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Region-Specific Characteristics of Astrocytes and Microglia: A Possible Involvement in Aging and Diseases
Abstract
Although different regions of the brain are dedicated to specific functions, the intra- and inter-regional heterogeneity of astrocytes and microglia in these regions has not yet been fully understood. Recently, an advancement in various technologies, such as single-cell RNA sequencing, has allowed for the discovery of astrocytes and microglia with distinct molecular fingerprints and varying functions in the brain. In addition, the regional heterogeneity of astrocytes and microglia exhibits different functions in several situations, such as aging and neurodegenerative diseases. Therefore, investigating the region-specific astrocytes and microglia is important in understanding the overall function of the brain. In this review, we summarize up-to-date research on various intra- and inter-regional heterogeneities of astrocytes and microglia, and provide information on how they can be applied to aging and neurodegenerative diseases.
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Previous studies have identified age-dependent heterogeneity in astrocytic reactivity profiles.
“Previous studies have reported increased astrocyte density in the hippocampus of LDLr−/− mice (de Oliveira et al. 2014; de Oliveira, Engel, de Paula, Dos Santos, et al. 2020) and have identified age‐dependent heterogeneity in astrocytic reactivity profiles (Clarke et al. 2018; Lee et al. 2022).”
From LDL Cholesterol Modulates Astrocyte Metabolism, Lipid Handling, and Morphology: Evidence From In Vitro and In Vivo Models (2026) · cites this paper as Lee et al. 2022
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Neurotoxic reactive astrocytes are induced by activated microglia
Liddelow, S. A., Guttenplan, K. A., Clarke, L. E., Bennett, F. C., Bohlen, C. J., Schirmer, L., Bennett, M. L., Münch, A. E., Chung, W.-S., Peterson, T. C., et al. (2017) · Nature · doi:10.1038/nature21029 · Cited by 7,971
Ageing as a risk factor for neurodegenerative disease
Hou, Y., Dan, X., Babbar, M., Wei, Y., Hasselbalch, S. G., Croteau, D. L., & Bohr, V. A. (2019) · Nature Reviews Neurology · doi:10.1038/s41582-019-0244-7 · Cited by 3,310
Knopman, D. S., Amieva, H., Petersen, R. C., Chételat, G., Holtzman, D. M., Hyman, B. T., Nixon, R. A., & Jones, D. T. (2021) · Nature Reviews Disease Primers · doi:10.1038/s41572-021-00269-y · Cited by 2,606
BDNF from microglia causes the shift in neuronal anion gradient underlying neuropathic pain
Coull, J. A. M., Beggs, S., Boudreau, D., Boivin, D., Tsuda, M., Inoue, K., Gravel, C., Salter, M. W., & De Koninck, Y. (2005) · Nature · doi:10.1038/nature04223 · Cited by 1,965
The human brain in numbers: a linearly scaled-up primate brain
Herculano-Houzel, S. (2009) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.031.2009 · Cited by 1,778
Microglia in neurodegeneration
Hickman, S., Izzy, S., Sen, P., Morsett, L., & El Khoury, J. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0242-x · Cited by 1,710
Pathology of Neurodegenerative Diseases
Dugger, B. N., & Dickson, D. W. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a028035 · Cited by 1,665
Microglia Shape Adult Hippocampal Neurogenesis through Apoptosis-Coupled Phagocytosis
Sierra, A., Encinas, J. M., Deudero, J. J. P., Chancey, J. H., Enikolopov, G., Overstreet-Wadiche, L. S., Tsirka, S. E., & Maletic-Savatic, M. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.08.014 · Cited by 1,622
β-Lactam antibiotics offer neuroprotection by increasing glutamate transporter expression
Rothstein, J. D., Patel, S., Regan, M. R., Haenggeli, C., Huang, Y. H., Bergles, D. E., Jin, L., Dykes Hoberg, M., Vidensky, S., Chung, D. S., et al. (2005) · Nature · doi:10.1038/nature03180 · Cited by 1,518
Disease-Associated Microglia: A Universal Immune Sensor of Neurodegeneration
Deczkowska, A., Keren-Shaul, H., Weiner, A., Colonna, M., Schwartz, M., & Amit, I. (2018) · Cell · doi:10.1016/j.cell.2018.05.003 · Cited by 1,474
Propagation of Tau Pathology in a Model of Early Alzheimer's Disease
de Calignon, A., Polydoro, M., Suárez-Calvet, M., William, C., Adamowicz, D. H., Kopeikina, K. J., Pitstick, R., Sahara, N., Ashe, K. H., Carlson, G. A., et al. (2012) · Neuron · doi:10.1016/j.neuron.2011.11.033 · Cited by 1,427
Autophagy in healthy aging and disease
Aman, Y., Schmauck-Medina, T., Hansen, M., Morimoto, R. I., Simon, A. K., Bjedov, I., Palikaras, K., Simonsen, A., Johansen, T., Tavernarakis, N., et al. (2021) · Nature Aging · doi:10.1038/s43587-021-00098-4 · Cited by 1,313
The hippocampus and memory: insights from spatial processing
Bird, C. M., & Burgess, N. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2335 · Cited by 1,313
Melanized dopaminergic neurons are differentially susceptible to degeneration in Parkinson's disease
Hirsch, E., Graybiel, A. M., & Agid, Y. A. (1988) · Nature · doi:10.1038/334345a0 · Cited by 1,301
TREM2 Maintains Microglial Metabolic Fitness in Alzheimer’s Disease
Ulland, T. K., Song, W. M., Huang, S. C.-C., Ulrich, J. D., Sergushichev, A., Beatty, W. L., Loboda, A. A., Zhou, Y., Cairns, N. J., Kambal, A., et al. (2017) · Cell · doi:10.1016/j.cell.2017.07.023 · Cited by 1,263
Normal aging induces A1-like astrocyte reactivity
Clarke, L. E., Liddelow, S. A., Chakraborty, C., Münch, A. E., Heiman, M., & Barres, B. A. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1800165115 · Cited by 1,237
Li, Q., Cheng, Z., Zhou, L., Darmanis, S., Neff, N. F., Okamoto, J., Gulati, G., Bennett, M. L., Sun, L. O., Clarke, L. E., et al. (2019) · Neuron · doi:10.1016/j.neuron.2018.12.006 · Cited by 1,129
Grubman, A., Chew, G., Ouyang, J. F., Sun, G., Choo, X. Y., McLean, C., Simmons, R. K., Buckberry, S., Vargas-Landin, D. B., Poppe, D., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0539-4 · Cited by 956
