Astrocytes and microglia in neurodegenerative diseases: Lessons from human in vitro models
Open accessAbstract
Both astrocytes and microglia fulfil homeostatic and immune functions in the healthy CNS. Dysfunction of these cell types have been implicated in the pathomechanisms of several neurodegenerative diseases. Understanding the cellular autonomy and early pathological changes in these cell types may inform drug screening and therapy development. While animal models and post-mortem tissue have been invaluable in understanding disease processes, the advent of human in vitro models provides a unique insight into disease biology as a manipulable model system obtained directly from patients. Here, we discuss the different human in vitro models of astrocytes and microglia and outline the phenotypes that have been recapitulated in these systems.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Astrocyte and microglia iPSC models partially recapitulate the transcriptomes of their in vivo counterparts and may capture authentic neurodegenerative disease phenotypes.
“Astrocyte and microglia iPSC models partially recapitulate the transcriptomes of their in vivo counterparts and may capture authentic neurodegenerative disease phenotypes [345,406,480,481,482,483,484].”
From Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy (2025) · cites this paper as [480]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Neuropathological stageing of Alzheimer-related changes.
Braak, H., & Braak, E. (1991) · Acta Neuropathologica · doi:10.1007/bf00308809 · Cited by 16,123 · see citing works
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 · see citing works
Astrocytes: Biology and pathology
Sofroniew, M. V., & Vinters, H. V. (2010) · Acta Neuropathologica · doi:10.1007/s00401-009-0619-8 · Cited by 5,196 · see citing works
A Lineage of Myeloid Cells Independent of Myb and Hematopoietic Stem Cells
Schulz, C., Perdiguero, E. G., Chorro, L., Szabo-Rogers, H., Cagnard, N., Kierdorf, K., Prinz, M., Wu, B., Jacobsen, S. E. W., Pollard, J. W., et al. (2012) · Science · doi:10.1126/science.1219179 · Cited by 2,578 · see citing works
Identification of a unique TGF-β–dependent molecular and functional signature in microglia
Butovsky, O., Jedrychowski, M. P., Moore, C. S., Cialic, R., Lanser, A. J., Gabriely, G., Koeglsperger, T., Dake, B., Wu, P. M., Doykan, C. E., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3599 · Cited by 2,543 · see citing works
Tissue-resident macrophages originate from yolk-sac-derived erythro-myeloid progenitors
Gomez Perdiguero, E., Klapproth, K., Schulz, C., Busch, K., Azzoni, E., Crozet, L., Garner, H., Trouillet, C., de Bruijn, M. F., Geissmann, F., et al. (2015) · Nature · doi:10.1038/nature13989 · Cited by 2,339 · see citing works
RAGE and amyloid-β peptide neurotoxicity in Alzheimer's disease
Yan, S. D., Chen, X., Fu, J., Chen, M., Zhu, H., Roher, A., Slattery, T., Zhao, L., Nagashima, M., Morser, J., et al. (1996) · Nature · doi:10.1038/382685a0 · Cited by 2,012 · see citing works
Astrocyte scar formation aids central nervous system axon regeneration
Anderson, M. A., Burda, J. E., Ren, Y., Ao, Y., O’Shea, T. M., Kawaguchi, R., Coppola, G., Khakh, B. S., Deming, T. J., & Sofroniew, M. V. (2016) · Nature · doi:10.1038/nature17623 · Cited by 1,851 · see citing works
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 · see citing works
Onset and Progression in Inherited ALS Determined by Motor Neurons and Microglia
Boillée, S., Yamanaka, K., Lobsiger, C. S., Copeland, N. G., Jenkins, N. A., Kassiotis, G., Kollias, G., & Cleveland, D. W. (2006) · Science · doi:10.1126/science.1123511 · Cited by 1,623 · see citing works
Microglia emerge from erythromyeloid precursors via Pu.1- and Irf8-dependent pathways
Kierdorf, K., Erny, D., Goldmann, T., Sander, V., Schulz, C., Perdiguero, E. G., Wieghofer, P., Heinrich, A., Riemke, P., Hölscher, C., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3318 · Cited by 1,457 · see citing works
Microglial Dysfunction and Defective β-Amyloid Clearance Pathways in Aging Alzheimer's Disease Mice
Hickman, S. E., Allison, E. K., & El Khoury, J. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.0616-08.2008 · Cited by 1,329 · cited 1× · see citing works
“However, evidence points to a combination of dysfunctional Aβ-clearing mechanisms (Hickman et al., 2008) and Aβ-induced activation of proinflammatory processes through upregulated secretion of cytokines and neurotoxins (Guillot-Sestier and Town, 2013).”
BackgroundAn environment-dependent transcriptional network specifies human microglia identity
Gosselin, D., Skola, D., Coufal, N. G., Holtman, I. R., Schlachetzki, J. C. M., Sajti, E., Jaeger, B. N., O’Connor, C., Fitzpatrick, C., Pasillas, M. P., et al. (2017) · Science · doi:10.1126/science.aal3222 · Cited by 1,220 · cited 2× · see citing works
“Human astrocytes and microglia display differences to their mouse counterparts in terms of their morphology, gene expression and function (Oberheim et al., 2012; Tarassishin et al., 2014; Zhang et al., 2016; Galatro et al., 2017; Gosselin et al., 2017).”
Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis
Yamanaka, K., Chun, S. J., Boillee, S., Fujimori-Tonou, N., Yamashita, H., Gutmann, D. H., Takahashi, R., Misawa, H., & Cleveland, D. W. (2008) · Nature Neuroscience · doi:10.1038/nn2047 · Cited by 1,140 · see citing works
Lin, Y.-T., Seo, J., Gao, F., Feldman, H. M., Wen, H.-L., Penney, J., Cam, H. P., Gjoneska, E., Raja, W. K., Cheng, J., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.05.008 · Cited by 1,125 · see citing works
Microglial signatures and their role in health and disease
Butovsky, O., & Weiner, H. L. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0057-5 · Cited by 1,046 · see citing works
Physiological Roles of Aquaporin-4 in Brain
Nagelhus, E. A., & Ottersen, O. P. (2013) · Physiological Reviews · doi:10.1152/physrev.00011.2013 · Cited by 766 · see citing works
Mertens, J., Paquola, A. C. M., Ku, M., Hatch, E., Böhnke, L., Ladjevardi, S., McGrath, S., Campbell, B., Lee, H., Herdy, J. R., et al. (2015) · Cell Stem Cell · doi:10.1016/j.stem.2015.09.001 · Cited by 765 · see citing works
Kondo, T., Asai, M., Tsukita, K., Kutoku, Y., Ohsawa, Y., Sunada, Y., Imamura, K., Egawa, N., Yahata, N., Okita, K., et al. (2013) · Cell Stem Cell · doi:10.1016/j.stem.2013.01.009 · Cited by 741 · see citing works
Transcriptomic analysis of purified human cortical microglia reveals age-associated changes
Galatro, T. F., Holtman, I. R., Lerario, A. M., Vainchtein, I. D., Brouwer, N., Sola, P. R., Veras, M. M., Pereira, T. F., Leite, R. E. P., Möller, T., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4597 · Cited by 741 · see citing works
A 3D human triculture system modeling neurodegeneration and neuroinflammation in Alzheimer’s disease
Park, J., Wetzel, I., Marriott, I., Dréau, D., D’Avanzo, C., Kim, D. Y., Tanzi, R. E., & Cho, H. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0175-4 · Cited by 644 · see citing works
Bruttger, J., Karram, K., Wörtge, S., Regen, T., Marini, F., Hoppmann, N., Klein, M., Blank, T., Yona, S., Wolf, Y., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.06.012 · Cited by 634 · see citing works
A new fate mapping system reveals context-dependent random or clonal expansion of microglia
Tay, T. L., Mai, D., Dautzenberg, J., Fernández-Klett, F., Lin, G., Sagar, Datta, M., Drougard, A., Stempfl, T., Ardura-Fabregat, A., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4547 · Cited by 597 · see citing works
Sloan, S. A., Darmanis, S., Huber, N., Khan, T. A., Birey, F., Caneda, C., Reimer, R., Quake, S. R., Barres, B. A., & Paşca, S. P. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.035 · Cited by 593 · see citing works
A combination of ontogeny and CNS environment establishes microglial identity
Bennett, F. C., Bennett, M. L., Yaqoob, F., Mulinyawe, S. B., Grant, G. A., Hayden Gephart, M., Plowey, E. D., & Barres, B. A. (2018) · Neuron · doi:10.1016/j.neuron.2018.05.014 · Cited by 524 · see citing works
Local generation of glia is a major astrocyte source in postnatal cortex
Ge, W.-P., Miyawaki, A., Gage, F. H., Jan, Y. N., & Jan, L. Y. (2012) · Nature · doi:10.1038/nature10959 · Cited by 507 · see citing works
Microglial activation correlates with severity in Huntington disease: A clinical and PET study
Pavese, N., Gerhard, A., Tai, Y. F., Ho, A. K., Turkheimer, F., Barker, R. A., Brooks, D. J., & Piccini, P. (2006) · Neurology · doi:10.1212/01.wnl.0000222734.56412.17 · Cited by 462 · see citing works
McQuade, A., Coburn, M., Tu, C. H., Hasselmann, J., Davtyan, H., & Blurton-Jones, M. (2018) · Molecular Neurodegeneration · doi:10.1186/s13024-018-0297-x · Cited by 449 · see citing works
di Domenico, A., Carola, G., Calatayud, C., Pons-Espinal, M., Muñoz, J. P., Richaud-Patin, Y., Fernandez-Carasa, I., Gut, M., Faella, A., Parameswaran, J., et al. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.12.011 · Cited by 372 · see citing works
PSEN1 Mutant iPSC-Derived Model Reveals Severe Astrocyte Pathology in Alzheimer's Disease
Oksanen, M., Petersen, A. J., Naumenko, N., Puttonen, K., Lehtonen, Š., Gubert Olivé, M., Shakirzyanova, A., Leskelä, S., Sarajärvi, T., Viitanen, M., et al. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.10.016 · Cited by 332 · see citing works
Jiang, R., Diaz-Castro, B., Looger, L. L., & Khakh, B. S. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.3693-15.2016 · Cited by 237 · see citing works
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 · see citing works
Buchrieser, J., James, W., & Moore, M. D. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2016.12.020 · Cited by 215 · see citing works
Lin, Y.-T., Seo, J., Gao, F., Feldman, H. M., Wen, H.-L., Penney, J., Cam, H. P., Gjoneska, E., Raja, W. K., Cheng, J., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.06.011 · Cited by 210 · see citing works
Varcianna, A., Myszczynska, M. A., Castelli, L. M., O'Neill, B., Kim, Y., Talbot, J., Nyberg, S., Nyamali, I., Heath, P. R., Stopford, M. J., et al. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2018.11.067 · Cited by 194 · see citing works
Hall, C. E., Yao, Z., Choi, M., Tyzack, G. E., Serio, A., Luisier, R., Harley, J., Preza, E., Arber, C., Crisp, S. J., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.05.024 · Cited by 179 · see citing works
