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Glial responses to implanted electrodes in the brain
Open accessAbstract
The use of implants that can electrically stimulate or record electrophysiological or neurochemical activity in nervous tissue is rapidly expanding. Despite remarkable results in clinical studies and increasing market approvals, the mechanisms underlying the therapeutic effects of neuroprosthetic and neuromodulation devices, as well as their side effects and reasons for their failure, remain poorly understood. A major assumption has been that the signal-generating neurons are the only important target cells of neural-interface technologies. However, recent evidence indicates that the supporting glial cells remodel the structure and function of neuronal networks and are an effector of stimulation-based therapy. Here, we reframe the traditional view of glia as a passive barrier, and discuss their role as an active determinant of the outcomes of device implantation. We also discuss the implications that this has on the development of bioelectronic medical devices.
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“The fibrotic capsule forming around the implant not only damages and displaces the target neuronal tissue, but also forms a high-impedance layer that dampens the weak electrical signals produced by neurons and dissipates stimulating electrode currents.”
From Foreign Body Reaction to Implanted Biomaterials and Its Impact in Nerve Neuroprosthetics (2021) · cites this paper as Salatino et al., 2017
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
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“Despite these differences, the general principles underlying FBR and the consequences (formation of a fibrotic capsule, inflammatory damage to the surrounding tissue) still apply (Polikov et al., 2005; Salatino et al., 2017).”
From Foreign Body Reaction to Implanted Biomaterials and Its Impact in Nerve Neuroprosthetics (2021) · cites this paper as Salatino et al., 2017
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The fibrotic capsule forming around the implant not only damages and displaces the target neuronal tissue, but also forms a high-impedance layer that dampens the weak electrical signals produced by neurons and dissipates stimulating electrode currents.”
From Foreign Body Reaction to Implanted Biomaterials and Its Impact in Nerve Neuroprosthetics (2021) · cites this paper as Salatino et al., 2017
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“FBR is currently the key culprit behind chronically-implanted neuroprosthetic implant failure (Polikov et al., 2005; Salatino et al., 2017), and poses a major hurdle to the clinical translation of new neuroprosthetic technologies.”
From Foreign Body Reaction to Implanted Biomaterials and Its Impact in Nerve Neuroprosthetics (2021) · cites this paper as Salatino et al., 2017
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Flexible implants in general show improved tissue compatibility compared to stiffer equivalents, minimizing trauma and FBR arising from shear damage (Lacour et al., 2016; Salatino et al., 2017).”
From Foreign Body Reaction to Implanted Biomaterials and Its Impact in Nerve Neuroprosthetics (2021) · cites this paper as Salatino et al., 2017
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“FBR occurs in response to any material that is implanted into the body (Anderson et al., 2008; Salatino et al., 2017).”
From Foreign Body Reaction to Implanted Biomaterials and Its Impact in Nerve Neuroprosthetics (2021) · cites this paper as Salatino et al., 2017
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“Material stiffness also greatly contributes to FBR, with softer materials (closer in stiffness to that of biological tissues) generating less mechanical trauma and therefore less FBR (Lacour et al., 2016; Salatino et al., 2017).”
From Foreign Body Reaction to Implanted Biomaterials and Its Impact in Nerve Neuroprosthetics (2021) · cites this paper as Salatino et al., 2017
In the citing paper
“It has been shown that all biocompatible materials used so far provoke an inflammatory response and some degree of foreign body reaction [174,175].”
From Advances in visual prostheses: engineering and biological challenges (2022) · cites this paper as [175]
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Citations
Cites
Strogatz, S. H. (2001) · Nature · doi:10.1038/35065725 · Cited by 8,236
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 · cited 1×
“The diversity of their roles is reflected in the recent identification of distinct subclasses of astrocytes that are characterized by differences in gene expression, function and reactive states during CNS injury 4,22–24 .”
Ionic channels of excitable membranes
(1985) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(85)90172-7 · Cited by 7,134
Geometric Control of Cell Life and Death
Chen, C. S., Mrksich, M., Huang, S., Whitesides, G. M., & Ingber, D. E. (1997) · Science · doi:10.1126/science.276.5317.1425 · Cited by 4,710
A perivascular origin for mesenchymal stem cells in multiple human organs
Crisan, M., Yap, S., Casteilla, L., Chen, C.-W., Corselli, M., Park, T. S., Andriolo, G., Sun, B., Zheng, B., Zhang, L., et al. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2008.07.003 · Cited by 3,991 · cited 1×
“It has been proposed that these cells have reparative potential through association with neurogenic niches 225,226 .”
Frequency Dependence of Signal Power and Spatial Reach of the Local Field Potential
Leski, S., Lindén, H., Tetzlaff, T., Pettersen, K. H., & Einevoll, G. T. (2013) · PubMed · doi:10.18154/rwth-conv-084442 · Cited by 3,667
Mechanisms underlying inflammation in neurodegeneration
Glass, C. K., Saijo, K., Winner, B., Marchetto, M. C., & Gage, F. H. (2010) · Cell · doi:10.1016/j.cell.2010.02.016 · Cited by 3,580
Cahoy, J. D., Emery, B., Kaushal, A., Foo, L. C., Zamanian, J. L., Christopherson, K. S., Xing, Y., Lubischer, J. L., Krieg, P. A., Krupenko, S. A., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-07.2008 · Cited by 3,129
Neurodegenerative Disorders: Parkinson's Disease and Huntington's Disease
Hague, S., Klaffke, S., & Bandmann, O. (2006) · IMPERIAL COLLEGE PRESS eBooks · doi:10.1142/9781860948961_0007 · Cited by 2,767
Molecular dissection of reactive astrogliosis and glial scar formation
Sofroniew, M. V. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.08.002 · Cited by 2,594
Glial and neuronal control of brain blood flow
Attwell, D., Buchan, A. M., Charpak, S., Lauritzen, M., MacVicar, B. A., & Newman, E. A. (2010) · Nature · doi:10.1038/nature09613 · Cited by 2,511
Neural synchrony in brain disorders: Relevance for cognitive dysfunctions and pathophysiology
Uhlhaas, P. J., & Singer, W. (2006) · Neuron · doi:10.1016/j.neuron.2006.09.020 · Cited by 2,194
Electrical stimulation of excitable tissue: design of efficacious and safe protocols