Microglia polarization from M1 to M2 in neurodegenerative diseases
Guo, S., Wang, H., & Yin, Y. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.815347 · Cited by 920
Astrocytes Control Synapse Formation, Function, and Elimination
Chung, W.-S., Allen, N. J., & Eroglu, C. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020370 · Cited by 839
Identification of region-specific astrocyte subtypes at single cell resolution
Batiuk, M. Y., Martirosyan, A., Wahis, J., de Vin, F., Marneffe, C., Kusserow, C., Koeppen, J., Viana, J. F., Oliveira, J. F., Voet, T., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-14198-8 · Cited by 805
Microglia Heterogeneity in the Single-Cell Era
Masuda, T., Sankowski, R., Staszewski, O., & Prinz, M. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.010 · Cited by 784
The role of adult hippocampal neurogenesis in brain health and disease
Toda, T., Parylak, S. L., Linker, S. B., & Gage, F. H. (2019) · Molecular Psychiatry · doi:10.1038/s41380-018-0036-2 · Cited by 719
Toll‐like receptor 4 is required for α‐synuclein dependent activation of microglia and astroglia
Fellner, L., Irschick, R., Schanda, K., Reindl, M., Klimaschewski, L., Poewe, W., Wenning, G. K., & Stefanova, N. (2013) · Glia · doi:10.1002/glia.22437 · Cited by 697
Friedman, B. A., Srinivasan, K., Ayalon, G., Meilandt, W. J., Lin, H., Huntley, M. A., Cao, Y., Lee, S.-H., Haddick, P. C. G., Ngu, H., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2017.12.066 · Cited by 662
Satb2 Regulates Callosal Projection Neuron Identity in the Developing Cerebral Cortex
Alcamo, E. A., Chirivella, L., Dautzenberg, M., Dobreva, G., Fariñas, I., Grosschedl, R., & McConnell, S. K. (2008) · Neuron · doi:10.1016/j.neuron.2007.12.012 · Cited by 658
Functional diversity of astrocytes in neural circuit regulation
Haim, L. B., & Rowitch, D. H. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.159 · Cited by 618
Microglia in Neuroinflammation and Neurodegeneration: From Understanding to Therapy
Muzio, L., Viotti, A., & Martino, G. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.742065 · Cited by 581
Single-cell analysis reveals T cell infiltration in old neurogenic niches
Dulken, B. W., Buckley, M. T., Navarro Negredo, P., Saligrama, N., Cayrol, R., Leeman, D. S., George, B. M., Boutet, S. C., Hebestreit, K., Pluvinage, J. V., et al. (2019) · Nature · doi:10.1038/s41586-019-1362-5 · Cited by 521
Synaptic degeneration in Alzheimer's disease
Arendt, T. (2009) · Acta Neuropathologica · doi:10.1007/s00401-009-0536-x · Cited by 517
Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex
Sipe, G. O., Lowery, Tremblay, M.-È., Kelly, E. A., Lamantia, C. E., & Majewska, A. K. (2016) · Nature Communications · doi:10.1038/ncomms10905 · Cited by 512
Microglia in Central Nervous System Inflammation and Multiple Sclerosis Pathology
Voet, S., Prinz, M., & van Loo, G. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2018.11.005 · Cited by 503
Cholesterol metabolism in neurons and astrocytes
Pfrieger, F. W., & Ungerer, N. (2011) · Progress in Lipid Research · doi:10.1016/j.plipres.2011.06.002 · Cited by 500
New insights into the role of TREM2 in Alzheimer’s disease
Gratuze, M., Leyns, C. E. G., & Holtzman, D. M. (2018) · Molecular Neurodegeneration · doi:10.1186/s13024-018-0298-9 · Cited by 489
Neuronal basis of age-related working memory decline
Wang, M., Gamo, N. J., Yang, Y., Jin, L. E., Wang, X.-J., Laubach, M., Mazer, J. A., Lee, D., & Arnsten, A. F. T. (2011) · Nature · doi:10.1038/nature10243 · Cited by 485
Epigenetic regulation of brain region-specific microglia clearance activity
Ayata, P., Badimon, A., Strasburger, H. J., Duff, M. K., Montgomery, S. E., Loh, Y.-H. E., Ebert, A., Pimenova, A. A., Ramirez, B. R., Chan, A. T., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0192-3 · Cited by 460
Exercise plasma boosts memory and dampens brain inflammation via clusterin
De Miguel, Z., Khoury, N., Betley, M. J., Lehallier, B., Willoughby, D., Olsson, N., Yang, A. C., Hahn, O., Lu, N., Vest, R. T., et al. (2021) · Nature · doi:10.1038/s41586-021-04183-x · Cited by 422
Astrocytes in Neurodegenerative Disease: Table 1.
Phatnani, H., & Maniatis, T. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020628 · Cited by 420
Microglia modulate neurodegeneration in Alzheimer’s and Parkinson’s diseases
Bartels, T., De Schepper, S., & Hong, S. (2020) · Science · doi:10.1126/science.abb8587 · Cited by 412
Impermanence of dendritic spines in live adult CA1 hippocampus
Attardo, A., Fitzgerald, J. E., & Schnitzer, M. J. (2015) · Nature · doi:10.1038/nature14467 · Cited by 399
Role of Microglia TLRs in Neurodegeneration
Fiebich, B. L., Batista, C. R. A., Saliba, S. W., Yousif, N. M., & de Oliveira, A. C. P. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00329 · Cited by 291
IL4-driven microglia modulate stress resilience through BDNF-dependent neurogenesis
Zhang, J., Rong, P., Zhang, L., He, H., Zhou, T., Fan, Y., Mo, L., Zhao, Q., Han, Y., Li, S., et al. (2021) · Science Advances · doi:10.1126/sciadv.abb9888 · Cited by 287
Lopes, K. D. P., Snijders, G. J. L., Humphrey, J., Allan, A., Sneeboer, M. A. M., Navarro, E., Schilder, B. M., Vialle, R. A., Parks, M., Missall, R., et al. (2022) · Nature Genetics · doi:10.1038/s41588-021-00976-y · Cited by 273
Sobue, A., Komine, O., Hara, Y., Endo, F., Mizoguchi, H., Watanabe, S., Murayama, S., Saito, T., Saido, T. C., Sahara, N., et al. (2021) · Acta Neuropathologica Communications · doi:10.1186/s40478-020-01099-x · Cited by 253
Tchieu, J., Calder, E. L., Guttikonda, S. R., Gutzwiller, E. M., Aromolaran, K. A., Steinbeck, J. A., Goldstein, P. A., & Studer, L. (2019) · Nature Biotechnology · doi:10.1038/s41587-019-0035-0 · Cited by 231
Microglia and Neuroinflammation: What Place for P2RY12?
