| Literature DB >> 33911021 |
José Antonio Noriega-Prieto1,2, Laura Eva Maglio1,3, Jonathan A Zegarra-Valdivia4,5,6, Jaime Pignatelli4,5, Ana M Fernandez4,5, Laura Martinez-Rachadell4,5, Jansen Fernandes4,7, Ángel Núñez1, Alfonso Araque2, Ignacio Torres-Alemán4,5, David Fernández de Sevilla8.
Abstract
Insulin-like growth factor-I (IGF-I) signaling plays a key role in learning and memory processes. While the effects of IGF-I on neurons have been studied extensively, the involvement of astrocytes in IGF-I signaling and the consequences on synaptic plasticity and animal behavior remain unknown. We have found that IGF-I induces long-term potentiation (LTPIGFI) of the postsynaptic potentials that is caused by a long-term depression of inhibitory synaptic transmission in mice. We have demonstrated that this long-lasting decrease in the inhibitory synaptic transmission is evoked by astrocytic activation through its IGF-I receptors (IGF-IRs). We show that LTPIGFI not only increases the output of pyramidal neurons, but also favors the NMDAR-dependent LTP, resulting in the crucial information processing at the barrel cortex since specific deletion of IGF-IR in cortical astrocytes impairs the whisker discrimination task. Our work reveals a novel mechanism and functional consequences of IGF-I signaling on cortical inhibitory synaptic plasticity and animal behavior, revealing that astrocytes are key elements in these processes.SIGNIFICANCE STATEMENT Insulin-like growth factor-I (IGF-I) signaling plays key regulatory roles in multiple processes of brain physiology, such as learning and memory. Yet, the underlying mechanisms remain largely undefined. Here we demonstrate that astrocytes respond to IGF-I signaling, elevating their intracellular Ca2+ and stimulating the release of ATP/adenosine, which triggers the LTD of cortical inhibitory synapses, thus regulating the behavioral task performance related to cortical sensory information processing. Therefore, the present work represents a major conceptual advance in our knowledge of the cellular basis of IGF-I signaling in brain function, by including for the first time astrocytes as key mediators of IGF-I actions on synaptic plasticity, cortical sensory information discrimination and animal behavior.Entities:
Keywords: IGF-I; astrocytes; barrel cortex; long-term depression; long-term potentiation; sensory discrimination
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Year: 2021 PMID: 33911021 PMCID: PMC8260162 DOI: 10.1523/JNEUROSCI.0005-21.2021
Source DB: PubMed Journal: J Neurosci ISSN: 0270-6474 Impact factor: 6.167