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X-WR-CALNAME:Bordeaux Neurocampus
X-ORIGINAL-URL:https://www.bordeaux-neurocampus.fr/en/
X-WR-CALDESC:Events for Bordeaux Neurocampus
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TZID:Europe/Paris
BEGIN:DAYLIGHT
TZOFFSETFROM:+0100
TZOFFSETTO:+0200
TZNAME:CEST
DTSTART:20250330T010000
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TZNAME:CET
DTSTART:20251026T010000
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BEGIN:VEVENT
DTSTART;VALUE=DATE:20250717
DTEND;VALUE=DATE:20250719
DTSTAMP:20260407T043941
CREATED:20250425T145852Z
LAST-MODIFIED:20250718T152006Z
UID:183440-1752710400-1752883199@www.bordeaux-neurocampus.fr
SUMMARY:Symposium - Focus on Brain Energy Metabolism
DESCRIPTION:Venue: Domaine du Haut-Carré \n\nOrganised by: \n\nAnne-Karine Bouzier-Sore (CRMSB\, département STS)\nAude Panatier (Neurocentre Magendie)\nHélène Roumes Rodriguez (CRMSB\, département STS)\n\nAbout the symposium\n\nDay 1 will focus on fundamental researc \, presenting the latest findings on metabolic interactions between different brain cell types\, with particular attention to lactate exchanges – not only the astrocyte-neuron lactate shuttle\, but also metabolic exchanges with microglia and oligodendrocytes.\nDay 2 will be dedicated to translational researc \, addressing the consequences of energy metabolism dysregulation in brain disorders\, with a focus on preclinical and clinical research and roundtable discussions between scientists and clinicians.\n\nA strong emphasis will be placed on young researchers\, with multiple opportunities for oral and poster presentations. Prizes will be awarded for the best contributions ! \nThe event will take place in a friendly and welcoming atmosphere\, including a wine & cheese poster session on the evening of Day 1. \n\nFull program: \nfbem.sciencesconf.org/resource/page/id/3 \nRegistration (deadline: June 15\, 11:59 PM):\nfbem.sciencesconf.org/registration?lang=en \nAbstract submission (young researchers\, dead-line June 15):\nfbem.sciencesconf.org/submission/submit?lang=en \n  \n
URL:https://www.bordeaux-neurocampus.fr/en/event/focus-on-brain-energy-metabolism/
CATEGORIES:For scientists,Symposium
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BEGIN:VEVENT
DTSTART;TZID=Europe/Paris:20250717T140000
DTEND;TZID=Europe/Paris:20250717T150000
DTSTAMP:20260407T043941
CREATED:20250523T091416Z
LAST-MODIFIED:20250627T144953Z
UID:184586-1752760800-1752764400@www.bordeaux-neurocampus.fr
SUMMARY:Seminar - Hwai-Jong Cheng
DESCRIPTION:Venue : CARF \n\nHwai-Jong Chen\nInstitute of Molecular Biology\, Academia Sinica\nTaipei\, Taiwan \nInvited by Emilie Pacary (Magendie) \nTitle\nIntegration of progenitor cells from adult brain into mature hippocampal circuits \nAbstract\nIn adult mammalian hippocampus\, neurogenesis is prominent in the subgranular zone of dentate gyrus (DG). These adult-born neurons are functionally integrated into the existing mature hippocampal circuitry. Abnormalities in adult hippocampal neurogenesis (AHN) are implicated in neurological disorders related to learning\, memory\, and emotion. AHN is less efficient with aging. Our lab has been studying how aging processes change AHN in mice (1). We developed an efficient method to culture neurospheres from adult and aged neural progenitors in DG\, and keep them as adult hippocampal neural progenitor cells (AHNPCs) (2). Single cell RNA (sc-RNA) sequencing analysis was performed on AHNPCs to identify intrinsic factors that might regulate aging changes of these progenitor cells. We transplanted AHNPCs into mouse DG in vivo to explore how these ectopic cells differentiate and integrate in the mature hippocampus. Spatial transcriptomic analysis was used to demonstrate transplanted AHNPCs exhibit same expression profile as neighboring endogenous granule cells. Our ultimate goal is to investigate whether the cultured AHNPCs can be utilized for treating neurological disorders. \n(1) Murray\, K.D.\, Liu\, X.-B.\, King\, A.N.\, Luu\, J. and Cheng\, H.-J..  Age-related changes in synaptic plasticity associated with mossy fiber terminal integration during adult neurogenesis.  eNeuro 7(3):ENEURO.0030-20 (2020) \n(2) Vafaeva\, O.\, Namchaiw\, P.\, Murray\, K.\, Diaz\, E.\, and Cheng\, H.-J..  Protocol for culturing neurospheres from progenitor cells in the dentate gyrus of aged mouse hippocampus. STAR Protoc. 6(1): 103692 (2025). \nBiosketch\nDr. Hwai-Jong Cheng’s research interest is to understand the formation of neural connectivity during development and in diseases. He has broad background in molecular and cellular neurobiology and has contributed to identify mechanisms regulating neural topographic connections\, axonal pruning\, and adult neurogenesis. His research group has been utilizing various techniques\, including mouse and C. elegans genetics\, imaging\, in vivo transplantation\, electron microscopic analysis\, and electrophysiological study\, to tackle these questions. Currently\, his research focuses on how the adult-born neurons are functionally integrated into pre-existing mature neural circuitry. \n
URL:https://www.bordeaux-neurocampus.fr/en/event/seminar-hwai-jong-cheng/
CATEGORIES:For scientists,home-event,Impromptu seminar,Magendie
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