Gómez Morillas, A., Besson, V. C., & Lerouet, D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041636 · Cited by 214
Toll-like receptor signaling in amyotrophic lateral sclerosis spinal cord tissue
Casula, M., Iyer, A. M., Spliet, W. G. M., Anink, J. J., Steentjes, K., Sta, M., Troost, D., & Aronica, E. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.02.001 · Cited by 200
Park, J.-S., Kam, T.-I., Lee, S., Park, H., Oh, Y., Kwon, S.-H., Song, J.-J., Kim, D., Kim, H., Jhaldiyal, A., et al. (2021) · Acta Neuropathologica Communications · doi:10.1186/s40478-021-01180-z · Cited by 192
Phenotypic Heterogeneity and Plasticity of Isocortical and Hippocampal Astrocytes in the Human Brain
Sosunov, A. A., Wu, X., Tsankova, N. M., Guilfoyle, E., McKhann, G. M., & Goldman, J. E. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4037-13.2014 · Cited by 185
A role for microglia in synaptic plasticity?
Tremblay, M.-È., & Majewska, A. K. (2011) · Communicative & Integrative Biology · doi:10.4161/cib.4.2.14506 · Cited by 176 · cited 1×
“Not only does the hippocampus contain a large number of synaptic connections between numerous neurons and single astrocytes [69], it also shows a synaptic plasticity that is actively regulated by both microglia and astrocytes [70,71].”
BackgroundThe Cuprizone Model: Dos and Do Nots
Zhan, J., Mann, T., Joost, S., Behrangi, N., Frank, M., & Kipp, M. (2020) · Cells · doi:10.3390/cells9040843 · Cited by 171 · cited 1×
“(2021) induced demyelination in the cortical region of a mouse brain using cuprizone, a copper chelator that induces the selective apoptosis of oligodendrocytes followed by the activation of microglia [61], microglia from different cortical layers showed distinguishable responses.”
BackgroundBernier, B. E., Lacagnina, A. F., Ayoub, A., Shue, F., Zemelman, B. V., Krasne, F. B., & Drew, M. R. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.3029-16.2017 · Cited by 168
Toll like receptor 4 mediates cell death in a mouse MPTP model of Parkinson disease
Noelker, C., Morel, L., Lescot, T., Osterloh, A., Alvarez-Fischer, D., Breloer, M., Henze, C., Depboylu, C., Skrzydelski, D., Michel, P. P., et al. (2013) · Scientific Reports · doi:10.1038/srep01393 · Cited by 164
An updated assessment of microglia depletion: current concepts and future directions
Han, J., Harris, R. A., & Zhang, X.-M. (2017) · Molecular Brain · doi:10.1186/s13041-017-0307-x · Cited by 141
Serotonin, neural markers, and memory
Meneses, A. (2015) · Frontiers in Pharmacology · doi:10.3389/fphar.2015.00143 · Cited by 90
Gomes, C., Cunha, C., Nascimento, F., Ribeiro, J. A., Vaz, A. R., & Brites, D. (2019) · Molecular Neurobiology · doi:10.1007/s12035-018-1220-8 · Cited by 79
Tada, M., Konno, T., Tada, M., Tezuka, T., Miura, T., Mezaki, N., Okazaki, K., Arakawa, M., Itoh, K., Yamamoto, T., et al. (2016) · Annals of Neurology · doi:10.1002/ana.24754 · Cited by 70
Uriarte Huarte, O., Kyriakis, D., Heurtaux, T., Pires-Afonso, Y., Grzyb, K., Halder, R., Buttini, M., Skupin, A., Mittelbronn, M., & Michelucci, A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.639613 · Cited by 52
Flagged first, then by citations
Research works printed but not linked: 176
- Gee, 2005, Astrocytes: Regulation of brain homeostasis via apolipoprotein E, Int. J. Biochem. Cell Biol., 37, 1145, 10.1016/j.biocel.2004.10.004 · DOI
- Li, 2018, Microglia and macrophages in brain homeostasis and disease, Nat. Rev. Immunol., 18, 225, 10.1038/nri.2017.125 · DOI · Paper page
- Sofroniew, 2010, Astrocytes: Biology and pathology, Acta Neuropathol., 119, 7, 10.1007/s00401-009-0619-8 · DOI · Paper page
- MacVicar, 2015, Astrocyte regulation of blood flow in the brain, Cold Spring Harb. Perspect. Biol., 7, a020388, 10.1101/cshperspect.a020388 · DOI
- Chever, 2013, How do astrocytes shape synaptic transmission? Insights from electrophysiology, Front. Cell. Neurosci., 7, 159
- Cowan, 2018, Microglia: Immune Regulators of Neurodevelopment, Front. Immunol., 9, 2576, 10.3389/fimmu.2018.02576 · DOI
- Sato, 2015, Effects of Microglia on Neurogenesis, Glia, 63, 1394, 10.1002/glia.22858 · DOI · Paper page
- Khakh, 2019, The Emerging Nature of Astrocyte Diversity, Annu. Rev. Neurosci., 42, 187, 10.1146/annurev-neuro-070918-050443 · DOI
- Matyash, 2010, Heterogeneity in astrocyte morphology and physiology, Brain Res. Rev., 63, 2, 10.1016/j.brainresrev.2009.12.001 · DOI
- Xin, 2018, Functional Astrocyte Heterogeneity and Implications for Their Role in Shaping Neurotransmission, Front. Cell. Neurosci., 12, 141, 10.3389/fncel.2018.00141 · DOI
- Tan, 2020, Microglial regional heterogeneity and its role in the brain, Mol. Psychiatry, 25, 351, 10.1038/s41380-019-0609-8 · DOI · Paper page
- Oberheim, 2012, Heterogeneity of astrocytic form and function, Methods Mol. Biol., 814, 23, 10.1007/978-1-61779-452-0_3 · DOI · Paper page
- Matias, 2019, Astrocyte Heterogeneity: Impact to Brain Aging and Disease, Front. Aging Neurosci., 11, 59, 10.3389/fnagi.2019.00059 · DOI · Paper page
- Hayashi, 2019, Heterogeneity of Oligodendrocytes and Their Precursor Cells, Adv. Exp. Med. Biol., 1190, 53, 10.1007/978-981-32-9636-7_5 · DOI
- Bøstrand, S.M.K., and Williams, A. (2021). Oligodendroglial Heterogeneity in Neuropsychiatric Disease. Life, 11. · DOI
- Floriddia, 2020, Distinct oligodendrocyte populations have spatial preference and different responses to spinal cord injury, Nat. Commun., 11, 5860, 10.1038/s41467-020-19453-x · DOI