Self-citationGarcia-Reitboeck, P., Phillips, A., Piers, T. M., Villegas-Llerena, C., Butler, M., Mallach, A., Rodrigues, C., Arber, C. E., Heslegrave, A., Zetterberg, H., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.07.094 · Cited by 162 · see citing works
Prion-like transmission of neuronal huntingtin aggregates to phagocytic glia in the Drosophila brain
Pearce, M. M. P., Spartz, E. J., Hong, W., Luo, L., & Kopito, R. R. (2015) · Nature Communications · doi:10.1038/ncomms7768 · Cited by 159 · see citing works
Microglial activation in the pathogenesis of Huntington's disease
Yang, H.-M., Yang, S., Huang, S.-S., Tang, B.-S., & Guo, J.-F. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00193 · Cited by 151 · see citing works
Human iPSC‐derived microglia: A growing toolset to study the brain's innate immune cells
Hasselmann, J., & Blurton‐Jones, M. (2020) · Glia · doi:10.1002/glia.23781 · Cited by 145 · see citing works
Induced pluripotent stem cell model recapitulates pathologic hallmarks of Gaucher disease
Panicker, L. M., Miller, D., Park, T. S., Patel, B., Azevedo, J. L., Awad, O., Masood, M. A., Veenstra, T. D., Goldin, E., Stubblefield, B. K., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1207889109 · Cited by 129 · see citing works
Flagged first, then by citations
Research works printed but not linked: 137
- Abramov A.Y. Canevari L. Duchen M.R. Changes in intracellular calcium and glutathione in astrocytes as the primary mechanism of amyloid neurotoxicity J. Neurosci. 23 12 2003 5088 5095 12832532 PMC6741151
- Abud E.M. Ramirez R.N. Martinez E.S. Healy L.M. Nguyen C.H.H. Newman S.A. iPSC-derived human microglia-like cells to study neurological diseases Neuron 94 2 2017 278 293 e9 28426964 PMC5482419
- Aflaki E. Stubblefield B.K. McGlinchey R.P. McMahon B. Ory D.S. Sidransky E. A characterization of Gaucher iPS-derived astrocytes: potential implications for Parkinson’s disease Neurobiol. Dis. 134 2020 104647 PMC6980699 31669751
- Allen S.P. Hall B. Castelli L.M. Francis L. Woof R. Siskos A.P. Astrocyte adenosine deaminase loss increases motor neuron toxicity in amyotrophic lateral sclerosis Brain 142 3 2019 586 605 30698736 PMC6391613
- Almeida S. Zhang Z. Coppola G. Mao W. Futai K. Karydas A. Induced pluripotent stem cell models of progranulin-deficient frontotemporal dementia uncover specific reversible neuronal defects Cell Rep. 2 4 2012 789 798 23063362 PMC3532907
- Amos P.J. Fung S. Case A. Kifelew J. Osnis L. Smith C.L. Modulation of hematopoietic lineage specification impacts TREM2 expression in microglia-like cells derived from human stem cells ASN Neuro 9 4 2017 1759091417716610 PMC5548325 28683563
- Banerjee P. Paza E. Perkins E.M. James O.G. Kenkhuis B. Lloyd A.F. Burr K. Story D. Yusuf D. He X. Backofen R. Dando O. Chandran S. Priller J. Generation of pure monocultures of human microglia-like cells from induced pluripotent stem cells Stem Cell Res. 49 2020 102046 10.1016/j.scr.2020.102046 33096385 · DOI
- Barbar L. Jain T. Zimmer M. Kruglikov I. Sadick J.S. Wang M. CD49f is a novel marker of functional and reactive human iPSC-derived astrocytes Neuron 107 3 2020 436 453 32485136 PMC8274549
- Bates G.P. Dorsey R. Gusella J.F. Hayden M.R. Kay C. Leavitt B.R. Huntington disease Nat. Rev. Dis. Primers 1 2015 15005 27188817
- Benraiss A. Wang S. Herrlinger S. Li X. Chandler-Militello D. Mauceri J. Human glia can both induce and rescue aspects of disease phenotype in Huntington disease Nat. Commun. 7 2016 11758 27273432 PMC4899632
- Birger A. Ben-Dor I. Ottolenghi M. Turetsky T. Gil Y. Sweetat S. Human iPSC-derived astrocytes from ALS patients with mutated C9ORF72 show increased oxidative stress and neurotoxicity EBioMedicine 50 2019 274 289 31787569 PMC6921360
- Booth H.D.E. Hirst W.D. Wade-Martins R. The role of astrocyte dysfunction in Parkinson’s disease pathogenesis Trends Neurosci. 40 6 2017 358 370 28527591 PMC5462417
- Booth H.D.E. Wessely F. Connor-Robson N. Rinaldi F. Vowles J. Browne C. RNA sequencing reveals MMP2 and TGFB1 downregulation in LRRK2 G2019S Parkinson’s iPSC-derived astrocytes Neurobiol. Dis. 129 2019 56 66 31085228
- Braak H. Sastre M. Del Tredici K. Development of alpha-synuclein immunoreactive astrocytes in the forebrain parallels stages of intraneuronal pathology in sporadic Parkinson’s disease Acta Neuropathol. 114 3 2007 231 241 17576580
- Bradford J. Shin J.Y. Roberts M. Wang C.E. Li X.J. Li S. Expression of mutant huntingtin in mouse brain astrocytes causes age-dependent neurological symptoms Proc. Natl. Acad. Sci. U. S. A. 106 52 2009 22480 22485 20018729 PMC2799722
- Bradley R.A. Shireman J. McFalls C. Choi J. Canfield S.G. Dong Y. Regionally specified human pluripotent stem cell-derived astrocytes exhibit different molecular signatures and functional properties Development 146 13 2019 PMC6633609 31189664
- Brownjohn P.W. Smith J. Solanki R. Lohmann E. Houlden H. Hardy J. Functional studies of missense TREM2 mutations in human stem cell-derived microglia Stem Cell Rep. 10 4 2018 1294 1307 PMC5998752 29606617
- Cavaliere F. Cerf L. Dehay B. Ramos-Gonzalez P. De Giorgi F. Bourdenx M. In vitro α-synuclein neurotoxicity and spreading among neurons and astrocytes using Lewy body extracts from Parkinson disease brains Neurobiol. Dis. 103 2017 101 112 28411117
