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Nanoscale and functional heterogeneity of the hippocampal extracellular space
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Astrocytes in the DG and CA3 regions may be more sensitive and susceptible to metabolic and inflammatory stress responses, perhaps because they are involved in adult neurogenesis, active synaptic remodeling and higher basal neuronal plasticity.
“Astrocytes in the DG and CA3 regions may be more sensitive and susceptible to metabolic and inflammatory stress responses, perhaps because they are involved in adult neurogenesis, active synaptic remodeling and higher basal neuronal plasticity81,82.”
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Cites
Glia as architects of central nervous system formation and function
Allen, N. J., & Lyons, D. A. (2018) · Science · doi:10.1126/science.aat0473 · Cited by 1,001
Thorne, R. G., & Nicholson, C. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509425103 · Cited by 641
The roles of perineuronal nets and the perinodal extracellular matrix in neuronal function
Fawcett, J. W., Oohashi, T., & Pizzorusso, T. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0196-3 · Cited by 589
The dual role of the extracellular matrix in synaptic plasticity and homeostasis
Dityatev, A., Schachner, M., & Sonderegger, P. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2898 · Cited by 559
Ultrastructural analysis of adult mouse neocortex comparing aldehyde perfusion with cryo fixation
Korogod, N., Petersen, C. C., & Knott, G. W. (2015) · eLife · doi:10.7554/elife.05793 · Cited by 408
Selective Neuronal Vulnerability in Alzheimer’s Disease: A Network-Based Analysis
Roussarie, J.-P., Yao, V., Rodriguez-Rodriguez, P., Oughtred, R., Rust, J., Plautz, Z., Kasturia, S., Albornoz, C., Wang, W., Schmidt, E. F., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.06.010 · Cited by 180
Reduced extracellular space in the brain of tenascin‐R‐ and HNK‐1‐sulphotransferase deficient mice
Syková, E., Voříšek, I., Mazel, T., Antonova, T., & Schachner, M. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04375.x · Cited by 73
Flagged first, then by citations
Research works printed but not linked: 30
- Syková, 2008, Diffusion in brain extracellular space, Physiol. Rev., 88, 1277, 10.1152/physrev.00027.2007 · DOI · Paper page
- Nicholson, 2000, Diffusion of molecules in brain extracellular space: theory and experiment, Prog. Brain Res., 125, 129, 10.1016/S0079-6123(00)25007-3 · DOI
- Rasmussen, 2022, Fluid transport in the brain, Physiol. Rev., 102, 1025, 10.1152/physrev.00031.2020 · DOI
- Godin, 2017, Single-nanotube tracking reveals the nanoscale organization of the extracellular space in the live brain, Nat. Nanotechnol., 12, 238, 10.1038/nnano.2016.248 · DOI · Paper page
- Tonnesen, 2018, Super-resolution imaging of the extracellular space in living brain tissue, Cell, 172, 1108, 10.1016/j.cell.2018.02.007 · DOI
- Goode, 2020, An integrated index: engrams, place cells, and hippocampal memory, Neuron, 107, 805, 10.1016/j.neuron.2020.07.011 · DOI
- Sherwood, 2021, NMDARs, coincidence detectors of astrocytic and neuronal activities, Int. J. Mol. Sci., 22, 7258, 10.3390/ijms22147258 · DOI
- Bartsch, 2015, Selective neuronal vulnerability of human hippocampal CA1 neurons: lesion evolution, temporal course, and pattern of hippocampal damage in diffusion-weighted MR imaging, J. Cerebr. Blood Flow Metabol., 35, 1836, 10.1038/jcbfm.2015.137 · DOI
- Alkadhi, 2019, Cellular and molecular differences between area CA1 and the dentate gyrus of the Hippocampus, Mol. Neurobiol., 56, 6566, 10.1007/s12035-019-1541-2 · DOI
- Zheng, 2017, Nanoscale diffusion in the synaptic cleft and beyond measured with time-resolved fluorescence anisotropy imaging, Sci. Rep., 7, 42022, 10.1038/srep42022 · DOI
- McBain, 1990, Regional variation of extracellular space in the hippocampus, Science, 249, 674, 10.1126/science.2382142 · DOI · Paper page
- Hrabetová, 2005, Extracellular diffusion is fast and isotropic in the stratum radiatum of hippocampal CA1 region in rat brain slices, Hippocampus, 15, 441, 10.1002/hipo.20068 · DOI