- Sherafat, 2021, Shaping of Regional Differences in Oligodendrocyte Dynamics by Regional Heterogeneity of the Pericellular Microenvironment, Front. Cell. Neurosci., 15, 337, 10.3389/fncel.2021.721376 · DOI
- MacDonald, 2021, Single Cell Transcriptomics of Ependymal Cells Across Age, Region and Species Reveals Cilia-Related and Metal Ion Regulatory Roles as Major Conserved Ependymal Cell Functions, Front. Cell. Neurosci., 15, 268, 10.3389/fncel.2021.703951 · DOI
- Shipp, 2007, Structure and function of the cerebral cortex, Curr. Biol., 17, R443, 10.1016/j.cub.2007.03.044 · DOI · Paper page
- Molyneaux, 2007, Neuronal subtype specification in the cerebral cortex, Nat. Rev. Neurosci., 8, 427, 10.1038/nrn2151 · DOI
- Naka, 2016, Inhibitory Circuits in Cortical Layer 5, Front. Neural Circuits, 10, 35, 10.3389/fncir.2016.00035 · DOI
- Hage, 2022, Synaptic connectivity to L2/3 of primary visual cortex measured by two-photon optogenetic stimulation, eLife, 11, e71103, 10.7554/eLife.71103 · DOI
- Kim, 2015, Three Types of Cortical Layer 5 Neurons That Differ in Brain-wide Connectivity and Function, Neuron, 88, 1253, 10.1016/j.neuron.2015.11.002 · DOI · Paper page
- Lanjakornsiripan, 2018, Layer-specific morphological and molecular differences in neocortical astrocytes and their dependence on neuronal layers, Nat. Commun., 9, 1623, 10.1038/s41467-018-03940-3 · DOI
- Bayraktar, 2020, Astrocyte layers in the mammalian cerebral cortex revealed by a single-cell in situ transcriptomic map, Nat. Neurosci., 23, 500, 10.1038/s41593-020-0602-1 · DOI · Paper page
- Takata, N., and Hirase, H. (2008). Cortical layer 1 and layer 2/3 astrocytes exhibit distinct calcium dynamics in vivo. PLoS ONE, 3. · DOI
- Kang, 2014, Astrocyte activation is suppressed in both normal and injured brain by FGF signaling, Proc. Natl. Acad. Sci. USA, 111, E2987, 10.1073/pnas.1320401111 · DOI
- Liu, 2018, Astrocyte-Secreted Chordin-like 1 Drives Synapse Maturation and Limits Plasticity by Increasing Synaptic GluA2 AMPA Receptors, Neuron, 100, 1116, 10.1016/j.neuron.2018.09.043 · DOI
- Rowland, 2018, Functional properties of stellate cells in medial entorhinal cortex layer II, eLife, 7, e36664, 10.7554/eLife.36664 · DOI
- Kaas, J.H. (2007). 3.08-The evolution of neuron classes in the neocortex of mammals. Evolution of Nervous Systems, Academic Press.
- Fazzari, 2020, Cortical distribution of GABAergic interneurons is determined by migration time and brain size, Development, 147, 1, 10.1242/dev.185033 · DOI
- Hartfuss, 2003, Reelin signaling directly affects radial glia morphology and biochemical maturation, Development, 130, 4597, 10.1242/dev.00654 · DOI · Paper page
- Imai, 2016, Dorsal Forebrain-Specific Deficiency of Reelin-Dab1 Signal Causes Behavioral Abnormalities Related to Psychiatric Disorders, Cereb. Cortex, 27, 3485, 10.1093/cercor/bhv334 · DOI
- Boisvert, 2018, The Aging Astrocyte Transcriptome from Multiple Regions of the Mouse Brain, Cell Rep., 22, 269, 10.1016/j.celrep.2017.12.039 · DOI · Paper page
- Li, 2022, Decoding the temporal and regional specification of microglia in the developing human brain, Cell Stem Cell, 29, 620, 10.1016/j.stem.2022.02.004 · DOI
- Weigel, 2021, Microtubule organization and dynamics in oligodendrocytes, astrocytes, and microglia, Dev. Neurobiol., 81, 310, 10.1002/dneu.22753 · DOI
- Gemma, 2013, The role of microglia in adult hippocampal neurogenesis, Front. Cell. Neurosci., 7, 229, 10.3389/fncel.2013.00229 · DOI
- Ziv, 2008, Immune-based regulation of adult neurogenesis: Implications for learning and memory, Brain Behav. Immun., 22, 167, 10.1016/j.bbi.2007.08.006 · DOI
- Olson, 2001, NeuroD2 is necessary for development and survival of central nervous system neurons, Dev. Biol., 234, 174, 10.1006/dbio.2001.0245 · DOI
- Tutukova, 2021, The Role of Neurod Genes in Brain Development, Function, and Disease, Front. Mol. Neurosci., 14, 662774, 10.3389/fnmol.2021.662774 · DOI
- Uittenbogaard, 2010, NeuroD6 genomic signature bridging neuronal differentiation to survival via the molecular chaperone network, J. Neurosci. Res., 88, 33, 10.1002/jnr.22182 · DOI
- Dobri, 2021, CD36 in Alzheimer’s Disease: An Overview of Molecular Mechanisms and Therapeutic Targeting, Neuroscience, 453, 301, 10.1016/j.neuroscience.2020.11.003 · DOI
- Attaai, 2020, Inhibition of Microglial TGFβ Signaling Increases Expression of Mrc1, Front. Cell. Neurosci., 14, 66, 10.3389/fncel.2020.00066 · DOI
- Jay, 2019, TREM2 is required for microglial instruction of astrocytic synaptic engulfment in neurodevelopment, Glia, 67, 1873, 10.1002/glia.23664 · DOI · Paper page
- Mallya, 2018, Microglial Pruning of Synapses in the Prefrontal Cortex During Adolescence, Cereb. Cortex, 29, 1634, 10.1093/cercor/bhy061 · DOI
- Roufagalas, 2021, Novel cell-based analysis reveals region-dependent changes in microglial dynamics in grey matter in a cuprizone model of demyelination, Neurobiol. Dis., 157, 105449, 10.1016/j.nbd.2021.105449 · DOI
- Choi, S., Guo, L., and Cordeiro, M.F. (2021). Retinal and Brain Microglia in Multiple Sclerosis and Neurodegeneration. Cells, 10. · DOI · Paper page
- Schuebel, 2017, Local Cues Establish and Maintain Region-Specific Phenotypes of Basal Ganglia Microglia, Neuron, 95, 341, 10.1016/j.neuron.2017.06.020 · DOI · Paper page
- Destrieux, 2013, Surgical anatomy of the hippocampus, Neurochirurgie, 59, 149, 10.1016/j.neuchi.2013.08.003 · DOI
- Bartsch, 2011, CA1 neurons in the human hippocampus are critical for autobiographical memory, mental time travel, and autonoetic consciousness, Proc. Natl. Acad. Sci. USA, 108, 17562, 10.1073/pnas.1110266108 · DOI
