Astrocytes locally translate transcripts in their peripheral processes
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Abstract
Significance: Cellular compartments are specialized for particular functions. In astrocytes, the peripheral, perisynaptic processes contain proteins specialized for reuptake of neurotransmitters and ions, and have been shown to alter their morphology in response to activity. Regulated transport of a specific subset of nuclear-derived mRNAs to specific compartments is thought to support the specialization of these compartments and allow for local regulation of translation. In neurons, local translation near activated synapses is thought to generate the proteins needed for the synaptic alterations that constitute memory. We demonstrate that astrocytes also have sequence-dependent local translation in their peripheral processes, including transcripts with roles in regulating synapses, and identify one mechanism regulating this translation. These findings suggest local translation in astrocyte processes may play a role in synapse modulation.
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The presence of Plxnb1 mRNA puncta in hypertrophic processes of reactive astrocytes signifies local translation.
“signifying local translation, a scenario described for Gfap and other key astrocyte genes35, 36.”
From Regulation of cell distancing in peri-plaque glial nets by Plexin-B1 affects glial activation and amyloid compaction in Alzheimer’s disease (2024) · cites this paper as [35]
The Discussion and Fig. 2 report local protein synthesis in peripheral astrocyte processes, and Fig. 5 includes Gfap among the mRNAs examined for localization. The paper does not study Plxnb1 or reactive, hypertrophic astrocytes; it also does not establish that mRNA puncta alone signify translation of a particular transcript. (LLM, conf=0.86)
Experimental — accuracy not yet measuredHA-tagged ribosomes are present throughout the astrocyte, including distal processes where local translation occurs.
“We further confirmed that HA-tagged ribosomes are present throughout the astrocyte, including distal processes where local translation occurs (Figure 1G; Sakers et al., 2017).”
From The aging astrocyte transcriptome from multiple regions of the mouse brain. (2018) · cites this paper as Sakers et al., 2017
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Lorenz, R., Bernhart, S. H., Höner zu Siederdissen, C., Tafer, H., Flamm, C., Stadler, P. F., & Hofacker, I. L. (2011) · Algorithms for Molecular Biology · doi:10.1186/1748-7188-6-26 · Cited by 5,098 · see citing works
Bailey, T., Johnson, J., Grant, C. E., & Noble, W. S. (2015) · Nucleic Acids Res. · doi:10.1093/nar/gkv416 · Cited by 4,916 · see citing works
Spatially resolved, highly multiplexed RNA profiling in single cells
Chen, K. H., Boettiger, A. N., Moffitt, J. R., Wang, S., & Zhuang, X. (2015) · Science · doi:10.1126/science.aaa6090 · Cited by 2,969 · see citing works
Gruber, A. R., Lorenz, R., Bernhart, S. H., Neuböck, R., & Hofacker, I. L. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn188 · Cited by 2,717 · see citing works
Rothstein, J. D., Dykes-Hoberg, M., Pardo, C. A., Bristol, L. A., Jin, L., Kuncl, R. W., Kanai, Y., Hediger, M. A., Wang, Y., Schielke, J. P., et al. (1996) · Neuron · doi:10.1016/s0896-6273(00)80086-0 · Cited by 2,534 · see citing works
Tripartite synapses: glia, the unacknowledged partner
Araque, A., Parpura, V., Sanzgiri, R. P., & Haydon, P. G. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01349-6 · Cited by 2,529 · see citing works
CNS synaptogenesis promoted by glia-derived cholesterol
Mauch, D. H., Nägler, K., Schumacher, S., Göritz, C., Müller, E.-C., Otto, A., & Pfrieger, F. W. (2001) · Science · doi:10.1126/science.294.5545.1354 · Cited by 1,711 · see citing works
SUnSET, a nonradioactive method to monitor protein synthesis
Schmidt, E. K., Clavarino, G., Ceppi, M., & Pierre, P. (2009) · Nature Methods · doi:10.1038/nmeth.1314 · Cited by 1,706 · see citing works
Thrombospondins are astrocyte-secreted proteins that promote CNS synaptogenesis
Christopherson, K. S., Ullian, E. M., Stokes, C. C. A., Mullowney, C. E., Hell, J. W., Agah, A., Lawler, J., Mosher, D. F., Bornstein, P., & Barres, B. A. (2005) · Cell · doi:10.1016/j.cell.2004.12.020 · Cited by 1,688 · see citing works
Multicolor Super-Resolution Imaging with Photo-Switchable Fluorescent Probes
Bates, M., Huang, B., Dempsey, G. T., & Zhuang, X. (2007) · Science · doi:10.1126/science.1146598 · Cited by 1,507 · see citing works
Uniquely Hominid Features of Adult Human Astrocytes
Oberheim, N. A., Takano, T., Han, X., He, W., Lin, J. H. C., Wang, F., Xu, Q., Wyatt, J. D., Pilcher, W., Ojemann, J. G., et al. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.4707-08.2009 · Cited by 1,488 · see citing works
Selective loss of glial glutamate transporter GLT‐1 in amyotrophic lateral sclerosis
Rothstein, J. D., Van Kammen, M., Levey, A. I., Martin, L. J., & Kuncl, R. W. (1995) · Annals of Neurology · doi:10.1002/ana.410380114 · Cited by 1,471 · see citing works
Nielsen, S. M., Nagelhus, E. A., Amiry-Moghaddam, M. R., Bourque, C. W., Agre, P. C., & Ottersen, O. P. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-01-00171.1997 · Cited by 1,440 · see citing works
Control of Synapse Number by Glia
Ullian, E. M., Sapperstein, S. K., Christopherson, K. S., & Barres, B. A. (2001) · Science · doi:10.1126/science.291.5504.657 · Cited by 1,380 · see citing works
Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways
Chung, W.-S., Clarke, L. E., Wang, G. X., Stafford, B. K., Sher, A., Chakraborty, C., Joung, J., Foo, L. C., Thompson, A., Chen, C., et al. (2013) · Nature · doi:10.1038/nature12776 · Cited by 1,377 · cited 1× · see citing works
“Furthermore, Mertk is a required engulfment receptor for astrocytemediated synapse elimination, in vitro and in vivo (29).”
