Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/127310
Title: Global proteomic and methylome analysis in human induced pluripotent stem cells reveals overexpression of a human TLR3 affecting proper innate immune response signaling
Author: Requena Osete, Jordi
Alvarez Palomo, Ana Belen
Codina Pascual, M.
Delgado-Morales, Raúl
Moran, Sebastian
Esteller, Manel
Sal, M.
Boronat Barado, Anna
Consiglio, Antonella
Addeleccia Bogle, O.
Wolwertang, E.
Ovchinnikov, D.
Álvarez, Iñaki
Jaraquemada, Dolores
Mezquita Pla, Jovita
Oliva, R.
Edel, Michael John
Keywords: Resposta immunitària
Cèl·lules mare
Inflamació
Citoquines
Immune response
Stem cells
Inflammation
Cytokines
Issue Date: 3-Jan-2019
Publisher: AlphaMed Press
Abstract: When considering the clinical applications of autologous cell replacement therapy of human iPSC‐derived cells there is a clear need to better understand what the immune response will be before we embark on extensive clinical trials to treat or model human disease. We performed a detailed assessment comparing human fibroblast cell lines (termed F1) reprogrammed into human iPSC and subsequently differentiated back to fibroblast cells (termed F2) or other human iPSC‐derived cells including neural stem cells made from either retroviral, episomal or synthetic mRNA cell reprogramming methods. Global proteomic analysis reveals the main differences in signal transduction and immune cell protein expression between F1 and F2 cells, implicating wild type toll like receptor protein 3 (TLR3). Furthermore, global methylome analysis identified an isoform of the human TLR3 gene that is not epigenetically reset correctly upon differentiation to F2 cells resulting in a hypomethylated transcription start site in the TLR3 isoform promoter and overexpression in most human iPSC‐derived cells not seen in normal human tissue. The human TLR3 isoform in human iPSC‐NSC functions to suppress NF‐KB p65 signaling pathway in response to virus (Poly IC), suggesting suppressed immunity of iPSC‐derived cells to viral infection. The sustained wild type TLR3 and TLR3 isoform over expression is central to understanding the altered immunogenicity of human iPSC‐derived cells calling for screening of human iPSC‐derived cells for TLR3 expression levels before applications.
Note: Versió postprint del document publicat a: https://doi.org/10.1002/stem.2966
It is part of: Stem Cells, 2019
URI: http://hdl.handle.net/2445/127310
Related resource: https://doi.org/10.1002/stem.2966
ISSN: 1066-5099
Appears in Collections:Articles publicats en revistes (Biomedicina)

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