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1.
Tianjin Medical Journal ; (12): 38-43, 2024.
Artigo em Chinês | WPRIM | ID: wpr-1020967

RESUMO

Cerebral organoids are three-dimensional nerve cultures induced by embryonic stem cells(ESCs)or induced pluripotent stem cells(iPSCs)that mimic the structure and function of human brain.With the continuous optimization of cerebral organoid culture technology and the combination with emerging technologies such as organ transplantation,gene editing and organoids-on-chip,complex brain tissue structures such as functional vascular structures and neural circuits have been produced,which provides new methods and ideas for studying human brain development and diseases.This article reviews the latest advances in brain organoid technology,describes its application in neurological diseases and advances in stroke modeling and transplantation treatment.

2.
Acta Anatomica Sinica ; (6): 383-391, 2023.
Artigo em Chinês | WPRIM | ID: wpr-1015192

RESUMO

Objective To understand the characteristics and developmental differences between cerebral organoids in vitro and normal cerebral cortices in vivo. Methods 1. Grouping: cerebral cortices in vivo group and cultured cerebral organoids in vitro group. 2. Sample collection: cortical tissues were collected from Kunming mouse embryos at embryonic day 7.5(E7.5), E9.5, E11.5, E14.5, and postnatal day 3 (P3) or P7. Three specimens were taken from each group. Meanwhile, cerebral organoids were cultured with mouse induced pluripotent stem cells (iPSCs), and samples at different culture time point were collected, and more than 3 samples were collected at each time point. 3. Detection method: the distribution of different types of cells in each group of specimens was analyzed by immunofluorescent staining. Results While relative similarities between in vivo cerebral cortical development and the cerebral organoids in vitro were observed, including the histogenesis, and the morphological differentiation of nerve cells and glial cells, the lamellar architecture of cerebral cortex in mouse brain was not observed in cerebral organoids. Conclusion The development of cerebral organoids in vitro has some similarity with body's cortical development. Therefore, cerebral organoids can be used to a substitution of cortex and diseases' models, but improvement of the existing technologies is necessary.

3.
Chinese Journal of Neuromedicine ; (12): 1076-1078, 2019.
Artigo em Chinês | WPRIM | ID: wpr-1035117

RESUMO

The 3D human brain organ is aninvitrocultured organ that can be implemented by a researcher in recent years in a standard tissue culture chamber. Its growth and development is very similar to the endogenous developmental program of the human brain. The 3D human brain organs can promote people's understanding of human brain characteristics, and thus, conduct more in-depth research on human brain neuropsychiatric diseases. This is a review of the development, application, obstacles and prospects of 3D human brain organs.

4.
Protein & Cell ; (12): 823-833, 2017.
Artigo em Inglês | WPRIM | ID: wpr-758016

RESUMO

The development of a cerebral organoid culture in vitro offers an opportunity to generate human brain-like organs to investigate mechanisms of human disease that are specific to the neurogenesis of radial glial (RG) and outer radial glial (oRG) cells in the ventricular zone (VZ) and subventricular zone (SVZ) of the developing neocortex. Modeling neuronal progenitors and the organization that produces mature subcortical neuron subtypes during early stages of development is essential for studying human brain developmental diseases. Several previous efforts have shown to grow neural organoid in culture dishes successfully, however we demonstrate a new paradigm that recapitulates neocortical development process with VZ, OSVZ formation and the lamination organization of cortical layer structure. In addition, using patient-specific induced pluripotent stem cells (iPSCs) with dysfunction of the Aspm gene from a primary microcephaly patient, we demonstrate neurogenesis defects result in defective neuronal activity in patient organoids, suggesting a new strategy to study human developmental diseases in central nerve system.


Assuntos
Humanos , Potenciais de Ação , Fisiologia , Biomarcadores , Metabolismo , Técnicas de Cultura de Células , Corpos Embrioides , Biologia Celular , Metabolismo , Expressão Gênica , Células-Tronco Pluripotentes Induzidas , Biologia Celular , Metabolismo , Ventrículos Laterais , Biologia Celular , Metabolismo , Microcefalia , Genética , Metabolismo , Patologia , Modelos Biológicos , Mutação , Neocórtex , Biologia Celular , Metabolismo , Proteínas do Tecido Nervoso , Genética , Neurogênese , Genética , Neurônios , Biologia Celular , Metabolismo , Organoides , Biologia Celular , Metabolismo , Fator de Transcrição PAX6 , Genética , Metabolismo , Técnicas de Patch-Clamp , Fatores de Transcrição SOXB1 , Genética , Metabolismo , Proteína da Zônula de Oclusão-1 , Genética , Metabolismo
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