Trophic Interactions Between Astroglial Cells and Hippocampal Neurons in Culture

Growth of a rat neuroblastoma cell line in serum-free supplemented medium.

Bottenstein, J. E., & SATO, G. H. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.1.514 · Cited by 2,268

Rat hippocampal neurons in dispersed cell culture.

Banker, G. A., & Cowan, W. M. (1977) · Brain Research · doi:10.1016/0006-8993(77)90594-7 · Cited by 1,110

Growth and cultivation of dissociated neurons and glial cells from embryonic chick, rat and human brain in flask cultures.

Booher, J., & Sensenbrenner, M. (1972) · PubMed · Cited by 760

Adult rat brain astrocytes support survival of both NGF-dependent and NGF-insensitive neurones

Lindsay, R. M. (1979) · Nature · doi:10.1038/282080a0 · Cited by 373

Trophic Mechanisms in the Peripheral Nervous System

Varon, S. S., & Bunge, R. P. (1978) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.01.030178.001551 · Cited by 326

Further observations on hippocampal neurons in dispersed cell culture

Banker, G. A., & Cowan, W. M. (1979) · Journal of Comparative Neurology · doi:10.1002/cne.901870302 · Cited by 285

Nerve Growth Factor

Bradshaw, R. A. (1978) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.47.070178.001203 · Cited by 246

Neuron-glia interactions.

Varon, S. S., & Gg, S. (1979) · PubMed · Cited by 244

Induction of neurite outgrowth by a conditioned-medium factor bound to the culture substratum

Collins, F. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.10.5210 · Cited by 241

Survival and development in culture of dissociated parasympathetic neurons from ciliary ganglia

Helfand, S. L., Smith, G. A., & Wessells, N. K. (1976) · Developmental Biology · doi:10.1016/0012-1606(76)90174-3 · Cited by 177

Influence of the culture substratum on the expression of choline acetyltransferase activity in purified motoneurons from rat embryos

Martinou, J., Bierer, F., Thaı̈, A. L. V., & Weber, M. J. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90180-6 · Cited by 21

The presence of non-neuronal cells influences somatostatin release from cultured cerebral cortical cells

Parés-Herbute, N., Bonet-Kerrache, A. A., Péraldi‐Roux, S., Pin, J., Gabrion, J., ASTIER, H. S., & Tapia‐Arancibia, L. (1988) · Developmental Brain Research · doi:10.1016/0165-3806(88)90011-9 · Cited by 21

INTRACEREBRAL GRAFTING OF DISSOCIATED CNS TISSUE SUSPENSIONS

Schmidt, R. H., Björklund, A., Stenevi, U., & Dunnett, S. B. (1983) · Elsevier eBooks · doi:10.1016/b978-0-12-635120-0.50022-9 · Cited by 21

Integration of circadian rhythms and immunotherapy for enhanced precision in brain cancer treatment

Quist, M., van Os, M., Laake, L. W. V., Bovenschen, N., & Crnko, S. (2024) · EBioMedicine · doi:10.1016/j.ebiom.2024.105395 · Cited by 21

Age-dependent survival-promoting activity of vitamin K on cultured CNS neurons

Nakajima, M., Furukawa, S., Hayashi, K., Yamada, A., Kawashima, T., & Hayashi, Y. (1993) · Developmental Brain Research · doi:10.1016/0165-3806(93)90041-8 · Cited by 20

Aberrant NLRP3 Inflammasome Activation Ignites the Fire of Inflammation in Neuromuscular Diseases

Péladeau, C. L., & Sandhu, J. K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22116068 · Cited by 20

In vitro methods to prepare astrocyte and motoneuron cultures for the investigation of potential in vivo interactions

Taylor, A., Robinson, M. B., & Milligan, C. (2007) · Nature Protocols · doi:10.1038/nprot.2007.208 · Cited by 22

Immunocytochemical study of S‐100 positive glial cells in the brainstem and spinal cord of the rat embryo

Gomez, L. A., Brusco, A., & Saavedra, J. P. (1990) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(90)90023-u · Cited by 20

Ultrastructural development of the medial superior olive (MSO) in the ferret

Brunso-Bechtold, J. K., Henkel, C. K., & Linville, C. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903240407 · Cited by 20

Intracerebral transplantation of cultured neurons after reaggregation in a plasma clot