- Cekanaviciute E. Dietrich H.K. Axtell R.C. Williams A.M. Egusquiza R. Wai K.M. Astrocytic TGF-β signaling limits inflammation and reduces neuronal damage during central nervous system Toxoplasma infection J. Immunol. 193 1 2014 139 149 24860191 PMC4075480
- Cho I.K. Hunter C.E. Ye S. Pongos A.L. Chan A.W.S. Combination of stem cell and gene therapy ameliorates symptoms in Huntington’s disease mice NPJ Regen. Med. 4 2019 7 30937182 PMC6435637
- Claes C. Van Den Daele J. Boon R. Schouteden S. Colombo A. Sebastian Monasor L. Fiers M. Ordovas L. Nami F. Bohrmann B. Tahirovic S. De Strooper B. Verfaille C.M. Human stem cell–derived monocytes and microglia‐like cells reveal impaired amyloid plaque clearance upon heterozygous or homozygous loss of TREM2 Alzheimers Dementia 15 3 2019 453 464 30442540
- Clarke B.E. Patani R. The microglial component of amyotrophic lateral sclerosis Brain 2020 awaa309 10.1093/brain/awaa309 PMC7805793 33427296 · DOI · Paper page
- Clarke B.E. Taha D.M. Tyzack G.E. Patani R. Regionally encoded functional heterogeneity of astrocytes in health and disease: a perspective Glia 69 1 2020 20 27 32749770
- Clarke B.E. Taha D.M. Ziff O.J. Alam A. Thelin E.P. Marco Garcia N. Helmy A. Patani R. Human stem cell-derived astrocytes exhibit region-specific heterogeneity in their secretory profiles Brain 143 10 2020 85 PMC7586081 32895697
- Colodner K.J. Montana R.A. Anthony D.C. Folkerth R.D. De Girolami U. Feany M.B. Proliferative potential of human astrocytes J. Neuropathol. Exp. Neurol. 64 2 2005 163 169 15751231
- Corder E.H. Saunders A.M. Strittmatter W.J. Schmechel D.E. Gaskell P.C. Small G.W. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer’s disease in late onset families Science 261 5123 1993 921 923 8346443
- Davalos D. Grutzendler J. Yang G. Kim J.V. Zuo Y. Jung S. ATP mediates rapid microglial response to local brain injury in vivo Nat. Neurosci. 8 6 2005 752 758 15895084
- Donnelly K.M. DeLorenzo O.R. Zaya A.D. Pisano G.E. Thu W.M. Luo L. Phagocytic glia are obligatory intermediates in transmission of mutant huntingtin aggregates across neuronal synapses Elife 2020 9 PMC7297539 32463364
- Doorn K.J. Moors T. Drukarch B. van de Berg W.Dj Lucassen P.J. van Dam A.M. Microglial phenotypes and toll-like receptor 2 in the substantia nigra and hippocampus of incidental Lewy body disease cases and Parkinson’s disease patients Acta Neuropathol. Commun. 2 2014 90 25099483 PMC4224021
- Douvaras P. Sun B. Wang M. Kruglikov I. Lallos G. Zimmer M. Directed differentiation of human pluripotent stem cells to microglia Stem Cell Rep. 8 6 2017 1516 1524 PMC5470097 28528700
- East E. Golding J.P. Phillips J.B. A versatile 3D culture model facilitates monitoring of astrocytes undergoing reactive gliosis J. Tissue Eng. Regener. Med. 3 8 2009 634 646 PMC2842570 19813215
- El Khoury J. Hickman S.E. Thomas C.A. Loike J.D. Silverstein S.C. Microglia, scavenger receptors, and the pathogenesis of Alzheimer’s disease Neurobiol. Aging 19 Suppl. 1 1998 S81 4 9562474
- Etemad S. Zamin R.M. Ruitenberg M.J. Filgueira L. A novel in vitro human microglia model: characterization of human monocyte-derived microglia J. Neurosci. Methods 209 1 2012 79 89 22659341
- Ferreira M. Massano J. An updated review of Parkinson’s disease genetics and clinicopathological correlations Acta Neurol. Scand. 135 3 2017 273 284 27273099
- Foo L.C. Allen N.J. Bushong E.A. Ventura P.B. Chung W.S. Zhou L. Development of a method for the purification and culture of rodent astrocytes Neuron 71 5 2011 799 811 21903074 PMC3172573
- Furihata T. Ito R. Kamiichi A. Saito K. Chiba K. Establishment and characterization of a new conditionally immortalized human astrocyte cell line J. Neurochem. 2016 92 105 26365151
- Garcia V.J. Rushton D.J. Tom C.M. Allen N.D. Kemp P.J. Svendsen C.N. Huntington’s disease patient-derived astrocytes display electrophysiological impairments and reduced neuronal support Front. Neurosci. 13 2019 669 31316341 PMC6610155
- Ginhoux F. Greter M. Leboeuf M. Nandi S. See P. Gokhan S. Fate mapping analysis reveals that adult microglia derive from primitive macrophages Science 330 6005 2010 841 845 20966214 PMC3719181
- Gowing G. Lalancette-Hébert M. Audet J.N. Dequen F. Julien J.P. Macrophage colony stimulating factor (M-CSF) exacerbates ALS disease in a mouse model through altered responses of microglia expressing mutant superoxide dismutase Exp. Neurol. 220 2 2009 267 275 19733170
- Grassivaro F. Menon R. Acquaviva M. Ottoboni L. Ruffini F. Bergamaschi A. Convergence between microglia and peripheral macrophages phenotype during development and neuroinflammation J. Neurosci. 40 4 2020 784 795 31818979 PMC6975289
- Gu X.L. Long C.X. Sun L. Xie C. Lin X. Cai H. Astrocytic expression of Parkinson’s disease-related A53T alpha-synuclein causes neurodegeneration in mice Mol. Brain 3 2010 12 20409326 PMC2873589
- Guillot-Sestier M.V. Town T. Innate immunity in Alzheimer’s disease: a complex affair CNS Neurol. Disord. Drug Targets 12 5 2013 593 607 23574177 PMC3792655
- Gupta K. Patani R. Baxter P. Serio A. Story D. Tsujita T. Human embryonic stem cell derived astrocytes mediate non-cell-autonomous neuroprotection through endogenous and drug-induced mechanisms Cell Death Differ. 19 5 2012 779 787 22095276 PMC3321621
