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@ARTICLE{Ulbrich:154294,
author = {Ulbrich, Philipp and Khoshneviszadeh, Mashima and Jandke,
Solveig and Schreiber, Stefanie and Dityatev, Alexander},
title = {{I}nterplay between perivascular and perineuronal
extracellular matrix remodelling in neurological and
psychiatric diseases.},
journal = {European journal of neuroscience},
volume = {53},
number = {12},
issn = {1460-9568},
address = {Oxford [u.a.]},
publisher = {Wiley},
reportid = {DZNE-2021-00148},
pages = {3811-3830},
year = {2021},
note = {ISSN 1460-9568 not unique: **3 hits**.},
abstract = {Vascular damage, central nervous system (CNS) injury,
seizure or even psychological stress may trigger activation
of microglia and infiltration of other immune cells,
accompanied by high levels of expression and activity of
extracellular proteases, such as matrix metalloproteinases
(MMPs), and degradation/remodelling of the perivascular and
perineuronal extracellular matrix (ECM). This acute response
is followed by the recovery/chronic phase, during which the
activation of astrocytes leads to the upregulated synthesis
of ECM molecules, which, in combination with elevated
expression of tissue inhibitor of metalloproteinases (TIMP)
proteins, increases the aggregation of ECM molecules. This
biphasic dysregulation of local balance between
extracellular proteases and the ECM activates multiple
temporally overlapping signalling cascades, involving
receptor-type protein tyrosine phosphatases, integrins,
Toll-like receptors, cell adhesion molecules, and ion
channels, resulting in impaired synaptic plasticity and
cognition. An additional level of complexity is related to
the leakage of blood plasma proteins, such as fibrinogen,
and the diffusion of perivascularly overproduced MMPs, TIMPs
and ECM molecules into the CNS parenchyma, leading to
diverse effects on neurons and incorporation of these
molecules into the interstitial neural ECM. This review aims
to outline these complex common mechanisms in stroke, CNS
injury, depression, epilepsy, multiple sclerosis and
cerebral small vessel disease and to discuss translational
strategies to advance the development of new therapies for
these neurological and psychiatric diseases.},
keywords = {Astrocytes / Extracellular Matrix / Humans / Matrix
Metalloproteinases / Mental Disorders / Nervous System
Diseases / Neurons / Tissue Inhibitor of Metalloproteinases
/ cerebral small vessel disease (Other) / perineuronal
extracellular matrix (Other) / perivascular extracellular
matrix (Other) / stroke (Other)},
cin = {AG Schreiber / AG Reymann / AG Dityatev},
ddc = {610},
cid = {I:(DE-2719)1310010 / I:(DE-2719)1310005 /
I:(DE-2719)1310007},
pnm = {353 - Clinical and Health Care Research (POF4-353) / 351 -
Brain Function (POF4-351)},
pid = {G:(DE-HGF)POF4-353 / G:(DE-HGF)POF4-351},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:32594588},
doi = {10.1111/ejn.14887},
url = {https://pub.dzne.de/record/154294},
}