Evidence map›Paper›PMID 38802562›Full record

ArticleNature biotechnology2025

Long-term intravital subcellular imaging with confocal scanning light-field microscopy.

Zhi Lu, Siqing Zuo, Minghui Shi, Jiaqi Fan, Jingyu Xie, Guihua Xiao, Li Yu, Jiamin Wu, Qionghai Dai

Abstract read
In one paragraph

Article in Nature biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

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  14. Correlative Imaging Platform Linking Taste Cell Function to Molecular Identity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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.

Zhi Lu *Department of Automation, Tsinghua University, Beijing, China.ORCID http://orcid.org/0000-0003-3739-8756
Siqing Zuo *Department of Automation, Tsinghua University, Beijing, China.
Minghui Shi *State Key Laboratory of Membrane Biology, Tsinghua University-Peking University Joint Center for Life Sciences, Beijing Frontier Research Center for Biological Structure, School of Life Sciences, Tsinghua University, Beijing, China.
Jiaqi FanInstitute for Brain and Cognitive Sciences, Tsinghua University, Beijing, China.ORCID http://orcid.org/0009-0001-1860-3729
Jingyu XieDepartment of Automation, Tsinghua University, Beijing, China.
Guihua XiaoDepartment of Automation, Tsinghua University, Beijing, China.
Li YuState Key Laboratory of Membrane Biology, Tsinghua University-Peking University Joint Center for Life Sciences, Beijing Frontier Research Center for Biological Structure, School of Life Sciences, Tsinghua University, Beijing, China. liyulab@tsinghua.edu.cn.
Jiamin WuDepartment of Automation, Tsinghua University, Beijing, China. wujiamin@tsinghua.edu.cn.ORCID http://orcid.org/0000-0003-3479-1026
Qionghai DaiDepartment of Automation, Tsinghua University, Beijing, China. qhdai@tsinghua.edu.cn.ORCID http://orcid.org/0000-0001-7043-3061

Funding

China Postdoctoral Science Foundation 2023M741963National Natural Science Foundation of China (National Science Foundation of China) 62071272National Natural Science Foundation of China (National Science Foundation of China) 62088102National Natural Science Foundation of China (National Science Foundation of China) 62222508National Natural Science Foundation of China (National Science Foundation of China) 62231018
6 · The paper itself

Abstract

Long-term observation of subcellular dynamics in living organisms is limited by background fluorescence originating from tissue scattering or dense labeling. Existing confocal approaches face an inevitable tradeoff among parallelization, resolution and phototoxicity. Here we present confocal scanning light-field microscopy (csLFM), which integrates axially elongated line-confocal illumination with the rolling shutter in scanning light-field microscopy (sLFM). csLFM enables high-fidelity, high-speed, three-dimensional (3D) imaging at near-diffraction-limit resolution with both optical sectioning and low phototoxicity. By simultaneous 3D excitation and detection, the excitation intensity can be reduced below 1 mW mm

Indexed as

Intravital MicroscopyAnimalsDrosophilaImaging, Three-DimensionalMiceMicroscopy, Confocal

Identifiers

PMID38802562
PMCPMC11994454

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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.