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    <subfield code="a">10.1016/j.neubiorev.2020.07.015</subfield>
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    <subfield code="a">pmid:32687884</subfield>
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    <subfield code="a">1873-7528</subfield>
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    <subfield code="a">DZNE-2022-00979</subfield>
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    <subfield code="a">English</subfield>
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    <subfield code="a">Spijker, Sabine</subfield>
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    <subfield code="a">Incubation of depression: ECM assembly and parvalbumin interneurons after stress.</subfield>
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    <subfield code="a">Amsterdam [u.a.]</subfield>
    <subfield code="c">2020</subfield>
    <subfield code="b">Elsevier Science</subfield>
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    <subfield code="a">Journal Article</subfield>
    <subfield code="b">journal</subfield>
    <subfield code="m">journal</subfield>
    <subfield code="0">PUB:(DE-HGF)16</subfield>
    <subfield code="s">1685012127_32153</subfield>
    <subfield code="2">PUB:(DE-HGF)</subfield>
    <subfield code="x">Review Article</subfield>
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    <subfield code="a">(CC-BY 4.0)</subfield>
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    <subfield code="a">The extracellular space is occupied by a complex network of proteins creating a mesh-like assembly known as the extracellular matrix (ECM). ECM assembles into dense net-like structures, perineuronal nets (PNNs), that envelope cell somas and proximal neurites of predominantly parvalbumin+-(PV+) interneurons. ECM regulates cell-to-cell communication, thereby modulating neuronal network function. Accumulating evidence points to the importance of network dysfunction in the pathophysiology of psychiatric diseases, in which stress acts as a major predisposing factor. Here we review stress-induced changes in ECM/PNNs and PV+-interneurons in preclinical models of (or for) depression, with a special focus on social stress. We argue that the direction of these alterations largely depends on stress recency, as well as on stress timing and the brain region under investigation. A biphasic temporal regulation of ECM/PNNs and PV+-interneuron function is typically observed after stress. Understanding the complex mechanisms underlying ECM organization in relation to stress-induced molecular, cellular and network changes is crucial to further decipher the implications of ECM remodeling in the incubation of depressive symptoms.</subfield>
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    <subfield code="0">G:(DE-HGF)POF4-899</subfield>
    <subfield code="c">POF4-899</subfield>
    <subfield code="f">POF IV</subfield>
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    <subfield code="a">Chronic mild/unpredictable stress</subfield>
    <subfield code="2">Other</subfield>
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    <subfield code="a">Early life stress</subfield>
    <subfield code="2">Other</subfield>
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  <datafield tag="650" ind1=" " ind2="7">
    <subfield code="a">Experience-dependent plasticity</subfield>
    <subfield code="2">Other</subfield>
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  <datafield tag="650" ind1=" " ind2="7">
    <subfield code="a">Hippocampus</subfield>
    <subfield code="2">Other</subfield>
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  <datafield tag="650" ind1=" " ind2="7">
    <subfield code="a">Hyper-excitability</subfield>
    <subfield code="2">Other</subfield>
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  <datafield tag="650" ind1=" " ind2="7">
    <subfield code="a">Hypo-excitability</subfield>
    <subfield code="2">Other</subfield>
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  <datafield tag="650" ind1=" " ind2="7">
    <subfield code="a">Prefrontal cortex</subfield>
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  <datafield tag="650" ind1=" " ind2="7">
    <subfield code="a">Restraint stress</subfield>
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    <subfield code="a">Social defeat stress</subfield>
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    <subfield code="a">Parvalbumins</subfield>
    <subfield code="2">NLM Chemicals</subfield>
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    <subfield code="a">Depression</subfield>
    <subfield code="2">MeSH</subfield>
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    <subfield code="a">Extracellular Matrix</subfield>
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    <subfield code="a">Interneurons</subfield>
    <subfield code="2">MeSH</subfield>
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    <subfield code="a">Neurons</subfield>
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  <datafield tag="650" ind1=" " ind2="2">
    <subfield code="a">Parvalbumins</subfield>
    <subfield code="2">MeSH</subfield>
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    <subfield code="a">Koskinen, Maija-Kreetta</subfield>
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    <subfield code="a">Riga, Danai</subfield>
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