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Objectives: Neural stem/progenitor cells derived from olfactory neuroepithelium (hereafter olfactory neural stem/progenitor cells, ONSPCs) are emerging as a potential tool in the exploration of psychiatric disorders. The present study intended to assess whether ONSPCs could help discern individuals with schizophrenia (SZ) from non-schizophrenic (NS) subjects by exploring specific cellular and molecular features.
Methods: ONSPCs were collected from 19 in-patients diagnosed with SZ and 31 NS individuals and propagated in basal medium. Mitochondrial ATP production, expression of β-catenin and cell proliferation, which are described to be altered in SZ, were examined in freshly isolated or newly thawed ONSPCs after a few culture passages.
Results: SZ-ONSPCs exhibited a lower mitochondrial ATP production and insensitivity to agents capable of positively or negatively affecting β-catenin expression with respect to NS-ONSPCs. As to proliferation, it declined in SZ-ONSPCs as the number of culture passages increased compared to a steady level of growth shown by NS-ONSPCs.
Conclusions: The ease and safety of sample collection as well as the differences observed between NS- and SZ-ONSPCs, may lay the groundwork for a new approach to obtain biological material from a large number of living individuals and gain a better understanding of the mechanisms underlying SZ pathophysiology.
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http://dx.doi.org/10.1080/15622975.2024.2357096 | DOI Listing |
Neural Regen Res
September 2025
Institute of Anatomy and Cell Biology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Human induced pluripotent stem cell-derived neural stem/progenitor cells are used in cell-replacement and regenerative therapeutic strategies after traumatic central nervous system injury. Traumatic injury alters the host microenvironment, which in turn affects the functionality of transplanted human neural stem/ progenitor cells and potentially limits their benefits for neurorepair. However, the underlying mechanisms through which the host environment alters the fate and functionality of transplanted human neural stem/progenitor cells remain poorly understood.
View Article and Find Full Text PDFCells
August 2025
Institute of Neurobiology, School of Basic Medical Sciences, Xian Jiaotong University Health Science Center, Xi'an 710061, China.
Neural stem/progenitor cells (NSPCs) in the subventricular zone (SVZ) of the central nervous system (CNS) are critical for tissue repair following injury or disease. These cells retain the capacity to proliferate, migrate, and differentiate into neurons, astrocytes, and oligodendrocytes, making them a promising therapeutic target for neurodegenerative disorders and traumatic injuries. However, the molecular mechanisms regulating their proliferation remain incompletely understood.
View Article and Find Full Text PDFJ Neurooncol
August 2025
Department of Neurological Surgery, University of California at San Francisco, San Francisco, CA, USA.
Background: Patients with brain cancers are diagnosed based on MRI in the clinical setting while molecular signatures offer potential therapeutic targets. The necessity to re-form molecular and imaging information motivated our meta-analysis to decipher the correlation between the MRI-classified tumor locations, gene expression, and protein signatures in GBM.
Methods: We analyzed spatial and omics data alongside the assessment of post-translational modifications.
J Mater Chem B
August 2025
Neural Circuit Research Group, Korea Brain Research Institute, 61, Cheomdan-ro, Dong-gu, Daegu, Republic of Korea.
Fluorescent dyes are widely used in biological systems, yet the number of fluorescent scaffolds with desirable photophysical properties remains limited. Herein, we report the synthesis of novel asymmetric pyridinium salts facile Rh(III) C-H activation. A structure-activity relationship (SAR) study led to the identification of a lead candidate, KD01, which exhibits a large Stokes shift (Ex/Em = 405/605 nm) and bright fluorescence only upon interaction with live brain cells.
View Article and Find Full Text PDFPharmacol Biochem Behav
October 2025
Department of Biological Science and Technology, Faculty of Advanced Engineering, Tokyo University of Science, Tokyo, Japan. Electronic address:
Calbindin-D28K (Calb1) is a calcium-binding protein that regulates intracellular calcium signaling and neuronal excitability. In the hippocampal dentate gyrus (DG), Calb1 expression increases with granule cell maturation but is downregulated following chronic antidepressant treatment. To elucidate the functional relevance of this antidepressant-associated downregulation, we used an adeno-associated virus-mediated knockdown approach in mice to reduce Calb1 expression in the DG.
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