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Patient-Specific iPSC-Derived Astrocytes Contribute to Non-Cell-Autonomous Neurodegeneration in Parkinson's Disease
Open accessAbstract
Parkinson's disease (PD) is associated with the degeneration of ventral midbrain dopaminergic neurons (vmDAns) and the accumulation of toxic α-synuclein. A non-cell-autonomous contribution, in particular of astrocytes, during PD pathogenesis has been suggested by observational studies, but remains to be experimentally tested. Here, we generated induced pluripotent stem cell-derived astrocytes and neurons from familial mutant LRRK2 G2019S PD patients and healthy individuals. Upon co-culture on top of PD astrocytes, control vmDAns displayed morphological signs of neurodegeneration and abnormal, astrocyte-derived α-synuclein accumulation. Conversely, control astrocytes partially prevented the appearance of disease-related phenotypes in PD vmDAns. We additionally identified dysfunctional chaperone-mediated autophagy (CMA), impaired macroautophagy, and progressive α-synuclein accumulation in PD astrocytes. Finally, chemical enhancement of CMA protected PD astrocytes and vmDAns via the clearance of α-synuclein accumulation. Our findings unveil a crucial non-cell-autonomous contribution of astrocytes during PD pathogenesis, and open the path to exploring novel therapeutic strategies aimed at blocking the pathogenic cross talk between neurons and glial cells.
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“in contrast to neuron-specific cell autonomous mechanisms that affect individual DA neurons within the SNc, non-cell autonomous mechanisms can cause dysfunction across the entire SNc, thereby leading to rapid DA neurodegeneration”
From Mitochondrial DNA Damage in Substantia Nigra Pars Compacta Astrocytes Exacerbates Dopaminergic Neuron Loss in a 6-Hydroxydopamine Mouse Model of Parkinsonism (2026) · cites this paper as di Domenico et al. 2019
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“Interestingly, astrocytes generated from hiPSC derived from fibroblasts obtained from patients with CNS diseases (usually with a genetic mutation causative of disease or a risk polymorphism) show pathological phenotypes, including dysregulation of lipid metabolism11, alteration in the contents of the extracellular vesicles released by astrocytes80, reduced autophagy81, or altered STAT3 signaling82”
From Reactive astrocyte nomenclature, definitions, and future directions (2021) · cites this paper as [81]
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Vos, T., Barber, R. M., Bell, B., Bertozzi-Villa, A., Biryukov, S., Bolliger, I., Charlson, F., Davis, A., Degenhardt, L., Dicker, D., et al. (2015) · The Lancet · doi:10.1016/s0140-6736(15)60692-4 · Cited by 6,414
Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling
Chambers, S. M., Fasano, C. A., Papapetrou, E. P., Tomishima, M., Sadelain, M., & Studer, L. (2009) · Nature Biotechnology · doi:10.1038/nbt.1529 · Cited by 3,620
Impaired Degradation of Mutant α-Synuclein by Chaperone-Mediated Autophagy
Cuervo, A. M., Stefanis, L., Fredenburg, R., Lansbury, P. T., & Sulzer, D. (2004) · Science · doi:10.1126/science.1101738 · Cited by 2,024 · cited 2×
“…in a-syn turnover in these cells. a-syn has previously been shown to undergo degradation both by the ubiquitin/proteasome system and by autophagy (Cuervo et al., 2004; Webb et al., 2003); therefore a-syn flux in the presence of lysosomal and proteasome inhibitors (leupeptin and lactacystin,…”
BackgroundSelf-citationKriks, S., Shim, J., Piao, J., Ganat, Y. M., Wakeman, D. R., Xie, Z., Carrillo‐Reid, L., Auyeung, G., Antonacci, C. L., Buch, A., et al. (2011) · Nature · doi:10.1038/nature10648 · Cited by 1,951
α-Synuclein Is Degraded by Both Autophagy and the Proteasome
Webb, J. L., Ravikumar, B., Atkins, J., Skepper, J. N., & Rubinsztein, D. C. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300227200 · Cited by 1,429
Lee, H.-J., Suk, J.-E., Patrick, C., Bae, E.-J., Cho, J.-H., Rho, S., Hwang, D., Masliah, E., & Lee, S.-J. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.081125 · Cited by 877
α-Synuclein impairs macroautophagy: implications for Parkinson’s disease
Winslow, A. R., Chen, C.-W., Corrochano, S., Acevedo-Arozena, A., Gordon, D. E., Peden, A. A., Lichtenberg, M., Menzies, F. M., Ravikumar, B., Imarisio, S., et al. (2010) · Journal of Cell Biology · doi:10.1083/jcb.201003122 · Cited by 825 · cited 2×
“Degradation of a-syn has been shown to occur by both proteasome and autophagic pathways, and conversely, high levels of a-syn have been demonstrated to be toxic for both systems (Tanaka et al., 2001; Webb et al., 2003; Winslow et al., 2010).”