BackgroundA translational profiling approach for the molecular characterization of CNS cell types
Heiman, M., Schaefer, A., Gong, S., Peterson, J. D., Day, M., Ramsey, K. E., Suárez-Fariñas, M., Schwarz, C., Stephan, D. A., Surmeier, D. J., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.028 · Cited by 1,134 · see citing works
mRNA localization: Gene expression in the spatial dimension
Martin, K. C., & Ephrussi, A. (2009) · Cell · doi:10.1016/j.cell.2009.01.044 · Cited by 1,048 · see citing works
A Requirement for Local Protein Synthesis in Neurotrophin-Induced Hippocampal Synaptic Plasticity
Kang, H., & Schuman, E. M. (1996) · Science · doi:10.1126/science.273.5280.1402 · Cited by 985 · see citing works
Application of a translational profiling approach for the comparative analysis of CNS cell types
Doyle, J. P., Dougherty, J. D., Heiman, M., Schmidt, E. F., Stevens, T. R., Ma, G., Bupp, S., Shrestha, P., Shah, R. D., Doughty, M. L., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.029 · Cited by 912 · see citing works
Self-citationGlutamate exocytosis from astrocytes controls synaptic strength
Jourdain, P., Bergersen, L. H., Bhaukaurally, K., Bezzi, P., Santello, M., Domercq, M., Matute, C., Tonello, F., Gundersen, V., & Volterra, A. (2007) · Nature Neuroscience · doi:10.1038/nn1849 · Cited by 806 · see citing works
Synaptic Efficacy Enhanced by Glial Cells in Vitro
Pfrieger, F. W., & Barres, B. A. (1997) · Science · doi:10.1126/science.277.5332.1684 · Cited by 793 · see citing works
Synaptic Islands Defined by the Territory of a Single Astrocyte
Halassa, M. M., Fellin, T., Takano, H., Dong, J.-H., & Haydon, P. G. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1419-07.2007 · Cited by 767 · see citing works
Han, T. W., Kato, M., Xie, S., Wu, L. C., Mirzaei, H., Pei, J., Chen, M., Xie, Y., Allen, J. D., Xiao, G., et al. (2012) · Cell · doi:10.1016/j.cell.2012.04.016 · Cited by 758 · see citing works
Astrocytic complexity distinguishes the human brain
Oberheim, N. A., Wang, X., Goldman, S., & Nedergaard, M. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.08.004 · Cited by 739 · see citing works
Superresolution Imaging of Chemical Synapses in the Brain
Dani, A., Huang, B., Bergan, J. F., Dulac, C. G., & Zhuang, X. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.021 · Cited by 718 · see citing works
Self-citationMotif Enrichment Analysis: a unified framework and an evaluation on ChIP data
McLeay, R. C., & Bailey, T. L. (2010) · BMC Bioinformatics · doi:10.1186/1471-2105-11-165 · Cited by 687 · see citing works
Steward, O., & Levy, W. (1982) · The Journal of Neuroscience · doi:10.1523/jneurosci.02-03-00284.1982 · Cited by 676 · see citing works
Control of excitatory CNS synaptogenesis by astrocyte-secreted proteins Hevin and SPARC
Kucukdereli, H., Allen, N. J., Lee, A. T., Feng, A., Ozlu, M. I., Conatser, L. M., Chakraborty, C., Workman, G., Weaver, M., Sage, E. H., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1104977108 · Cited by 642 · see citing works
Mutant Mice (Quaking and Jimpy) with Deficient Myelination in the Central Nervous System
Sidman, R. L., Dickie, M. M., & Appel, S. H. (1964) · Science · doi:10.1126/science.144.3616.309 · Cited by 603 · see citing works
Sharova, L. V., Sharov, A. A., Nedorezov, T., Piao, Y., Shaik, N., & Ko, M. S. H. (2009) · DNA Research · doi:10.1093/dnares/dsn030 · Cited by 591 · see citing works
Burgin, K., Waxham, M., Rickling, S., Westgate, S., Mobley, W. C., & Kelly, P. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-06-01788.1990 · Cited by 564 · see citing works
Production and purification of serotype 1, 2, and 5 recombinant adeno-associated viral vectors
Zolotukhin, S., Potter, M., Zolotukhin, I., Sakai, Y., Loiler, S., Fraites, T. J., Chiodo, V. A., Philipsberg, T., Muzyczka, N., Hauswirth, W. W., et al. (2002) · Methods · doi:10.1016/s1046-2023(02)00220-7 · Cited by 556 · see citing works
Miller, S., Yasuda, M., Coats, J., Jones, Y., Martone, M. E., & Mayford, M. R. (2002) · Neuron · doi:10.1016/s0896-6273(02)00978-9 · Cited by 507 · see citing works
Neuronal Regulation of Glutamate Transporter Subtype Expression in Astrocytes
Swanson, R. A., Liu, J., Miller, J. W., Rothstein, J. D., Farrell, K., Stein-Behrens, B., & Longuemare, M. C. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-03-00932.1997 · Cited by 500 · see citing works
Danbolt, N. C., Storm‐Mathisen, J., & Kanner, B. I. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90316-t · Cited by 438 · see citing works
Synthesis and incorporation of myelin polypeptides into CNS myelin.