Merrill, D. R., Bikson, M., & Jefferys, J. G. R. (2005) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2004.10.020 · Cited by 2,078
The stem-cell niche as an entity of action
Scadden, D. T. (2006) · Nature · doi:10.1038/nature04957 · Cited by 1,902
The role of inflammation in epilepsy
Vezzani, A., French, J., Bartfai, T., & Baram, T. Z. (2011) · Nature Reviews Neurology · doi:10.1038/nrneurol.2010.178 · Cited by 1,876
Capillary pericytes regulate cerebral blood flow in health and disease
Hall, C. N., Reynell, C., Gesslein, B., Hamilton, N. B., Mishra, A., Sutherland, B. A., O’Farrell, F. M., Buchan, A. M., Lauritzen, M., & Attwell, D. (2014) · Nature · doi:10.1038/nature13165 · Cited by 1,870
High-performance neuroprosthetic control by an individual with tetraplegia
Collinger, J. L., Wodlinger, B., Downey, J. E., Wang, W., Tyler-Kabara, E. C., Weber, D. J., McMorland, A. J., Velliste, M., Boninger, M. L., & Schwartz, A. B. (2013) · The Lancet · doi:10.1016/s0140-6736(12)61816-9 · Cited by 1,848
Ion Channels/Excitable Membranes
Terlau, H., & Kirchhoff, F. (2006) · Springer eBooks · doi:10.1007/3-540-29623-9_5640 · Cited by 1,805
Dissolvable films of silk fibroin for ultrathin conformal bio-integrated electronics
Kim, D.-H., Viventi, J., Amsden, J. J., Xiao, J., Vigeland, L., Kim, Y.-S., Blanco, J. A., Panilaitis, B., Frechette, E. S., Contreras, D., et al. (2010) · Nature Materials · doi:10.1038/nmat2745 · Cited by 1,721
Synaptic scaling mediated by glial TNF-α
Stellwagen, D., & Malenka, R. C. (2006) · Nature · doi:10.1038/nature04671 · Cited by 1,715
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
Webber, M. J., Appel, E. A., Meijer, E. W., & Langer, R. (2015) · Nature Materials · doi:10.1038/nmat4474 · Cited by 1,609
Cortical control of a prosthetic arm for self-feeding
Velliste, M., Perel, S., Spalding, M. C., Whitford, A. S., & Schwartz, A. B. (2008) · Nature · doi:10.1038/nature06996 · Cited by 1,591
Optical Deconstruction of Parkinsonian Neural Circuitry
Gradinaru, V., Mogri, M., Thompson, K. R., Henderson, J. M., & Deisseroth, K. A. (2009) · Science · doi:10.1126/science.1167093 · Cited by 1,568
Microglia in neurodegenerative disease
Perry, V. H., Nicoll, J. A. R., & Holmes, C. (2010) · Nature Reviews Neurology · doi:10.1038/nrneurol.2010.17 · Cited by 1,543
Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation
Zonta, M., Angulo, M. C., Gobbo, S., Rosengarten, B., Hossmann, K.-A., Pozzan, T., & Carmignoto, G. (2002) · Nature Neuroscience · doi:10.1038/nn980 · Cited by 1,446
Lü, Y., Aimetti, A. A., Langer, R., & Gu, Z. (2016) · Nature Reviews Materials · doi:10.1038/natrevmats.2016.75 · Cited by 1,440
Control of Synaptic Strength by Glial TNFα
Beattie, E. C., Stellwagen, D., Morishita, W., Bresnahan, J. C., Ha, B. K., Von Zastrow, M., Beattie, M. S., & Malenka, R. C. (2002) · Science · doi:10.1126/science.1067859 · Cited by 1,344
Diversity of astrocyte functions and phenotypes in neural circuits
Khakh, B. S., & Sofroniew, M. V. (2015) · Nature Neuroscience · doi:10.1038/nn.4043 · Cited by 1,239
Injectable, Cellular-Scale Optoelectronics with Applications for Wireless Optogenetics
Kim, T.-I., McCall, J. G., Jung, Y. H., Huang, X., Siuda, E. R., Li, Y., Song, J., Song, Y. M., Pao, H. A., Kim, R.-H., et al. (2013) · Science · doi:10.1126/science.1232437 · Cited by 1,174
Astrocyte-mediated control of cerebral blood flow
Takano, T., Tian, G.-F., Peng, W., Lou, N., Libionka, W., Han, X., & Nedergaard, M. (2005) · Nature Neuroscience · doi:10.1038/nn1623 · Cited by 1,137
Inflammation and white matter degeneration persist for years after a single traumatic brain injury
Johnson, V. E., Stewart, J. E., Begbie, F. D., Trojanowski, J. Q., Smith, D. H., & Stewart, W. (2013) · Brain · doi:10.1093/brain/aws322 · Cited by 1,045
Fellin, T., Pascual, O., Gobbo, S., Pozzan, T., Haydon, P. G., & Carmignoto, G. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.011 · Cited by 1,005
Stimuli-Responsive Polymer Nanocomposites Inspired by the Sea Cucumber Dermis
Capadona, J. R., Shanmuganathan, K., Tyler, D. J., Rowan, S. J., & Weder, C. (2008) · Science · doi:10.1126/science.1153307 · Cited by 965
PDGFRA/NG2 glia generate myelinating oligodendrocytes and piriform projection neurons in adult mice
Rivers, L. E., Young, K. M., Rizzi, M., Jamen, F., Psachoulia, K., Wade, A., Kessaris, N., & Richardson, W. D. (2008) · Nature Neuroscience · doi:10.1038/nn.2220 · Cited by 961
Intracellular Features Predicted by Extracellular Recordings in the Hippocampus In Vivo
Henze, D. A., Borhegyi, Z., Csicsvari, J., Mamiya, A., Harris, K. D., & Buzsáki, G. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.1.390 · Cited by 942
Biran, R., Martin, D. C., & Tresco, P. A. (2005) · Experimental Neurology · doi:10.1016/j.expneurol.2005.04.020 · Cited by 893
Polydendrocytes (NG2 cells): multifunctional cells with lineage plasticity
Nishiyama, A., Komitova, M., Suzuki, R., & Zhu, X. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2495 · Cited by 865
Stretchable nanoparticle conductors with self-organized conductive pathways
Kim, Y., Zhu, J. G., Yeom, B., Prima, M. A. D., Su, X., Kim, J.-G., Yoo, S. J., Uher, C., & Kotov, N. A. (2013) · Nature · doi:10.1038/nature12401 · Cited by 854
Soft, stretchable, fully implantable miniaturized optoelectronic systems for wireless optogenetics
Park, S. I., Brenner, D. S., Shin, G., Morgan, C. D., Copits, B. A., Chung, H. U., Pullen, M. Y., Noh, K. N., Davidson, S., Oh, S. J., et al. (2015) · Nature Biotechnology · doi:10.1038/nbt.3415 · Cited by 794
Astrocyte roles in traumatic brain injury
Burda, J. E., Bernstein, A. M., & Sofroniew, M. V. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.03.020 · Cited by 791
Cunningham, C., Wilcockson, D. C., Campion, S., Lunnon, K., & Perry, V. H. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2614-05.2005 · Cited by 768
Materials and technologies for soft implantable neuroprostheses
Lacour, S. P., Courtine, G., & Guck, J. (2016) · Nature Reviews Materials · doi:10.1038/natrevmats.2016.63 · Cited by 738
Astrocytes Potentiate Transmitter Release at Single Hippocampal Synapses
Perea, G., & Araque, A. (2007) · Science · doi:10.1126/science.1144640 · Cited by 727
Carbon nanotube coating improves neuronal recordings
Keefer, E. W., Botterman, B. R., Romero, M. I., Rossi, A. F., & Gross, G. W. (2008) · Nature Nanotechnology · doi:10.1038/nnano.2008.174 · Cited by 721
Kozai, T. D. Y., Langhals, N. B., Patel, P. R., Deng, X., Zhang, H., Smith, K. L., Lahann, J., Kotov, N. A., & Kipke, D. R. (2012) · Nature Materials · doi:10.1038/nmat3468 · Cited by 721
Self-citationSofroniew, M. V. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020420 · Cited by 695 · cited 2×
“Gradients of damage-associated cues regulate the expression of extracellular-signalling molecules, of intracellular transducers and of transcription factors that instruct subtype specification 25 .”