- Haenseler W. Rajendran L. Concise Review: Modeling Neurodegenerative Diseases with Human Pluripotent Stem Cell-Derived Microglia Stem Cells 37 6 2019 724 730 30801863 PMC6849818
- Haenseler W. Sansom S.N. Buchrieser J. Newey S.E. Moore C.S. Nicholls F.J. A highly efficient human pluripotent stem cell microglia model displays a neuronal-co-culture-specific expression profile and inflammatory response Stem Cell Rep. 8 6 2017 1727 1742 PMC5470330 28591653
- Haenseler W. Zambon F. Lee H. Vowles J. Rinaldi F. Duggal G. Excess α-synuclein compromises phagocytosis in iPSC-derived macrophages Sci. Rep. 7 1 2017 9003 28827786 PMC5567139
- Haidet-Phillips A.M. Doreswamy A. Gross S.K. Tang X. Campanelli J.T. Maragakis N.J. Human glial progenitor engraftment and gene expression is independent of the ALS environment Exp. Neurol. 264 2015 188 199 25523812 PMC5411013
- Hall-Roberts H. Agarwal D. Obst J. Smith T.B. Monzón-Sandoval J. Di Daniel E. Webber C. James W.S. Mead E. Davis J.B. Cowley S.A. TREM2 Alzheimer’s variant R47H causes similar transcriptional dysregulation to knockout, yet only subtle functional phenotypes in human iPSC-derived macrophages Alzheimers Res Ther. 12 2020 151 10.1186/s13195-020-00709-z PMC7667762 33198789 · DOI · Paper page
- Han X. Chen M. Wang F. Windrem M. Wang S. Shanz S. Forebrain engraftment by human glial progenitor cells enhances synaptic plasticity and learning in adult mice Cell Stem Cell 12 3 2013 342 353 23472873 PMC3700554
- Hardiman O. Al-Chalabi A. Chio A. Corr E.M. Logroscino G. Robberecht W. Amyotrophic lateral sclerosis Nat. Rev. Dis. Primers 3 2017 17071 28980624
- Härtlova A. Herbst S. Peltier J. Rodgers A. Bilkei-Gorzo O. Fearns A. LRRK2 is a negative regulator of EMBO J. 37 12 2018 PMC6003659 29789389
- Heman-Ackah S.M. Bassett A.R. Wood M.J. Precision modulation of neurodegenerative disease-related gene expression in human iPSC-derived neurons Sci. Rep. 6 2016 28420 27341390 PMC4920027
- Hsiao H.Y. Chen Y.C. Chen H.M. Tu P.H. Chern Y. A critical role of astrocyte-mediated nuclear factor-κB-dependent inflammation in Huntington’s disease Hum. Mol. Genet. 22 9 2013 1826 1842 23372043
- Imaizumi K. Sone T. Ibata K. Fujimori K. Yuzaki M. Akamatsu W. Controlling the regional identity of hPSC-derived neurons to uncover neuronal subtype specificity of neurological disease phenotypes Stem Cell Rep. 5 6 2015 1010 1022 PMC4682123 26549851
- Imamura K. Hishikawa N. Sawada M. Nagatsu T. Yoshida M. Hashizume Y. Distribution of major histocompatibility complex class II-positive microglia and cytokine profile of Parkinson’s disease brains Acta Neuropathol. 106 6 2003 518 526 14513261
- Janabi N. Peudenier S. Heron B. Ng K. Tardieu M. Establishment of human microglial cell lines after transfection of primary cultures of embryonic microglial cells with the SV40 large T antigen Neurosci. Lett. 1995 105 108 7478261
- Juopperi Ta Kim Wr Chiang Ch Yu H. Margolis Rl Ross Ca Astrocytes generated from patient induced pluripotent stem cells recapitulate features of Huntington’s disease patient cells Mol. Brain 5 2012 17 22613578 PMC3506453
- Kamakura S. Oishi K. Yoshimatsu T. Nakafuku M. Masuyama N. Gotoh Y. Hes binding to STAT3 mediates crosstalk between Notch and JAK-STAT signalling Nat. Cell Biol. 6 6 2004 547 554 15156153
- Kang P. Lee H.K. Glasgow S.M. Finley M. Donti T. Gaber Z.B. Sox9 and NFIA coordinate a transcriptional regulatory cascade during the initiation of gliogenesis Neuron 74 1 2012 79 94 22500632 PMC3543821
- Karran E. De Strooper B. The amyloid cascade hypothesis: are we poised for success or failure? J. Neurochem. 139 Suppl. 2 2016 237 252 27255958
- Kelley K.W. Ben Haim L. Schirmer L. Tyzack G.E. Tolman M. Miller J.G. Kir4.1-dependent astrocyte-fast motor neuron interactions are required for peak strength Neuron 98 2 2018 306 319 e7 29606582 PMC5919779
- Konttinen H. Cabral-da-Silva M.E.C. Ohtonen S. Wojciechowski S. Shakirzyanova A. Caligola S. PSEN1ΔE9, APPswe, and APOE4 confer disparate phenotypes in human iPSC-derived microglia Stem Cell Rep. 13 4 2019 669 683 PMC6829767 31522977
- Krencik R. Weick J.P. Liu Y. Zhang Z.J. Zhang S.C. Specification of transplantable astroglial subtypes from human pluripotent stem cells Nat. Biotechnol. 29 6 2011 528 534 21602806 PMC3111840
- Krencik R. Seo K. van Asperen J.V. Basu N. Cvetkovic C. Barlas S. Systematic three-dimensional coculture rapidly recapitulates interactions between human neurons and astrocytes Stem Cell Rep. 9 6 2017 1745 1753 PMC5785708 29198827
- Langley R.R. Fan D. Guo L. Zhang C. Qingtang L. Brantley E.C. Generation of an immortalized astrocyte cell line from H-2Kb-tsA58 mice to study the role of astrocytes in brain metastasis Int. J. Oncol. 2009 665 672 PMC2882684 19724901
- Lee H.J. Suk J.E. Patrick C. Bae E.J. Cho J.H. Rho S. Direct transfer of alpha-synuclein from neuron to astroglia causes inflammatory responses in synucleinopathies J. Biol. Chem. 285 12 2010 9262 9272 20071342 PMC2838344
- Lee H. Flynn R. Sharma I. Haberman E. Carling P.J. Nicholls F.J. LRRK2 is recruited to phagosomes and co-recruits RAB8 and RAB10 in human pluripotent stem cell-derived macrophages Stem Cell Rep. 14 5 2020 940 955 PMC7221108 32359446
- Li X. Tao Y. Bradley R. Du Z. Kong L. Dong Y. Fast generation of functional subtype astrocytes from human pluripotent stem cells Stem Cell Rep. 11 4 2018 998 1008 PMC6178885 30269954
