دورية أكاديمية

Identification of thyrotropin-releasing hormone as hippocampal glutaminyl cyclase substrate in neurons and reactive astrocytes

التفاصيل البيبلوغرافية
العنوان: Identification of thyrotropin-releasing hormone as hippocampal glutaminyl cyclase substrate in neurons and reactive astrocytes
المؤلفون: Waniek, Alexander, Hartlage-Rübsamen, Maike, Höfling, Corinna, Kehlen, Astrid, Schilling, Stephan, Demuth, Hans-Ulrich, Roßner, Steffen
سنة النشر: 2015
المجموعة: Publikationsdatenbank der Fraunhofer-Gesellschaft
مصطلحات موضوعية: Glutaminyl cyclase, hippocampus, thyrotropin-releasing hormone, amyloid pathology
الوقت: 610
الوصف: S.146-155 ; Recently, Av peptide variants with an N-terminal truncation and pyroglutamate modification were identified and shown to be highly neurotoxic and prone to aggregation. This modification of Av is catalyzed by glutaminyl cyclase (QC) and pharmacological inhibition of QC diminishes Av deposition and accompanying gliosis and ameliorates memory impairment in transgenic mouse models of Alzheimer's disease (AD). QC expression was initially described in the hypothalamus, where thyrotropin-releasing hormone (TRH) is one of its physiological substrates. In addition to its hormonal role, a novel neuroprotective function of TRH following excitotoxicity and Av-mediated neurotoxicity has been reported in the hippocampus. Functionally matching this finding, we recently demonstrated QC expression by hippocampal interneurons in mouse brain. Here, we detected neuronal co-expression of QC and TRH in the hippocampus of young adult wild type mice using double immunofluorescence labeling. This provides evidence for TRH being a physiological QC substrate in hippocampus. Additionally, in neocortex of aged but not of young mice transgenic for amyloid precursor protein an increase of QC mRNA levels was found compared to wild type littermates. This phenomenon was not observed in hippocampus, which is later affected by Av pathology. However, in hippocampus of transgenic - but not of wild type mice - a correlation between QC and TRH mRNA levels was revealed. This co-regulation of the enzyme QC and its substrate TRH was reflected by a co-induction of both proteins in reactive astrocytes in proximity of Av deposits. Also, in primary mouse astrocytes a co-induction of QC and TRH was demonstrated upon Av stimulation. ; 1852 ; Nr.1
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: Biochimica et biophysica acta. Molecular basis of disease; 0316033A; 0316033B; RO 2226/13-1; https://publica.fraunhofer.de/handle/publica/239426Test
DOI: 10.1016/j.bbadis.2014.11.011
الإتاحة: https://doi.org/10.1016/j.bbadis.2014.11.011Test
https://publica.fraunhofer.de/handle/publica/239426Test
رقم الانضمام: edsbas.CD80AB4E
قاعدة البيانات: BASE