Single-cell sequencing and organoids: applications in organ development and disease

The integration of single-cell sequencing and organoid technologies has been transformative for biomedical research, enabling investigations of organ development, disease mechanisms, and therapeutic innovation at even finer resolutions. Organoids serve as 3D in vitro models that replicate the structural and functional complexity of human tissues, while single-cell sequencing can resolve cellular heterogeneity, transcriptional dynamics, and lineage trajectories at high resolution. This review systematically explores the synergistic potential of these two technologies across multiple domains. First, it describes their application in studying the developmental mechanisms of organs including the brain, lungs, heart, liver, intestines, and kidneys, revealing key signaling pathways and cellular interaction networks. Then, it details their application in studying in vitro models of various diseases, including neurodegenerative disorders, genetic diseases, infectious diseases, metabolic syndrome, and tumors, advancing the in-depth analysis of pathological mechanisms. By leveraging patient-derived organoid biobanks, combining these two technologies can accelerate drug screening and precision, while utilizing transplantable tissue constructs to pioneer regenerative medicine strategies. This review also highlights the strengths of combining these two technologies in dynamically decoding cellular behavior and communication networks. By constructing physiologically relevant multifunctional research platforms, the integration of single-cell sequencing with organoid models will accelerate the elucidation of disease mechanisms and drive innovative breakthroughs in precision medicine and regenerative medicine. Looking ahead, the deep integration of single-cell sequencing with organoids, combined with cutting-edge technologies such as spatial transcriptomics and gene editing, will continue to propel life sciences toward a transformative leap from descriptive research to mechanism-driven, precision-oriented, and personalized approaches.

Authors

Institutions

Publication Details

Journal
Molecular Biomedicine
Published
2025-12-08
DOI
https://doi.org/10.1186/s43556-025-00364-6
Citations
2
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
1.61
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Single-cell sequencing and organoids: applications in organ development and disease

Boqiang Tao, Qirong Li, Jianmei Yin, Dongxu Wang et al.
2 citations
Molecular Biomedicine
Single-cell and spatial transcriptomics
1.61
article

Single-cell sequencing and organoids: applications in organ development and disease

Boqiang Tao, Qirong Li, Jianmei Yin, Dongxu Wang, Qiang Feng, Tiantian Li, Hao Ming, Chao Lin, Hao Yang, Yanxin Liu, Wei Gao
article en
2 citations

Abstract

The integration of single-cell sequencing and organoid technologies has been transformative for biomedical research, enabling investigations of organ development, disease mechanisms, and therapeutic innovation at even finer resolutions. Organoids serve as 3D in vitro models that replicate the structural and functional complexity of human tissues, while single-cell sequencing can resolve cellular heterogeneity, transcriptional dynamics, and lineage trajectories at high resolution. This review systematically explores the synergistic potential of these two technologies across multiple domains. First, it describes their application in studying the developmental mechanisms of organs including the brain, lungs, heart, liver, intestines, and kidneys, revealing key signaling pathways and cellular interaction networks. Then, it details their application in studying in vitro models of various diseases, including neurodegenerative disorders, genetic diseases, infectious diseases, metabolic syndrome, and tumors, advancing the in-depth analysis of pathological mechanisms. By leveraging patient-derived organoid biobanks, combining these two technologies can accelerate drug screening and precision, while utilizing transplantable tissue constructs to pioneer regenerative medicine strategies. This review also highlights the strengths of combining these two technologies in dynamically decoding cellular behavior and communication networks. By constructing physiologically relevant multifunctional research platforms, the integration of single-cell sequencing with organoid models will accelerate the elucidation of disease mechanisms and drive innovative breakthroughs in precision medicine and regenerative medicine. Looking ahead, the deep integration of single-cell sequencing with organoids, combined with cutting-edge technologies such as spatial transcriptomics and gene editing, will continue to propel life sciences toward a transformative leap from descriptive research to mechanism-driven, precision-oriented, and personalized approaches.

Molecular BiomedicineVol. 6(1)
Jilin University (CN), Wenzhou Vocational College of Science and Technology (CN), First Hospital of Jilin University (CN), Jilin Province Science and Technology Department (CN), Jilin Agricultural University (CN), WengFu Group (China) (CN), Jilin Business and Technology College
Openalex Percentile: Top 14%
Single-cell and spatial transcriptomics
1.61
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.