Colman, D., Kreibich, G., Frey, A. B., & Sabatini, D. D. (1982) · The Journal of Cell Biology · doi:10.1083/jcb.95.2.598 · Cited by 424 · see citing works
Zhang, H. L., Eom, T., Oleynikov, Y., Shenoy, S. M., Liebelt, D. A., Dictenberg, J. B., Singer, R. H., & Bassell, G. J. (2001) · Neuron · doi:10.1016/s0896-6273(01)00357-9 · Cited by 387 · see citing works
Glial contributions to excitatory neurotransmission in cultured hippocampal cells
Mennerick, S. J., & Zorumski, C. F. (1994) · Nature · doi:10.1038/368059a0 · Cited by 352 · see citing works
Dougherty, J. D., Schmidt, E. F., Nakajima, M., & Heintz, N. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq130 · Cited by 344 · see citing works
Self-citationTo localize or not to localize: mRNA fate is in 3′UTR ends
Andreassi, C., & Riccio, A. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.06.001 · Cited by 338 · see citing works
Kislauskis, E. (1993) · The Journal of Cell Biology · doi:10.1083/jcb.123.1.165 · Cited by 328 · see citing works
Mayford, M. R., Baranes, D., Podsypanina, K., & Kandel, E. R. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.23.13250 · Cited by 323 · see citing works
Remote Control of Gene Function by Local Translation
Jung, H., Gkogkas, C. G., Sonenberg, N., & Holt, C. E. (2014) · Cell · doi:10.1016/j.cell.2014.03.005 · Cited by 302 · see citing works
Target RNA motif and target mRNAs of the Quaking STAR protein
Galarneau, A., & Richard, S. (2005) · Nature Structural & Molecular Biology · doi:10.1038/nsmb963 · Cited by 285 · see citing works
Facilitation of dendritic mRNA transport by CPEBPreprint
Huang, Y., Carson, J. H., Barbarese, E., & Richter, J. D. (2003) · Genes & Development · doi:10.1101/gad.1053003 · Cited by 265 · see citing works
Emerging Roles of Disordered Sequences in RNA-Binding Proteins
Calabretta, S., & Richard, S. (2015) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2015.08.012 · Cited by 240 · see citing works
How and why does β‐actin mRNA target?
Condeelis, J. S., & Singer, R. H. (2005) · Biology of the Cell · doi:10.1042/bc20040063 · Cited by 240 · see citing works
Dopaminergic Cell Loss Induced by Human A30P α -Synuclein Gene Transfer to the Rat Substantia Nigra
Klein, R. L., King, M. A., Hamby, M. E., & Meyer, E. M. (2002) · Human Gene Therapy · doi:10.1089/10430340252837206 · Cited by 209 · see citing works
Derouiche, A., & Frotscher, M. (2001) · Glia · doi:10.1002/glia.1120 · Cited by 197 · see citing works
Sun, S., Sun, Y., Ling, S., Ferraiuolo, L., McAlonis‐Downes, M., Zou, Y., Drenner, K., Wang, Y., Ditsworth, D., Tokunaga, S., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1520639112 · Cited by 194 · see citing works
Neural Cell Type-Specific Expression of QKI Proteins Is Altered inquakingviableMutant Mice
Hardy, R. J., Loushin, C., Friedrich, V. L., Chen, Q., Ebersole, T. A., Lazzarini, R. A., & Artzt, K. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-24-07941.1996 · Cited by 184 · see citing works
Nuclear Retention of MBP mRNAs in the Quaking Viable Mice
Larocque, D., Pilotte, J., Chen, T., Cloutier, F., Bernard Massie, B., Pedraza, L., Couture, R., Lasko, P. F., Almazán, G., & Richard, S. (2002) · Neuron · doi:10.1016/s0896-6273(02)01055-3 · Cited by 167 · see citing works
Li, Z., Zhang, Y., Li, D., & Feng, Y. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-13-04944.2000 · Cited by 150 · see citing works
Dynamic mRNA Transport and Local Translation in Radial Glial Progenitors of the Developing Brain
Pilaz, L., Lennox, A. L., Rouanet, J. P., & Silver, D. L. (2016) · Current Biology · doi:10.1016/j.cub.2016.10.040 · Cited by 144 · see citing works
Glia selectively approach synapses on thin dendritic spines
Medvedev, N. I., Popov, V. I., Henneberger, C., Kraev, I., Rusakov, D. A., & Stewart, M. G. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2014.0047 · Cited by 107 · see citing works
Okaty, B. W., Sugino, K., & Nelson, S. B. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016493 · Cited by 104 · see citing works
Berger, U. V., DeSilva, T. M., Chen, W., & Rosenberg, P. A. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20737 · Cited by 104 · see citing works
Greco, T. M., Seeholzer, S. H., Mak, A., Spruce, L. A., & Ischiropoulos, H. (2010) · Journal of Proteome Research · doi:10.1021/pr100134n · Cited by 104 · see citing works
A single transcription factor is sufficient to induce and maintain secretory cell architecturePreprint
Lo, H. G., Jin, R. U., Sibbel, G., Liu, D., Karki, A., Joens, M. S., Madison, B., Zhang, B., Blanc, V., Fitzpatrick, J. A. J., et al. (2017) · Genes & Development · doi:10.1101/gad.285684.116 · Cited by 82 · see citing works
Dougherty, J. D., Fomchenko, E. I., Akuffo, A. A., Schmidt, E. F., Helmy, K. Y., Bazzoli, E., Brennan, C., Holland, E. C., & Milosevic, A. (2012) · Cancer Research · doi:10.1158/0008-5472.can-11-2632 · Cited by 67 · see citing works
Self-citationEndogenous 24S-hydroxycholesterol modulates NMDAR-mediated function in hippocampal slices
Sun, M., Izumi, Y., Benz, A. M., Zorumski, C. F., & Mennerick, S. J. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00890.2015 · Cited by 64 · see citing works