BackgroundA common LRRK2 mutation in idiopathic Parkinson's disease
Gilks, W. P., Abou-Sleiman, P. M., Gandhi, S., Jain, S., Singleton, A., Lees, A. J., Shaw, K., Bhatia, K. P., Bonifati, V., Quinn, N. P., et al. (2005) · The Lancet · doi:10.1016/s0140-6736(05)17830-1 · Cited by 774
LRRK2 Mutant iPSC-Derived DA Neurons Demonstrate Increased Susceptibility to Oxidative Stress
Nguyen, H. N., Byers, B., Cord, B. J., Shcheglovitov, A., Byrne, J., Gujar, P., Kee, K., Schüle, B., Dolmetsch, R. E., Langston, J. W., et al. (2011) · Cell stem cell · doi:10.1016/j.stem.2011.01.013 · Cited by 768
A novel TALE nuclease scaffold enables high genome editing activity in combination with low toxicity
Mussolino, C., Morbitzer, R., Lütge, F., Dannemann, N., Lahaye, T., & Cathomen, T. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr597 · Cited by 714
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Items 301–373 of 373
Convergent transcriptomic signature in iPSC-dopaminergic neurons of hereditary Parkinson’s disease
Kopylova, I. V., Ivanov, A. B., Eidelman, L. R., Zaitseva, E. N., Kulikova, E. D., Grekhnev, D. A., Bogomazova, A. N., Vigont, V. A., Kaznacheyeva, E. V., Lagarkova, M. A., et al. (2026) · Life Science Alliance · doi:10.26508/lsa.202503551 · Cited by 1
Li, Y., Li, Q., Wang, Y., Wang, X., Di, G., Niu, M., Xu, Z., & Huang, Y. (2026) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-026-01218-7 · Cited by 1
Organoids: the third dimension of human brain development and disease
Kouroupi, G., Prodromidou, K., Papastefanaki, F., Taoufik, E., & Matsas, R. (2021) · The International Journal of Developmental Biology · doi:10.1387/ijdb.210158gk · Cited by 1
Grochowska, M. M., Ferraro, F., Mascaro, A. C., Natale, D., Winkelaar, A. B., Boumeester, V., Breedveld, G. J., Bonifati, V., & Mandemakers, W. J. (2023) · Disease Models & Mechanisms · doi:10.1242/dmm.049980 · Cited by 1
Stem cell engineering approaches for investigating glial cues in central nervous system disorders
Vardhan, S., Jordan, T., & Sakiyama‐Elbert, S. E. (2024) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2024.103131 · Cited by 1
Sam, R., Han, T., Sidransky, E., & Chen, Y. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823884-4.00011-0 · Cited by 1
Can Leucine‐Rich Repeat Kinase 2 Inhibition Benefit GBA–Parkinson's Disease?