- Liddelow S.A. Barres B.A. Reactive astrocytes: production, function, and therapeutic potential Immunity 46 6 2017 957 967 28636962
- Liévens J.C. Woodman B. Mahal A. Spasic-Boscovic O. Samuel D. Kerkerian-Le Goff L. Impaired glutamate uptake in the R6 Huntington’s disease transgenic mice Neurobiol. Dis. 8 5 2001 807 821 11592850
- Liu C.C. Kanekiyo T. Xu H. Bu G. Apolipoprotein E and Alzheimer disease: risk, mechanisms and therapy Nat. Rev. Neurol. 9 2 2013 106 118 23296339 PMC3726719
- Loria F. Vargas J.Y. Bousset L. Syan S. Salles A. Melki R. α-Synuclein transfer between neurons and astrocytes indicates that astrocytes play a role in degradation rather than in spreading Acta Neuropathol. 134 5 2017 789 808 28725967
- Madill M. McDonagh K. Ma J. Vajda A. McLoughlin P. O’Brien T. Amyotrophic lateral sclerosis patient iPSC-derived astrocytes impair autophagy via non-cell autonomous mechanisms Mol. Brain 10 1 2017 22 28610619 PMC5470320
- Mancuso R. Van Den Daele J. Fattorelli N. Leen W. Balusu S. Burton O. Liston A. Sierksma A. Fourne Y. Poovathingal S. Arranz-Mendiguren A. Sala Frigerio C. Claes C. Serneels L. Theys T. Perry H.V. Verfaillie C. Fiers M. De Strooper B. Stem-cell-derived human microglia transplanted in mouse brain to study human disease Nat. Neurosci. 22 2019 2111 2116 31659342 PMC7616913
- McQuade A. Kang Y.J. Hasselmann J. Jairaman A. Sotelo A. Coburn M. Gene expression and functional deficits underlie TREM2-knockout microglia responses in human models of Alzheimer’s disease Nat. Commun. 11 1 2020 5370 33097708 PMC7584603
- Meyer K. Ferraiuolo L. Miranda Cj Likhite S. McElroy S. Renusch S. Direct conversion of patient fibroblasts demonstrates non-cell autonomous toxicity of astrocytes to motor neurons in familial and sporadic ALS Proc. Natl. Acad. Sci. U. S. A. 111 2 2014 829 832 24379375 PMC3896192
- Miklossy J. Doudet D.D. Schwab C. Yu S. McGeer E.G. McGeer P.L. Role of ICAM-1 in persisting inflammation in Parkinson disease and MPTP monkeys Exp. Neurol. 197 2 2006 275 283 16336966
- Moehle M.S. Webber P.J. Tse T. Sukar N. Standaert D.G. DeSilva T.M. LRRK2 inhibition attenuates microglial inflammatory responses J. Neurosci. 32 5 2012 1602 1611 22302802 PMC3532034
- Muffat J. Li Y. Yuan B. Mitalipova M. Omer A. Corcoran S. Efficient derivation of microglia-like cells from human pluripotent stem cells Nat. Med. 22 11 2016 1358 1367 27668937 PMC5101156
- Nalls M.A. Duran R. Lopez G. Kurzawa-Akanbi M. McKeith I.G. Chinnery P.F. A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies JAMA Neurol. 70 6 2013 727 735 23588557 PMC3841974
- Nguyen H.N. Byers B. Cord B. Shcheglovitov A. Byrne J. Gujar P. LRRK2 mutant iPSC-derived DA neurons demonstrate increased susceptibility to oxidative stress Cell Stem Cell 8 3 2011 267 280 21362567 PMC3578553
- Nimmerjahn A. Kirchhoff F. Helmchen F. Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo Science 308 5726 2005 1314 1318 15831717
- Oberheim N.A. Goldman S.A. Nedergaard M. Heterogeneity of astrocytic form and function Methods Mol. Biol. 814 2012 23 45 22144298 PMC3506190
- Ohgidani M. Kato T.A. Setoyama D. Sagata N. Hashimoto R. Shigenobu K. Direct induction of ramified microglia-like cells from human monocytes: dynamic microglial dysfunction in Nasu-Hakola disease Sci. Rep. 4 2014 4957 24825127 PMC4019954
- Panagiotakopoulou V. Ivanyuk D. De Cicco S. Interferon-γ signaling synergizes with LRRK2 in neurons and microglia derived from human induced pluripotent stem cells Nat. Commun. 11 2020 5163 10.1038/s41467-020-18755-4 33057020 PMC7560616 · DOI
- Pandya H. Shen M.J. Ichikawa D.M. Sedlock A.B. Choi Y. Johnson K.R. Differentiation of human and murine induced pluripotent stem cells to microglia-like cells Nat. Neurosci. 20 5 2017 753 759 28253233 PMC5404968
- Panicker L.M. Miller D. Awad O. Bose V. Lun Y. Park T.S. Gaucher iPSC-derived macrophages produce elevated levels of inflammatory mediators and serve as a new platform for therapeutic development Stem Cells 32 9 2014 2338 2349 24801745 PMC4138241
- Patani R. Lewis P.A. Trabzuni D. Puddifoot C.A. Wyllie D.J. Walker R. Investigating the utility of human embryonic stem cell-derived neurons to model ageing and neurodegenerative disease using whole-genome gene expression and splicing analysis J. Neurochem. 122 4 2012 738 751 22681703 PMC3504076
- Perriot S. Mathias A. Perriard G. Canales M. Jonkmans N. Merienne N. Human induced pluripotent stem cell-derived astrocytes are differentially activated by multiple sclerosis-associated cytokines Stem Cell Rep. 11 5 2018 1199 1210 PMC6234919 30409508
- Philips T. Rothstein J.D. Glial cells in amyotrophic lateral sclerosis Exp. Neurol. 262 Pt B 2014 111 120 24859452 PMC4241182
- Piers T.M. Cosker K. Mallach A. Johnson G.T. Guerreiro R. Hardy J. A locked immunometabolic switch underlies TREM2 R47H loss of function in human iPSC-derived microglia FASEB J. 34 2 2020 2436 2450 31907987 PMC7027848
- Pocock J.M. Piers T.M. Modelling microglial function with induced pluripotent stem cells: an update Nat. Rev. Neurosci. 19 8 2018 445 452 29977068
- Price T.N.C. Burke J.F. L.V M A novel human astrocyte cell line (A735) with astrocyte-specific neurotransmitter function In Vitro Cellular & Developmental Biology – Animal 1999 Springer 279 288 10475274