Ike, H., Kosugi, A., Kato, A., Iino, R., Hirano, H., Fujiwara, T. K., Ritchie, K. P., & Kusumi, A. (2003) · ChemPhysChem · doi:10.1002/cphc.200300670 · Cited by 62 · see citing works
Gerstner, J. R., Vanderheyden, W. M., LaVaute, T. M., Westmark, C. J., Rouhana, L., Pack, A. I., Wickens, M., & Landry, C. F. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3228-11.2012 · Cited by 61 · see citing works
Lie, Y. S., & Macdonald, P. M. (1999) · Development · doi:10.1242/dev.126.6.1129 · Cited by 59 · see citing works
A Comprehensive Analysis of Cell Type–Specific Nuclear RNA From Neurons and Glia of the Brain
Reddy, A. S., O’Brien, D., Pisat, N., Weichselbaum, C. T., Sakers, K., Lisci, M., Dalal, J. S., & Dougherty, J. D. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.02.021 · Cited by 50 · see citing works
Self-citationThomsen, R., Pallesen, J., Daugaard, T. F., Børglum, A. D., & Nielsen, A. L. (2013) · Glia · doi:10.1002/glia.22569 · Cited by 40 · see citing works
Westmark, P. R., Westmark, C. J., Jeevananthan, A., & Malter, J. S. (2011) · Journal of Visualized Experiments · doi:10.3791/3196 · Cited by 36 · see citing works
RNA-binding protein QKI regulates Glial fibrillary acidic protein expression in human astrocytes
Radomska, K. J., Halvardson, J., Reinius, B., Carlström, E. L., Emilsson, L., Feuk, L., & JAZIN, E. E. (2013) · Human Molecular Genetics · doi:10.1093/hmg/dds553 · Cited by 28 · see citing works
Mishra, P. J., Guo, T. W., Zaidi, R., Davis, S. R., Arnheiter, H., Walker, R. L., Meltzer, P. S., & Merlino, G. T. (2012) · Cancer Research · doi:10.1158/1538-7445.am2012-4856 · Cited by 13 · see citing works
Ribosome-associated membrane contacts between astrocytes in the anoxic brain
Špaček, J. (1982) · Acta Neuropathologica · doi:10.1007/bf00692182 · Cited by 7 · see citing works
Westmark, P. R., Westmark, C. J., Jeevananthan, A., & Malter, J. S. (2011) · Journal of Visualized Experiments · doi:10.3791/3196-v · Cited by 4 · see citing works
Kislauskis, E. H., Li, Z., Singer, R. H., & Taneja, K. L. (1993) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · Cited by 4 · see citing works
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Cell Biology of Astrocyte-Synapse Interactions
Allen, N. J., & Eroğlu, Ç. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.056 · Cited by 1,031 · see citing works
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 · see citing works
Astrocyte function from information processing to cognition and cognitive impairment
Santello, M., Toni, N., & Volterra, A. (2019) · Nature Neuroscience · doi:10.1038/s41593-018-0325-8 · Cited by 737 · see citing works
The aging astrocyte transcriptome from multiple regions of the mouse brain.
Boisvert, M. M., Erikson, G. A., Shokhirev, M. N., & Allen, N. J. (2018) · Cell Reports · doi:10.1016/j.celrep.2017.12.039 · Cited by 702 · see citing works
Dejanovic, B., Wu, T., Tsai, M.-C., Graykowski, D., Gandham, V. D., Rose, C. M., Bakalarski, C. E., Ngu, H., Wang, Y., Pandey, S., et al. (2022) · Nature Aging · doi:10.1038/s43587-022-00281-1 · Cited by 341 · see citing works
Merkurjev, D., Hong, W., Iida, K., Oomoto, I., Goldie, B. J., Yamaguti, H., Ohara, T., Kawaguchi, S., Hirano, T., Martin, K. C., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0173-6 · Cited by 237 · see citing works
Astroglial Glutamate Signaling and Uptake in the Hippocampus
Rose, C. R., Felix, L., Zeug, A., Dietrich, D., Reiner, A., & Henneberger, C. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00451 · Cited by 224 · see citing works
Baldwin, K. T., Murai, K. K., & Khakh, B. S. (2023) · Trends in Cell Biology · doi:10.1016/j.tcb.2023.09.006 · Cited by 230 · see citing works
Compartmentalized Signaling in Neurons: From Cell Biology to Neuroscience
Terenzio, M., Schiavo, G., & Fainzilber, M. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.015 · Cited by 139 · see citing works
Mattioli, C. C., Rom, A., Franke, V., Imami, K., Arrey, G., Terne, M., Woehler, A., Akalin, A., Ulitsky, I., & Chekulaeva, M. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky1270 · Cited by 125 · see citing works
A Paranigral VTA Nociceptin Circuit that Constrains Motivation for Reward
Parker, K. E., Pedersen, C. E., Gomez, A. M., Spangler, S. M., Walicki, M. C., Feng, S., Stewart, S., Otis, J. M., Al‐Hasani, R., McCall, J. G., et al. (2019) · Cell · doi:10.1016/j.cell.2019.06.034 · Cited by 113 · see citing works
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Werner, C. D., Sauer, M., & Geis, C. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.0c01174 · Cited by 111 · see citing works
Sapkota, D., Lake, A. M., Yang, W., Yang, C., Wesseling, H., Guise, A. J., Uncu, C., Dalal, J. S., Kraft, A. W., Lee, J., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2018.12.077 · Cited by 111 · see citing works
Self-citationMartins, D., Giacomel, A., Williams, S., Turkheimer, F., Dipasquale, O., & Veronese, M. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.110173 · Cited by 94 · see citing works
Farris, S., Ward, J. M., Carstens, K. E., Samadi, M., Wang, Y., & Dudek, S. M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.08.093 · Cited by 94 · see citing works
Calcium Signals in Astrocyte Microdomains, a Decade of Great Advances
