Evidence map›Paper›PMID 41646420›Full record

ArticleResearch square2026

A modular tissue-clearing framework integrated with light-field microscopy enables rapid volumetric phenotyping of cardiac tissue.

Shi Lin, Denise Schichines, Hua-Man Hsu, Yen-Ling Hung, Kaushik Chowdhury, I-Ting Lin, Chieh-Ju Wang, Min-Ju Tsai, Zi-Yuan Liu, Kai-Chien Yang and 3 more

Abstract readPreprint
In one paragraph

Article in Research square, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Shi LinDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.
Denise SchichinesDepartment of Plant and Microbial Biology, University of California, Berkeley, CA, USA.
Hua-Man HsuDivision of Research Microscopy Solutions, Carl Zeiss Co., Ltd., Hsinchu, Taiwan.
Yen-Ling HungDepartment and Graduate Institute of Pharmacology, National Taiwan University College of Medicine, Taipei, Taiwan.
Kaushik ChowdhuryInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
I-Ting LinInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Chieh-Ju WangInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Min-Ju TsaiResearch Center for Applied Sciences, Academia Sinica, Taipei, Taiwan.
Zi-Yuan LiuDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.
Kai-Chien YangDepartment and Graduate Institute of Pharmacology, National Taiwan University College of Medicine, Taipei, Taiwan.
Shih-Lei Ben LaiInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Bi-Chang ChenResearch Center for Applied Sciences, Academia Sinica, Taipei, Taiwan.ORCID https://orcid.org/0000-0002-1876-7432
Rebecca HealdDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.

Funding

A Zeiss LSM 710 confocal microscope for the Biological Imaging Facility at the US10RR026866 · NCRR · UNIVERSITY OF CALIFORNIA BERKELEY · PI RUZIN, STEVEN EARL · 2010 to 2010
$419k
NCRR NIH HHS S10 RR026866
6 · The paper itself

Abstract

Tissue clearing has transformed volumetric imaging by improving optical access to thick tissues, yet most existing protocols remain rigid and fail to accommodate the biochemical diversity of different samples. Here, we introduce a question-oriented modular framework that enables flexible assembly of clearing and imaging pipelines tailored to specific biological objectives. By systematically optimizing each module to preserve endogenous fluorescence, antigenicity, and tissue integrity while achieving high transparency and protein retention, we demonstrate its use across diverse cardiac applications-development, infarction and regeneration, as well as immune and vascular mapping-showing that different questions require distinct module assemblies and parameters. Coupled with light-field microscopy (LFM), the workflow efficiently captures submillimeter sections with 30-100-fold smaller datasets and rapid computational reconstruction, enabling high-throughput quantitative volumetric analysis. Together, this modular framework and imaging integration provide a rational and practical foundation for adaptable and interoperable 3D analyses of regenerative, pathological, and comparative systems across vertebrate models.

Identifiers

PMID41646420
PMCPMC12869691

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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.