Lindsay, R. M., Raisman, G., & Seeley, P. J. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90030-3 · Cited by 20

Role of astroglial cell clones in the survival and differentiation of cerebellar embryonic neurons

Alliot, F., Delhaye‐Bouchaud, N., Geffard, M., & Pessac, B. (1988) · Developmental Brain Research · doi:10.1016/0165-3806(88)90223-4 · Cited by 20

Sphingosine 1‐phosphate‐primed astrocytes enhance differentiation of neuronal progenitor cells

Spohr, T. C. L. D. S. E., Dezonne, R. S., Nones, J., Souza, C. D. S., Einicker‐Lamas, M., Gomes, F. C. A., & Rehen, S. K. (2012) · Journal of Neuroscience Research · doi:10.1002/jnr.23076 · Cited by 19

Comparison of alterations in amino acids content in cultured astrocytes or neurons exposed to methylmercury separately or in co-culture

Yin, Z., Albrecht, J., Syversen, T. L. M., Jiang, H., Summar, M. L., da Rocha, J. B. T., Farina, M., & Aschner, M. (2009) · Neurochemistry International · doi:10.1016/j.neuint.2009.01.015 · Cited by 19

Neurotrophic effects of conditioned media of astrocytes isolated from different brain regions on hippocampal and cortical neurons

Yoshida, M., Saitō, H., & Katsuki, H. (1995) · Cellular and Molecular Life Sciences · doi:10.1007/bf01929356 · Cited by 19

Axonal regrowth in the amyelinated optic nerve of the myelin‐deficient rat: Ultrastructural observations and effects of ganglioside administration

Marciano, F. F., Gocht, A., Dentinger, M. P., Hof, L., Csiza, C. K., & Barron, K. D. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902950206 · Cited by 19

MK-801 affects the potassium-induced increase of glial fibrillary acidic protein immunoreactivity in rat brain

Herrera, D. G., & Cuello, A. C. (1992) · Brain Research · doi:10.1016/0006-8993(92)90195-f · Cited by 19

Subcultured astrocytes suppress the proliferation of neuroblasts in vitro

Yoshida, K., Kohsaka, S., Nii, S., Idei, T., Otani, M., Toya, S., & Tsukada, Y. (1986) · Neuroscience Letters · doi:10.1016/0304-3940(86)90433-7 · Cited by 19

Dissecting the non-neuronal cell contribution to Parkinson’s disease pathogenesis using induced pluripotent stem cells

Pons-Espinal, M., Blasco-Agell, L., & Consiglio, A. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03700-x · Cited by 18

Effects of ethanol on cultured embryonic neurons from the cerebral cortex of the rat

Bingham, S. M., Mudd, L. M., Lopez, T. F., & Montague, J. R. (2004) · Alcohol · doi:10.1016/j.alcohol.2003.12.003 · Cited by 18

Chapter 25 Chapter Growth factors and growth factor receptors in the hippocampus. Role in plasticity and response to injury

Nieto‐Sampedro, M., & Bovolenta, P. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)61261-3 · Cited by 18

MPP+ Injection into Rat Substantia Nigra Causes Secondary Glial Activation but Not Cell Death in the Ipsilateral Striatum

Canudas, A. M., Fríguls, B., Planas, A. M., Gabriel, C., Escubedo, E., Camarasa, J., Camins, A., & Pallàs, M. (2000) · Neurobiology of Disease · doi:10.1006/nbdi.2000.0308 · Cited by 18

Marked neurotrophic effects of diffusible substances released from non-target cerebellar cells on thalamic neurons in culture

Hisanaga, K., & Sharp, F. R. (1990) · Developmental Brain Research · doi:10.1016/0165-3806(90)90137-n · Cited by 18

Effect of a Conditioning Lesion on Axonal Transport During Regeneration

McQuarrie, I. G. (1984) · Springer eBooks · doi:10.1007/978-1-4684-1197-3_12 · Cited by 18

Comparison between sub-chronic and chronic sleep deprivation-induced behavioral and neuroimmunological abnormalities in mice: Focusing on glial cell phenotype polarization

Niazi, N. U. K., Huang, C.-Y., Yang, Z., Zhang, Y., & Song, C. (2024) · Behavioural Brain Research · doi:10.1016/j.bbr.2024.115067 · Cited by 17

