index to fluorescence, inherits the advantages of both high-specificity fluorescence imaging and label-free RI imaging. Importantly, full 3D modelling of absolute and unbiased RI improves generalization, such that the approach is applicable to a broad range of new samples without retraining to facilitate immediate applicability. The performance, reliability and scalability of this technology are extensively characterized, and its various applications within single-cell profiling at unprecedented scales (which can generate new experimentally testable hypotheses) are demonstrated.

Indexed as

Deep Learning3T3 CellsActinsAnimalsCell Line, TumorCell MembraneCell NucleolusCell NucleusChlorocebus aethiopsCOS CellsElectron Microscope TomographyHEK293 CellsHeLa CellsHumansImaging, Three-DimensionalLipid DropletsActins

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Registered trials

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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.