Syringe-injectable electronics
Liu, J., Fu, T.-M., Cheng, Z., Hong, G., Zhou, T., Jin, L., Duvvuri, M., Jiang, Z., Kruskal, P., Xie, C., et al. (2015) · Nature Nanotechnology · doi:10.1038/nnano.2015.115 · Cited by 687
Neuromodulatory properties of inflammatory cytokines and their impact on neuronal excitability
Vezzani, A., & Viviani, B. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.10.027 · Cited by 670
Neural recording and modulation technologies
Chen, R., Canales, A., & Anikeeva, P. (2017) · Nature Reviews Materials · doi:10.1038/natrevmats.2016.93 · Cited by 655
How does adenosine inhibit transmitter release?
Fredholm, B. B., & Dunwiddie, T. V. (1988) · Trends in Pharmacological Sciences · doi:10.1016/0165-6147(88)90194-0 · Cited by 640
Ludwig, K. A., Uram, J. D., Yang, J., Martin, D. C., & Kipke, D. R. (2006) · Journal of Neural Engineering · doi:10.1088/1741-2560/3/1/007 · Cited by 638
Self-citationPerry, V. H., & Teeling, J. L. (2013) · Seminars in Immunopathology · doi:10.1007/s00281-013-0382-8 · Cited by 638
Silent synapses and the emergence of a postsynaptic mechanism for LTP
Kerchner, G. A., & Nicoll, R. A. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2501 · Cited by 635
Ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration
Luan, L., Wei, X., Zhao, Z., Siegel, J. J., Potnis, O., Tuppen, C. A., Lin, S. Q., Kazmi, S., Fowler, R. A., Holloway, S., et al. (2017) · Science Advances · doi:10.1126/sciadv.1601966 · Cited by 628
Brain Tissue Responses to Neural Implants Impact Signal Sensitivity and Intervention Strategies
Kozai, T. D. Y., Jaquins-Gerstl, A. S., Vazquez, A. L., Michael, A. C., & Cui, X. T. (2015) · ACS Chemical Neuroscience · doi:10.1021/cn500256e · Cited by 622
Self-citationNew roles for astrocytes: Regulation of synaptic transmission
Newman, E. A. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00237-6 · Cited by 619
Failure mode analysis of silicon-based intracortical microelectrode arrays in non-human primates
Barrese, J. C., Rao, N., Paroo, K., Triebwasser, C., Vargas-Irwin, C., Franquemont, L., & Donoghue, J. P. (2013) · Journal of Neural Engineering · doi:10.1088/1741-2560/10/6/066014 · Cited by 600
Gesammelte Abhandlungen zur wissenschaftlichen Medicin
Virchow, R. (1862) · Cited by 590
A Review of Organic and Inorganic Biomaterials for Neural Interfaces
Fattahi, P., Yang, G., Kim, G., & Abidian, M. R. (2014) · Advanced Materials · doi:10.1002/adma.201304496 · Cited by 580
Astrocyte heterogeneity: an underappreciated topic in neurobiology
Zhang, Y., & Barres, B. A. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.06.005 · Cited by 569
Henry, C. J., Huang, Y., Wynne, A. M., & Godbout, J. P. (2009) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2008.09.002 · Cited by 565
Mechanisms of deep brain stimulation
Herrington, T. M., Cheng, J. J., & Eskandar, E. N. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00281.2015 · Cited by 551
Mechanotransduction at Cell-Matrix and Cell-Cell Contacts
Chen, C. S., Tan, J. L., & Tien, J. (2004) · Annual Review of Biomedical Engineering · doi:10.1146/annurev.bioeng.6.040803.140040 · Cited by 544
Engineering Immunomodulatory Biomaterials To Tune the Inflammatory Response
Vishwakarma, A., Bhise, N. S., Evangelista, M. B., Rouwkema, J., Dokmeci, M. R., Ghaemmaghami, A. M., Vrana, N. E., & Khademhosseini, A. (2016) · Trends in biotechnology · doi:10.1016/j.tibtech.2016.03.009 · Cited by 516
Wadhwa, R., Lagenaur, C. F., & Cui, X. T. (2005) · Journal of Controlled Release · doi:10.1016/j.jconrel.2005.10.027 · Cited by 498
Loane, D. J., Kumar, A., Stoica, B. A., Cabatbat, R., & Faden, A. I. (2014) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0000000000000021 · Cited by 498
History, Applications, and Mechanisms of Deep Brain Stimulation
Miocinovic, S., Somayajula, S., Chitnis, S., & Vitek, J. L. (2013) · JAMA Neurology · doi:10.1001/2013.jamaneurol.45 · Cited by 496
Axons, but not cell bodies, are activated by electrical stimulation in cortical gray matter
Nowak, L. G., & Bullier, J. (1998) · Experimental Brain Research · doi:10.1007/s002210050304 · Cited by 492
McConnell, G. C., Rees, H. D., Levey, A. I., Gutekunst, C.-A., Gross, R. E., & Bellamkonda, R. V. (2009) · Journal of Neural Engineering · doi:10.1088/1741-2560/6/5/056003 · Cited by 480
Neural probe design for reduced tissue encapsulation in CNS
Seymour, J. P., & Kipke, D. R. (2007) · Biomaterials · doi:10.1016/j.biomaterials.2007.03.024 · Cited by 462
Long-term motor cortex plasticity induced by an electronic neural implant
Andrew, J. O., Mavoori, J., & Fetz, E. E. (2006) · Nature · doi:10.1038/nature05226 · Cited by 454
Multifunctional Nanobiomaterials for Neural Interfaces
Abidian, M. R., & Martin, D. C. (2009) · Advanced Functional Materials · doi:10.1002/adfm.200801473 · Cited by 427
Using a Common Average Reference to Improve Cortical Neuron Recordings From Microelectrode Arrays
Ludwig, K. A., Miriani, R. M., Langhals, N. B., Joseph, M. D., Anderson, D. J., & Kipke, D. R. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90989.2008 · Cited by 426
Self-citationChaos and commotion in the wake of cortical spreading depression and spreading depolarizations
Pietrobon, D., & Moskowitz, M. A. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3770 · Cited by 424
Electrical wound-healing assay for cells in vitro
Keese, C. R., Wegener, J., Walker, S. R., & Giæver, I. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0307588100 · Cited by 423
Suner, S., Fellows, M. R., Vargas-Irwin, C., Nakata, G. K., & Donoghue, J. P. (2005) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2005.857687 · Cited by 415 · cited 3×
“…attests to the role of reactive gliosis in the remodelling and reshaping of neural circuitry during healing, yet relatively few reports have linked glial activity to the therapeutic effects of neuromodulation 38,45 or explored the relationship between glial responses and recording quality 62,63 .”