Bonet-Ponce, L., & Cookson, M. R. (2020) · Movement Disorders · doi:10.1002/mds.28029 · Cited by 1
LRP10 as a novel α-synuclein regulator in Lewy body diseasesPreprint
Mascaro, A. C., Grochowska, M. M., Boumeester, V., Dits, N. F. J., Bilgiҫ, E. N., Breedveld, G. J., Vergouw, L. J. M., de Jong, F. J., van Royen, M. E., Bonifati, V., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.12.540510 · Cited by 1
Astrocyte-specific secretome profiling reveals its correlation with neurological disordersPreprint
Liu, J., Gao, J., Guo, L., Ma, G., Guan, M., Xia, C., He, J., Yang, Y., Wu, Y., Xu, J., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.21.624658 · Cited by 1
Testa, V., Montero-Muñoz, J., Baruffi, V., Alzeer, M., Mularoni, L., Fernández‐Carasa, I., Simmini, G., Comellas-Comaposada, N., Ake, F. A., Richaud, Y., et al. (2025) · SSRN Electronic Journal · doi:10.1101/2025.08.01.668099 · Cited by 1
Self-citationLRRK2 I1371V Impairs Astrocytic Glucose Metabolism and Triggers Multi-Organellar Dysfunction in PDPreprint
Banerjee, R., Santhoshkumar, R., Holla, V. V., Kamble, N. L., Yadav, R., Pal, P. K., & Datta, I. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.19.700314 · Cited by 1
Jang, W. E., Srivastava, U., Brandelli, A. D., Kumar, P., Espinosa‐García, C., Kour, D., Kumari, R., & Rangaraju, S. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.21.700735 · Cited by 3
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Kibria, A. S. M. G., Nawaz, S., DİKMEN, T., AKKAYA, Ö. Ö., & Yağcı, A. (2020) · Kocatepe Veterinary Journal · doi:10.30607/kvj.751139
Gruschus, J. M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85707-9.00004-6
Sonninen, T.-M., Plotnikova, L. M., Laham-Karam, N., Goldsteins, G., Koıstınaho, J., & Lehtonen, Š. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85764-2.00009-0
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Ofir, R. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85764-2.00001-6
Astrocytes in neurodegenerative disorders
Jacquet, A. D. R. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823884-4.00007-9
Human induced pluripotent stem cell–derived astrocytes progenitors as discovery platforms
Taga, A., & Maragakis, N. J. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85545-7.00005-3
Vahsen, B. F. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8894
Molecular and clinical determinants of pathogenic protein aggregation
de Mattos, E. P. (2022) · University of Groningen research database (University of Groningen / Centre for Information Technology) · doi:10.33612/diss.220760500
Oun, A. (2022) · doi:10.33612/diss.253651629
Grochowska, M. M., Ferraro, F., Mascaro, A. C., Natale, D., Winkelaar, A. B., Boumeester, V., Breedveld, G. J., Bonifati, V., & Mandemakers, W. J. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.08.515628
Sun, X., Badachhape, A., Chin, J., Annapragada, A., & Tanifum, E. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.25.550555
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Yang, M., You, D., Liu, G., Lu, Y., Yang, G., O’Brien, T., Henshall, D. C., Hardiman, O. M., Liu, M., & Shen, S. (2023) · Research Square · doi:10.21203/rs.3.rs-3369126/v1
Changes in neural progenitor lineage composition during astrocytic differentiation of human iPSCsPreprint
Li, Z., Cardo, L. F., Rokicki, M., Monzón‐Sandoval, J., Volpato, V., Wessely, F., Webber, C., & Li, M. (2024) · eLife · doi:10.7554/elife.96423 · Cited by 2
Differential growth and transcriptomic profile of stem cell-derived midbrain astrocytesPreprint
Li, Z., Cardo, L. F., Rokicki, M., Monzón‐Sandoval, J., Volpato, V., Wessely, F., Webber, C., & Li, M. (2024) · eLife · doi:10.7554/elife.96423.1 · Cited by 2
Wolters, E. C. (2025) · Cambridge University Press eBooks · doi:10.1017/9781108989855.013
Qiu, B., & Caiazzo, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.13.648609
Changes in neural progenitor lineage constituent during astrocytic differentiation of human iPSCsPreprint