Lia, A., Henriques, V. J., Zonta, M., Chiavegato, A., Carmignoto, G., Gómez‐Gonzalo, M., & Losi, G. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.673433 · Cited by 96 · see citing works
Mazaré, N., Oudart, M., Moulard, J., Cheung, G. T. Y., Tortuyaux, R., Mailly, P., Mazaud, D., Bemelmans, A., Boulay, A.-C., Blugeon, C., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108076 · Cited by 90 · see citing works
No Longer Underappreciated: The Emerging Concept of Astrocyte Heterogeneity in Neuroscience
Pestana, F., Edwards‐Faret, G., Belgard, T. G., Martirosyan, A., & Holt, M. G. (2020) · Brain Sciences · doi:10.3390/brainsci10030168 · Cited by 86 · see citing works
Distribution and Function of the Bestrophin-1 (Best1) Channel in the Brain
Oh, S., & Lee, C. J. (2017) · Experimental Neurobiology · doi:10.5607/en.2017.26.3.113 · Cited by 77 · see citing works
Astrocyte-Neuron Signaling in Synaptogenesis
Shan, L., Zhang, T., Fan, K. S., Cai, W., & Liu, H. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.680301 · Cited by 76 · see citing works
Galea, E., Weinstock, L. D., Larramona-Arcas, R., Pybus, A. F., Giménez-Llort, L., Escartin, C., & Wood, L. B. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105655 · Cited by 83 · see citing works
Hayashi, M. K. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19041177 · Cited by 72 · see citing works
Cellular and regional vulnerability in frontotemporal tauopathies
Forrest, S. L., Kril, J. J., & Halliday, G. M. (2019) · Acta Neuropathologica · doi:10.1007/s00401-019-02035-7 · Cited by 71 · see citing works
Role of glia and extracellular matrix in controlling neuroplasticity in the central nervous system
Dzyubenko, E., & Hermann, D. M. (2023) · Seminars in Immunopathology · doi:10.1007/s00281-023-00989-1 · Cited by 67 · see citing works
Transcriptomic Analysis of Ribosome-Bound mRNA in Cortical Neurites In Vivo
Ouwenga, R., Lake, A. M., O'Brien, D., Mogha, A., Dani, A., & Dougherty, J. D. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3044-16.2017 · Cited by 65 · see citing works
Self-citationDroplet-based transcriptome profiling of individual synapses
Niu, M., Cao, W., Wang, Y., Zhu, Q., Luo, J., Wang, B., Zheng, H., Weitz, D. A., & Zong, C. C. (2023) · Nature Biotechnology · doi:10.1038/s41587-022-01635-1 · Cited by 62 · see citing works
Dynamism of an Astrocyte In Vivo: Perspectives on Identity and Function
Poskanzer, K. E., & Molofsky, A. (2017) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021317-121125 · Cited by 58 · see citing works
Astrocyte heterogeneity and interactions with local neural circuits
Holt, M. G. (2023) · Essays in Biochemistry · doi:10.1042/ebc20220136 · Cited by 56 · see citing works
Aqp4 stop codon readthrough facilitates amyloid-β clearance from the brain
Sapkota, D., Florian, C. P., Doherty, B. M., White, K. M., Reardon, K. M., Ge, X., Garbow, J. R., Yuede, C. M., Cirrito, J. R., & Dougherty, J. D. (2022) · Brain · doi:10.1093/brain/awac199 · Cited by 55 · see citing works
Self-citationAstrocyte structural heterogeneity in the mouse hippocampus
Viana, J. F., Machado, J. L., Abreu, D. S., Veiga, A., Barsanti, S., Tavares, G., Martins, M., Sardinha, V. M., Guerra‐Gomes, S., Domingos, C., et al. (2023) · Glia · doi:10.1002/glia.24362 · Cited by 59 · see citing works
Scofield, M. D. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.10.029 · Cited by 52 · see citing works
Subcellular and regional localization of mRNA translation in midbrain dopamine neurons
Hobson, B. D., Kong, L., Angelo, M. F., Lieberman, O. J., Mosharov, E. V., Herzog, É., Sulzer, D. L., & Sims, P. A. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110208 · Cited by 49 · see citing works
Activity-dependent translation dynamically alters the proteome of the perisynaptic astrocyte process
Sapkota, D., Kater, M. S. J., Sakers, K., Nygaard, K. R., Liu, Y., Koester, S. K., Fass, S. B., Lake, A. M., Khazanchi, R., Khankan, R. R., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111474 · Cited by 49 · see citing works
Self-citationChipman, P. H., Fung, C. C. A., Fernández, A. P., Sawant, A., Tedoldi, A., Kawai, A., Gautam, S. G., Kurosawa, M., Abe, M., Sakimura, K., et al. (2021) · eLife · doi:10.7554/elife.70818 · Cited by 50 · see citing works
Astrocyte-synapse interactions during brain development
Farizatto, K. L. G., & Baldwin, K. T. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102704 · Cited by 46 · see citing works
The Quaking RNA ‐binding proteins as regulators of cell differentiation
Neumann, D., Goodall, G. J., & Gregory, P. A. (2022) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1724 · Cited by 45 · see citing works
The Nanoworld of the Tripartite Synapse: Insights from Super-Resolution Microscopy
Heller, J. P., & Rusakov, D. A. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00374 · Cited by 44 · see citing works
Huang, Y., Wang, M., Ni, H., Zhang, J., Li, A., Hu, B., Junqueira Alves, C., Wahane, S., Rios de Anda, M., Ho, L., et al. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01664-w · Cited by 42 · see citing works
“Interestingly, Plxnb1 mRNA puncta were not only detected in cell somas, but also in hypertrophic processes of reactive astrocytes, signifying local translation, which has been also described for Gfap and other key astrocyte genes 35,36 .”