Dunwiddie, T. V., Diao, L., & Proctor, W. R. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-20-07673.1997 · Cited by 414
Norden, D. M., Muccigrosso, M. M., & Godbout, J. P. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.10.028 · Cited by 413
Monai, H., Ohkura, M., Tanaka, M., Oe, Y., Konno, A., Hirai, H., Mikoshiba, K., Itohara, S., Nakai, J., Iwai, Y., et al. (2016) · Nature Communications · doi:10.1038/ncomms11100 · Cited by 410
Hippocampal Short- and Long-Term Plasticity Are Not Modulated by Astrocyte Ca 2+ Signaling
Agulhon, C., Fiacco, T. A., & McCarthy, K. D. (2010) · Science · doi:10.1126/science.1184821 · Cited by 409
Conducting Polymers for Neural Prosthetic and Neural Interface Applications
Green, R. A., & Abidian, M. R. (2015) · Advanced Materials · doi:10.1002/adma.201501810 · Cited by 405
Abidian, M. R., Corey, J. M., Kipke, D. R., & Martin, D. C. (2010) · Small · doi:10.1002/smll.200901868 · Cited by 405
Three-dimensional macroporous nanoelectronic networks as minimally invasive brain probes
Xie, C., Liu, J., Fu, T.-M., Dai, X., Zhou, W., & Lieber, C. M. (2015) · Nature Materials · doi:10.1038/nmat4427 · Cited by 404
Complex impedance spectroscopy for monitoring tissue responses to inserted neural implants
Williams, J. C., Hippensteel, J. A., Dilgen, J., Shain, W. G., & Kipke, D. R. (2007) · Journal of Neural Engineering · doi:10.1088/1741-2560/4/4/007 · Cited by 402
Williams, J. C., Rennaker, R. L., & Kipke, D. R. (1999) · Brain Research Protocols · doi:10.1016/s1385-299x(99)00034-3 · Cited by 400
Moshayedi, P., Ng, G., Kwok, J. C. F., Yeo, G. S. H., Bryant, C. E., Fawcett, J. W., Franze, K., & Guck, J. R. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.01.038 · Cited by 397
Astrocytes in the Epileptic Brain
Wetherington, J. P., Serrano, G. E., & Dingledine, R. J. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.002 · Cited by 391
A Materials Roadmap to Functional Neural Interface Design
Wellman, S. M., Eles, J. R., Ludwig, K. A., Seymour, J. P., Michelson, N. J., McFadden, W. E., Vazquez, A. L., & Kozai, T. D. Y. (2018) · Advanced Functional Materials · doi:10.1002/adfm.201701269 · Cited by 389
Self-citationProgress towards biocompatible intracortical microelectrodes for neural interfacing applications
Jorfi, M., Skousen, J. L., Weder, C., & Capadona, J. R. (2015) · Journal of Neural Engineering · doi:10.1088/1741-2560/12/1/011001 · Cited by 384
McIntyre, C. C., & Grill, W. M. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.4.1592 · Cited by 383
Astroglial networks scale synaptic activity and plasticity
Pannasch, U., Vargová, L., Reingruber, J., Ezan, P., Holcman, D., Giaume, C., Syková, E., & Rouach, N. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016650108 · Cited by 383
Chronic microsensors for longitudinal, subsecond dopamine detection in behaving animals
Clark, J. J., Sandberg, S. G., Wanat, M. J., Gan, J. O., Horne, E. A., Hart, A. S., Akers, C. A., Parker, J. G., Willuhn, I., Martinez, V., et al. (2010) · Nature Methods · doi:10.1038/nmeth.1412 · Cited by 378
Kipke, D. R., Vetter, R. J., Williams, J. C., & Hetke, J. F. (2003) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2003.814443 · Cited by 364
Nanotools for Neuroscience and Brain Activity Mapping
Alivisatos, A. P., Andrews, A. M., Boyden, E. S., Chun, M., Church, G. M., Deisseroth, K. A., Donoghue, J. P., Fraser, S. E., Lippincott‐Schwartz, J., Looger, L. L., et al. (2013) · ACS Nano · doi:10.1021/nn4012847 · Cited by 358
Buffo, A., Rolando, C., & Ceruti, S. (2009) · Biochemical Pharmacology · doi:10.1016/j.bcp.2009.09.014 · Cited by 338
Stable long-term chronic brain mapping at the single-neuron level
Tian-ming Fu, B., Hong, G., Zhou, T., Schuhmann, T. G., Viveros, R. D., & Lieber, C. M. (2016) · Nature Methods · doi:10.1038/nmeth.3969 · Cited by 330
mRNA up-regulation of MHC II and pivotal pro-inflammatory genes in normal brain aging
Frank, M. G., Barrientos, R. M., Biedenkapp, J. C., Rudy, J. W., Watkins, L. R., & Maier, S. F. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.03.013 · Cited by 327
Zhong, Y., & Bellamkonda, R. V. (2007) · Brain Research · doi:10.1016/j.brainres.2007.02.024 · Cited by 326
NG2-glia as multipotent neural stem cells: fact or fantasy?