Glia determine the course of brain-derived neurotrophic factor-mediated dendritogenesis and provide a soluble inhibitory cue to dendritic growth in the brainstem

Martin, J., Brown, A. L., & Bałkowiec, A. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.01.013 · Cited by 17

The effects of peripherally-subacute treatment with irisin on hippocampal dendritogenesis and astrocyte-secreted factors

Kim, M.-H., & Leem, Y. (2019) · Physical Activity and Nutrition · doi:10.20463/jenb.2019.0029 · Cited by 17

Schwann cell-derived factors support serotoninergic neuron survival and promote neurite outgrowth

Pellitteri, R., Zicca, A., Mancardi, G., Savio, T., & Cadoni, A. (2009) · European Journal of Histochemistry · doi:10.4081/1645 · Cited by 17

P2Y1 receptor mediated neuronal fibre outgrowth in organotypic brain slice co-cultures

Heine, C., Sygnecka, K., Scherf, N., Grohmann, M., Braesigk, A., & Franke, H. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.02.001 · Cited by 17

The effect of basic fibroblast growth factor on glutamate-injured neuroarchitecture and arachidonic acid release in adult hippocampal neurons

Himmelseher, S., Henninger, E., & Georgieff, M. (1996) · Brain Research · doi:10.1016/0006-8993(95)01220-6 · Cited by 17

Retinal ganglion cell survival is mediated by cell contact with immature rat astroglia

McCaffery, C. A., Raju, T. R., & Bennett, M. R. (1985) · Neuroscience Letters · doi:10.1016/0304-3940(85)90512-9 · Cited by 17

Both survival and development of spontaneously active rat hypothalamic neurons in dissociated culture are dependent on membrane depolarization

Ling, D. S. F., Petroski, R. E., & Geller, H. M. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90034-g · Cited by 17

Non-neuronal cell proliferation in tissue culture: Implications for axonal regeneration in the central nervous system

Oorschot, D. E., & Jones, D. G. (1986) · Brain Research · doi:10.1016/0006-8993(86)91041-3 · Cited by 17

CNS white matter can be altered to support neuronal outgrowth

Carpenter, M. K., Hassinge, T. D., Whalen, L. R., & Kater, S. B. (1994) · Journal of Neuroscience Research · doi:10.1002/jnr.490370103 · Cited by 17

Septal deafferentation enhances the neurotrophic effects of rat hippocampus on cultured neural cells from the central nervous system

Yoshida, K., Kohsaka, S., Idei, T., Nii, S., Otani, M., Toya, S., & Tsukada, Y. (1986) · Neuroscience Letters · doi:10.1016/0304-3940(86)90187-4 · Cited by 17

Neurite outgrowth from cerebral cortical neurons is promoted by medium conditioned over heart cells

KLIGMAN, D. E. (1982) · Journal of Neuroscience Research · doi:10.1002/jnr.490080218 · Cited by 17

Transplantation of septal neurons maintained in long-term culture

Gibbs, R. B., Pixley, S. K., & Cotman, C. W. (1986) · Brain Research · doi:10.1016/0006-8993(86)91354-5 · Cited by 17

Phloroglucinol attenuates oligomeric amyloid beta peptide1-42-induced astrocytic activation by reducing oxidative stress

Yang, E.-J., Kim, H.-J., Kim, H.-S., & Chang, M. (2021) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2021.01.008 · Cited by 16

Dendritic Polyglycerol Amine: An Enhanced Substrate to Support Long-Term Neural Cell Culture

Clément, J.-P., Al-Alwan, L. A., Glasgow, S. D., Stolow, A., Ding, Y., Melo, T. Q., Khayachi, A., Liu, Y., Hellmund, M., Haag, R., et al. (2022) · ASN NEURO · doi:10.1177/17590914211073276 · Cited by 17

Enhancing the Self-Repairing Potential of the CNS After Injury

Cotman, C. W., Nieto‐Sampedro, M., & Gibbs, R. B. (1984) · Central Nervous System Trauma · doi:10.1089/cns.1984.1.3 · Cited by 16

Ultrastructure of Müller cells in the developing human retina

Rhodes, R. H. (1984) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/bf02134260 · Cited by 16

The mechanism of cytosine arabinoside toxicity on quiescent astrocytes in vitro appears to be analogous to in vivo brain injury

