Publication:
Human cerebral organoids: Complex, versatile, and human-relevant models of neural development and brain diseases.

dc.contributor.authorCoronel Lopez, Raquel
dc.contributor.authorGonzález-Sastre, Rosa
dc.contributor.authorMateos-Martínez, Patricia
dc.contributor.authorMaeso Cuesta, Laura
dc.contributor.authorLlorente-Beneyto, Elena
dc.contributor.authorMartín-Benito, Sabela
dc.contributor.authorCosta Gagosian, Viviana S
dc.contributor.authorFoti, Leonardo
dc.contributor.authorGonzález-Caballero, MCarmen
dc.contributor.authorLópez-Alonso, Victoria
dc.contributor.authorListe-Noya, Isabel
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderMinisterio de Ciencia, Innovación y Universidades (España)
dc.contributor.funderAgencia Estatal de Investigación (España)
dc.contributor.funderComunidad de Madrid (España)
dc.date.accessioned2026-08-20T15:03:10Z
dc.date.available2026-08-20T15:03:10Z
dc.date.issued2026-03-01
dc.description.abstractThe brain is the most complex human organ, and commonly used models, such as two-dimensional-cell cultures and animal brains, often lack the sophistication needed to accurately use in research. In this context, human cerebral organoids have emerged as valuable tools offering a more complex, versatile, and human-relevant system than traditional animal models, which are often unable to replicate the intricate architecture and functionality of the human brain. Since human cerebral organoids are a state-of-the-art model for the study of neurodevelopment and different pathologies affecting the brain, this field is currently under constant development, and work in this area is abundant. In this review, we give a complete overview of human cerebral organoids technology, starting from the different types of protocols that exist to generate different human cerebral organoids. We continue with the use of brain organoids for the study of brain pathologies, highlighting neurodevelopmental, psychiatric, neurodegenerative, brain tumor, and infectious diseases. Because of the potential value of human cerebral organoids, we describe their use in transplantation, drug screening, and toxicology assays. We also discuss the technologies available to study cell diversity and physiological characteristics of organoids. Finally, we summarize the limitations that currently exist in the field, such as the development of vasculature and microglia, and highlight some of the novel approaches being pursued through bioengineering.
dc.description.peerreviewed
dc.description.sponsorshipThis work was supported by the Grant PID2021-126715OB-I00 financed by MCIN/AEI/10.13039/501100011033 and “ERDF A way of making Europe”, by the Grant PI22CIII/00055 funded by Instituto de Salud Carlos III (ISCIII), and the UFIECPY 398/19 (PEJ2018-004965) grant to RGS funded by AEI (Spain), the UFIECPY-396/19 (PEJ2018-004961) grant financed by MCIN (Spain) and FI23CIII/00003 grant funded by ISCIII-PFIS (Spain) to PMM, the UFIECPY 328/22 (PEJ-2021-TL/BMD-21001) grant to LM financed by CAM (Spain), and the grant by CAPES (Coordination for the Improvement of Higher Education Personnel), through the PDSE program (Programa de Doutorado Sanduíche no Exterior), to VSCG financed by MEC (Brazil).
dc.format.number3
dc.format.page837-854
dc.format.volume21
dc.identifier.citationCoronel, R., González-Sastre, R., Mateos-Martínez, P., Maeso, L., Llorente-Beneyto, E., Martín-Benito, S., Costa Gagosian, V. S., Foti, L., González-Caballero, M. C., López-Alonso, V., & Liste, I. (2025). Human cerebral organoids: Complex, versatile, and human-relevant models of neural development and brain diseases. Neural Regeneration Research, 21(3), 837–854. https://doi.org/10.4103/NRR.NRR-D-24-01639.
dc.identifier.doi10.4103/NRR.NRR-D-24-01639
dc.identifier.journalNeural Regeneration Research
dc.identifier.pubmedID40364645
dc.identifier.urihttps://hdl.handle.net/20.500.12105/27674
dc.language.isoeng
dc.publisherWolters Kluwer
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-126715OB-I00/ES/IMPLICACIONES DE LA PROTEINA PRECURSORA AMILOIDE (APP): NEURODESARROLLO Y ENFERMEDAD DE ALZHEIMER/
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII/AESI/PI22CIII%2F00055/ES/Modelos humanos neurales para estudiar la evolución celular y proteómica en la enfermedad de Alzheimer/
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI//UFIECPY 398%2F19 (PEJ2018-004965)/ES//
dc.relation.projectIDinfo:eu-repo/grantAgreement/MCIN//UFIECPY-396%2F19 (PEJ2018-004961)/ES//
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII//FI23CIII%2F00003/ES//
dc.relation.projectIDinfo:eu-repo/grantAgreement/CAM//UFIECPY 328%2F22 (PEJ-2021-TL%2FBMD-21001)/ES//
dc.relation.publisherversionhttps://doi.org/10.4103/NRR.NRR-D-24-01639
dc.repisalud.centroISCIII::Unidad Funcional de Investigación de Enfermedades Crónicas (UFIEC)
dc.repisalud.centroISCIII::Centro Nacional de Sanidad Ambiental (CNSA)
dc.repisalud.institucionISCIII
dc.rights.accessRightsopen access
dc.rights.licenseAttribution-NonCommercial-ShareAlike 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectAssembloids
dc.subjectBioengineering
dc.subjectChallenges
dc.subjectDisease modeling
dc.subjectDrug screening and toxicology
dc.subjectHuman brain organoids
dc.subjectHuman pluripotent stem cells
dc.subjectNeurodegenerative diseases
dc.subjectNeurodevelopment
dc.subjectVascularization
dc.titleHuman cerebral organoids: Complex, versatile, and human-relevant models of neural development and brain diseases.
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication
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