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Structural and quantitative analysis of astrocytes in the mouse hippocampus
Abstract
We revealed the structural features of astrocytes by means of light microscopy, confocal laser scanning microscopy and high voltage electron microscopy, and estimated their numerical densities in the mouse hippocampus. The high voltage electron microscope examinations of Golgi-impregnated astrocytes clearly disclosed their fine leaflet-like processes in the masses occupied by individual astrocytes. The intracellular injection of two different fluorescent tracers into two neighboring astrocytes revealed that each astrocyte occupied a discrete area with a limited overlap only at its peripheral portion. In a quantitative analysis using an optical dissector, the numerical densities of astrocytes identified as S100-immunoreactive cells were only slightly different in their areal and laminar distributions. The numerical densities were higher in the stratum lacunosum-moleculare and dentate hilus, while they were slightly lower in the principal cell layers than the average (24.2 x 10(3) mm(-3)) in whole hippocampal regions. As for the dorsoventral difference, the numerical densities were significantly larger at the ventral level in the dentate gyrus, whereas such tendency was not apparent in the hippocampus proper. The projection area of the astrocytes estimated from Golgi-impregnated samples was roughly in inverse relation to the numerical densities; the areas in the stratum lacunosum-moleculare were somewhat smaller than the other layers, where the numerical densities were high. Th…
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Protoplasmic astrocytes were densely tiled in layers 2-6.
“The compact and complicated arbors of protoplasmic astrocytes were densely tiled in layers 2–6 as described previously (39–41).”
From A petavoxel fragment of human cerebral cortex reconstructed at nanoscale resolution (2024) · cites this paper as [40]
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Research works printed but not linked: 38
- Alvarez-Buylla, 2001, A unified hypothesis on the lineage of neural stem cells, Nat. Rev. Neurosci., 2, 287, 10.1038/35067582 · DOI
- Anderson, 2000, Astrocyte glutamate transport: review of properties, regulation, and physiological functions, Glia, 32, 1, 10.1002/1098-1136(200010)32:1<1::AID-GLIA10>3.0.CO;2-W · DOI
- Azmitia, 1990, S100B but not NGF, EGF, insulin or calmodulin is a CNS serotonergic growth factor, Brain Res., 516, 354, 10.1016/0006-8993(90)90942-5 · DOI
- Bass, 1971, Quantitative cytoarchitectonic distribution of neurons, glia, and DNA in rat cerebral cortex, J. Comp. Neurol., 143, 481, 10.1002/cne.901430405 · DOI
- Bjugn, 1993, Estimate of the total number of neurons and glial and endothelial cells in the rat spinal cord by means of the optical disector, J. Comp. Neurol., 328, 406, 10.1002/cne.903280307 · DOI
- Erecinska, 1990, Metabolism and role of glutamate in mammalian brain, Prog. Neurobiol., 35, 245, 10.1016/0301-0082(90)90013-7 · DOI
- Fujise, 1999, Mossy cells in the mouse dentate gyrus: identification in the dorsal hilus and their distribution along the dorsoventral axis, Brain Res., 816, 500, 10.1016/S0006-8993(98)01202-5 · DOI
- Grosche, 1999, Microdomains for neuron-glia interaction: parallel fiber signaling to Bergmann glial cells, Nat. Neurosci., 2, 139, 10.1038/5692 · DOI
- Haan, 1982, Production and characterization of monoclonal antibodies against the ‘brain-specific’ proteins 14-3-2 and S-100, Proc. Natl. Acad. Sci. USA, 79, 7585, 10.1073/pnas.79.23.7585 · DOI
- Haydon, 2001, GLIA: listening and talking to the synapse, Nat. Rev. Neurosci., 2, 185, 10.1038/35058528 · DOI
- Heizmann, 1998, New perspectives on S100 proteins: a multi-functional Ca(2+)-, Zn(2+)- and Cu(2+)-binding protein family, Biometals, 11, 383, 10.1023/A:1009212521172 · DOI
- Hertz, 1999, Astrocytes: glutamate producers for neurons, J. Neurosci. Res., 57, 417, 10.1002/(SICI)1097-4547(19990815)57:4<417::AID-JNR1>3.0.CO;2-N · DOI
- Hu, 1996, S100β stimulates inducible nitric oxide synthase activity and mRNA levels in rat cortical astrocytes, J. Biol. Chem., 271, 2543, 10.1074/jbc.271.5.2543 · DOI · Paper page
- Iino, 2001, Glia–synapse interaction through Ca2+-permeable AMPA receptors in Bergmann glia, Science, 292, 926, 10.1126/science.1058827 · DOI
- Ilg, 1996, Expression pattern of S100 calcium-binding proteins in human tumors, Int. J. Cancer., 68, 325, 10.1002/(SICI)1097-0215(19961104)68:3<325::AID-IJC10>3.0.CO;2-7 · DOI