- Schafer, 2016, Adult Neurogenesis in the Hippocampus: From Stem Cells to Behavior, Cell, 167, 897, 10.1016/j.cell.2016.10.021 · DOI · Paper page
- Chai, 2017, Neural Circuit-Specialized Astrocytes: Transcriptomic, Proteomic, Morphological, and Functional Evidence, Neuron, 95, 531, 10.1016/j.neuron.2017.06.029 · DOI · Paper page
- Ota, 2013, The Role of Astrocytes in the Regulation of Synaptic Plasticity and Memory Formation, Neural Plast., 2013, 185463, 10.1155/2013/185463 · DOI
- Doe, 2021, The role of astrocyte-mediated plasticity in neural circuit development and function, Neural Dev., 16, 1, 10.1186/s13064-020-00151-9 · DOI
- Huang, 2020, Region-Specific Transcriptional Control of Astrocyte Function Oversees Local Circuit Activities, Neuron, 106, 992, 10.1016/j.neuron.2020.03.025 · DOI
- Yu, 2017, Identification of diverse astrocyte populations and their malignant analogs, Nat. Neurosci., 20, 396, 10.1038/nn.4493 · DOI · Paper page
- Dale, 2016, Effects of serotonin in the hippocampus: How SSRIs and multimodal antidepressants might regulate pyramidal cell function, CNS Spectr., 21, 143, 10.1017/S1092852915000425 · DOI
- Iigaya, 2018, An effect of serotonergic stimulation on learning rates for rewards apparent after long intertrial intervals, Nat. Commun., 9, 2477, 10.1038/s41467-018-04840-2 · DOI · Paper page
- Schade, 2021, Serotonin receptor 4 regulates hippocampal astrocyte morphology and function, Glia, 69, 872, 10.1002/glia.23933 · DOI
- Khakh, 2015, Diversity of astrocyte functions and phenotypes in neural circuits, Nat. Neurosci., 18, 942, 10.1038/nn.4043 · DOI · Paper page
- Ando, 2019, Identification of an early cell fate regulator by detecting dynamics in transcriptional heterogeneity and co-regulation during astrocyte differentiation, Npj Syst. Biol. Appl., 5, 18, 10.1038/s41540-019-0095-2 · DOI
- Zepeda, 2013, Role of wnt signaling in the control of adult hippocampal functioning in health and disease: Therapeutic implications, Curr. Neuropharmacol., 11, 465, 10.2174/1570159X11311050001 · DOI
- 2012, Astrocytes as neural stem cells in the adult brain, J. Stem Cells, 7, 181
- Lawson, 1990, Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain, Neuroscience, 39, 151, 10.1016/0306-4522(90)90229-W · DOI · Paper page
- Salamanca, 2019, MIC-MAC: An automated pipeline for high-throughput characterization and classification of three-dimensional microglia morphologies in mouse and human postmortem brain samples, Glia, 67, 1496, 10.1002/glia.23623 · DOI
- Parkhurst, 2013, Microglia promote learning-dependent synapse formation through brain-derived neurotrophic factor, Cell, 155, 1596, 10.1016/j.cell.2013.11.030 · DOI · Paper page
- Cherubini, 2015, The CA3 region of the hippocampus: How is it? What is it for? How does it do it?, Front. Cell. Neurosci., 9, 19, 10.3389/fncel.2015.00019 · DOI
- Ohgomori, 2021, A unique subtype of ramified microglia associated with synapses in the rat hippocampus, Eur. J. Neurosci., 54, 4740, 10.1111/ejn.15330 · DOI
- Akiyoshi, 2018, Microglia Enhance Synapse Activity to Promote Local Network Synchronization, Eneuro, 5, 1, 10.1523/ENEURO.0088-18.2018 · DOI
- Sheppard, 2019, Lipopolysaccharide-induced neuroinflammation induces presynaptic disruption through a direct action on brain tissue involving microglia-derived interleukin 1 beta, J. Neuroinflammation, 16, 106, 10.1186/s12974-019-1490-8 · DOI
- Peng, 2019, Microglial P2Y12 receptor regulates ventral hippocampal CA1 neuronal excitability and innate fear in mice, Mol. Brain, 12, 71, 10.1186/s13041-019-0492-x · DOI
- Grabert, 2016, Microglial brain region−dependent diversity and selective regional sensitivities to aging, Nat. Neurosci., 19, 504, 10.1038/nn.4222 · DOI · Paper page
- Theocharidis, 2009, Network visualization and analysis of gene expression data using BioLayout Express3D, Nat. Protoc., 4, 1535, 10.1038/nprot.2009.177 · DOI
- Bernardo, 2006, PPAR-gamma agonists as regulators of microglial activation and brain inflammation, Curr. Pharm. Des., 12, 93, 10.2174/138161206780574579 · DOI
- Wen, 2018, Polarization of Microglia to the M2 Phenotype in a Peroxisome Proliferator-Activated Receptor Gamma-Dependent Manner Attenuates Axonal Injury Induced by Traumatic Brain Injury in Mice, J. Neurotrauma, 35, 2330, 10.1089/neu.2017.5540 · DOI
- Dentesano, 2014, CD200R1 and CD200 expression are regulated by PPAR-γ in activated glial cells, Glia, 62, 982, 10.1002/glia.22656 · DOI
- Mestre, 2012, CD200-CD200R1 interaction contributes to neuroprotective effects of anandamide on experimentally induced inflammation, Glia, 60, 1437, 10.1002/glia.22366 · DOI
- Biber, 2007, Neuronal ‘On’ and ‘Off’ signals control microglia, Trends Neurosci., 30, 596, 10.1016/j.tins.2007.08.007 · DOI · Paper page
- Polazzi, 2013, Copper-Zinc Superoxide Dismutase (SOD1) Is Released by Microglial Cells and Confers Neuroprotection against 6-OHDA Neurotoxicity, Neurosignals, 21, 112, 10.1159/000337115 · DOI
- Gruol, D.L., Koibuchi, N., Manto, M., Molinari, M., Schmahmann, J.D., and Shen, Y. (2016). A brief history of the cerebellum. Essentials of Cerebellum and Cerebellar Disorders: A Primer for Graduate Students, Springer International Publishing. · DOI
- Apps, 2005, Anatomical and physiological foundations of cerebellar information processing, Nat. Rev. Neurosci., 6, 297, 10.1038/nrn1646 · DOI