Li, Z., Cardo, L. F., Rokicki, M., Monzón‐Sandoval, J., Volpato, V., Wessely, F., Webber, C., & Li, M. (2025) · eLife · doi:10.7554/elife.96423.2
Low-frequency genetic variants in GAK enhance Golgi function and protect against Parkinson’s diseasePreprint
Calatayud, C., Fernández‐Carasa, I., Spataro, N., Mussolino, C., Richaud‐Patín, Y., Faella, A., Fernández‐Santiago, R., Ezquerra, M., Courtin, T., Bandrés‐Ciga, S., et al. (2025) · medRxiv · doi:10.1101/2025.08.13.25333123
Self-citationBlumenthal, Y., Imamura, K., & Inoue, H. (2025) · Current human cell research and applications · doi:10.1007/978-981-95-0587-6_10
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Wagener, A., Mayeen, N. F., Müller, S. A., Tschirner, S. K., Nuscher, B., Mencke, P., Lichtenthaler, S. F., Boussaad, I., Krüger, R., & Burbulla, L. F. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.02.685006
Roy, I., Fiorini, M., Thomas, R. A., Ambriz, G. J., Farhan, S. M. K., Piscopo, V. E. C., & Durcan, T. M. (2026) · BMC Genomic Data · doi:10.1186/s12863-026-01462-2
Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329492
Vicente-Acosta, A., Giménez-Cassina, A., Díaz‐Nido, J., & Loría, F. (2022) · Figshare · doi:10.6084/m9.figshare.19588803
Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329513
Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329501
Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329528
Supakul, S., Murakami, R., Oyama, C., Shindo, T., Hatakeyama, Y., Itsuno, M., Bannai, H., Shibata, S., Maeda, S., & Okano, H. (2024) · Figshare · doi:10.6084/m9.figshare.26686686
Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329489
Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329525
Supakul, S., Murakami, R., Oyama, C., Shindo, T., Hatakeyama, Y., Itsuno, M., Bannai, H., Shibata, S., Maeda, S., & Okano, H. (2024) · Figshare · doi:10.6084/m9.figshare.26686680
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Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329531
Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329516
Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329498
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Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329522
Supakul, S., Murakami, R., Oyama, C., Shindo, T., Hatakeyama, Y., Itsuno, M., Bannai, H., Shibata, S., Maeda, S., & Okano, H. (2024) · Figshare · doi:10.6084/m9.figshare.26686683
Lee, J. H., Han, J.-H., Joe, E., & Jou, I. (2021) · Figshare · doi:10.6084/m9.figshare.14921111
Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329519
Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329510
Supakul, S., Murakami, R., Oyama, C., Shindo, T., Hatakeyama, Y., Itsuno, M., Bannai, H., Shibata, S., Maeda, S., & Okano, H. (2024) · Figshare · doi:10.6084/m9.figshare.26686677
Bowles, K. R., Pugh, D. A., Liu, Y., Patel, T., Renton, A. E., Bandrés‐Ciga, S., Gan‐Or, Z., Heutink, P., Siitonen, A., Bertelsen, S. E., et al. (2022) · Figshare · doi:10.6084/m9.figshare.20329495
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Novosadova, E. V., & Grivennikov, I. A. (2025) · Neurochemical Journal · doi:10.1134/s1819712425700692
Tang, X., Cui, H., & Cui, H. (2026) · Biofabrication · doi:10.1088/1758-5090/ae4895
Interaction entre autophagie et exosomes au niveau synaptique dans la maladie de Parkinson
Sanchez-Mirasierra, I. (2023) · theses.fr (ABES) · doi:10.70675/7104d6d5z945ez494eza917zda9e6be1eea6
Poulot-Becq-Giraudon, Y. (2024) · theses.fr (ABES) · doi:10.70675/0d7a8b92z8393z4d76z82a8z87efe0790346
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Zolin, A., Weber, S. A., Xie, Y. X., & Burré, J. (2026) · Molecular Neurodegeneration Advances · doi:10.1186/s44477-026-00038-9
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Datta, I., & Sahu, D. D. (2026) · Advances in immunology · doi:10.1016/bs.ai.2026.04.005
Hastings, N., Rahman, S. M. J., Kuan, W., Alfaidi, M., Fox, S., Erkamp, N. A., Andrzejewska, E., Whitehead, M., Zakirov, A., Unwin, R. D., et al. (2026) · Experimental Neurology · doi:10.1016/j.expneurol.2026.115897