Richardson, W. D., Young, K. M., Tripathi, R. B., & McKenzie, I. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.013 · Cited by 300
Prasad, A., Xue, Q.-S., Sankar, V., Nishida, T., Shaw, G., Streit, W. J., & Sanchez, J. C. (2012) · Journal of Neural Engineering · doi:10.1088/1741-2560/9/5/056015 · Cited by 298
Adenosine is crucial for deep brain stimulation–mediated attenuation of tremor
Bekar, L. K., Libionka, W., Tian, G.-F., Xu, Q., Torres, A., Wang, X., Lovatt, D., Williams, E. K., Takano, T., Schnermann, J. B., et al. (2007) · Nature Medicine · doi:10.1038/nm1693 · Cited by 291
Weissberg, I., Wood, L., Kamintsky, L., Vazquez, O. N., Milikovsky, D. Z., Alexander, A., Oppenheim, H., Ardizzone, C., Becker, A. J., Frigerio, F., et al. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.02.029 · Cited by 291
Nerve conduction block utilising high-frequency alternating current
Kilgore, K. L., & Bhadra, N. (2004) · Medical & Biological Engineering & Computing · doi:10.1007/bf02344716 · Cited by 287
Ludwig, K. A., Langhals, N. B., Joseph, M. D., Richardson-Burns, S. M., Hendricks, J. L., & Kipke, D. R. (2011) · Journal of Neural Engineering · doi:10.1088/1741-2560/8/1/014001 · Cited by 283
Self-citationNG 2‐glia and their functions in the central nervous system
Dimou, L., & Gallo, V. (2015) · Glia · doi:10.1002/glia.22859 · Cited by 275
Mechanically-compliant intracortical implants reduce the neuroinflammatory response
Nguyen, J. K., Park, D. J., Skousen, J. L., Hess-Dunning, A. E., Tyler, D. J., Rowan, S. J., Weder, C., & Capadona, J. R. (2014) · Journal of Neural Engineering · doi:10.1088/1741-2560/11/5/056014 · Cited by 274
Liu, X., McCreery, D. B., Carter, R. R., Bullara, L. A., Yuen, T. G. H., & Agnew, W. F. (1999) · IEEE Transactions on Rehabilitation Engineering · doi:10.1109/86.788468 · Cited by 272
The impact of chronic blood–brain barrier breach on intracortical electrode function
Saxena, T. K., Karumbaiah, L., Gaupp, E. A., Patkar, R., Patil, K., Betancur, M. I., Stanley, G. B., & Bellamkonda, R. V. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.03.007 · Cited by 270
Abidian, M. R., Ludwig, K. A., Marzullo, T., Martin, D. C., & Kipke, D. R. (2009) · Advanced Materials · doi:10.1002/adma.200900887 · Cited by 263
Self-citationFidler, P. S., Schütte, K., Asher, R. A., Dobbertin, A., Thornton, S. R., Calle, Y., Muir, E. M., Levine, J. M., Geller, H. M., ROGERS, J. H., et al. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-20-08778.1999 · Cited by 261
Calcium Dynamics in Cortical Astrocytes and Arterioles During Neurovascular Coupling
Filosa, J. A., Bonev, A. D., & Nelson, M. T. (2004) · Circulation Research · doi:10.1161/01.res.0000148636.60732.2e · Cited by 257
TNFα in synaptic function: switching gears
Santello, M., & Volterra, A. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.06.001 · Cited by 253
Emerging role for astroglial networks in information processing: from synapse to behavior
Pannasch, U., & Rouach, N. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.04.004 · Cited by 251
The linear and non-linear electrical properties of the electrode-electrolyte interface
McAdams, E. T., Lackermeier, A., McLaughlin, J. A., Macken, D., & JOSSINET, J. (1995) · Biosensors and Bioelectronics · doi:10.1016/0956-5663(95)96795-z · Cited by 243
Perge, J. A., Homer, M. L., Malik, W. Q., Cash, S., Eskandar, E., Friehs, G., Donoghue, J. P., & Hochberg, L. R. (2013) · Journal of Neural Engineering · doi:10.1088/1741-2560/10/3/036004 · Cited by 243
Relationship between intracortical electrode design and chronic recording function
Karumbaiah, L., Saxena, T., Carlson, D., Patil, K., Patkar, R., Gaupp, E. A., Betancur, M., Stanley, G. B., Carin, L., & Bellamkonda, R. V. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.07.016 · Cited by 241
Glia: The many ways to modulate synaptic plasticity
Achour, S. B., & Pascual, O. (2010) · Neurochemistry International · doi:10.1016/j.neuint.2010.02.013 · Cited by 240
In vivo impedance spectroscopy of deep brain stimulation electrodes
Lempka, S. F., Miocinovic, S., Johnson, M. D., Vitek, J. L., & McIntyre, C. C. (2009) · Journal of Neural Engineering · doi:10.1088/1741-2560/6/4/046001 · Cited by 226
State-of-the-art MEMS and microsystem tools for brain research
Seymour, J. P., Wu, F., Wise, K. D., & Yoon, E. (2017) · Microsystems & Nanoengineering · doi:10.1038/micronano.2016.66 · Cited by 221
Molecular mechanisms of astrocyte-induced synaptogenesis
Baldwin, K. T., & Eroğlu, Ç. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.05.006 · Cited by 219
Adenosine Receptors and Neurological Disease: Neuroprotection and Neurodegeneration
Stone, T. W., Ceruti, S., & Abbracchio, M. P. (2009) · Handbook of experimental pharmacology · doi:10.1007/978-3-540-89615-9_17 · Cited by 216
Kozai, T. D. Y., Vazquez, A. L., Weaver, C. L., Kim, S.-G., & Cui, X. T. (2012) · Journal of Neural Engineering · doi:10.1088/1741-2560/9/6/066001 · Cited by 215
Self-citationKozai, T. D. Y., Catt, K. A., Li, X., Gugel, Z. V., Olafsson, V. T., Vazquez, A. L., & Cui, X. T. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.10.040 · Cited by 214
Self-citationDiffusion barriers evoked in the rat cortex by reactive astrogliosis
Roitbak, T., & Sykov�, E. (1999) · Glia · doi:10.1002/(sici)1098-1136(199910)28:1 · Cited by 211
The regulation of adult rodent hippocampal neurogenesis by deep brain stimulation
Toda, H., Hamani, C., Fawcett, A. P., Hutchison, W. D., & Lozano, A. M. (2008) · Journal of neurosurgery · doi:10.3171/jns/2008/108/01/0132 · Cited by 204
Dunwiddie, T. V., & Fredholm, B. B. (1989) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)23256-6 · Cited by 203
Kozai, T. D. Y., Gugel, Z., Li, X., Gilgunn, P. J., Khilwani, R., Ozdoganlar, O. B., Fedder, G. K., Weber, D. J., & Cui, X. T. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.07.039 · Cited by 193