Patel, A. J., Hunt, A., & Seaton, P. (1988) · Brain Research · doi:10.1016/0006-8993(88)91579-x · Cited by 16

Labeling of Neural Cells by Gold-Filled Sendai Virus Envelopes Before Intracerebral Transplantation

Ardizzoni, S. C., Michaels, A. S., & Arendash, G. W. (1988) · Science · doi:10.1126/science.2829355 · Cited by 16

Conductance properties of GABA-activated chloride currents recorded from cultured hippocampal neurons

Allen, C. N., & Albuquerque, E. X. (1987) · Brain Research · doi:10.1016/s0006-8993(87)80039-2 · Cited by 16

Regeneration in the optic nerve of adult rats: influences of cultured astrocytes and optic nerve grafts of different ontogenetic stages

Sievers, J., Bamberger, C., Debus, O. M., & Lucius, R. (1995) · Journal of Neurocytology · doi:10.1007/bf01191214 · Cited by 16

Association of sympathetic axons in denervated hippocampus to intracerebral vasculature

McGinty, J. F., Milner, T. A., & Loy, R. (1982) · Anatomy and Embryology · doi:10.1007/bf00301882 · Cited by 16

Development of glutamate‐stimulated phosphatidylinositol metabolism in primary neuronal and astrocyte cultures

DeCoster, M. A., & Yourick, D. L. (1994) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(94)90044-2 · Cited by 16

Image analysis of CNS neurotrophic factor effects on neuronal survival and neurite outgrowth

Matsumoto, T., Oshima, K., Miyamoto, A., Sakurai, M., Goto, M., & Hayashi, S. (1990) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(90)90160-h · Cited by 15

Isolation, Culture and Functional Characterization of Glia and Endothelial Cells From Adult Pig Brain

Tanti, G. K., Srivastava, R., Kalluri, S. R., Nowak, C., & Hemmer, B. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00333 · Cited by 15

A peroxisome deficiency–induced reductive cytosol state up-regulates the brain-derived neurotrophic factor pathway

Abe, Y., Honsho, M., Kawaguchi, R., Matsuzaki, T., Ichiki, Y., Fujitani, M., Fujiwara, K., Hirokane, M., Oku, M., Sakai, Y., et al. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.011989 · Cited by 15

Ultrastructural and immunohistochemical analysis of axonal regrowth and myelination in membranes which form over lesion sites in the rat visual system

Dyson, S. E., Harvey, A. R., Trapp, B. D., & Heath, J. W. (1988) · Journal of Neurocytology · doi:10.1007/bf01216707 · Cited by 15

Cultures of cells from fetal rat brain: Methods to control composition, morphology, and biochemical activity

Mahoney, M. J., & Saltzman, W. M. (1999) · Biotechnology and Bioengineering · doi:10.1002/(sici)1097-0290(19990220)62:4 · Cited by 15

Glial activity during axonal regrowth following cryogenic injury of rat spinal cord

Collins, G. H., & West, N. R. (1989) · Brain Research Bulletin · doi:10.1016/0361-9230(89)90130-5 · Cited by 15

Schwann cell-conditioned medium promotes neurite outgrowth from explants of fetal rat retina and tectum in vitro

McLoon, L. K., & McLoon, S. C. (1988) · Developmental Brain Research · doi:10.1016/0165-3806(88)90067-3 · Cited by 15

Axonal growth and its inhibition

Berry, M., Hall, S., Shewan, D. A., & Cohen, J. (1994) · Eye · doi:10.1038/eye.1994.53 · Cited by 15

Neurotrophic and Neurite Promoting Activities in Astroglial Conditioned Medium

Beckh, S., Müller, H. W., & Seifert, W. E. (1987) · Springer eBooks · doi:10.1007/978-3-642-71381-1_24 · Cited by 15

Dynamic indentation reveals differential viscoelastic properties of white matter versus gray matter-derived astrocytes upon treatment with lipopolysaccharide

Antonovaité, N., van Wageningen, T. A., Paardekam, E. J., van Dam, A., & Iannuzzi, D. (2020) · Journal of the mechanical behavior of biomedical materials/Journal of mechanical behavior of biomedical materials · doi:10.1016/j.jmbbm.2020.103783 · Cited by 14