Astrocyte Molecular Clock Function in the Nucleus Accumbens Is Important for Reward-Related Behavior
Becker‐Krail, D. D., Ketchesin, K. D., Burns, J. N., Zong, W., Hildebrand, M. A., DePoy, L. M., Vadnie, C. A., Tseng, G. C., Logan, R. W., Huang, Y. H., et al. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.02.007 · Cited by 42 · see citing works
Astrocytes functionally integrate multiple synapses via specialized leaflet domains
Benoit, L., Hristovska, I., Liaudet, N., Jouneau, P., Fertin, A., Ceglia, R. D., Litvin, D. G., Castro, M. A. D., Jevtic, M., Zalachoras, I., et al. (2025) · Cell · doi:10.1016/j.cell.2025.08.036 · Cited by 48 · see citing works
Gilbert, A., Elorza‐Vidal, X., Estévez, R., Cohen‐Salmon, M., & Boulay, A.-C. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01832-w · Cited by 39 · see citing works
Translational control in aging and neurodegeneration
Skariah, G., & Todd, P. K. (2020) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1628 · Cited by 40 · see citing works
Sakers, K., Liu, Y., Llaci, L., Lee, S. M., Vasek, M. J., Rieger, M. A., Brophy, S., Tycksen, E., Lewis, R. M., Maloney, S. E., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21703-5 · Cited by 37 · see citing works
Self-citationCa 2+ activity maps of astrocytes tagged by axoastrocytic AAV transfer
Georgiou, L., Echeverría, A., Georgiou, A., & Kühn, B. (2022) · Science Advances · doi:10.1126/sciadv.abe5371 · Cited by 38 · see citing works
Essential Role of Astrocytes in Learning and Memory
Escalada, P., Ezkurdia, A., Ramírez, M. J., & Solas, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25031899 · Cited by 42 · see citing works
Disruption of Glutamate Transport and Homeostasis by Acute Metabolic Stress
Passlick, S., Rose, C. R., Petzold, G. C., & Henneberger, C. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.637784 · Cited by 38 · see citing works
The Expanding Toolkit of Translating Ribosome Affinity Purification
Dougherty, J. D. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1929-17.2017 · Cited by 37 · see citing works
Self-citationmRNA Transport and Local Translation in Glia
Meservey, L. M., Topkar, V. V., & Fu, M. (2021) · Trends in Cell Biology · doi:10.1016/j.tcb.2021.03.006 · Cited by 37 · see citing works
Local translation in microglial processes is required for efficient phagocytosis
Vasek, M. J., Mueller, S. M., Fass, S. B., Deajon-Jackson, J. D., Liu, Y., Crosby, H. W., Koester, S. K., Yi, J., Li, Q., & Dougherty, J. D. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01353-0 · Cited by 35 · see citing works
Self-citationPerez, J. D., Fusco, C. M., & Schuman, E. M. (2021) · Annual Review of Genetics · doi:10.1146/annurev-genet-030321-054851 · Cited by 36 · see citing works
GFAP-isoforms in the nervous system: Understanding the need for diversity
de Reus, A. J. E. M., Başak, O., Dykstra, W., van Asperen, J. V., van Bodegraven, E. J., & Hol, E. M. (2024) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2024.102340 · Cited by 35 · see citing works
Imaging tripartite synapses using super-resolution microscopy
Heller, J. P., Odii, T., Zheng, K., & Rusakov, D. A. (2019) · Methods · doi:10.1016/j.ymeth.2019.05.024 · Cited by 35 · see citing works
Tapella, L., Dematteis, G., Moro, M., Pistolato, B., Tonelli, E., Vanella, V. V., Giustina, D., Forgia, A. L., Restelli, E., Barberis, E., et al. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05324-4 · Cited by 34 · see citing works
Astrocytic TRPV4 Channels and Their Role in Brain Ischemia
Turečková, J., Heřmanová, Z., Marchetti, V., & Anděrová, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24087101 · Cited by 34 · see citing works
Manninen, T., Saudargienė, A., & Linne, M. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008360 · Cited by 32 · see citing works
Kilfeather, P., Khoo, J. H., Wagner, K., Liang, H., Caiazza, M. C., An, Y., Zhang, X., Chen, X., Connor‐Robson, N., Shang, Z., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113784 · Cited by 32 · see citing works
Vitronectin from brain pericytes promotes adult forebrain neurogenesis by stimulating CNTF
Jia, C., Keasey, M. P., Malone, H. M., Lovins, C., Sante, R. R., Razskazovskiy, V., & Hagg, T. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.11.002 · Cited by 31 · see citing works
Díaz, A., Merino, P., Manrique, L. G., Cheng, L., & Yepes, M. (2018) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x18783653 · Cited by 30 · see citing works
The computational power of the human brain
Gebicke‐Haerter, P. J. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1220030 · Cited by 30 · see citing works
Astrocyte diversity and subtypes: aligning transcriptomics with multimodal perspectives
Hennes, M., Richter, M. L., Fischer-Sternjak, J., & Götz, M. (2025) · EMBO Reports · doi:10.1038/s44319-025-00529-y · Cited by 35 · see citing works
AstroDot – a new method for studying the spatial distribution of mRNA in astrocytes