Self-citationMechanically adaptive intracortical implants improve the proximity of neuronal cell bodies
Harris, J. P., Capadona, J. R., Miller, R. H., Healy, B. C., Shanmuganathan, K., Rowan, S. J., Weder, C., & Tyler, D. J. (2011) · Journal of Neural Engineering · doi:10.1088/1741-2560/8/6/066011 · Cited by 192
Kozai, T. D. Y., Marzullo, T., Hooi, F. M., Langhals, N. B., Majewska, A. K., Brown, E. B., & Kipke, D. R. (2010) · Journal of Neural Engineering · doi:10.1088/1741-2560/7/4/046011 · Cited by 184
Self-citationNolta, N. F., Christensen, M. B., Crane, P. D., Skousen, J. L., & Tresco, P. A. (2015) · Biomaterials · doi:10.1016/j.biomaterials.2015.02.081 · Cited by 181
Abiotic-biotic characterization of Pt/Ir microelectrode arrays in chronic implants
Prasad, A., Xue, Q.-S., Dieme, R., Sankar, V., Mayrand, R. C., Nishida, T., Streit, W. J., & Sanchez, J. C. (2014) · Frontiers in Neuroengineering · doi:10.3389/fneng.2014.00002 · Cited by 178
Compact Movable Microwire Array for Long-Term Chronic Unit Recording in Cerebral Cortex of Primates
Jackson, A., & Fetz, E. E. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00569.2007 · Cited by 174
Untangling GABAergic wiring in the cortical microcircuit
Kubota, Y. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.10.003 · Cited by 172
Borton, D., Micera, S., Millán, J. D. R., & Courtine, G. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3005968 · Cited by 171
Safety and Efficacy of Transcranial Direct Current Stimulation in Acute Experimental Ischemic Stroke
Peruzzotti‐Jametti, L., Cambiaghi, M., Bacigaluppi, M., Gallizioli, M., Gaude, E., Mari, S., Sandrone, S., Cursi, M., Teneud, L., Comı, G., et al. (2013) · Stroke · doi:10.1161/strokeaha.113.001687 · Cited by 169
Timmermann, L., Jain, R., Chen, L., Maarouf, M., Barbe, M., Allert, N., Brücke, T., Kaiser, I., Beirer, S., Sejio, F., et al. (2015) · Lancet Neurology · doi:10.1016/s1474-4422(15)00087-3 · Cited by 167
Fabrication of Responsive, Softening Neural Interfaces
Ware, T. H., Simon, D., Arreaga‐Salas, D., Reeder, J. T., Rennaker, R. L., Keefer, E. W., & Voit, W. (2012) · Advanced Functional Materials · doi:10.1002/adfm.201200200 · Cited by 166
Lin, T., Kim, G.-M., Chen, J.-J., Cheung, W.-M., He, Y. Y., & Hsu, C. Y. (2003) · Stroke · doi:10.1161/01.str.0000047100.84604.ba · Cited by 165
Quantifying long-term microelectrode array functionality using chronic in vivo impedance testing
Prasad, A., & Sanchez, J. C. (2012) · Journal of Neural Engineering · doi:10.1088/1741-2560/9/2/026028 · Cited by 164
Deep brain stimulation mechanisms: the control of network activity via neurochemistry modulation
McIntyre, C. C., & Anderson, R. W. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13649 · Cited by 162
3D Parylene sheath neural probe for chronic recordings
Kim, B. J., Kuo, J. T. W., Hara, S. A., Lee, C. D., Liu, Y., Gutierrez, C. A., Hoang, T., Pikov, V., & Meng, E. F. (2013) · Journal of Neural Engineering · doi:10.1088/1741-2560/10/4/045002 · Cited by 159
Impedance characteristics of deep brain stimulation electrodes in vitro and in vivo
Wei, X. F., & Grill, W. M. (2009) · Journal of Neural Engineering · doi:10.1088/1741-2560/6/4/046008 · Cited by 159
Rao, L., Zhou, H., Li, T., Li, C., & Duan, Y. Y. (2012) · Acta Biomaterialia · doi:10.1016/j.actbio.2012.03.001 · Cited by 159
Grahn, P. J., Mallory, G. W., Khurram, O. U. H., Berry, B. M., Hachmann, J. T., Bieber, A. J., Bennet, K. E., Min, H.-K. P., Chang, S.-Y., Lee, K. H., et al. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00169 · Cited by 158
Application of an optogenetic byway for perturbing neuronal activity via glial photostimulation
Sasaki, T., Beppu, K., Tanaka, K. F., Fukazawa, Y., Shigemoto, R., & Matsui, K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1213458109 · Cited by 156
Deep Brain Stimulation Results in Local Glutamate and Adenosine Release
Tawfik, V. L., Chang, S.-Y., Hitti, F. L., Roberts, D. W., Leiter, J. C., Jovanovic, S., & Lee, K. H. (2010) · Neurosurgery · doi:10.1227/01.neu.0000371988.73620.4c · Cited by 154
Rueger, M. A., Keuters, M. H., Walberer, M., Braun, R., Klein, R., Sparing, R., Fink, G. R., Graf, R., & Schroeter, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043776 · Cited by 151
Neuropathology of the blood–brain barrier and pharmaco-resistance in human epilepsy
Liu, J. Y. W., Thom, M., Catarino, C. B., Martinian, L., Figarella-Branger, D. F., Bartoloméi, F., Koepp, M. J., & Sisodiya, S. M. (2012) · Brain · doi:10.1093/brain/aws147 · Cited by 141
Ware, T., Simon, D., Hearon, K., Liu, C., Shah, S., Reeder, J., Khodaparast, N., Kilgard, M. P., Maitland, D. J., Rennaker, R. L., et al. (2012) · Macromolecular Materials and Engineering · doi:10.1002/mame.201200241 · Cited by 138
Deep brain stimulation and the role of astrocytes
Vedam‐Mai, V., van Battum, E. Y., Kamphuis, W., Feenstra, M. G. P., Denys, D. A. J. P., Reynolds, B. A., Okun, M. S., & Hol, E. M. (2011) · Molecular Psychiatry · doi:10.1038/mp.2011.61 · Cited by 137
Kozai, T. D. Y., Li, X., Bodily, L. M., Caparosa, E. M., Zenonos, G. A., Carlisle, D. L., Friedlander, R. M., & Cui, X. T. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.08.006 · Cited by 136
Self-citationTien, L. W., Wu, F., Tang‐Schomer, M. D., Yoon, E., Omenetto, F. G., & Kaplan, D. L. (2013) · Advanced Functional Materials · doi:10.1002/adfm.201203716 · Cited by 136
Otto, K. J., Johnson, M. D., & Kipke, D. R. (2006) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2005.862530 · Cited by 132
Repeated voltage biasing improves unit recordings by reducing resistive tissue impedances
Johnson, M. D., Otto, K. J., & Kipke, D. R. (2005) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2005.847373 · Cited by 131
In Vivo Electrical Impedance Spectroscopy of Tissue Reaction to Microelectrode Arrays
