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  1. Article ; Online: RNA Editing Alterations Define Disease Manifestations in the Progression of Experimental Autoimmune Encephalomyelitis (EAE).

    Dafou, Dimitra / Kanata, Eirini / Pettas, Spyros / Bekas, Nikolaos / Dimitriadis, Athanasios / Kempapidou, Garyfalia / Lagoudaki, Roza / Theotokis, Paschalis / Touloumi, Olga / Delivanoglou, Nikoleta / Kesidou, Evangelia / Xanthopoulos, Konstantinos / Grigoriadis, Nikolaos / Papavasiliou, Fotini Nina / Sklaviadis, Theodoros

    Cells

    2022  Volume 11, Issue 22

    Abstract: RNA editing is an epitranscriptomic modification, leading to targeted changes in RNA transcripts. It is mediated by the action of ADAR (adenosine deaminases acting on double-stranded (ds) RNA and APOBEC (apolipoprotein B mRNA editing enzyme catalytic ... ...

    Abstract RNA editing is an epitranscriptomic modification, leading to targeted changes in RNA transcripts. It is mediated by the action of ADAR (adenosine deaminases acting on double-stranded (ds) RNA and APOBEC (apolipoprotein B mRNA editing enzyme catalytic polypeptide-like) deaminases and appears to play a major role in the pathogenesis of many diseases. Here, we assessed its role in experimental autoimmune encephalomyelitis (EAE), a widely used non-clinical model of autoimmune inflammatory diseases of the central nervous system (CNS), which resembles many aspects of human multiple sclerosis (MS). We have analyzed in silico data from microglia isolated at different timepoints through disease progression to identify the global editing events and validated the selected targets in murine tissue samples. To further evaluate the functional role of RNA editing, we induced EAE in transgenic animals lacking expression of APOBEC-1. We found that RNA-editing events, mediated by the APOBEC and ADAR deaminases, are significantly reduced throughout the course of disease, possibly affecting the protein expression necessary for normal neurological function. Moreover, the severity of the EAE model was significantly higher in APOBEC-1 knock-out mice, compared to wild-type controls. Our results implicate regulatory epitranscriptomic mechanisms in EAE pathogenesis that could be extrapolated to MS and other neurodegenerative disorders (NDs) with common clinical and molecular features.
    MeSH term(s) Humans ; Mice ; Animals ; RNA Editing/genetics ; APOBEC-1 Deaminase/genetics ; Encephalomyelitis, Autoimmune, Experimental/genetics ; RNA, Double-Stranded ; Mutagenesis, Site-Directed ; Mice, Knockout
    Chemical Substances APOBEC-1 Deaminase (EC 3.5.4.36) ; RNA, Double-Stranded
    Language English
    Publishing date 2022-11-12
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2661518-6
    ISSN 2073-4409 ; 2073-4409
    ISSN (online) 2073-4409
    ISSN 2073-4409
    DOI 10.3390/cells11223582
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Oxygen-Glucose Deprivation (OGD) Modulates the Unfolded Protein Response (UPR) and Inflicts Autophagy in a PC12 Hypoxia Cell Line Model.

    Vavilis, Theofanis / Delivanoglou, Nikoleta / Aggelidou, Eleni / Stamoula, Eleni / Mellidis, Kyriakos / Kaidoglou, Aikaterini / Cheva, Angeliki / Pourzitaki, Chryssa / Chatzimeletiou, Katerina / Lazou, Antigone / Albani, Maria / Kritis, Aristeidis

    Cellular and molecular neurobiology

    2016  Volume 36, Issue 5, Page(s) 701–712

    Abstract: Hypoxia is the lack of sufficient oxygenation of tissue, imposing severe stress upon cells. It is a major feature of many pathological conditions such as stroke, traumatic brain injury, cerebral hemorrhage, perinatal asphyxia and can lead to cell death ... ...

    Abstract Hypoxia is the lack of sufficient oxygenation of tissue, imposing severe stress upon cells. It is a major feature of many pathological conditions such as stroke, traumatic brain injury, cerebral hemorrhage, perinatal asphyxia and can lead to cell death due to energy depletion and increased free radical generation. The present study investigates the effect of hypoxia on the unfolded protein response of the cell (UPR), utilizing a 16-h oxygen-glucose deprivation protocol (OGD) in a PC12 cell line model. Expression of glucose-regulated protein 78 (GRP78) and glucose-regulated protein 94 (GRP94), key players of the UPR, was studied along with the expression of glucose-regulated protein 75 (GRP75), heat shock cognate 70 (HSC70), and glyceraldehyde 3-phosphate dehydrogenase, all with respect to the cell death mechanism(s). Cells subjected to OGD displayed upregulation of GRP78 and GRP94 and concurrent downregulation of GRP75. These findings were accompanied with minimal apoptotic cell death and induction of autophagy. The above observation warrants further investigation to elucidate whether autophagy acts as a pro-survival mechanism that upon severe and prolonged hypoxia acts as a concerted cell response leading to cell death. In our OGD model, hypoxia modulates UPR and induces autophagy.
    MeSH term(s) Animals ; Apoptosis/drug effects ; Autophagy/physiology ; Cell Hypoxia ; Cell Survival ; Glucose/metabolism ; Neurons/metabolism ; Oxygen/metabolism ; PC12 Cells ; Rats ; Unfolded Protein Response/physiology
    Chemical Substances Glucose (IY9XDZ35W2) ; Oxygen (S88TT14065)
    Language English
    Publishing date 2016-07
    Publishing country United States
    Document type Journal Article
    ZDB-ID 283404-2
    ISSN 1573-6830 ; 0272-4340
    ISSN (online) 1573-6830
    ISSN 0272-4340
    DOI 10.1007/s10571-015-0250-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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