Oudart, M., Tortuyaux, R., Mailly, P., Mazaré, N., Boulay, A.-C., & Cohen‐Salmon, M. (2020) · Journal of Cell Science · doi:10.1242/jcs.239756 · Cited by 28 · see citing works
Mazaré, N., Oudart, M., & Cohen‐Salmon, M. (2021) · Journal of Cell Science · doi:10.1242/jcs.251629 · Cited by 28 · see citing works
Blanco‐Urrejola, M., Gaminde‐Blasco, A., Gamarra, M., de la Cruz, A., Vecino, E., Alberdi, E. M., & Baleriola, J. (2021) · Cells · doi:10.3390/cells10030632 · Cited by 23 · see citing works
Cellular neurometabolism: a tentative to connect cell biology and metabolism in neurology
García‐Cazorla, À., & Saudubray, J. (2018) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-018-0226-8 · Cited by 28 · see citing works
Dvorzhak, A., Helassa, N., Török, K., Schmitz, D., & Grantyn, R. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2865-18.2019 · Cited by 27 · see citing works
Arizono, M., & Nägerl, U. V. (2021) · Glia · doi:10.1002/glia.24103 · Cited by 28 · see citing works
Heterogeneity of the astrocytic AMPA‐receptor transcriptome
Mölders, A., Koch, A., Menke, R., & Klöcker, N. (2018) · Glia · doi:10.1002/glia.23514 · Cited by 27 · see citing works
Intracellular spatial transcriptomic analysis toolkit (InSTAnT)
Kumar, A., Schrader, A. W., Aggarwal, B., Ebrahimpour-Boroojeny, A., Asadian, M., Lee, J., Song, Y. J., Zhao, S. D., Han, H., & Sinha, S. (2024) · Nature Communications · doi:10.1038/s41467-024-49457-w · Cited by 26 · see citing works
Local gene regulation in radial glia: Lessons from across the nervous system
D’Arcy, B. R., & Silver, D. L. (2020) · Traffic · doi:10.1111/tra.12769 · Cited by 25 · see citing works
De novo proteomic methods for examining the molecular mechanisms underpinning long-term memory
Evans, H. T., Blackmore, D. G., Götz, J., & Bodea, L. (2021) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2020.12.015 · Cited by 25 · see citing works
A cAMP-Related Gene Network in Microglia Is Inversely Regulated by Morphine Tolerance and Withdrawal
Coffey, K. R., Lesiak, A. J., Marx, R. E., Vo, E. K., Garden, G. A., & Neumaier, J. F. (2021) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2021.07.011 · Cited by 25 · see citing works
Ayana, R., Zandecki, C., houcke, J. V., Mariën, V., Seuntjens, E., & Arckens, L. (2024) · Aging Cell · doi:10.1111/acel.14251 · Cited by 23 · see citing works
A transcriptomic atlas of astrocyte heterogeneity across space and time in mouse and marmoset
Schroeder, M. E., McCormack, D. M., Metzner, L. R., Kang, J., Li, K. X., Yu, E., Melamed, L., Levandowski, K. M., Zaniewski, H., Zhang, Q., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.09.011 · Cited by 26 · see citing works
Kuo, Y.-M., Hsu, P.-C., Hung, C., Hu, Y.-Y., Huang, Y., Gan, Y., Lin, C.-H., Shie, F., Chang, W., Kao, L., et al. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-01669-8 · Cited by 23 · see citing works
Rurak, G. M., Woodside, B. C., Aguilar‐Valles, A., & Salmaso, N. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2020.100897 · Cited by 23 · see citing works
Monitoring regional astrocyte diversity by cell type‐specific proteomic labeling in vivo
Prabhakar, P., Pielot, R., Landgraf, P., Wissing, J. B., Bayrhammer, A., van Ham, M., Gundelfinger, E. D., Jänsch, L., Dieterich, D. C., & Müller, A. (2022) · Glia · doi:10.1002/glia.24304 · Cited by 21 · see citing works
Ultrastructural Analysis of Thalamus Damages in a Mouse Model of Osmotic-Induced Demyelination
Bouchat, J., Gilloteaux, J., Suain, V., Vlaender, D. V., Brion, J., & Nicaise, C. (2019) · Neurotoxicity Research · doi:10.1007/s12640-019-00041-x · Cited by 23 · see citing works
Diacylglycerol lipase alpha in astrocytes is involved in maternal care and affective behaviors
Schüle, L., Glasmacher, S., Gertsch, J., Roggan, M. D., Transfeld, J. L., Bîndilă, L., Lutz, B., Kolbe, C., Bilkei‐Gorzó, A., Zimmer, A., et al. (2020) · Glia · doi:10.1002/glia.23903 · Cited by 23 · see citing works
PRDM16-DT is a novel lncRNA that regulates astrocyte function in Alzheimer’s disease
Schröder, S., Fuchs, U., Gisa, V., Peña, T., Krüger, D. M., Hempel, N., Burkhardt, S., Salinas, G., Schütz, A., Delalle, I., et al. (2024) · Acta Neuropathologica · doi:10.1007/s00401-024-02787-x · Cited by 27 · see citing works
A viral toolkit for recording transcription factor–DNA interactions in live mouse tissues
Cammack, A. J., Moudgil, A., Chen, J., Vasek, M. J., Shabsovich, M., McCullough, K. B., Yen, A., Lagunas, T., Maloney, S. E., He, J., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1918241117 · Cited by 22 · see citing works
Self-citationNG2 Glia: Novel Roles beyond Re-/Myelination
Parolisi, R., & Boda, E. (2018) · Neuroglia · doi:10.3390/neuroglia1010011 · Cited by 21 · see citing works
Rǎdulescu, A., Todd, G. C., Williams, C., Bennink, B., Lemus, A. A., Chesbro, H. E., Bourgeois, J. R., Kopec, A. M., Zuloaga, D. G., & Scimemi, A. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009845 · Cited by 21 · see citing works