- Puschmann T.B. Zandén C. De Pablo Y. Kirchhoff F. Pekna M. Liu J. Pekny M. Bioactive 3D cell culture system minimizes cellular stress and maintains the in vivo-like morphological complexity of astroglial cells Glia 61 3 2013 432 440 23292921
- Qian K. Huang H. Peterson A. Hu B. Maragakis N.J. Ming G.L. Sporadic ALS astrocytes induce neuronal degeneration in vivo Stem Cell Rep. 8 4 2017 843 855 PMC5390239 28366455
- Ransohoff R.M. A polarizing question: do M1 and M2 microglia exist? Nat. Neurosci. 19 8 2016 987 991 27459405
- Rossi C. Cusimano M. Zambito M. Finardi A. Capotondo A. Garcia-Manteiga J.M. Interleukin 4 modulates microglia homeostasis and attenuates the early slowly progressive phase of amyotrophic lateral sclerosis Cell Death Dis. 9 2 2018 250 29445154 PMC5833860
- Rowland H.A. Hooper N.M. Kellett K.A.B. Modelling sporadic Alzheimer’s disease using induced pluripotent stem cells Neurochem. Res. 43 12 2018 2179 2198 30387070 PMC6267251
- Ryan K.J. White C.C. Patel K. Xu J. Olah M. Replogle J.M. A human microglia-like cellular model for assessing the effects of neurodegenerative disease gene variants Sci. Transl. Med. 9 421 2017 PMC5945290 29263232
- Sabogal-Guáqueta A.M. Marmolejo-Garza A. de Pádua V.P. Eggen B. Boddeke E. Dolga A.M. Microglia alterations in neurodegenerative diseases and their modeling with human induced pluripotent stem cell and other platforms Prog. Neurobiol. 190 2020 101805 32335273
- Salter M.W. Stevens B. Microglia emerge as central players in brain disease Nat. Med. 23 9 2017 1018 1027 28886007
- Sánchez-Danés A. Richaud-Patin Y. Carballo-Carbajal I. Jiménez-Delgado S. Caig C. Mora S. Disease-specific phenotypes in dopamine neurons from human iPS-based models of genetic and sporadic Parkinson’s disease EMBO Mol. Med. 4 5 2012 380 395 22407749 PMC3403296
- Sapp E. Kegel K.B. Aronin N. Hashikawa T. Uchiyama Y. Tohyama K. Early and progressive accumulation of reactive microglia in the Huntington disease brain J. Neuropathol. Exp. Neurol. 60 2 2001 161 172 11273004
- Schon E.A. Przedborski S. Mitochondria: the next (neurode)generation Neuron 70 6 2011 1033 1053 21689593 PMC3407575
- Serio A. Bilican B. Barmada S.J. Ando D.M. Zhao C. Siller R. Astrocyte pathology and the absence of non-cell autonomy in an induced pluripotent stem cell model of TDP-43 proteinopathy Proc. Natl. Acad. Sci. U. S. A. 110 12 2013 4697 4702 23401527 PMC3607024
- Sidransky E. Nalls M.A. Aasly J.O. Aharon-Peretz J. Annesi G. Barbosa E.R. Multicenter analysis of glucocerebrosidase mutations in Parkinson’s disease N. Engl. J. Med. 361 17 2009 1651 1661 19846850 PMC2856322
- Simard A.R. Soulet D. Gowing G. Julien J.P. Rivest S. Bone marrow-derived microglia play a critical role in restricting senile plaque formation in Alzheimer’s disease Neuron 49 4 2006 489 502 16476660
- Simmons D.A. Casale M. Alcon B. Pham N. Narayan N. Lynch G. Ferritin accumulation in dystrophic microglia is an early event in the development of Huntington’s disease Glia 55 10 2007 1074 1084 17551926
- Sloan S.A. Barres B.A. Mechanisms of astrocyte development and their contributions to neurodevelopmental disorders Curr. Opin. Neurobiol. 27 2014 75 81 24694749 PMC4433289
- Smethurst P. Risse E. Tyzack G.E. Mitchell J.S. Taha D.M. Chen Y.R. Distinct responses of neurons and astrocytes to TDP-43 proteinopathy in amyotrophic lateral sclerosis Brain 143 2 2020 430 440 32040555 PMC7009461
- Soreq L. Rose J. Soreq E. Hardy J. Trabzuni D. Cookson M.R. Major shifts in glial regional identity are a transcriptional hallmark of human brain aging Cell Rep. 18 2 2017 557 570 28076797 PMC5263238
- Svoboda D.S. Barrasa M.I. Shu J. Rietjens R. Zhang S. Mitalipova M. Human iPSC-derived microglia assume a primary microglia-like state after transplantation into the neonatal mouse brain Proc. Natl. Acad. Sci. U. S. A. 116 50 2019 25293 25303 31772018 PMC6911218
- Taga A. Dastgheyb R. Habela C. Joseph J. Richard J.P. Gross S.K. Role of human-induced pluripotent stem cell-derived spinal cord astrocytes in the functional maturation of motor neurons in a multielectrode array system Stem Cells Transl. Med. 8 12 2019 1272 1285 31631575 PMC6877769
- Takahashi K. Yamanaka S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors Cell 126 4 2006 663 676 16904174
- Takahashi K. Tanabe K. Ohnuki M. Narita M. Ichisaka T. Tomoda K. Induction of pluripotent stem cells from adult human fibroblasts by defined factors Cell 131 5 2007 861 872 18035408
- Tarassishin L. Suh H.S. Lee S.C. LPS and IL-1 differentially activate mouse and human astrocytes: role of CD14 Glia 62 6 2014 999 1013 24659539 PMC4015139
- Thelin E.P. Hall C.E. Tyzack G.E. Frostell A. Giorgi-Coll S. Alam A. Delineating astrocytic cytokine responses in a human stem cell model of neural trauma J. Neurotrauma 37 1 2020 93 105 31452443 PMC6921298
- Tien A.C. Tsai H.H. Molofsky A.V. McMahon M. Foo L.C. Kaul A. Regulated temporal-spatial astrocyte precursor cell proliferation involves BRAF signalling in mammalian spinal cord Development 139 14 2012 2477 2487 22675209 PMC3383225
- Tiryaki V.M. Ayres V.M. Ahmed I. Shreiber D.I. Differentiation of reactive-like astrocytes cultured on nanofibrillar and comparative culture surfaces Nanomedicine 10 4 2015 529 545 24985141
