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AMPK-regulated miRNA-210-3p is activated during ischaemic neuronal injury and modulates PI3K-p70S6K signalling
journal contributionposted on 20.04.2021, 16:20 by Shona PfeifferShona Pfeiffer, Anna Tomašcová, Uta Mamrak, Stefan HaunsbergerStefan Haunsberger, Niamh ConnollyNiamh Connolly, Alexa Resler, Heiko DuessmannHeiko Duessmann, Petronela Weisová, Elisabeth JirströmElisabeth Jirström, Beatrice D’Orsi, Gang ChenGang Chen, Mattia CremonaMattia Cremona, Bryan T Hennessy, Nikolaus Plesnila, Jochen PrehnJochen Prehn
Progressive neuronal injury following ischaemic stroke is associated with glutamate-induced depolarization, energetic stress and activation of AMP-activated protein kinase (AMPK). We here identify a molecular signature associated with neuronal AMPK activation, as a critical regulator of cellular response to energetic stress following ischaemia. We report a robust induction of microRNA miR-210-3p both in vitro in primary cortical neurons in response to acute AMPK activation and following ischaemic stroke in vivo. Bioinformatics and reverse phase protein array analysis of neuronal protein expression changes in vivo following administration of a miR-210-3p mimic revealed altered expression of phosphatase and tensin homolog (PTEN), 3-phosphoinositide-dependent protein kinase 1 (PDK1), ribosomal protein S6 kinase (p70S6K) and ribosomal protein S6 (RPS6) signalling in response to increasing miR-210-3p. In vivo, we observed a corresponding reduction in p70S6K activity following ischaemic stroke. Utilizing models of glutamate receptor over-activation in primary neurons, we demonstrated that induction of miR-210-3p was accompanied by sustained suppression of p70S6K activity and that this effect was reversed by miR-210-3p inhibition. Collectively, these results provide new molecular insight into the regulation of cell signalling during ischaemic injury, and suggest a novel mechanism whereby AMPK regulates miR-210-3p to control p70S6K activity in ischaemic stroke and excitotoxic injury. (Figure presented.).
SFI (13/IA/1881; 17/COEN/3474)
Munich Cluster of Systems Neurology (SyNergy; Project ID EXC2145/ID390857198)
RCSI International StAR Ph.D. studentship
CommentsThis is the peer reviewed version of the following article: Pfeiffer S, Tomašcová A, Mamrak U, Haunsberger SJ, Connolly NMC, Resler A, Düssmann H, Weisová P, Jirström E, D'Orsi B, Chen G, Cremona M, Hennessy BT, Plesnila N, Prehn JHM. AMPK-regulated miRNA-210-3p is activated during ischaemic neuronal injury and modulates PI3K-p70S6K signalling. Journal of Neurochemistry. 2021, which has been published in final form at https://doi.org/10.1111/jnc.15347 This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
Published CitationPfeiffer S, Tomašcová A, Mamrak U, Haunsberger SJ, Connolly NMC, Resler A, Düssmann H, Weisová P, Jirström E, D'Orsi B, Chen G, Cremona M, Hennessy BT, Plesnila N, Prehn JHM. AMPK-regulated miRNA-210-3p is activated during ischaemic neuronal injury and modulates PI3K-p70S6K signalling. Journal of Neurochemistry. 2021.
Publication Date11 March 2021
- Beaumont Hospital
- Centre for Systems Medicine
- FutureNeuro Centre
- Molecular Medicine
- Physiology and Medical Physics
- Neurological and Psychiatric Disorders
- Accepted Version (Postprint)