- Lisberger, 2021, Diversity and dynamism in the cerebellum, Nat. Neurosci., 24, 160, 10.1038/s41593-020-00754-9 · DOI
- Cook, 2021, Losing the Beat: Contribution of Purkinje Cell Firing Dysfunction to Disease, and Its Reversal, Neuroscience, 462, 247, 10.1016/j.neuroscience.2020.06.008 · DOI
- Cerminara, 2015, Redefining the cerebellar cortex as an assembly of non-uniform Purkinje cell microcircuits, Nat. Rev. Neurosci., 16, 79, 10.1038/nrn3886 · DOI
- Lippman, 2008, Morphogenesis and regulation of Bergmann glial processes during Purkinje cell dendritic spine ensheathment and synaptogenesis, Glia, 56, 1463, 10.1002/glia.20712 · DOI
- Witcher, 2010, Three-dimensional relationships between perisynaptic astroglia and human hippocampal synapses, Glia, 58, 572, 10.1002/glia.20946 · DOI
- Araujo, 2019, The Role of Astrocytes in the Development of the Cerebellum, Cerebellum, 18, 1017, 10.1007/s12311-019-01046-0 · DOI
- Cerrato, V., Parmigiani, E., Figueres-Oñate, M., Betizeau, M., Aprato, J., Nanavaty, I., Berchialla, P., Luzzati, F., de’Sperati, C., and López-Mascaraque, L. (2018). Multiple origins and modularity in the spatiotemporal emergence of cerebellar astrocyte heterogeneity. PLoS Biol., 16. · DOI
- Farmer, 2016, Neurons diversify astrocytes in the adult brain through sonic hedgehog signaling, Science, 351, 849, 10.1126/science.aab3103 · DOI
- Xu, 2013, Bergmann glia function in granule cell migration during cerebellum development, Mol. Neurobiol., 47, 833, 10.1007/s12035-013-8405-y · DOI
- Buffo, 2013, Origin, lineage and function of cerebellar glia, Prog. Neurobiol., 109, 42, 10.1016/j.pneurobio.2013.08.001 · DOI
- Hoogland, 2010, Recent Developments in the Understanding of Astrocyte Function in the Cerebellum In Vivo, Cerebellum, 9, 264, 10.1007/s12311-009-0139-z · DOI
- Tang, 2009, Heterogeneity of Kir4.1 channel expression in glia revealed by mouse transgenesis, Glia, 57, 1706, 10.1002/glia.20882 · DOI
- Palay, 1972, The form of velate astrocytes in the cerebellar cortex of monkey and rat: High voltage electron microscopy of rapid Golgi preparations, Z. Für Anat. Und Entwickl., 138, 1, 10.1007/BF00519921 · DOI
- Farmer, 2017, Resolving Astrocyte Heterogeneity in the CNS, Front. Cell. Neurosci., 11, 300, 10.3389/fncel.2017.00300 · DOI
- Stowell, 2018, Cerebellar microglia are dynamically unique and survey Purkinje neurons in vivo, Dev. Neurobiol., 78, 627, 10.1002/dneu.22572 · DOI · Paper page
- Brown, 2018, C-type lectins in immunity and homeostasis, Nat. Rev. Immunol., 18, 374, 10.1038/s41577-018-0004-8 · DOI
- Holling, 2004, Function and regulation of MHC class II molecules in T-lymphocytes: Of mice and men, Hum. Immunol., 65, 282, 10.1016/j.humimm.2004.01.005 · DOI · Paper page
- Harms, 2013, MHCII Is Required for α-Synuclein-Induced Activation of Microglia, CD4 T Cell Proliferation, and Dopaminergic Neurodegeneration, J. Neurosci., 33, 9592, 10.1523/JNEUROSCI.5610-12.2013 · DOI · Paper page
- Siew, 2018, Microglial Lectins in Health and Neurological Diseases, Front. Mol. Neurosci., 11, 158, 10.3389/fnmol.2018.00158 · DOI
- Fumagalli, 2017, Pharmacological inhibition of mannose-binding lectin ameliorates neurobehavioral dysfunction following experimental traumatic brain injury, J. Cereb. Blood Flow Metab., 37, 938, 10.1177/0271678X16647397 · DOI
- Waller, R., Baxter, L., Fillingham, D.J., Coelho, S., Pozo, J.M., Mozumder, M., Frangi, A.F., Ince, P.G., Simpson, J.E., and Highley, J.R. (2019). Iba-1-/CD68+ microglia are a prominent feature of age-associated deep subcortical white matter lesions. PLoS ONE, 14. · DOI
- Perego, 2011, Temporal pattern of expression and colocalization of microglia/macrophage phenotype markers following brain ischemic injury in mice, J. Neuroinflammation, 8, 174, 10.1186/1742-2094-8-174 · DOI
- Routh, 2010, Glucose Sensing Neurons in the Ventromedial Hypothalamus, Sensors, 10, 9002, 10.3390/s101009002 · DOI
- Yoon, 2021, Hypothalamic glucose-sensing mechanisms, Diabetologia, 64, 985, 10.1007/s00125-021-05395-6 · DOI
- Quarta, 2016, Astrocytic Insulin Signaling Couples Brain Glucose Uptake with Nutrient Availability, Cell, 166, 867, 10.1016/j.cell.2016.07.028 · DOI
- Morel, 2017, Molecular and Functional Properties of Regional Astrocytes in the Adult Brain, J. Neurosci., 37, 8706, 10.1523/JNEUROSCI.3956-16.2017 · DOI · Paper page
- Griemsmann, 2014, Heterogeneity in expression of functional ionotropic glutamate and GABA receptors in astrocytes across brain regions: Insights from the thalamus, Philos. Trans. R Soc. Lond. B Biol. Sci., 369, 20130602, 10.1098/rstb.2013.0602 · DOI
- Matthias, 2003, Segregated Expression of AMPA-Type Glutamate Receptors and Glutamate Transporters Defines Distinct Astrocyte Populations in the Mouse Hippocampus, J. Neurosci., 23, 1750, 10.1523/JNEUROSCI.23-05-01750.2003 · DOI
- Lalo, 2006, NMDA Receptors Mediate Neuron-to-Glia Signaling in Mouse Cortical Astrocytes, J. Neurosci., 26, 2673, 10.1523/JNEUROSCI.4689-05.2006 · DOI
- Altman, 1962, Are new neurons formed in the brains of adult mammals?, Science, 135, 1127, 10.1126/science.135.3509.1127 · DOI
- Altman, 1965, Autoradiographic and histological evidence of postnatal hippocampal neurogenesis in rats, J. Comp. Neurol., 124, 319, 10.1002/cne.901240303 · DOI · Paper page
- Kaplan, 1977, Neurogenesis in the adult rat: Electron microscopic analysis of light radioautographs, Science, 197, 1092, 10.1126/science.887941 · DOI
- Ponti, 2013, Lineage progression from stem cells to new neurons in the adult brain ventricular-subventricular zone, Cell Cycle, 12, 1649, 10.4161/cc.24984 · DOI
