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      Abnormalities in perineuronal nets and behavior in mice lacking CSGalNAcT1, a key enzyme in chondroitin sulfate synthesis

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          Abstract

          Chondroitin sulfate (CS) is an important glycosaminoglycan and is mainly found in the extracellular matrix as CS proteoglycans. In the brain, CS proteoglycans are highly concentrated in perineuronal nets (PNNs), which surround synapses and modulate their functions. To investigate the importance of CS, we produced and precisely examined mice that were deficient in the CS synthesizing enzyme, CSGalNAcT1 (T1KO). Biochemical analysis of T1KO revealed that loss of this enzyme reduced the amount of CS by approximately 50% in various brain regions. The amount of CS in PNNs was also diminished in T1KO compared to wild-type mice, although the amount of a major CS proteoglycan core protein, aggrecan, was not changed. In T1KO, we observed abnormalities in several behavioral tests, including the open-field test, acoustic startle response, and social preference. These results suggest that T1 is important for plasticity, probably due to regulation of CS-dependent PNNs, and that T1KO is a good model for investigation of PNNs.

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          The online version of this article (10.1186/s13041-017-0328-5) contains supplementary material, which is available to authorized users.

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          Most cited references21

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          Perineuronal nets protect fear memories from erasure.

          In adult animals, fear conditioning induces a permanent memory that is resilient to erasure by extinction. In contrast, during early postnatal development, extinction of conditioned fear leads to memory erasure, suggesting that fear memories are actively protected in adults. We show here that this protection is conferred by extracellular matrix chondroitin sulfate proteoglycans (CSPGs) in the amygdala. The organization of CSPGs into perineuronal nets (PNNs) coincided with the developmental switch in fear memory resilience. In adults, degradation of PNNs by chondroitinase ABC specifically rendered subsequently acquired fear memories susceptible to erasure. This result indicates that intact PNNs mediate the formation of erasure-resistant fear memories and identifies a molecular mechanism closing a postnatal critical period during which traumatic memories can be erased by extinction.
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            Experience-dependent transfer of Otx2 homeoprotein into the visual cortex activates postnatal plasticity.

            Neural circuits are shaped by experience in early postnatal life. Distinct GABAergic connections within visual cortex determine the timing of the critical period for rewiring ocular dominance to establish visual acuity. We find that maturation of the parvalbumin (PV)-cell network that controls plasticity onset is regulated by a selective re-expression of the embryonic Otx2 homeoprotein. Visual experience promoted the accumulation of non-cell-autonomous Otx2 in PV-cells, and cortical infusion of exogenous Otx2 accelerated both PV-cell development and critical period timing. Conversely, conditional removal of Otx2 from non-PV cells or from the visual pathway abolished plasticity. Thus, the experience-dependent transfer of a homeoprotein may establish the physiological milieu for postnatal plasticity of a neural circuit.
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              Very long-term memories may be stored in the pattern of holes in the perineuronal net.

              R Tsien (2013)
              A hypothesis and the experiments to test it propose that very long-term memories, such as fear conditioning, are stored as the pattern of holes in the perineuronal net (PNN), a specialized ECM that envelops mature neurons and restricts synapse formation. The 3D intertwining of PNN and synapses would be imaged by serial-section EM. Lifetimes of PNN vs. intrasynaptic components would be compared with pulse-chase (15)N labeling in mice and (14)C content in human cadaver brains. Genetically encoded indicators and antineoepitope antibodies should improve spatial and temporal resolution of the in vivo activity of proteases that locally erode PNN. Further techniques suggested include genetic KOs, better pharmacological inhibitors, and a genetically encoded snapshot reporter, which will capture the pattern of activity throughout a large ensemble of neurons at a time precisely defined by the triggering illumination, drive expression of effector genes to mark those cells, and allow selective excitation, inhibition, or ablation to test their functional importance. The snapshot reporter should enable more precise inhibition or potentiation of PNN erosion to compare with behavioral consequences. Finally, biosynthesis of PNN components and proteases would be imaged.
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                Author and article information