Mutti, V., Bono, F., Tomasoni, Z., Fadel, D., Gnutti, C., Sbrini, G., Gaudenzi, C., Salvi, V., Bosisio, D., Russo, I., et al. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70510
Written in the Stars: Astrocyte Biology From Evolution to Disease
Falcone, C., Arckens, L., Baiula, M., Bedini, A., Bocchi, R., Broadhead, M. J., Caprini, M., Cavaliere, F., Cesca, F., Chowdhury, H. H., et al. (2026) · Acta Physiologica · doi:10.1111/apha.70289
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Bach, D., & Nguyen, T. L. (2026) · Cell Communication and Signaling · doi:10.1186/s12964-026-03197-0
Viljoen, S. J., Chaves, J. C. S., Peall, I. W., White, A. R., & Oikari, L. E. (2026) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2026.126168
Vázquez-Jiménez, A., Marqués, M. M., Sánchez-López, J. M., Agulla, J., Lapresa, R., Trigal, M., Fernández-Alonso, R., Merino, G., Fernández, A., Consiglio, A., et al. (2026) · Antioxidants · doi:10.3390/antiox15091151
Self-citationAstrocytes in Neurodegeneration: Spatial States, Crosstalk, and Emerging Therapies
Steger, L., Rothhammer, V., & Zunke, F. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-06142-x
Burdman, G., Hanna, M., Yndart, A., Vashist, A., & Lakshmana, M. K. (2026) · Cells · doi:10.3390/cells15191768
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Kaushik, S., & Cuervo, A. M. (2026) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-026-01023-6
Self-citationAl-Kuraishy, H. M., Naji, M., Hasan, R. R. A., Eliwa, D., & Batiha, G. E. (2026) · Neurodegenerative Disease Management · doi:10.1080/17582024.2026.2744191
Liu, Y., Halliday, G. M., & Fu, Y. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.10.06.757209
Metadata
- Authors
- 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., Soriano, J., Ferrer, I., Tolosa, E., Zorzano, A., Cuervo, A. M., Raya, A., & Consiglio, A.
- Affiliations
- Bellvitge University Hospital (ES)
- Institute for Research in Biomedicine (ES)
- Centro Nacional de Análisis Genómico (ES)
- Universitat de Barcelona (ES)
- Biomedical Research Networking Center on Neurodegenerative Diseases (ES)
- Corresponding author
- Consiglio, Antonella
- ORCID
- Venue
- Stem Cell Reports
- Publisher
- Elsevier BV
- Published
- 2019-02
- Volume
- 12
- Issue
- 2
- Pages
- 213-229
- ISSN
- 2213-6711 (ISSN-L)
- PMC
- PMC6372974
- OpenAlex
- W2911036111
- Cited by
- 372
- References
- 49
- Citations by year
- 2026: 32 · 2025: 38 · 2024: 44 · 2023: 45 · 2022: 65 · 2021: 69 · 2020: 53 · 2019: 26
- FWCI
- 36.04
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Stem Cell Reports (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona) (publishedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Institutional Research Information System (Università degli Studi di Brescia) (submittedVersion)
- Repositori digital de la UPF (Universitat Pompeu Fabra) (submittedVersion, cc-by)
- Funders
- Agència de Gestió d'Ajuts Universitaris i de Recerca (2014-SGR-878, 2017-SGR-899)
- Ministerio de Educación, Cultura y Deporte (BES-2014-069603, FPU12/03332)
- Ministerio de Economía y Competitividad (BFU2016-80870-P, FIS2016-78507-C2-2-P, SAF2015-69706-R)
- Instituto de Salud Carlos III
- European Regional Development Fund (RD16/0011/0024)
- Generalitat de Catalunya
- European Research Council (2012-StG-311736-PD-HUMMODEL)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- Parkinson's disease, astrocytes, non-cell autonomous neurodegeneration, induced pluripotent stem cell-derived astrocytes, dopaminergic neurons, ventral midbrain, LRRK2 G2019S, familial Parkinson's disease, alpha-synuclein accumulation, chaperone-mediated autophagy, macroautophagy, neuron-glia interactions
- MeSH terms
- Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Astrocytes, Autophagy, Cell Differentiation, Cells, Cultured, Humans, Mesencephalon, Neuroglia, Parkinson Disease, Phenotype, Coculture Techniques, alpha-Synuclein, Induced Pluripotent Stem Cells, Dopaminergic Neurons
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 ›
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