Morphogenetic Designs, and Disease Models in Central Nervous System Organoids DOI Open Access
Minsung Bock, Sung Jun Hong, Songzi Zhang

и другие.

International Journal of Molecular Sciences, Год журнала: 2024, Номер 25(14), С. 7750 - 7750

Опубликована: Июль 15, 2024

Since the emergence of first cerebral organoid (CO) in 2013, advancements have transformed central nervous system (CNS) research. Initial efforts focused on studying morphogenesis COs and creating reproducible models. Numerous methodologies been proposed, enabling design brain to represent specific regions spinal cord structures. CNS organoids now facilitate study a wide range diseases, from infections tumors, which were previously difficult investigate. We summarize major organoids, concerning morphogenetic designs disease examine development fabrication procedures how these enabled generation region-specific highlight application various demonstrating versatility potential models advancing our understanding complex conditions. discuss current challenges field, including issues related reproducibility, scalability, accurate recapitulation vivo environment. provide an outlook prospective studies future directions. This review aims comprehensive overview state-of-the-art research, highlighting key developments, challenges, prospects field.

Язык: Английский

An optimized method for directed differentiation of hypothalamic neural stem cells in a 3D culture system DOI

Jiao Luo,

Qiaoyan Tang,

Teng‐Nan Lin

и другие.

Research Square (Research Square), Год журнала: 2025, Номер unknown

Опубликована: Май 6, 2025

Abstract Hypothalamic neurogenesis is a complex process that plays crucial role in neuroendocrine homeostasis, making vivo studies of the hypothalamus particularly challenging. In this study, we present an optimized protocol for isolating and culturing hypothalamic neural stem cells (htNSCs) from neonatal (P1) mice, followed by their directed differentiation three-dimensional (3D) Matrigel environment. We successfully established primary culture system supports stability, growth, distinct characteristics htNSCs. Notably, demonstrate htNSCs can differentiate into GnRH-like neurons within Matrigel-based 3D system. These differentiated exhibit typical neuronal morphology functional characteristics. Our findings highlight potential as invaluable model studying function neurogenesis. Furthermore, method provides novel platform basic research may serve important implications further pathological mechanism disorders hypothalamus.

Язык: Английский

Процитировано

0

RosetteArray Platform for Quantitative High-Throughput Screening of Human Neurodevelopmental Risk DOI Creative Commons
Brady F. Lundin, Gavin Knight, Nikolai J. Fedorchak

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Апрель 2, 2024

SUMMARY Neural organoids have revolutionized how human neurodevelopmental disorders (NDDs) are studied. Yet, their utility for screening complex NDD etiologies and in drug discovery is limited by a lack of scalable quantifiable derivation formats. Here, we describe the RosetteArray ® platform’s ability to be used as an off-the-shelf, 96-well plate assay that standardizes incipient forebrain spinal cord organoid morphogenesis micropatterned, 3-D, singularly polarized neural rosette tissues (>9000 per plate). RosetteArrays seeded from cryopreserved pluripotent stem cells, cultured over 6-8 days, immunostained images can quantified using artificial intelligence-based software. We demonstrate suitability developmental neurotoxicity genetic environmental factors known cause tube defect risk. Given presence perturbation models NDDs neurodegenerative disorders, platform could enable quantitative high-throughput (qHTS) risk across regulatory precision medicine applications.

Язык: Английский

Процитировано

2

Polarization of organoids by bioengineered symmetry breaking DOI Creative Commons

Jae Ryun Ryu,

Kahee Ko,

Woong Sun

и другие.

IBRO Neuroscience Reports, Год журнала: 2024, Номер 17, С. 22 - 31

Опубликована: Май 21, 2024

Язык: Английский

Процитировано

2

Brain organoid as a model to study the role of mitochondria in neurodevelopmental disorders: achievements and weaknesses DOI Creative Commons
Raquel Coronel,

Enrique García-Moreno,

Emilio Siendones

и другие.

Frontiers in Cellular Neuroscience, Год журнала: 2024, Номер 18

Опубликована: Июнь 24, 2024

Mitochondrial diseases are a group of severe pathologies that cause complex neurodegenerative disorders for which, in most cases, no therapy or treatment is available. These organelles critical regulators both neurogenesis and homeostasis the neurological system. Consequently, mitochondrial damage dysfunction can occur as consequence neurodevelopmental diseases. As genetic knowledge advances, associations have been identified between genes encode proteins symptoms, such neuropathy, encephalomyopathy, ataxia, seizures, developmental delays, among others. Understanding how alter these processes essential researching rare Three-dimensional (3D) cell cultures, which self-assemble to form specialized structures composed different types, represent an accessible manner model organogenesis disorders. In particular, brain organoids revolutionizing study mitochondrial-based since they organ-specific model-generated from patient’s cell, thereby overcoming some limitations traditional animal models. this review, we collected functions recapitulate types reported organoids, focusing on those generated models addition advancements generation techniques, approaches studying neuronal physiology, drug screening repositioning studies performed with also reviewed. This scope review will summarize evidence function dynamics mitochondria organoids.

Язык: Английский

Процитировано

1

Morphogenetic Designs, and Disease Models in Central Nervous System Organoids DOI Open Access
Minsung Bock, Sung Jun Hong, Songzi Zhang

и другие.

International Journal of Molecular Sciences, Год журнала: 2024, Номер 25(14), С. 7750 - 7750

Опубликована: Июль 15, 2024

Since the emergence of first cerebral organoid (CO) in 2013, advancements have transformed central nervous system (CNS) research. Initial efforts focused on studying morphogenesis COs and creating reproducible models. Numerous methodologies been proposed, enabling design brain to represent specific regions spinal cord structures. CNS organoids now facilitate study a wide range diseases, from infections tumors, which were previously difficult investigate. We summarize major organoids, concerning morphogenetic designs disease examine development fabrication procedures how these enabled generation region-specific highlight application various demonstrating versatility potential models advancing our understanding complex conditions. discuss current challenges field, including issues related reproducibility, scalability, accurate recapitulation vivo environment. provide an outlook prospective studies future directions. This review aims comprehensive overview state-of-the-art research, highlighting key developments, challenges, prospects field.

Язык: Английский

Процитировано

1