Neurotrophin regulation of sodium and calcium channels in human neuroblastoma cells

Urbano, F. J., & Buño, W. (2000) · Neuroscience · doi:10.1016/s0306-4522(99)00552-7 · Cited by 14

Neuroprotective effects of L-carnitine against oxygen-glucose deprivation in rat primary cortical neurons

Kim, Y. J., Kim, S. Y., Sung, D. K., Chang, Y. S., & Park, W. S. (2012) · Korean Journal of Pediatrics · doi:10.3345/kjp.2012.55.7.238 · Cited by 14

Enzyme histochemical changes after transection or hemisection of the spinal cord of the rat

Krikorian, J. G., Guth, L., Barrett, C. P., & Donati, E. J. (1982) · Experimental Neurology · doi:10.1016/0014-4886(82)90130-3 · Cited by 14

Target cell stimulation and inhibition of norepinephrine uptake in dissociated rat locus coeruleus cultures

Sklair‐Tavron, L., & Segal, M. (1990) · Developmental Brain Research · doi:10.1016/0165-3806(90)90235-q · Cited by 14

Homologous conditioned medium enhances expression of TRH in hypothalamic neurons in primary culture

Charli, J., Cruz, C., Redondo, J. L., Guerra, C. E., & Joseph‐Bravo, P. (1995) · Developmental Brain Research · doi:10.1016/0165-3806(95)00134-y · Cited by 14

Modelling α-Synuclein Aggregation and Neurodegeneration with Fibril Seeds in Primary Cultures of Mouse Dopaminergic Neurons

Tourville, A., Akbar, D., Corti, O., Prehn, J. H. M., Melki, R., Hunot, S., & Michel, P. P. (2022) · Cells · doi:10.3390/cells11101640 · Cited by 13

Impact of Aβ40 and Aβ42 Fibrils on the Transcriptome of Primary Astrocytes and Microglia

Zhu, X. A., Schrader, J. M., Irizarry, B. A., Smith, S. O., & Nostrand, W. E. V. (2022) · Biomedicines · doi:10.3390/biomedicines10112982 · Cited by 14

Downregulation of Oxytocin Receptor Decreases the Length of Projections Stimulated by Retinoic Acid in the U-87MG Cells

Lestanova, Z., Puerta, F., Alanazi, M. M., Bačová, Z., Kiss, A., Castejon, A. M., & Bakoš, J. (2016) · Neurochemical Research · doi:10.1007/s11064-016-2133-4 · Cited by 13

Fast Regulation of GABAAR Diffusion Dynamics by Nogo-A Signaling

Fricke, S., Metzdorf, K., Ohm, M., Haak, S., Heine, M., Körte, M., & Zagrebelsky, M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.09.015 · Cited by 13

Advanced Bio-Based Polymers for Astrocyte Cell Models

Gradišnik, L., Bošnjak, R., Maver, T., & Velnar, T. (2021) · Materials · doi:10.3390/ma14133664 · Cited by 13

Astrocytes exert a pro-apoptotic effect on neurons in postnatal hippocampal cultures

Shute, A. A., Cormier, R. J., Moulder, K. L., Benz, A. M., Isenberg, K. E., Zorumski, C. F., & Mennerick, S. J. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2004.11.025 · Cited by 13

GROWTH STIMULATION AND CHEMOTROPIC ATTRACTION OF RAT RETINAL GANGLION CELL AXONS IN VITRO BY CO-CULTURED OPTIC NERVES, ASTROCYTES AND ASTROCYTE CONDITIONED MEDIUM

Lucius, R., Young, H. P., Tidow, S., & Sievers, J. (1996) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(96)00031-7 · Cited by 13

A novel way of removing quiescent astrocytes in a culture of subcortical neurons grown in a chemically defined medium

Patel, A. J., Seaton, P., & Hunt, A. (1988) · Developmental Brain Research · doi:10.1016/0165-3806(88)90246-5 · Cited by 13

Some practical and theoretical issues concerning fetal brain tissue grafts as therapy for brain dysfunctions

Stein, D. G., & Glasier, M. M. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037250 · Cited by 13

Transcellular retrograde labeling of radial glial cells with WGA‐HRP and diI in neonatal rat and hamster

Kageyama, G. H., & Robertson, R. T. (1993) · Glia · doi:10.1002/glia.440090109 · Cited by 13

