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      Scale Invariant Disordered Nanotopography Promotes Hippocampal Neuron Development and Maturation with Involvement of Mechanotransductive Pathways

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          Abstract

          The identification of biomaterials which promote neuronal maturation up to the generation of integrated neural circuits is fundamental for modern neuroscience. The development of neural circuits arises from complex maturative processes regulated by poorly understood signaling events, often guided by the extracellular matrix (ECM). Here we report that nanostructured zirconia surfaces, produced by supersonic cluster beam deposition of zirconia nanoparticles and characterized by ECM-like nanotopographical features, can direct the maturation of neural networks. Hippocampal neurons cultured on such cluster-assembled surfaces displayed enhanced differentiation paralleled by functional changes. The latter was demonstrated by single-cell electrophysiology showing earlier action potential generation and increased spontaneous postsynaptic currents compared to the neurons grown on the featureless unnaturally flat standard control surfaces. Label-free shotgun proteomics broadly confirmed the functional changes and suggests furthermore a vast impact of the neuron/nanotopography interaction on mechanotransductive machinery components, known to control physiological in vivo ECM-regulated axon guidance and synaptic plasticity. Our results indicate a potential of cluster-assembled zirconia nanotopography exploitable for the creation of efficient neural tissue interfaces and cell culture devices promoting neurogenic events, but also for unveiling mechanotransductive aspects of neuronal development and maturation.

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          Mitochondrial transport in neurons: impact on synaptic homeostasis and neurodegeneration.

          Mitochondria have a number of essential roles in neuronal function. Their complex mobility patterns within neurons are characterized by frequent changes in direction. Mobile mitochondria can become stationary or pause in regions that have a high metabolic demand and can move again rapidly in response to physiological changes. Defects in mitochondrial transport are implicated in the pathogenesis of several major neurological disorders. Research into the mechanisms that regulate mitochondrial transport is thus an important emerging frontier.
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            Recovery of learning and memory is associated with chromatin remodelling.

            Neurodegenerative diseases of the central nervous system are often associated with impaired learning and memory, eventually leading to dementia. An important aspect in pre-clinical research is the exploration of strategies to re-establish learning ability and access to long-term memories. By using a mouse model that allows temporally and spatially restricted induction of neuronal loss, we show here that environmental enrichment reinstated learning behaviour and re-established access to long-term memories after significant brain atrophy and neuronal loss had already occurred. Environmental enrichment correlated with chromatin modifications (increased histone-tail acetylation). Moreover, increased histone acetylation by inhibitors of histone deacetylases induced sprouting of dendrites, an increased number of synapses, and reinstated learning behaviour and access to long-term memories. These data suggest that inhibition of histone deacetylases might be a suitable therapeutic avenue for neurodegenerative diseases associated with learning and memory impairment, and raises the possibility of recovery of long-term memories in patients with dementia.
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              Cell death during development of the nervous system.

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                Author and article information

                Contributors
                Journal
                Front Cell Neurosci
                Front Cell Neurosci
                Front. Cell. Neurosci.
                Frontiers in Cellular Neuroscience
                Frontiers Media S.A.
                1662-5102
                18 November 2016
                2016
                : 10
                : 267
                Affiliations
                [1] 1Dipartimento di Fisica, Centro Interdisciplinare Materiali e Interfacce Nanostrutturate, Università degli Studi di Milano Milan, Italy
                [2] 2Fondazione Filarete Milan, Italy
                [3] 3Neurobiology of Learning Unit, Division of Neuroscience, Scientific Institute San Raffaele, Università Vita-Salute San Raffaele Milan, Italy
                [4] 4Dipartimento di Medicina Veterinaria, Università degli Studi di Milano Milan, Italy
                [5] 5SEMM - European School of Molecular Medicine Milan, Italy
                Author notes

                Edited by: Tommaso Pizzorusso, National Research Council, Italy

                Reviewed by: Erik B. Malarkey, University of Alabama at Birmingham, USA; Jennifer Larimore, Agnes Scott College, USA

                *Correspondence: Carsten Schulte carsten.schulte@ 123456unimi.it

                †These authors have contributed equally to this work.

                ‡Co-last authors.

                Article
                10.3389/fncel.2016.00267
                5114288
                27917111
                ff925701-0afa-4bb6-b721-02d5514b3c84
                Copyright © 2016 Schulte, Ripamonti, Maffioli, Cappelluti, Nonnis, Puricelli, Lamanna, Piazzoni, Podestà, Lenardi, Tedeschi, Malgaroli and Milani.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 27 July 2016
                : 01 November 2016
                Page count
                Figures: 7, Tables: 0, Equations: 0, References: 187, Pages: 22, Words: 18261
                Funding
                Funded by: Ministero dell'Istruzione, dell'Università e della Ricerca 10.13039/501100003407
                Award ID: FIRB RBA-P11AYN
                Award ID: PRIN 2012
                Funded by: European Commission 10.13039/501100000780
                Award ID: FP7-NMP-2013-LARGE-7
                Funded by: Fondazione Cariplo 10.13039/501100002803
                Categories
                Neuroscience
                Original Research

                Neurosciences
                neuronal differentiation,neuronal network maturation,biomaterial,mechanotransduction,proteomics,synaptic activity,integrin adhesion complex,neuronal cell adhesion molecules

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