Mercanzini, A., Colin, P., Bensadoun, J., Bertsch, A., & Renaud, P. (2009) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2009.2018457 · Cited by 130
McCreery, D. B., Yuen, T. G. H., Agnew, W. F., & Bullara, L. A. (1997) · IEEE Transactions on Biomedical Engineering · doi:10.1109/10.634645 · Cited by 130
Plasma-treated PET surfaces improve the biocompatibility of human endothelial cells
Ramires, P. A., Mirenghi, L., Romano, A. R., Palumbo, F., & Nicolardi, G. (2000) · Journal of Biomedical Materials Research · doi:10.1002/1097-4636(20000905)51:3 · Cited by 128
Oberlaender, M., Boudewijns, Z. S. R. M., Kleele, T., Mansvelder, H. D., Sakmann, B. J., & de Kock, C. P. J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1100647108 · Cited by 128
Thiol‐ene/acrylate substrates for softening intracortical electrodes
Ware, T. H., Simon, D., Liu, H. C., Musa, T., Vasudevan, S., Sloan, A. M., Keefer, E. W., Rennaker, R. L., & Voit, W. (2013) · Journal of Biomedical Materials Research Part B Applied Biomaterials · doi:10.1002/jbmb.32946 · Cited by 126
Hong, G., Tian-ming Fu, B., Zhou, T., Schuhmann, T. G., Huang, J., & Lieber, C. M. (2015) · Nano Letters · doi:10.1021/acs.nanolett.5b02987 · Cited by 126
Neurogenic hippocampal targets of deep brain stimulation
Encinas, J. M., Hamani, C., Lozano, A. M., & Enikolopov, G. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22503 · Cited by 125
Meléndez, R. I., Vuthiganon, J., & Kalivas, P. W. (2005) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.104.081521 · Cited by 123
Electron microscopy of tissue adherent to explanted electrodes in dystonia and Parkinson's disease
Moss, J. (2004) · Brain · doi:10.1093/brain/awh292 · Cited by 122
Eles, J. R., Vazquez, A. L., Snyder, N. R., Lagenaur, C. F., Murphy, M. C., Kozai, T. D. Y., & Cui, X. T. (2016) · Biomaterials · doi:10.1016/j.biomaterials.2016.10.054 · Cited by 117
Self-citationHascup, E. R., Hascup, K. N., Humeidan, M., Pomerleau, F., Huettl, P. F., Gratton, A. P., & Gerhardt, G. A. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.07066.x · Cited by 116
Braun, R., Klein, R. M., Walter, H. L., Ohren, M., Freudenmacher, L., Getachew, K., Ladwig, A., Lülling, J., Neumaier, B., Endepols, H., et al. (2016) · Experimental Neurology · doi:10.1016/j.expneurol.2016.02.018 · Cited by 116
Diniz, L. P., Tortelli, V., Garcia, M. N., Araújo, A. P. B., Melo, H. M., da Silva, G. S. S., Felice, F. G. D., Alves‐Leon, S. V., de Souza, J. M., Romão, L. F., et al. (2014) · Glia · doi:10.1002/glia.22713 · Cited by 115
A Novel Anti‐inflammatory Surface for Neural Electrodes
He, W. J., McConnell, G. C., Schneider, T. M., & Bellamkonda, R. V. (2007) · Advanced Materials · doi:10.1002/adma.200700943 · Cited by 114
Glia: A Neglected Player in Non-invasive Direct Current Brain Stimulation
Gellner, A., Reis, J., & Fritsch, B. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00188 · Cited by 114
Role of connexin43 in central nervous system injury
Chew, S. S. L., Johnson, C. S., Green, C. R., & Danesh-Meyer, H. V. (2010) · Experimental Neurology · doi:10.1016/j.expneurol.2010.07.014 · Cited by 113
Skousen, J. L., Merriam, S. M. E., Srivannavit, O., Perlin, G., Wise, K. D., & Tresco, P. A. (2011) · Progress in Brain Research · doi:10.1016/b978-0-444-53815-4.00009-1 · Cited by 111
Critical guidelines for validation of the selectivity of in-vivo chemical microsensors
Phillips, P. E. M., & Wightman, R. M. (2003) · TrAC Trends in Analytical Chemistry · doi:10.1016/s0165-9936(03)00907-5 · Cited by 110
Karumbaiah, L., Norman, S. E., Rajan, N. B., Anand, S., Saxena, T. K., Betancur, M. I., Patkar, R., & Bellamkonda, R. V. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.05.021 · Cited by 107
Hampson, R. E., Gerhardt, G. A., Marmarelis, V. Z., Song, D. B., Opriș, I. C., Santos, L. M., Berger, T. W., & Deadwyler, S. A. (2012) · Journal of Neural Engineering · doi:10.1088/1741-2560/9/5/056012 · Cited by 104
Chang, S.-Y., Kim, I., Marsh, M. P., Jang, D. P., Hwang, S.-C., Gompel, J. J. V., Goerss, S. J., Kimble, C. J., Bennet, K. E., Garris, P. A., et al. (2012) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2012.05.006 · Cited by 101
Mechanically adaptive nanocomposites for neural interfacing
Capadona, J. R., Tyler, D. J., Zorman, C. A., Rowan, S. J., & Weder, C. (2012) · MRS Bulletin · doi:10.1557/mrs.2012.97 · Cited by 101
Hascup, E. R., af Bjerkén, S., Hascup, K. N., Pomerleau, F., Huettl, P. F., Strömberg, I., & Gerhardt, G. A. (2009) · Brain Research · doi:10.1016/j.brainres.2009.06.084 · Cited by 100
Purinergic signaling induces thrombospondin-1 expression in astrocytes
Tran, M. D., & Neary, J. T. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0603146103 · Cited by 100
Hess‐Dunning, A., Capadona, J. R., Shanmuganathan, K., Hsu, L., Rowan, S. J., Weder, C., Tyler, D. J., & Zorman, C. A. (2011) · Journal of Micromechanics and Microengineering · doi:10.1088/0960-1317/21/5/054009 · Cited by 96
Robblee, L. S., McHardy, J., Agnew, W. F., & Bullara, L. A. (1983) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(83)90062-6 · Cited by 95
Novel multi-sided, microelectrode arrays for implantable neural applications
Seymour, J. P., Langhals, N. B., Anderson, D. J., & Kipke, D. R. (2011) · Biomedical Microdevices · doi:10.1007/s10544-011-9512-z · Cited by 95
Elastomeric and soft conducting microwires for implantable neural interfaces
Kolarcik, C. L., Luebben, S. D., Sapp, S. A., Hanner, J., Snyder, N. R., Kozai, T. D. Y., Chang, E., Nabity, J., Nabity, S. T., Lagenaur, C. F., et al. (2015) · Soft Matter · doi:10.1039/c5sm00174a · Cited by 90
Self-citationIncreased cortical extracellular adenosine correlates with seizure termination
Gompel, J. J. V., Bower, M. R., Worrell, G. A., Stead, M., Chang, S., Goerss, S. J., Kim, I., Bennet, K. E., Meyer, F. B., Marsh, W. R., et al. (2014) · Epilepsia · doi:10.1111/epi.12511 · Cited by 88
Deep Brain Stimulation: Are Astrocytes a Key Driver Behind the Scene?