- Iversen, 1975, Uptake and metabolism of τ-aminobutyric acid by neurones and glial cells, Biochem. Pharmacol., 24, 933, 10.1016/0006-2952(75)90422-0 · DOI
- Jinno, 1998, Quantitative analysis of GABAergic neurons in the mouse hippocampus, with optical disector using confocal laser scanning microscope, Brain Res., 814, 55, 10.1016/S0006-8993(98)01075-0 · DOI
- Kimelberg, 1986, Regional differences in 5-hydroxytryptamine and catecholamine uptake in primary astrocyte cultures, J. Neurochem., 47, 1647, 10.1111/j.1471-4159.1986.tb00808.x · DOI
- Kitamura, 1987, GFA-protein expression on the astroglia in cow and rat brains, Brain Res., 423, 189, 10.1016/0006-8993(87)90839-0 · DOI
- Kosaka, 1986, Three-dimensional structure of astrocytes in the rat dentate gyrus, J. Comp. Neurol., 249, 242, 10.1002/cne.902490209 · DOI
- Ling, 1973, Investigation of glial cells in semithin sections. II. Variation with age in the numbers of the various glial cell types in rat cortex and corpus callosum, J. Comp. Neurol., 149, 73, 10.1002/cne.901490105 · DOI
- Long, 1998, Stereological analysis of astrocyte and microglia in aging mouse hippocampus, Neurobiol. Aging, 19, 497, 10.1016/S0197-4580(98)00088-8 · DOI · Paper page
- Ludwin, 1976, The topographical distribution of S100 and GFA proteins in the adult rat brain: an immunohistochemical study using horseradish peroxidase-labelled antibodies, J. Comp. Neurol., 165, 197, 10.1002/cne.901650206 · DOI
- Nixdorf-Bergweiler, 1994, Developmental changes in the number, size, and orientation of GFAP-positive cells in the CA1 region of rat hippocampus, Glia, 12, 180, 10.1002/glia.440120304 · DOI
- Nomura, 1997, Distribution of nonprincipal neurons in the rat hippocampus, with special reference to their dorsoventral difference, Brain Res., 751, 64, 10.1016/S0006-8993(96)01395-9 · DOI
- Oliet, 2001, Control of glutamate clearance and synaptic efficacy by glial coverage of neurons, Science, 292, 923, 10.1126/science.1059162 · DOI
- Pinol, 1990, Poly- and monoclonal antibodies against recombinant rat brain calbindin D-28K were produced to map its selective distribution in the central nervous system, J. Neurochem., 54, 1827, 10.1111/j.1471-4159.1990.tb04879.x · DOI
- Rickmann, 1995, S100 protein expression in subpopulations of neurons of rat brain, Neuroscience, 67, 977, 10.1016/0306-4522(94)00615-C · DOI
- Rickmann, 1995, Modifications of S100-protein immunoreactivity in rat brain induced by tissue preparation, Histochem. Cell Biol., 103, 135, 10.1007/BF01454011 · DOI
- Savchenko, 2000, Microglia and astrocytes in the adult rat brain: Comparative immunocytochemical analysis demonstrates the efficacy of lipocortin 1 immunoreactivity, Neurosci., 96, 195, 10.1016/S0306-4522(99)00538-2 · DOI
- Teixeira, 2000, Differential regulation of cyclin D1 and D3 expression in the control of astrocyte proliferation induced by endothelin-1, J. Neurochem., 74, 1034, 10.1046/j.1471-4159.2000.0741034.x · DOI
- Thompson, 1942. Growth and Form, 2nd edn. Cambridge University Press, Cambridge. (Yanagida, T., Endo, I., Furusawa, T., Matsuyama, H., Takagi, R., 1973. Abridged Japanese edition. Tokyo University Press, Tokyo.)
- Tout, 1993, Contact-spacing among astrocytes is independent of neighbouring structures: in vivo and in vitro evidence, J. Comp. Neurol., 332, 433, 10.1002/cne.903320405 · DOI
- Walz, 2000, Role of astrocytes in the clearance of excess extracellular potassium, Neurochem. Int., 36, 291, 10.1016/S0197-0186(99)00137-0 · DOI
- Walz, 1998, Immunocytochemical evidence for a distinct GFAP-negative subpopulation of astrocytes in the adult rat hippocampus, Neurosci. Lett., 257, 127, 10.1016/S0304-3940(98)00813-1 · DOI
- Wei, 2001, Compartmentalized and binary behavior of terminal dendrites in hippocampal pyramidal neurons, Science, 293, 2272, 10.1126/science.1061198 · DOI
- Yang, 1995, S-100β has a neuronal localization in the rat hindbrain revealed by an antigen retrieval method, Brain Res., 696, 49, 10.1016/0006-8993(95)00755-F · DOI
- Zhang, 1997, Gliogenesis in postnatal rat optic nerve: LC1+ microglia and S100-β+astrocytes, Dev. Brain Res., 101, 27, 10.1016/S0165-3806(97)00025-4 · DOI
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Metadata
- Authors
- Ogata, K., & Kosaka, T.
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 2002-08
- Volume
- 113
- Issue
- 1
- Pages
- 221-233
- ISSN
- 0306-4522
- Cited by
- 357
- References
- 0
- Language
- en
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