- Tong X. Ao Y. Faas G.C. Nwaobi S.E. Xu J. Haustein M.D. Astrocyte Kir4.1 ion channel deficits contribute to neuronal dysfunction in Huntington’s disease model mice Nat. Neurosci. 17 5 2014 694 703 24686787 PMC4064471
- Tsai H.H. Li H. Fuentealba L.C. Molofsky A.V. Taveira-Marques R. Zhuang H. Regional astrocyte allocation regulates CNS synaptogenesis and repair Science 337 6092 2012 358 362 22745251 PMC4059181
- Tsuchiya S. Yamabe M. Yamaguchi Y. Kobayashi Y. Konno T. Tada K. Establishment and characterization of a human acute monocytic leukemia cell line (THP-1) Int. J. Cancer 1980 171 176 6970727
- Tyzack G. Lakatos A. Patani R. Human stem cell-derived astrocytes: specification and relevance for neurological disorders Curr. Stem Cell Rep. 2 2016 236 247 27547709 PMC4972864
- Tyzack G.E. Hall C.E. Sibley C.R. Cymes T. Forostyak S. Carlino G. A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models Nat. Commun. 8 1 2017 1164 29079839 PMC5660125
- Utz S.G. See P. Mildenberger W. Thion M.S. Silvin A. Lutz M. Early fate defines microglia and non-parenchymal brain macrophage development Cell 181 3 2020 557 573 e18 32259484
- Vasile F. Dossi E. Rouach N. Human astrocytes: structure and functions in the healthy brain Brain Struct. Funct. 222 5 2017 2017 2029 28280934 PMC5504258
- Veeraraghavalu K. Zhang C. Zhang X. Tanzi R.E. Sisodia S.S. Age-dependent, non-cell-autonomous deposition of amyloid from synthesis of β-amyloid by cells other than excitatory neurons J. Neurosci. 34 10 2014 3668 3673 24599465 PMC3942582
- Wakabayashi K. Hayashi S. Yoshimoto M. Kudo H. Takahashi H. NACP/alpha-synuclein-positive filamentous inclusions in astrocytes and oligodendrocytes of Parkinson’s disease brains Acta Neuropathol. 99 1 2000 14 20 10651022
- Xu M. Zhang L. Liu G. Jiang N. Zhou W. Zhang Y. Pathological changes in Alzheimer’s disease analyzed using induced pluripotent stem cell-derived human microglia-like cells J. Alzheimers Dis. 67 1 2019 357 368 30562902
- Watson P.M.D. Kavanagh E. Allenby G. Vassey M. Bioengineered 3D Glial Cell Culture Systems and Applications for Neurodegeneration and Neuroinflammation SLAS Discovery 22 5 2017 583 601 28346104
- Xu R. Li X. Boreland A.J. Posyton A. Kwan K. Hart R.P. Human iPSC-derived mature microglia retain their identity and functionally integrate in the chimeric mouse brain Nat. Commun. 11 1 2020 1577 32221280 PMC7101330
- Zhang Y. Sloan S.A. Clarke L.E. Caneda C. Plaza C.A. Blumenthal P.D. Purification and characterization of progenitor and mature human astrocytes reveals transcriptional and functional differences with mouse Neuron 89 1 2016 37 53 26687838 PMC4707064
- Zhang L. Xu M. Ren Q. Liu G. Meng S. Xiahou K. Human-induced pluripotent stem cell-derived neural cells from Alzheimer’s disease patients exhibited different susceptibility to oxidative stress Stem Cells Dev. 29 22 2020 1444 1456 32988331
- Zhao J. Davis M.D. Martens Y.A. Shinohara M. Graff-Radford N.R. Younkin S.G. APOE ε4/ε4 diminishes neurotrophic function of human iPSC-derived astrocytes Hum. Mol. Genet. 26 14 2017 2690 2700 28444230 PMC5886091
- Zhao C. Devlin A.C. Chouhan A.K. Selvaraj B.T. Stavrou M. Burr K. Mutant C9orf72 human iPSC-derived astrocytes cause non-cell autonomous motor neuron pathophysiology Glia 68 5 2020 1046 1064 31841614 PMC7078830
- Ziff O.J. Patani R. Harnessing cellular aging in human stem cell models of amyotrophic lateral sclerosis Aging Cell 18 1 2019 e12862 PMC6351881 30565851
- Zwilling D. Huang S.Y. Sathyasaikumar K.V. Notarangelo F.M. Guidetti P. Wu H.Q. Kynurenine 3-monooxygenase inhibition in blood ameliorates neurodegeneration Cell 145 6 2011 863 874 21640374 PMC3118409
Cited by
Sorted by citations
Microglia in neurodegenerative diseases: mechanism and potential therapeutic targets
Gao, C., Jiang, J., Tan, Y., & Chen, S. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01588-0 · Cited by 1,616 · see citing works
Human iPSC-derived glia models for the study of neuroinflammation
Stöberl, N., Maguire, E., Salis, E., Shaw, B., & Hall-Roberts, H. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02919-2 · Cited by 71 · see citing works
Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy
Bougnères, P., & Le Stunff, C. (2025) · Genes · doi:10.3390/genes16050590 · Cited by 11 · see citing works
- Authors
- Franklin, H., Clarke, B. E., & Patani, R.
- Affiliations
- The Francis Crick Institute (GB)
- Corresponding author
- Patani, Rickie
- Venue
- Progress in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2021-05
- Volume
- 200
- Pages
- 101973
- ISSN
- 0301-0082 (ISSN-L)
- PMC
- PMC8052192
- OpenAlex
- W3112409504
- Cited by
- 66
- References
- 41
- Citations by year
- 2026: 10 · 2025: 16 · 2024: 12 · 2023: 10 · 2022: 11 · 2021: 7
- FWCI
- 0.70
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Progress in Neurobiology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Figshare (submittedVersion, cc-by)
- Funders
- Medical Research Council
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Keywords
- astrocytes, microglia, neurodegenerative diseases, human in vitro models, disease modeling, astrocyte dysfunction, microglial dysfunction, CNS homeostasis, drug screening, disease phenotypes
- MeSH terms
- Animals, Astrocytes, Humans, Microglia, Neurodegenerative Diseases
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review