Fenoy, A. J., Goetz, L., Chabardès, S., & Xia, Y. (2014) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12223 · Cited by 88
Two-photon imaging of chronically implanted neural electrodes: Sealing methods and new insights
Kozai, T. D. Y., Eles, J. R., Vazquez, A. L., & Cui, X. T. (2015) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2015.10.007 · Cited by 88
Self-citationZuidema, J. M., Hyzinski‐García, M. C., Vlasselaer, K. V., Zaccor, N. W., Plopper, G. E., Mongin, A. A., & Gilbert, R. J. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.10.079 · Cited by 86
Controlled release nanoparticle-embedded coatings reduce the tissue reaction to neuroprostheses
Mercanzini, A., Reddy, S. T., Velluto, D., Colin, P., Maillard, A., Bensadoun, J., Hubbell, J. A., & Renaud, P. (2010) · Journal of Controlled Release · doi:10.1016/j.jconrel.2010.04.025 · Cited by 78
McCreery, D. B., Agnew, W. F., & Bullara, L. A. (2002) · Annals of Biomedical Engineering · doi:10.1114/1.1430748 · Cited by 77
Up-regulation of Connexin43 in the glial scar following photothrombotic ischemic injury.
Haupt, C., Witte, O., & Frahm, C. (2007) · Molecular and cellular neurosciences · doi:10.1016/j.mcn.2007.02.005 · Cited by 76
Zhao, H.-P., Steiger, A., Nohner, M., & Ye, H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0129625 · Cited by 75
McCreery, D. B., Cogan, S. F., Kane, S. R., & Pikov, V. (2016) · Journal of Neural Engineering · doi:10.1088/1741-2560/13/3/036012 · Cited by 69
Gutowski, S. M., Shoemaker, J. T., Templeman, K. L., Wei, Y., Latour, R. A., Bellamkonda, R. V., LaPlaca, M. C., & Garcı́a, A. J. (2015) · Biomaterials · doi:10.1016/j.biomaterials.2014.12.009 · Cited by 68
Matsuo, H., Uchida, K., Nakajima, H., Guerrero, A. R., Watanabe, S., Takeura, N., Sugita, D., Shimada, S., Nakatsuka, T., & Baba, H. (2014) · Pain · doi:10.1016/j.pain.2014.06.022 · Cited by 67
Sun, D. A., Yu, H., Spooner, J., Tatsas, A. D., Davis, T. L., Abel, T. W., Kao, C., & Konrad, P. E. (2008) · Journal of neurosurgery · doi:10.3171/jns/2008/109/8/0325 · Cited by 66
Interaction of macrophages with fibrous materials in vitro
Bernatchez, S. F., Parks, P. J., & Gibbons, D. F. (1996) · Biomaterials · doi:10.1016/0142-9612(96)00014-2 · Cited by 64
Flavopiridol reduces the impedance of neural prostheses in vivo without affecting recording quality
Purcell, E. K., Thompson, D. E., Ludwig, K. A., & Kipke, D. R. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2009.06.026 · Cited by 62
Self-citationSkousen, J. L., Bridge, M. J., & Tresco, P. A. (2015) · Biomaterials · doi:10.1016/j.biomaterials.2014.08.039 · Cited by 61
Silchenko, A. N., & Tass, P. A. (2007) · Biological Cybernetics · doi:10.1007/s00422-007-0196-7 · Cited by 59
Kolarcik, C. L., Bourbeau, D., Azemi, E., Rost, E., Zhang, L., Lagenaur, C. F., Weber, D. J., & Cui, X. T. (2012) · Acta Biomaterialia · doi:10.1016/j.actbio.2012.06.034 · Cited by 59
Research works printed but not linked: 1
- Humphrey, D. R. & Schmidt, E. M. in Neurophysiological Techniques Vol. II (eds Boulton, A. A., Baker, G. B. & Vanderwolf, C. H.) 1–64 (Humana Press, New York, 1990).
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Liu, Y., Liu, J., Chen, S., Lei, T., Kim, Y., Niu, S., Wang, H., Wang, X., Foudeh, A. M., Tok, J. B.-H., et al. (2019) · Nature Biomedical Engineering · doi:10.1038/s41551-018-0335-6 · Cited by 811
Nam, S., & Mooney, D. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.0c00798 · Cited by 764
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Metadata
- Authors
- Salatino, J. W., Ludwig, K. A., Kozai, T. D. Y., & Purcell, E. K.
- Affiliations
- Michigan State University (US)
- Mayo Clinic (US)
- University of Pittsburgh (US)
- Corresponding author
- Purcell, Erin K.
- Venue
- Nature Biomedical Engineering
- Published
- 2017-11-10
- Volume
- 1
- Issue
- 11
- Pages
- 862-877
- ISSN
- 2157-846X (ISSN-L)
- PMC
- PMC6261524
- OpenAlex
- W2765960015
- Cited by
- 642
- References
- 231
- Citations by year
- 2026: 77 · 2025: 110 · 2024: 92 · 2023: 95 · 2022: 68 · 2021: 76 · 2020: 61 · 2019: 38 · 2018: 24 · 2017: 1
- FWCI
- 16.46
- Type
- journal article
- Language
- en
- Update notices
- correction (2017-12-07)
- Open access
- green
- europepmc.org
- Licence
- Locations
- Nature Biomedical Engineering (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Grainger Foundation
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (R03NS095202, R21NS094900, R01NS094396)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neural Engineering
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Neurology › Vagus Nerve Stimulation Research
- Keywords
- glial cells, implanted electrodes, neuroprosthetics, neuromodulation, neural interfaces, device implantation outcomes
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