Growth Factors Regulating Autonomic Nerve Development

Coughlin, M. D. (1984) · Advances in cellular neurobiology · doi:10.1016/b978-0-12-008305-3.50007-6 · Cited by 13

Morphological differentiation of neuropeptide Y neurons in aggregate cultures of dissociated fetal cortical cells: a model system for glia-neuron paracrine interactions

Barnea, A., Anthony, E. L. P., Lu, G., & Cho, G. (1993) · Brain Research · doi:10.1016/0006-8993(93)91074-3 · Cited by 13

Chapter 39 The role of trophic factors in behavioral recovery and integration of transplants

Cotman, C. W., & Kesslak, J. P. (1988) · Progress in brain research · doi:10.1016/s0079-6123(08)60298-8 · Cited by 13

Effect of fluorodeoxyuridine on neurons and non-neuronal cells in cerebral explants

Oorschot, D. E. (1989) · Experimental Brain Research · doi:10.1007/bf00230692 · Cited by 12

Primary cultures of neurons for testing neuroprotective drug effects

Oberpichler-Schwenk, H., & Krieglstein, J. (1994) · Springer eBooks · doi:10.1007/978-3-7091-9350-1_1 · Cited by 12

Phencyclidine and some of its analogues have distinct effects on NMDA receptors of rat hippocampal neurons

Ramoa, A. S., & Albuquerque, E. X. (1988) · FEBS Letters · doi:10.1016/0014-5793(88)81254-7 · Cited by 12

Changes of extracellular proteins in hippocampus during depolarization

Nyström, B., Hamberger, A., & KARLSSON, J. (1986) · Neurochemistry International · doi:10.1016/0197-0186(86)90031-8 · Cited by 12

Current evidence for a role of glucose as a regulator of hypothalamic function and caloric homeostasis

Young, J. K. (1981) · Psychoneuroendocrinology · doi:10.1016/0306-4530(81)90014-7 · Cited by 12

Transient and long-lasting beneficial behavioral effects of grafts in the damaged hippocampus of rat

Sprick, U. (1991) · Behavioural Brain Research · doi:10.1016/s0166-4328(05)80010-5 · Cited by 12

Electrical and chemical modulation of homogeneous and heterogeneous human-iPSCs-derived neuronal networks on high density arrays

Parodi, G., Zanini, G., Chiappalone, M., & Martinoia, S. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1304507 · Cited by 11

Neuron–Astrocyte Liaison to Maintain Lipid Metabolism of Brain

Mukherjee, S., & Suresh, S. (2019) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2019.07.018 · Cited by 11

Aging and age-related diseases with a focus on therapeutic potentials of young blood/plasma

Hosseini, L., Shahabi, P., Fakhari, A., Zangbar, H. S., Seyedaghamiri, F., Sadeghzadeh, J., & Abolhasanpour, N. (2023) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-023-02657-5 · Cited by 11

Possible Involvement of Astrocytes in Neuroprotection by the Cognitive Enhancer T-588

Yamamuro, A., Ago, Y., Takuma, K., Maeda, S., Sakai, Y., Baba, A., & Matsuda, T. (2003) · Neurochemical Research · doi:10.1023/a:1026103304490 · Cited by 11

[H3]-nitrendipine binding in non-neuronal cell cultures

Litzinger, M. J., Foster, G. A., & Brenneman, D. E. (1986) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(86)90508-5 · Cited by 11

Extended neuronal protection induced after sublethal ischemia adjacent to the area with delayed neuronal death

Kitagawa, K., Matsumoto, M., Ohtsuki, T., Kuwabara, K., Mabuchi, T., Yagita, Y., Hori, M., & Yanagihara, T. (2000) · Neuroscience · doi:10.1016/s0306-4522(99)00555-2 · Cited by 11

Neuronal vs. glial somatostatin in the hypothalamus: a cell culture study of the ontogenesis of cellular location, content and release

Davidson, K., & Gillies, G. E. (1993) · Brain Research · doi:10.1016/0006-8993(93)90062-r · Cited by 11

Is the architecture of astrocytic membrane crucial for axonal regeneration in the central nervous system?

