Publication:
Human cerebral organoids: cellular composition and subcellular morphological features

dc.contributor.authorMateos-Martínez, Patricia
dc.contributor.authorCoronel Lopez, Raquel
dc.contributor.authorSachse, Martin
dc.contributor.authorGonzález-Sastre, Rosa
dc.contributor.authorMaeso Cuesta, Laura
dc.contributor.authorRodríguez, María Josefa
dc.contributor.authorTerrón-Orellana, Maria Carmen
dc.contributor.authorLópez-Alonso, Victoria
dc.contributor.authorListe-Noya, Isabel
dc.contributor.funderMinisterio de Ciencia e Innovación (España)
dc.contributor.funderAgencia Estatal de Investigación (España)
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
dc.date.accessioned2024-10-29T13:27:00Z
dc.date.available2024-10-29T13:27:00Z
dc.date.issued2024
dc.descriptionSupplementary figure S1: (A) Uniform manifold approximation and projection (UMAP) plot from unsupervised clustering of scRNAseq of the hCOs after culturing for 45 days and 60 days. Colors represent the cell clusters annotated as excitatory neurons (EN), interneurons (IN), neurons (N), intermediate precursor cells (IPC), oligodendrocyte precursors cells (OPC), astrocytes (AS), outer radial glia and astroglia (oRG + Astroglia), apical radial glia (aRG), and proliferative radial glia (pro-RG). (B) Bar plot displaying the proportion of each cluster of cells for hCOs after culturing for 45 days and 60 days. A dot plot indicating the expression of cell type-specific marker genes. The dot size represents the percentage of cells expressing the gene and the color gradient from low (blue) to high (red) indicates the average relative expression. (C) Violin plots showing the expression for VIM, SOX2, DCX, and MAP2 for hCOs after culturing for 45 days and 60 days. (D) The dot plot showing the expression for the cellular cluster of marker genes of CR: Cajal-Retzius; CP: choroid plexus; FD: forebrain dorsal; FV: forebrain ventral; HY: hippocampus; and MB/HB: midbrain and hindbrain. (E) Representation of enriched GO terms for upregulated and downregulated DEGs of the hCOs after culturing for 60 days versus after culturing for 45 days in the excitatory neurons cluster (Done from ReviGO).
dc.description.abstractIntroduction: Human cerebral organoids (hCOs) derived from pluripotent stem cells are very promising for the study of neurodevelopment and the investigation of the healthy or diseased brain. To help establish hCOs as a powerful research model, it is essential to perform the morphological characterization of their cellular components in depth. Methods: In this study, we analyzed the cell types consisting of hCOs after culturing for 45 days using immunofluorescence and reverse transcriptase qualitative polymerase chain reaction (RT-qPCR) assays. We also analyzed their subcellular morphological characteristics by transmission electron microscopy (TEM). Results: Our results show the development of proliferative zones to be remarkably similar to those found in human brain development with cells having a polarized structure surrounding a central cavity with tight junctions and cilia. In addition, we describe the presence of immature and mature migrating neurons, astrocytes, oligodendrocyte precursor cells, and microglia-like cells. Discussion: The ultrastructural characterization presented in this study provides valuable information on the structural development and morphology of the hCO, and this information is of general interest for future research on the mechanisms that alter the cell structure or function of hCOs.
dc.description.peerreviewed
dc.description.sponsorshipThe author(s) declare that financial support was received for the research, authorship, and/or publication of this article. The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: Grant PID2021-126715OB-I00 financed by MCIN/AEI/10.13039/501100011033, “ERDF A way of making Europe,” by the Grant of Instituto de Salud Carlos III (ISCIII) PI22CIII/00055, grant RTI2018-101663-B-100 financed by MCIN/AEI/, the UFIECPY 328/22, and PEJ-2021-TL/BMD-21001, a grant to LM financed by MCI, and a grant to PMM financed by MCIN-the UFIECPY-396/19, PEJ2018-004961.
dc.format.page1406839
dc.format.volume18
dc.identifier.citationFront Cell Neurosci. 2024 Jun 12:18:1406839.
dc.identifier.doi10.3389/fncel.2024.1406839
dc.identifier.e-issn1662-5102
dc.identifier.journalFrontiers in cellular neuroscience
dc.identifier.pubmedID38933177
dc.identifier.urihttps://hdl.handle.net/20.500.12105/25371
dc.language.isoeng
dc.publisherFrontiers Media
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PID2021-126715OB-I00
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PI22CIII/00055
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RTI2018-101663-B-100
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/UFIECPY328/22
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PEJ-2021-TL/BMD-21001
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/UFIECPY-396/19
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PEJ2018-004961
dc.relation.publisherversionhttps://doi.org/10.3389/fncel.2024.1406839
dc.repisalud.centroISCIII::Unidades Centrales Científico-Técnicas (UCCTs)
dc.repisalud.centroISCIII::Unidad Funcional de Investigación de Enfermedades Crónicas (UFIEC)
dc.repisalud.institucionISCIII
dc.rights.accessRightsopen access
dc.rights.licenseAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectGlial cells
dc.subjectHuman brain organoids
dc.subjectHuman pluripotent stem cells
dc.subjectMini-brains
dc.subjectNeural stem cells
dc.subjectNeurodevelopment
dc.subjectTransmission electron microscopy
dc.subjectUltrastructural characterization
dc.titleHuman cerebral organoids: cellular composition and subcellular morphological features
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication
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