                Contributors
                nzyoshioka@med.niigata-u.ac.jp
                miyata@agr.nagoya-u.ac.jp
                tamada@med.niigata-u.ac.jp
                ywatana@med.niigata-u.ac.jp
                akawasaki@med.niigata-u.ac.jp
                kitagawa@kobepharma-u.ac.jp
                takao@cts.u-toyama.ac.jp
                miyakawa@fujita-hu.ac.jp
                koseitak@aichi-med-u.ac.jp
                +81-25-227-2083 , tarokaja@med.niigata-u.ac.jp
                Journal
                Mol Brain
                Mol Brain
                Molecular Brain
                BioMed Central (London )
                1756-6606
                5 October 2017
                5 October 2017
                2017
                : 10
                : 47
                Affiliations
                [1 ]ISNI 0000 0001 0671 5144, GRID grid.260975.f, Department of Neurochemistry and Molecular Cell Biology, , Niigata University Graduate School of Medical and Dental Sciences, ; 1-757 Asahimachi, Chuo-ku, Niigata, 951-8510 Japan
                [2 ]ISNI 0000 0001 0671 5144, GRID grid.260975.f, Transdiciplinary Research Program, , Niigata University, ; Asahi-machi, Niigata, 951-8510 Japan
                [3 ]ISNI 0000 0004 0371 6549, GRID grid.411100.5, Department of Biochemistry, , Kobe Pharmaceutical University, ; Motoyamakita-machi, Kobe, 658-8558 Japan
                [4 ]ISNI 0000 0001 0943 978X, GRID grid.27476.30, Institute for Advanced Research, , Nagoya University, ; Furo-cho, Nagoya, 464-8601 Japan
                [5 ]ISNI 0000 0004 1754 9200, GRID grid.419082.6, PRESTO, Japan Science and Technology Agency (JST), ; Chiyoda-ku, Tokyo, 102-0075 Japan
                [6 ]ISNI 0000 0001 2272 1771, GRID grid.467811.d, Section of Behavior Patterns, National Institute of Physiological Sciences, ; Okazaki, Aichi 444-8787 Japan
                [7 ]ISNI 0000 0001 2171 836X, GRID grid.267346.2, Division of Experimental Animal Resource and Development, Life Science Research Center, , Toyama University, ; Toyama, 930-0194 Japan
                [8 ]ISNI 0000 0004 1761 798X, GRID grid.256115.4, Division of Systems Medical Science, Institute for Comprehensive Medical Science, , Fujita Health University, ; Toyoake, Aichi 470-1192 Japan
                [9 ]ISNI 0000 0001 0727 1557, GRID grid.411234.1, Department of Medical Biology, School of Medicine, , Aichi Medical University, ; Nagakute, Aichi 480-1103 Japan
                [10 ]ISNI 0000 0001 0671 5144, GRID grid.260975.f, Present address: Divisions of Neurobiology and Anatomy, , Niigata University Graduate School of Medical and Dental Sciences, ; Niigata, Japan
                [11 ]ISNI 0000 0001 0671 5144, GRID grid.260975.f, Present address: Divisions of Preventive Medicine, , Niigata University Graduate School of Medical and Dental Sciences, ; Niigata, Japan
                Author information
                http://orcid.org/0000-0003-1474-3385
                Article
                328
                10.1186/s13041-017-0328-5
                5629790
                28982363
                099e787b-dc14-49c8-a99f-609ef8971ae7
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 7 June 2017
                : 26 September 2017
                Funding
                Funded by: KAKENHI
                Award ID: #17023019, #22240040, and #24111515
                Award Recipient :
                Funded by: Sasakawa Scientific Research Grant
                Funded by: Platform of Advanced Animal Model Support from MEXT of Japan
                Funded by: Uehara Memorial Science Promoting Foundation
                Categories
                Research
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                © The Author(s) 2017

                Neurosciences
                Neurosciences

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