Wolburg, H., & K�stner, R. (1984) · Die Naturwissenschaften · doi:10.1007/bf00455908 · Cited by 11

Sprouting of sympathetic fibers in the hippocampus in the absence of major target cell candidates

Peterson, G. M., & Loy, R. (1983) · Brain Research · doi:10.1016/0006-8993(83)91117-4 · Cited by 11

Are neurons of the arcuate nucleus necessary for pathfinding by GnRH fibers arising from third ventricular grafts?

Silverman, R. C., Gibson, M. J., Charlton, H. M., & Silverman, A. (1990) · Experimental Neurology · doi:10.1016/0014-4886(90)90075-4 · Cited by 11

Neuropeptide Regulation of Mitosis

Gozes, I., Brenneman, D. E., Lilling, G., Davidson, A., & Moody, T. W. (1994) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1994.tb19827.x · Cited by 11

Immortalization of Fetal Mouse Brain Glial Cells by Human Papillomavirus Type 16 E7 Genes.

Ishii, K., Inoue, H., Hakura, A., Araki, W., & Masuda, T. (1992) · Cell Structure and Function · doi:10.1247/csf.17.197 · Cited by 11

Role of fragile X messenger ribonucleoprotein 1 in the pathophysiology of brain disorders: a glia perspective

D’Antoni, S., Spatuzza, M., Bonaccorso, C. M., & Catania, M. V. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105731 · Cited by 11

Infralow Frequencies and Ultradian Rhythms

Kaiser, D. A. (2013) · Seminars in Pediatric Neurology · doi:10.1016/j.spen.2013.10.005 · Cited by 10

Metabolism of steroids in pure cultures of neurons and glial cells: Role of intracellular signalling

Melcangi, R. C., Ballabio, M., Magnaghi, V., & Celotti, F. (1995) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/0960-0760(95)00071-7 · Cited by 10

Cytotoxic effects of acrylamide and its related compounds assessed by protein content, LDH activity and cumulative glucose consumption of neuron-rich cultures in a chemically defined medium

Hayashi, M., Tanii, H., Horiguchi, M., & Hashimoto, K. (1989) · Archives of Toxicology · doi:10.1007/bf00278644 · Cited by 10

Neonatal thyroid deficiency has differential effects on cell specific markers for astrocytes and oligodendrocytes in the rat brain

Patel, A. J., Hunt, A., & Kiss, J. Z. (1989) · Neurochemistry International · doi:10.1016/0197-0186(89)90107-1 · Cited by 10

Development of a culture system for pure rat neurons: advantages of a sandwich technique

Lucius, R., & Mentlein, R. (1995) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/s0940-9602(11)80152-4 · Cited by 10

Involvement of protein kinase C in the axonal growth‐promoting effect on spinal cord neurons by target‐derived astrocytes

Qian, J., Wang, H., Fischer, I., Friedman, E., & Levitt, P. R. (1994) · Journal of Neurobiology · doi:10.1002/neu.480251211 · Cited by 10

A simple, yet versatile, co-culture method for examining neuron-glia interactions

Sass, J. B., Ang, L. C., & Juurlink, B. H. J. (1993) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(93)90027-o · Cited by 10

A neurotrophic factor (NTF) released from primary glial cultures supports survival and fiber outgrowth of cultured hippocampal neurons

Müller, H. W., & Seifert, W. E. (1982) · Journal of Neuroscience Research · doi:10.1002/jnr.490080209 · Cited by 179

The output of neuronotrophic and neurite-promoting agents from rat brain astroglial cells: a microculture method for screening potential regulatory molecules

Rudge, J. S., Manthorpe, M., & Varon, S. S. (1985) · Developmental Brain Research · doi:10.1016/0165-3806(85)90188-9 · Cited by 145

Interactions of astroglia derived factors with hippocampal neurons

Matthiessen, H. P., Schmalenbach, C., & Müller, H. W. (1987) · Journal of Neuroimmunology · doi:10.1016/0165-5728(87)90311-0

A Neuron-Astrocyte Co-Culture System to Investigate Astrocyte-Secreted Factors in Mouse Neuronal Development

Jones, E. V., Cook, D., & Murai, K. K. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-452-0_22 · Cited by 60

Divergent Trophic Actions of Glioma Conditioned Media on Cultured Rat Hippocampal Neurons.

Okuda, S., Saitō, H., & Katsuki, H. (1994) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.17.735 · Cited by 3