- Saghyan, 2012, Extracellular diffusion in laminar brain structures exemplified by hippocampus, J. Neurosci. Methods, 205, 110, 10.1016/j.jneumeth.2011.12.008 · DOI
- Arranz, 2014, Hyaluronan deficiency due to Has3 knock-out causes altered neuronal activity and seizures via reduction in brain extracellular space, J. Neurosci., 34, 6164, 10.1523/JNEUROSCI.3458-13.2014 · DOI · Paper page
- Pérez-Pinzón, 1995, Extracellular potassium, volume fraction, and tortuosity in rat hippocampal CA1, CA3, and cortical slices during ischemia, J. Neurophysiol., 74, 565, 10.1152/jn.1995.74.2.565 · DOI
- Varela, 2016, Targeting neurotransmitter receptors with nanoparticles in vivo allows single-molecule tracking in acute brain slices, Nat. Commun., 7, 10947, 10.1038/ncomms10947 · DOI
- Wang, 2021, Real-time dissecting the dynamics of drug transportation in the live brain, Nano Lett., 21, 642, 10.1021/acs.nanolett.0c04216 · DOI
- Wegner, 2015, Quantum dots: bright and versatile in vitro and in vivo fluorescence imaging biosensors, Chem. Soc. Rev., 44, 4792, 10.1039/C4CS00532E · DOI
- Dahan, 2003, Diffusion dynamics of glycine receptors revealed by single-quantum dot tracking, Science, 302, 442, 10.1126/science.1088525 · DOI
- Groc, 2020, Linking glutamate receptor movements and synapse function, Science, 368, eaay4631, 10.1126/science.aay4631 · DOI · Paper page
- Groc, 2004, Differential activity-dependent regulation of the lateral mobilities of AMPA and NMDA receptors, Nat. Neurosci., 7, 695, 10.1038/nn1270 · DOI
- Murphy-Royal, 2015, Surface diffusion of astrocytic glutamate transporters shapes synaptic transmission, Nat. Neurosci., 18, 219, 10.1038/nn.3901 · DOI · Paper page
- Rosendale, 2021, A bottom-up approach to red-emitting molecular-based nanoparticles with natural stealth properties and their use for single-particle tracking deep in brain tissue, Adv. Mater., 33, e2006644, 10.1002/adma.202006644 · DOI
- Park, 2012, Influence of synaptic vesicle position on release probability and exocytotic fusion mode, Science, 335, 1362, 10.1126/science.1216937 · DOI
- Neef, 2014, Modes and regulation of endocytic membrane retrieval in mouse auditory hair cells, J. Neurosci., 34, 705, 10.1523/JNEUROSCI.3313-13.2014 · DOI
- Larsen, 2019, Developmental maturation of activity-induced K(+) and pH transients and the associated extracellular space dynamics in the rat hippocampus, J. Physiol., 597, 583, 10.1113/JP276768 · DOI
- Hrabetova, 2018, Unveiling the extracellular space of the brain: from super-resolved microstructure to in vivo function, J. Neurosci., 38, 9355, 10.1523/JNEUROSCI.1664-18.2018 · DOI
- Mazel, 1998, Diffusion heterogeneity and anisotropy in rat hippocampus, Neuroreport, 9, 1299, 10.1097/00001756-199805110-00008 · DOI
- Griffiths, 2019, Age-dependent sexual dimorphism in hippocampal cornu ammonis-1 perineuronal net expression in rats, Brain Behav., 9, e01265, 10.1002/brb3.1265 · DOI
- Levet, 2020, SpineJ: a software tool for quantitative analysis of nanoscale spine morphology, Methods, 174, 49, 10.1016/j.ymeth.2020.01.020 · DOI
Cited by
Sorted by citations
Niu, T., Wang, S., Zhang, H., Zhu, W., Liu, K., Zhou, X., Sun, R., Niu, D., & Yuan, Y. (2025) · Experimental & Molecular Medicine · doi:10.1038/s12276-025-01534-w · Cited by 7
Metadata
- Authors
- Grassi, D., Idziak, A., Lee, A., Calaresu, I., Sibarita, J.-B., Cognet, L., Nägerl, U. V., & Groc, L.
- ORCID
- Groc, Laurent
- Venue
- Cell Reports
- Publisher
- Elsevier BV
- Published
- 2023-05
- Volume
- 42
- Issue
- 5
- Pages
- 112478
- ISSN
- 2211-1247
- PMC
- PMC10242443
- Cited by
- 25
- References
- 7
- Language
- en
- Licence
- Funders
- Conseil Régional Aquitaine
- Human Frontier Science Program (RGP0019, RGP0041/2019)
- Agence Nationale de la Recherche (ANR-14-OHRI-0001-01, ANR-15-CE16-0004-03)
- Fondation pour la Recherche Médicale
- Fondation ARC pour la Recherche sur le Cancer
- Université de Bordeaux (845542)
- European Research Council (951294)
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