Evidence map›Paper›PMID 40855880›Full record

ArticleAdvanced intelligent discovery2025

Generative Ai for Cardiovascular Cell Type-Specific Fluorescence Colorization of Live-Cell hPSC-Derived Cardiac Organoids.

Arun Kumar Reddy Kandula, Tanakit Phamornratanakun, Angello Huerta Gomez, Marcel El-Mokahal, Zhen Ma, Yunhe Feng, Huaxiao Yang

Abstract read
In one paragraph

Article in Advanced intelligent discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Proceedings of the ... AAAI Conference on Artificial Intelligence. AAAI Conference on Artificial Intelligence · 2026
    Article
  5. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Arun Kumar Reddy KandulaDepartment of Biomedical Engineering, University of North Texas, Denton, Texas, USA.
Tanakit PhamornratanakunDepartment of Biomedical Engineering, University of North Texas, Denton, Texas, USA.
Angello Huerta GomezDepartment of Biomedical Engineering, University of North Texas, Denton, Texas, USA.
Marcel El-MokahalDepartment of Biomedical Engineering, University of North Texas, Denton, Texas, USA.
Zhen MaDepartment of Biomedical & Chemical Engineering, Syracuse University, Syracuse, New York, USA.
Yunhe FengDepartment of Computer Science & Engineering, University of North Texas, Denton, Texas, USA.
Huaxiao YangDepartment of Biomedical Engineering, University of North Texas, Denton, Texas, USA.ORCID 0000-0001-9335-8201

Funding

Establishing an In Vitro Embryotoxicity Risk Classification System Based on Human Cardiac Organoid ModelR01HD101130 · NICHD · SYRACUSE UNIVERSITY · PI MA, ZHEN · 2020 to 2025
$2.3M
G-RISE at the University of North TexasT32GM136501 · NIGMS · UNIVERSITY OF NORTH TEXAS · PI BURGGREN, WARREN, HUGHES, LEE · 2021 to 2024
$1.8M
Assessing Tyrosine Kinase Inhibitors-induced Cardiotoxicity with an Organoid-AI SystemR56HL174856 · NHLBI · UNIVERSITY OF NORTH TEXAS · PI YANG, HUAXIAO · 2024 to 2024
$547k
NOTCH signaling on the underdeveloped cardiac vascularization of hypoplastic left heart syndrome in the hiPSC-derived vascularized cardiac organoidsR15HD108720 · NICHD · UNIVERSITY OF NORTH TEXAS · PI YANG, HUAXIAO · 2022 to 2022
$438k
NHLBI NIH HHS R56 HL174856NICHD NIH HHS R01 HD101130NICHD NIH HHS R15 HD108720NIGMS NIH HHS T32 GM136501
6 · The paper itself

Abstract

Human pluripotent stem cell (hPSC)-derived cardiac organoids (COs) are the most recent three-dimensional tissue structure that mimics the human heart's structure and functionality for modeling heart development and disease. Fluorescent labeling and imaging are commonly utilized to characterize the cellular information in COs. However, the additional step of fluorescence labeling and imaging is time-consuming, inefficient, and typically for end-timepoint characterization. Meanwhile, the COs are routinely examined by brightfield/phase contrast microscope to track live-cell organoid formation in structure and morphology. Although the brightfield microscope provides essential information about COs, such as morphology and overall structure, it limits our understanding of cardiovascular cells (e.g., cardiomyocytes, CMs and endothelial cells, ECs) and corresponding quantifications in COs. Is it possible to overcome these limitations of bright-field microscopic imaging and provide cardiovascular cell type-specific information similar to the fluorescence-labeled imaging acquisition in COs? This research addresses this limitation by proposing a generative AI system for colorizing phase contrast images of COs from bright-field microscopic imaging using conditional generative adversarial networks (cGANs) to generate cardiovascular cell type-specific fluorescence images of COs. By giving these phase contrast images with multichannel fluorescence colorization, this intelligence system unlocks cell type and quantifications of COs in high efficiency and accuracy.

Indexed as

bright-field microscopecardiac organoidsfluorescence imaginggenerative adversarial networkshuman pluripotent stem cell (hPSC)image colorization

Identifiers

PMID40855880
PMCPMC12373119

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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.