ciRS-7 and miR-7 regulate ischemia induced neuronal death via glutamatergic signaling

Author:

Scoyni FlaviaORCID,Sitnikova Valeriia,Giudice Luca,Korhonen Paula,Trevisan Davide M,Hernandez de Sande Ana,Gomez-Budia Mireia,Giniatullina Raisa,Ugidos Irene FORCID,Dhungana Hiramani,Pistono Cristiana,Korvenlaita Nea,Välimäki Nelli-Noora,Kangas Salla M,Hiltunen Anniina E,Gribchenko Emma,Kaikkonen-Määttä Minna UORCID,Koistinaho Jari,Ylä-Herttuala Seppo,Hinttala ReettaORCID,Venø Morten T,Su Junyi,Stoffel Markus,Schaefer Anne,Rajewsky Nikolaus,Kjems Jørgen,LaPierre Mary P,Piwecka Monika,Jolkkonen Jukka,Giniatullin Rashid,Hansen Thomas B,Malm TarjaORCID

Abstract

ABSTRACTBrain functionality relies on finely tuned regulation of gene expression by networks of non-coding RNAs (ncRNAs) such as the one composed by the circular RNA ciRS-7 (also known as CDR1as), the microRNA miR-7 and the long non-coding RNA Cyrano. Here we describe ischemia induced alterations in the ncRNA network bothin vitroandin vivoand in transgenic mice lacking ciRS-7 or miR-7. Our data show that cortical neurons downregulate ciRS-7 and Cyrano and upregulate miR-7 expression upon ischemic insults. Mice lacking ciRS-7 show reduced lesion size and motor impairment, whilst the absence of miR-7 alone leads to an increase in the ischemia induced neuronal death. Moreover, miR-7 levels in pyramidal excitatory neurons regulate dendrite morphology and glutamatergic signaling suggesting a potential molecular link to thein vivophenotype. Our data reveal that ciRS-7 and miR-7 contribute to the outcome of ischemic stroke and shed new light into the pathophysiological roles of intracellular networks of non-coding RNAs in the brain.

Publisher

Cold Spring Harbor Laboratory

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