- Jurkowski, 2020, Beyond the Hippocampus and the SVZ: Adult Neurogenesis Throughout the Brain, Front. Cell. Neurosci., 14, 576444, 10.3389/fncel.2020.576444 · DOI
- Kempermann, 2015, Neurogenesis in the Adult Hippocampus, Cold Spring Harb. Perspect Biol., 7, a018812, 10.1101/cshperspect.a018812 · DOI · Paper page
- Kress, 2015, A Distinct Population of Microglia Supports Adult Neurogenesis in the Subventricular Zone, J. Neurosci., 35, 11848, 10.1523/JNEUROSCI.1217-15.2015 · DOI · Paper page
- Hohsfield, 2021, Subventricular zone/white matter microglia reconstitute the empty adult microglial niche in a dynamic wave, Elife, 10, 1, 10.7554/eLife.66738 · DOI
- Pereira, 2015, IL-10 regulates adult neurogenesis by modulating ERK and STAT3 activity, Front. Cell. Neurosci., 9, 57, 10.3389/fncel.2015.00057 · DOI
- Mattson, 2018, Hallmarks of Brain Aging: Adaptive and Pathological Modification by Metabolic States, Cell Metab., 27, 1176, 10.1016/j.cmet.2018.05.011 · DOI · Paper page
- Lemaitre, 2012, Normal age-related brain morphometric changes: Nonuniformity across cortical thickness, surface area and gray matter volume?, Neurobiol. Aging, 33, 617.e1, 10.1016/j.neurobiolaging.2010.07.013 · DOI
- Samson, 2013, Impact of aging brain circuits on cognition, Eur. J. Neurosci., 37, 1903, 10.1111/ejn.12183 · DOI
- Sanz, 2009, Cell-type-specific isolation of ribosome-associated mRNA from complex tissues, Proc. Natl. Acad. Sci. USA, 106, 13939, 10.1073/pnas.0907143106 · DOI · Paper page
- Idriss, 2017, Prenatal betaine exposure modulates hypothalamic expression of cholesterol metabolic genes in cockerels through modifications of DNA methylation, Poult. Sci., 96, 1715, 10.3382/ps/pew437 · DOI
- Palmer, 2018, Astrocytes and Aging, Front. Aging Neurosci., 10, 337, 10.3389/fnagi.2018.00337 · DOI
- Zhang, 2015, Cholesterol metabolism and homeostasis in the brain, Protein Cell, 6, 254, 10.1007/s13238-014-0131-3 · DOI · Paper page
- Fukui, 2015, Effect of cholesterol reduction on receptor signaling in neurons, J. Biol. Chem., 290, 26383, 10.1074/jbc.M115.664367 · DOI
- Naseem, 1987, Cytotoxicity of cholesterol oxides and their effects on cholesterol metabolism in cultured human aortic smooth muscle cells, Biochem. Int., 14, 71
- Takamiya, 2002, Inflammation induces serine protease inhibitor 3 expression in the rat pineal gland, Neuroscience, 113, 387, 10.1016/S0306-4522(02)00198-7 · DOI
- Zamanian, 2012, Genomic Analysis of Reactive Astrogliosis, J. Neurosci., 32, 6391, 10.1523/JNEUROSCI.6221-11.2012 · DOI · Paper page
- Yang, 2015, Glial fibrillary acidic protein: From intermediate filament assembly and gliosis to neurobiomarker, Trends Neurosci., 38, 364, 10.1016/j.tins.2015.04.003 · DOI · Paper page
- Pandya, 2021, Region-specific vulnerability in neurodegeneration: Lessons from normal ageing, Ageing Res. Rev., 67, 101311, 10.1016/j.arr.2021.101311 · DOI
- Li, 2013, Phagocyte dysfunction, tissue aging and degeneration, Ageing Res. Rev., 12, 1005, 10.1016/j.arr.2013.05.006 · DOI
- Colton, 2009, Heterogeneity of Microglial Activation in the Innate Immune Response in the Brain, J. Neuroimmune Pharmacol., 4, 399, 10.1007/s11481-009-9164-4 · DOI
- Butovsky, 2006, Microglia activated by IL-4 or IFN-gamma differentially induce neurogenesis and oligodendrogenesis from adult stem/progenitor cells, Mol. Cell Neurosci., 31, 149, 10.1016/j.mcn.2005.10.006 · DOI · Paper page
- Gan, 2018, Converging pathways in neurodegeneration, from genetics to mechanisms, Nat. Neurosci., 21, 1300, 10.1038/s41593-018-0237-7 · DOI
- Katsuno, 2018, Preclinical progression of neurodegenerative diseases, Nagoya J. Med. Sci., 80, 289
- Xu, 2019, Regional protein expression in human Alzheimer’s brain correlates with disease severity, Commun. Biol., 2, 43, 10.1038/s42003-018-0254-9 · DOI
- Buosi, 2018, Heterogeneity in Synaptogenic Profile of Astrocytes from Different Brain Regions, Mol. Neurobiol., 55, 751, 10.1007/s12035-016-0343-z · DOI
- Jana, 2008, Fibrillar amyloid-beta peptides activate microglia via TLR2: Implications for Alzheimer’s disease, J. Immunol., 181, 7254, 10.4049/jimmunol.181.10.7254 · DOI
- Zhang, 2021, Microglia in Alzheimer’s Disease: A Target for Therapeutic Intervention, Front. Cell Neurosci., 15, 749587, 10.3389/fncel.2021.749587 · DOI
- Bi, 2013, Reactive astrocytes secrete lcn2 to promote neuron death, Proc. Natl. Acad. Sci. USA, 110, 4069, 10.1073/pnas.1218497110 · DOI · Paper page
- Guttenplan, 2021, Neurotoxic reactive astrocytes induce cell death via saturated lipids, Nature, 599, 102, 10.1038/s41586-021-03960-y · DOI · Paper page
- Li, 2019, Reactive Astrocytes in Neurodegenerative Diseases, Aging Dis., 10, 664, 10.14336/AD.2018.0720 · DOI · Paper page
- Macdonald, 2014, Early detection of cerebral glucose uptake changes in the 5XFAD mouse, Curr. Alzheimer Res., 11, 450, 10.2174/1567205011666140505111354 · DOI · Paper page
- Braak, 1995, Staging of alzheimer’s disease-related neurofibrillary changes, Neurobiol. Aging, 16, 271, 10.1016/0197-4580(95)00021-6 · DOI · Paper page
- Grober, 1999, Memory and mental status correlates of modified Braak staging, Neurobiol. Aging, 20, 573, 10.1016/S0197-4580(99)00063-9 · DOI
- Cuervo, 2000, When lysosomes get old☆, Exp. Gerontol., 35, 119, 10.1016/S0531-5565(00)00075-9 · DOI
- Zhang, 2022, Impairment of the autophagy-lysosomal pathway in Alzheimer’s diseases: Pathogenic mechanisms and therapeutic potential, Acta Pharm. Sin. B, 12, 1019, 10.1016/j.apsb.2022.01.008 · DOI
