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During development, cortical interneurons generated from the ventral telencephalon migrate tangentially into the dorsal telencephalon. Although Achaete-scute family bHLH transcription factor 1 (Ascl1) plays important roles in the developing telencephalon, whether Ascl1 regulates tangential migration remains unclear. Here, we found that Ascl1 promoted tangential migration along the ventricular zone/subventricular zone (VZ/SVZ) and intermediate zone (IZ) of the dorsal telencephalon. Distal-less homeobox 2 (Dlx2) acted downstream of Ascl1 in promoting tangential migration along the VZ/SVZ but not IZ. We further identified Eph receptor B2 (Ephb2) as a direct target of Ascl1. Knockdown of EphB2 disrupted the separation of the VZ/SVZ and IZ migratory routes. Ephrin-A5, a ligand of EphB2, was sufficient to repel both Ascl1-expressing cells in vitro and tangentially migrating cortical interneurons in vivo. Together, our results demonstrate that Ascl1 induces expression of Dlx2 and Ephb2 to maintain distinct tangential migratory routes in the dorsal telencephalon.
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http://dx.doi.org/10.1038/srep42895 | DOI Listing |
Mol Psychiatry
September 2025
The Vivian L. Smith Department of Neurosurgery, University of Texas Health Science Center, 6431 Fannin St. MSB 7.147, Houston, TX, 77030, USA.
During cortical development, newly born neurons migrate radially or tangentially from their origin to expand the cortex. Simultaneously, neuron-derived factors support angiogenesis, and an elaborate network of blood cerebral vessels develops in the cortex. Traditionally, blood cerebral vessels were considered to support the growing cortex or migrating neurons by providing nutrients and oxygen.
View Article and Find Full Text PDFNat Commun
July 2025
RWTH Aachen University, Division of Neuroepigenetics, Institute of Zoology (Biology 2), Worringerweg 3, Aachen, Germany.
The coordinated development of cortical circuits composed of excitatory and inhibitory neurons is critical for proper brain function, and disruptions are linked to a spectrum of neuropsychiatric disorders. While excitatory neurons are generated locally in the cortical proliferative zones, inhibitory cortical interneurons (cINs) originate in the basal telencephalon and migrate tangentially into the cortex. Here, we show that DNA methyltransferase 1 (DNMT1) is essential for the migration and integration of somatostatin (SST)-expressing interneurons in mice.
View Article and Find Full Text PDFAnal Chem
July 2025
State Key Laboratory of Medicinal Chemical Biology, Tianjin Key Laboratory of Molecular Recognition and Biosensing, Frontiers Science Center for New Organic Matter, College of Chemistry, Nankai University, Tianjin 30071, China.
Small extracellular vesicles (sEVs) are nanoscale, lipid bilayer-enclosed vesicles that carry diverse biomolecules and hold considerable potential in disease diagnosis, monitoring, and therapeutic interventions. Efficient and scalable isolation of sEVs is essential for both biomedical research and clinical translation; however, conventional techniques, such as ultracentrifugation (UC), are time-consuming, low-throughput, and insufficient for separating sEV subpopulations by size. In this study, we present a high-throughput isolation platform utilizing cassette-based tangential flow filtration (CTFF) with membrane encapsulation.
View Article and Find Full Text PDFMol Psychiatry
July 2025
Université de Strasbourg, Centre National de la Recherche Scientifique (CNRS) UMR7104, Institut National de la Santé et de la Recherche Médicale (INSERM) U1258, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch-Graffenstaden, F-67404, France.
Interneuron development is a crucial step of brain corticogenesis. When affected it often leads to brain dysfunctions like epilepsy, intellectual disabilities and autism spectrum disorder. Such defects are observed in the DYRK1A-haploinsufficiency syndrome, caused by mutations in DYRK1A, and commonly associated to cortical excitatory/inhibitory imbalance.
View Article and Find Full Text PDFFEBS J
June 2025
Sunnybrook Research Institute, Biological Sciences Platform, Toronto, Canada.
The neocortex, which is the site of higher-order cognitive functioning, is comprised of two main neuronal types: excitatory (E) and inhibitory (I). Neurodevelopmental disorders that disrupt the balance of E:I neurotransmission predispose individuals to atypical brain function, highlighting the importance of generating the correct numbers of each neuronal type. During development, neurons with E and I neurotransmission profiles are primarily generated from neural stem and progenitor cells (NPCs), located in the dorsal and ventral telencephalon, respectively.
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