Makarava, N., Mychko, O., Molesworth, K., Chang, J. C., Henry, R. J., Tsymbalyuk, N., Gerzanich, V., Simard, J. M., Loane, D. J., & Baskakov, I. V. (2023) · Cells · doi:10.3390/cells12172172 · Cited by 19 · see citing works
Multifarious astrocyte–neuron dialog in shaping neural circuit architecture
Ngoc, K. H., Jeon, Y., Ko, J., & Um, J. W. (2024) · Trends in Cell Biology · doi:10.1016/j.tcb.2024.05.002 · Cited by 23 · see citing works
Megat, S., & Price, T. J. (2018) · Neurobiology of Pain · doi:10.1016/j.ynpai.2018.02.001 · Cited by 21 · see citing works
Ouwenga, R., Lake, A. M., Aryal, S., Lagunas, T., & Dougherty, J. D. (2018) · eNeuro · doi:10.1523/eneuro.0320-18.2018 · Cited by 21 · see citing works
Self-citationLearning and memory formation in zebrafish: Protein dynamics and molecular tools
Reemst, K., Shahin, H., & Shahar, O. D. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1120984 · Cited by 20 · see citing works
Foster, J. B., Zhao, F., Wang, X., Xu, Z., Lin, K. J., Askwith, C. C., Hodgetts, K. J., & Lin, C. G. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.07.028 · Cited by 20 · see citing works
RNA-binding protein quaking: a multifunctional regulator in tumour progression
Zhu, W., Yang, W., Sun, G., & Huang, J. (2024) · Annals of Medicine · doi:10.1080/07853890.2024.2443046 · Cited by 19 · see citing works
Negro, S., Stazi, M., Marchioretto, M., Tebaldi, T., Rodella, U., Duregotti, E., Gerke, V., Quattrone, A., Montecucco, C., Rigoni, M., et al. (2018) · RNA · doi:10.1261/rna.064816.117 · Cited by 19 · see citing works
Astrocyte-Synapse Structural Plasticity in Neurodegenerative and Neuropsychiatric Diseases
Badia‐Soteras, A., Mak, A., Blok, T. M., Boers-Escuder, C., van den Oever, M. C., Min, R., Smit, A. B., & Verheijen, M. H. G. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.04.011 · Cited by 18 · see citing works
Oudart, M., Avila‐Gutierrez, K., Moch, C., Dossi, E., Milior, G., Boulay, A.-C., Gaudey, M., Moulard, J., Lombard, B., Loew, D., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112456 · Cited by 18 · see citing works
Charron, A. J., Ward, S. L., North, B. J., Cerón, S., & Leib, D. A. (2019) · Journal of Virology · doi:10.1128/jvi.02246-18 · Cited by 18 · see citing works
SCD Inhibition Protects from α-Synuclein-Induced Neurotoxicity But Is Toxic to Early Neuron Cultures
Nicholatos, J. W., de Groot, J. C. W., Dhokai, S., Tran, D. T., Hrdlicka, L., Carlile, T. M., Bennion, M., Dalkilic-Liddle, I., Hirst, W. D., & Weihofen, A. (2021) · eNeuro · doi:10.1523/eneuro.0166-21.2021 · Cited by 18 · see citing works
Adenosine A1 Receptor mRNA Expression by Neurons and Glia in the Auditory Forebrain
Hackett, T. A. (2018) · The Anatomical Record · doi:10.1002/ar.23907 · Cited by 16 · see citing works
The brain's dark transcriptome: Sequencing RNA in distal compartments of neurons and glia
Ament, S. A., & Poulopoulos, A. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102725 · Cited by 14 · see citing works
Boulay, A.-C., Mazaré, N., Saubaméa, B., & Cohen‐Salmon, M. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9068-9_8 · Cited by 16 · see citing works
Photonics tools begin to clarify astrocyte calcium transients
Gorzo, K. A., & Gordon, G. R. (2022) · Neurophotonics · doi:10.1117/1.nph.9.2.021907 · Cited by 14 · see citing works
Could an Impairment in Local Translation of mRNAs in Glia be Contributing to Pathogenesis in ALS?
Barton, S. K., Gregory, J. M., Chandran, S., & Turner, B. J. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00124 · Cited by 15 · see citing works
- Authors
- Sakers, K., Lake, A. M., Khazanchi, R., Ouwenga, R., Vasek, M. J., Dani, A., & Dougherty, J. D.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Dougherty, Joseph D.
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2017-04-24
- Volume
- 114
- Issue
- 19
- Pages
- E3830-E3838
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC5441704
- OpenAlex
- W2951270532
- Cited by
- 202
- References
- 72
- Citations by year
- 2026: 24 · 2025: 17 · 2024: 20 · 2023: 25 · 2022: 22 · 2021: 27 · 2020: 20 · 2019: 20 · 2018: 19 · 2017: 8
- FWCI
- 2.26
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nd)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Children's Discovery Institute (MD-II-2013-269)
- HHS | National Institutes of Health (DA038458-01, MH099798-01)
- WUSTL Interface of Psychology Neuroscience and Genetics Training Grant (5T32 GM081739)
- WUSTL Neurosciences Program Training Grant (T32 GM008151)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Keywords
- astrocytes, local translation, mRNA transport, synaptic regulation
- MeSH terms
- Animals, Astrocytes, Cell Nucleus, Humans, Memory, Neurons, RNA, Messenger, Synapses, Protein Biosynthesis
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