Non-Cell-Autonomous Effect of Human SOD1G37R Astrocytes on Motor Neurons Derived from Human Embryonic Stem Cells
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Conditioned media from SOD1-G93A astrocytes is toxic to motor neurons.
“Consistent with previous studies [23–26], we validated that the conditioned media from these cultures is toxic to motor neurons.”
From Distinct repertoires of microRNAs present in mouse astrocytes compared to astrocyte-secreted exosomes (2017) · cites this paper as [24]
Astrocytes seem to secrete toxic factor(s) that are detrimental to motor neuron health.
“Moreover, astrocytes seem to secrete toxic factor(s) that are detrimental to motor neuron health [23–26].”
From Distinct repertoires of microRNAs present in mouse astrocytes compared to astrocyte-secreted exosomes (2017) · cites this paper as [24]
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Rosen, D. R., Siddique, T., Patterson, D., Figlewicz, D. A., Sapp, P., Hentati, A., Donaldson, D., Goto, J., O'Regan, J. P., Deng, H.-X., et al. (1993) · Nature · doi:10.1038/362059a0 · Cited by 7,062 · see citing works
Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons
Nagai, M., Re, D. B., Nagata, T., Chalazonitis, A., Jessell, T. M., Wichterle, H., & Przedborski, S. (2007) · Nature Neuroscience · doi:10.1038/nn1876 · Cited by 1,220 · see citing works
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
Design, power, and interpretation of studies in the standard murine model of ALS
Scott, S., Kranz, J. E., Cole, J., Lincecum, J. M., Thompson, K., Kelly, N., Bostrom, A., Theodoss, J., Al‐Nakhala, B. M., Vieira, F. G., et al. (2008) · Amyotrophic Lateral Sclerosis · doi:10.1080/17482960701856300 · Cited by 504 · see citing works
Urushitani, M., Sik, A., Sakurai, T., Nukina, N., Takahashi, R., & Julien, J.-P. (2006) · Nature Neuroscience · doi:10.1038/nn1603 · Cited by 419 · see citing works
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Research works printed but not linked: 16
- [1]1. Almer, G. ∙ Vukosavic, S. ∙ Romero, N. ... Inducible nitric oxide synthase up-regulation in a transgenic mouse model of familial amyotrophic lateral sclerosis J. Neurochem. 1999; 72:2415-2425 Crossref Scopus (204) PubMed Google Scholar
- [2]2. Anneser, J. Molecular basis of treatment in motor neurone disease Neurol. Sci. 2000; 21:S913-S918 Crossref PubMed Google Scholar
- [3]3. Arce, V. ∙ Garces, A. ∙ de Bovis, B. ... Cardiotrophin-1 requires LIFRbeta to promote survival of mouse motoneurons purified by a novel technique J. Neurosci. Res. 1999; 55:119-126 Crossref Scopus (134) PubMed Google Scholar
- [4]4. Barbeito, L.H. ∙ Pehar, M. ∙ Cassina, P. ... A role for astrocytes in motor neuron loss in amyotrophic lateral sclerosis Brain Res. Brain Res. Rev. 2004; 47:263-274 Crossref Scopus (265) PubMed Google Scholar
- [5]5. Barber, S.C. ∙ Mead, R.J. ∙ Shaw, P.J. Oxidative stress in ALS: a mechanism of neurodegeneration and a therapeutic target Biochim. Biophys. Acta. 2006; 1762:1051-1067 Crossref Scopus (377) PubMed Google Scholar
- [6]6. Boillee, S. ∙ Vande Velde, C. ∙ Cleveland, D.W. ALS: a disease of motor neurons and their nonneuronal neighbors Neuron. 2006; 52:39-59 Full Text Full Text (PDF) Scopus (1200) PubMed Google Scholar
- [7]7. Clement, A.M. ∙ Nguyen, M.D. ∙ Roberts, E.A. ... Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice Science. 2003; 302:113-117 Crossref Scopus (945) PubMed Google Scholar
- [8]8. Consiglio, A. ∙ Gritti, A. ∙ Dolcetta, D. ... Robust in vivo gene transfer into adult mammalian neural stem cells by lentiviral vectors Proc. Natl. Acad. Sci. USA. 2004; 101:14835-14840 Crossref Scopus (153) PubMed Google Scholar
- [9]9. Deng, H.X. ∙ Hentati, A. ∙ Tainer, J.A. ... Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase Science. 1993; 261:1047-1051 Crossref Scopus (1417) PubMed Google Scholar
- [10]10. DiBernardo, A.B. ∙ Cudkowicz, M.E. Translating preclinical insights into effective human trials in ALS Biochim. Biophys. Acta. 2006; 1762:1139-1149 Crossref Scopus (35) PubMed Google Scholar
- [11]11. Di Giorgio, F.P. ∙ Carrasco, M.A. ∙ Siao, M.C. ... Non-cell autonomous effect of glia on motor neurons in an embryonic stem cell-based ALS model Nat. Neurosci. 2007; 10:608-614 Crossref Scopus (680) PubMed Google Scholar
- [12]12. Di Giorgio, F.P. ∙ Boulting, G.L. ∙ Bobrowicz, S. ... Human-embryonic-stem-cell-derived motor neurons are sensitive to the toxic effect of glial cells carrying an ALS-causing mutation Cell Stem Cell. 2008; 3:637-648 this issue Full Text Full Text (PDF) Scopus (393) PubMed Google Scholar
- [13]13. Doble, A. The pharmacology and mechanism of action of riluzole Neurology. 1996; 47:S233-S241 Crossref PubMed Google Scholar
- [14]14. Grisham, M.B. ∙ Johnson, G.G. ∙ Lancaster, Jr., J.R. Quantitation of nitrate and nitrite in extracellular fluids Methods Enzymol. 1996; 268:237-246 Crossref PubMed Google Scholar
- [15]15. Harraz, M.M. ∙ Marden, J.J. ∙ Zhou, W. ... SOD1 mutations disrupt redox-sensitive Rac regulation of NADPH oxidase in a familial ALS model J. Clin. Invest. 2008; 118:659-670 PubMed Google Scholar
- [16]16. Henderson, C.E. ∙ Bloch-Gallego, E. ∙ Camu, W. ... Motoneuron survival factors: biological roles and therapeutic potential Neuromuscul. Disord. 1993; 3:455-458
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- Authors
- Marchetto, M. C. N., Muotri, A. R., Mu, Y., Smith, A. M., Cezar, G. G., & Gage, F. H.
- Venue
- Cell Stem Cell
- Publisher
- Elsevier BV
- Published
- 2008-12
- Volume
- 3
- Issue
- 6
- Pages
- 649-657
- ISSN
- 1934-5909
- Cited by
- 424
- References
- 5
- Language
- en
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1725 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
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