dc.contributor.author | Santos, Renata | |
dc.contributor.author | Vadodaria, Krishna C. | |
dc.contributor.author | Jaeger, Baptiste N. | |
dc.contributor.author | Mei, Arianna | |
dc.contributor.author | Lefcochilos-Fogelquist, Sabrina | |
dc.contributor.author | Mendes, Ana P. D. | |
dc.contributor.author | Erikson, Galina | |
dc.contributor.author | Shokhirev, Maxim | |
dc.contributor.author | Randolph-Moore, Lynne | |
dc.contributor.author | Fredlender, Callie | |
dc.contributor.author | Dave, Sonia | |
dc.contributor.author | Oefner, Ruth | |
dc.contributor.author | Fitzpatrick, Conor | |
dc.contributor.author | Pena, Monique | |
dc.contributor.author | Barron, Jerika J. | |
dc.contributor.author | Ku, Manching | |
dc.contributor.author | Denli, Ahmet M. | |
dc.contributor.author | Kerman, Bilal Ersen | |
dc.contributor.author | Charnay, Patrick | |
dc.contributor.author | Kelsoe, John R. | |
dc.contributor.author | Marchetto, Maria C. | |
dc.contributor.author | Gage, Fred H. | |
dc.date.accessioned | 10.07.201910:49:13 | |
dc.date.accessioned | 2019-07-10T20:03:08Z | |
dc.date.available | 10.07.201910:49:13 | |
dc.date.available | 2019-07-10T20:03:08Z | |
dc.date.issued | 2017 | en_US |
dc.identifier.citation | Santos, R., Vadodaria, K. C., Jaeger, B. N., Mei, A., Lefcochilos-Fogelquist, S., Mendes, Ana P. D. ... Gage, F. H. (2017). Stem Cell Reports, 8(6), 1757-1769. https://dx.doi.org/10.1016/j.stemcr.2017.05.011 | en_US |
dc.identifier.issn | 2213-6711 | |
dc.identifier.uri | https://dx.doi.org/10.1016/j.stemcr.2017.05.011 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12511/3813 | |
dc.description | WOS: 000402964700027 | en_US |
dc.description | PubMed ID: 28591655 | en_US |
dc.description.abstract | Astrocyte dysfunction and neuroinflammation are detrimental features in multiple pathologies of the CNS. Therefore, the development of methods that produce functional human astrocytes represents an advance in the study of neurological diseases. Here we report an efficient method for inflammation-responsive astrocyte generation from induced pluripotent stem cells (iPSCs) and embryonic stem cells. This protocol uses an intermediate glial progenitor stage and generates functional astrocytes that show levels of glutamate uptake and calcium activation comparable with those observed in human primary astrocytes. Stimulation of stem cell-derived astrocytes with interleukin-1 beta or tumor necrosis factor a elicits a strong and rapid pro-inflammatory response. RNA-sequencing transcriptome profiling confirmed that similar gene expression changes occurred in iPSC-derived and primary astrocytes upon stimulation with interleukin-1 beta. This protocol represents an important tool for modeling in-a-dish neurological diseases with an inflammatory component, allowing for the investigation of the role of diseased astrocytes in neuronal degeneration. | en_US |
dc.description.sponsorship | Paul G. Allen Family Foundation; JPB Foundation; Leona M. and Harry B. Helmsley Charitable Trust [2012-PG-MED002]; Annette C. Merle-Smith [R01 MH095741, U19MH106434]; G. Harold & Leila Y. Mathers Foundation; Flow Cytometry Core Facility of the Salk Institute; NIH-NCI CCSG [P30 014195]; Next Generation Sequencing Core Facility of the Salk Institute; Chapman Foundation; Helmsley Charitable Trust; Razavi Newman Integrative Genomics and Bioinformatics Core Facility of the Salk Institute; Swiss-NSF outgoing PD fellowship; Lynn and Edward Streim fellowship; EMBO long-term fellowship; Bettencourt Schueller Foundation; Philippe Foundation; Bob and Mary Jane Engman | en_US |
dc.description.sponsorship | For the production of the iPSCs, the authors would like to acknowledge financial support from Janssen Pharmaceuticals. This work was supported by the Paul G. Allen Family Foundation, Bob and Mary Jane Engman, The JPB Foundation, The Leona M. and Harry B. Helmsley Charitable Trust grant # 2012-PG-MED002, Annette C. Merle-Smith, R01 MH095741 (F.H.G.), U19MH106434 (F.H.G.), and The G. Harold & Leila Y. Mathers Foundation. This work was supported by the Flow Cytometry Core Facility of the Salk Institute with funding from NIH-NCI CCSG: P30 014195; the Next Generation Sequencing Core Facility of the Salk Institute with funding from NIH-NCI CCSG: P30 014195; the Chapman Foundation and the Helmsley Charitable Trust and by The Razavi Newman Integrative Genomics and Bioinformatics Core Facility of the Salk Institute with funding from NIH-NCI CCSG: P30 014195. This research was also supported by the Swiss-NSF outgoing PD fellowship (K.C.V.), Lynn and Edward Streim fellowship (K.C.V.), EMBO long-term fellowship (B.N.J.), the Bettencourt Schueller Foundation (B.N.J.), and the Philippe Foundation (B. N. J.). The authors would like to thank M. L. Gage for editorial comments. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Cell Press | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | * |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Inflammation-Responsive Astrocytes | en_US |
dc.subject | Glial Progenitors Generated | en_US |
dc.subject | Pluripotent Stem Cells | en_US |
dc.title | Differentiation of inflammation-responsive astrocytes from glial progenitors generated from human induced pluripotent stem cells | en_US |
dc.type | article | en_US |
dc.relation.ispartof | Stem Cell Reports | en_US |
dc.department | İstanbul Medipol Üniversitesi, Rektörlük, Rejeneratif ve Restoratif Tıp Araştırmaları Merkezi (REMER) | en_US |
dc.authorid | 0000-0003-1106-3288 | en_US |
dc.identifier.volume | 8 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.startpage | 1757 | en_US |
dc.identifier.endpage | 1769 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.doi | 10.1016/j.stemcr.2017.05.011 | en_US |
dc.identifier.wosquality | Q1 | en_US |
dc.identifier.scopusquality | Q1 | en_US |