- Wolfe, 2013, Autophagy failure in Alzheimer’s disease and the role of defective lysosomal acidification, Eur. J. Neurosci., 37, 1949, 10.1111/ejn.12169 · DOI
- Wu, 2016, Neuronal activity enhances tau propagation and tau pathology in vivo, Nat. Neurosci., 19, 1085, 10.1038/nn.4328 · DOI · Paper page
- Cole, 2018, TFEB enhances astroglial uptake of extracellular tau species and reduces tau spreading, J. Exp. Med., 215, 2355, 10.1084/jem.20172158 · DOI · Paper page
- Garaschuk, O., and Verkhratsky, A. (2019). Microglia in neurodegenerative disorders. Microglia: Methods and Protocols, Springer. · DOI
- Streit, 2021, The Role of Microglia in Sporadic Alzheimer’s Disease, J. Alzheimers Dis., 79, 961, 10.3233/JAD-201248 · DOI
- Spinrad, 2017, A Unique Microglia Type Associated with Restricting Development of Alzheimer’s Disease, Cell, 169, 1276, 10.1016/j.cell.2017.05.018 · DOI · Paper page
- Konishi, 2018, Microglial TREM2/DAP12 Signaling: A Double-Edged Sword in Neural Diseases, Front. Cell. Neurosci., 12, 206, 10.3389/fncel.2018.00206 · DOI · Paper page
- Otero, 2009, Macrophage colony-stimulating factor induces the proliferation and survival of macrophages via a pathway involving DAP12 and β-catenin, Nat. Immunol., 10, 734, 10.1038/ni.1744 · DOI · Paper page
- Koychev, 2020, Correlation of Alzheimer Disease Neuropathologic Staging with Amyloid and Tau Scintigraphic Imaging Biomarkers, J. Nucl. Med., 61, 1413, 10.2967/jnumed.119.230458 · DOI
- Krasemann, 2017, The TREM2-APOE Pathway Drives the Transcriptional Phenotype of Dysfunctional Microglia in Neurodegenerative Diseases, Immunity, 47, 566, 10.1016/j.immuni.2017.08.008 · DOI · Paper page
- Rangaraju, 2018, Identification and therapeutic modulation of a pro-inflammatory subset of disease-associated-microglia in Alzheimer’s disease, Mol. Neurodegener., 13, 24, 10.1186/s13024-018-0254-8 · DOI · Paper page
- Hu, 2021, Replicative senescence dictates the emergence of disease-associated microglia and contributes to Aβ pathology, Cell Rep., 35, 109228, 10.1016/j.celrep.2021.109228 · DOI · Paper page
- Dauer, 2003, Parkinson’s Disease: Mechanisms and Models, Neuron, 39, 889, 10.1016/S0896-6273(03)00568-3 · DOI · Paper page
- Kostuk, 2019, Subregional differences in astrocytes underlie selective neurodegeneration or protection in Parkinson’s disease models in culture, Glia, 67, 1542, 10.1002/glia.23627 · DOI
- Mullican, 2018, Uniting GDF15 and GFRAL: Therapeutic Opportunities in Obesity and Beyond, Trends Endocrinol. Metab., 29, 560, 10.1016/j.tem.2018.05.002 · DOI · Paper page
- Chen, 2017, Neuroprotective Role of the PI3 Kinase/Akt Signaling Pathway in Zebrafish, Front. Endocrinol., 8, 21, 10.3389/fendo.2017.00021 · DOI
- Naoi, 2019, Neuroprotection of multifunctional phytochemicals as novel therapeutic strategy for neurodegenerative disorders: Antiapoptotic and antiamyloidogenic activities by modulation of cellular signal pathways, Future Neurol., 14, FNL9, 10.2217/fnl-2018-0028 · DOI
- Kwon, 2020, Neuroinflammation in neurodegenerative disorders: The roles of microglia and astrocytes, Transl. Neurodegener., 9, 42, 10.1186/s40035-020-00221-2 · DOI · Paper page
- Araki, T. (2021). Astrocytes in Amyotrophic Lateral Sclerosis. Amyotrophic Lateral Sclerosis, Exon publications. · DOI
- Miller, 2017, Astroglial transcriptome dysregulation in early disease of an ALS mutant SOD1 mouse model, J. Neurogenet., 31, 37, 10.1080/01677063.2016.1260128 · DOI
- Trias, 2011, Phenotypically aberrant astrocytes that promote motoneuron damage in a model of inherited amyotrophic lateral sclerosis, Proc. Natl. Acad. Sci. USA, 108, 18126, 10.1073/pnas.1110689108 · DOI
- Gomes, 2020, Astrocyte regional diversity in ALS includes distinct aberrant phenotypes with common and causal pathological processes, Exp. Cell Res., 395, 112209, 10.1016/j.yexcr.2020.112209 · DOI
- Pajarillo, 2019, The role of astrocytic glutamate transporters GLT-1 and GLAST in neurological disorders: Potential targets for neurotherapeutics, Neuropharmacology, 161, 107559, 10.1016/j.neuropharm.2019.03.002 · DOI
- Axelsson, 1984, Hereditary diffuse leucoencephalopathy with spheroids, Acta Psychiatr. Scand. Suppl., 314, 1
- Han, 2020, Microglial replacement therapy: A potential therapeutic strategy for incurable CSF1R-related leukoencephalopathy, Acta Neuropathol. Commun., 8, 217, 10.1186/s40478-020-01093-3 · DOI · Paper page
- Han, 2019, Enforced microglial depletion and repopulation as a promising strategy for the treatment of neurological disorders, Glia, 67, 217, 10.1002/glia.23529 · DOI
- Kana, 2019, CSF-1 controls cerebellar microglia and is required for motor function and social interaction, J. Exp. Med., 216, 2265, 10.1084/jem.20182037 · DOI · Paper page
Cited by
Sorted by citations
Baumart, G. J., Rodrigues, M. S., Sholl, J. N., de Sousa, A. C., Weber, A. F., Costa‐Beber, L. C., Farias, H. R., Costa, M. V., Peres, A. M., de Camargo, P. R., et al. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70403 · Cited by 2
Metadata
- Authors
- Lee, J., Kim, S. W., & Kim, K.-T.
- Affiliations
- Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea
- Venue
- Cells
- Publisher
- MDPI AG
- Published
- 2022-06-12
- Volume
- 11
- Issue
- 12
- Pages
- 1902
- ISSN
- 2073-4409
- PMC
- PMC9220858
- Cited by
- 34
- References
- 58
- Language
- en
- Funders
- Rural Development Administration of the Republic of Korea (PJ01640202)
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