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Background: Understanding the genetic foundations of brain development has been made possible by the use of traditional biological models. However, these models frequently fail to capture the complexity of human brain development, particularly the considerable cortical expansion that sets humans apart from other vertebrates and non-human primates.
Objectives: The purpose of this review is to outline the methodology, applications, and potential prospects for using human brain organoids as sophisticated models for researching brain development and illness mechanisms.
Methods: Organoids, or three-dimensional (3-D) structures, are generated by utilizing adult or embryonic stem cells to mimic the main structural and functional features of the human brain. The present investigation emphasizes the advantages of these organoids over traditional two-dimensional (2-D) monolayer models in relation to cellular variety and the ability to create complex 3-D networks, addressing various methods established by researchers to culture these cells.
Results: Organoids precisely mimic numerous features of human brain development, overcoming the limitations of conventional models. They have demonstrated significant utility in investigating the mechanisms that contribute to neurodegenerative diseases like Parkinson's and Alzheimer's, in addition to tumor biology, providing a valuable understanding of both the normal physiological processes and the underlying cause of the human brain.
Conclusion: Human brain organoids signify a notable progression in the field of neuroscience research, facilitating enhanced modeling of brain disorders. Future investigations will further enhance these methodologies and examine their applications, leading to innovative therapeutic strategies and broadening the knowledge of human brain disorders.
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http://dx.doi.org/10.2174/0125899775369286250206050006 | DOI Listing |
J Infect Dis
September 2025
Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA USA.
Sequestration of Plasmodium falciparum-infected erythrocytes (IE) in the microvasculature is a major virulence determinant. While the sequestration of mature stage parasites (trophozoite and schizonts) to vascular endothelium is well established, the conditions that promote ring-stage IE sequestration is less understood. Here, we observed in ring-stage parasites that febrile exposure increased transcript levels of several exported parasite genes involved in the trafficking of the P.
View Article and Find Full Text PDFJ Neurophysiol
September 2025
Max Planck Research Group Pain Perception, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.
Repetition suppression, the reduced neural response upon repeated presentation of a stimulus, can be explained by models focussing on bottom-up (i.e. adaptation) or top-down (i.
View Article and Find Full Text PDFSci Transl Med
September 2025
Roche Pharma Research and Early Development, Pharmaceutical Sciences, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd., 4070 Basel, Switzerland.
Oligodendrocytes, the myelinating cells of the central nervous system (CNS), are essential for the formation of myelin sheaths and pivotal for maintaining axonal integrity and conduction. Disruption of these cells and the myelin sheaths they produce is a hallmark of demyelinating conditions like multiple sclerosis or those resulting from certain drug side effects, leading to profound neurological impairments. In this study, we created a human brain organoid comprising neurons, astrocytes, and myelinating oligodendrocytes.
View Article and Find Full Text PDFBioinformatics
September 2025
The Second Affiliated Hospital and School of Public Health, Zhejiang University School of Medicine, Hangzhou, China.
Motivation: Drug repositioning presents a streamlined and cost-efficient way to expand the range of therapeutic possibilities. Drugs with human genetic evidence are more likely to advance successfully through clinical trials towards FDA approval. Single gene-based drug repositioning methods have been implemented, but approaches leveraging a broad spectrum of molecular signatures remain underexplored.
View Article and Find Full Text PDFJ Gerontol A Biol Sci Med Sci
September 2025
Department of Epidemiology and Biostatistics, College of Human Medicine, Michigan State University, East Lansing, MI.
Background: Poor olfaction may be associated with incident heart failure (HF) in older adults, but empirical evidence is scant.
Methods: We included 5,217 participants free of clinical HF and with a smell assessment in 2011-2013 from the Atherosclerosis Risk in Communities Study. Olfaction was measured by the 12-item Sniffin' Sticks odor identification test and defined as good (score 11-12), moderate (9-10), or poor (≤8).