Evidence map›Paper›PMID 33467671›Full record

ReviewCells2021

MMP-9 Signaling Pathways That Engage Rho GTPases in Brain Plasticity.

Izabela Figiel, Patrycja K Kruk, Monika Zaręba-Kozioł, Paulina Rybak, Monika Bijata, Jakub Wlodarczyk, Joanna Dzwonek

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Izabela FigielNencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, 02-093 Warsaw, Poland.ORCID 0000-0001-5028-0168
Patrycja K KrukNencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, 02-093 Warsaw, Poland.ORCID 0000-0002-5038-9718
Monika Zaręba-KoziołNencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, 02-093 Warsaw, Poland.
Paulina RybakNencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, 02-093 Warsaw, Poland.
Monika BijataNencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, 02-093 Warsaw, Poland.ORCID 0000-0003-0589-4771
Jakub WlodarczykNencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, 02-093 Warsaw, Poland.
Joanna DzwonekNencki Institute of Experimental Biology, Polish Academy of Sciences, 3 Pasteur Street, 02-093 Warsaw, Poland.ORCID 0000-0002-3834-2175
Instytut Biologii Doświadczalnej im. Marcelego Nenckiego · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The extracellular matrix (ECM) has been identified as a critical factor affecting synaptic function. It forms a functional scaffold that provides both the structural support and the reservoir of signaling molecules necessary for communication between cellular constituents of the central nervous system (CNS). Among numerous ECM components and modifiers that play a role in the physiological and pathological synaptic plasticity, matrix metalloproteinase 9 (MMP-9) has recently emerged as a key molecule. MMP-9 may contribute to the dynamic remodeling of structural and functional plasticity by cleaving ECM components and cell adhesion molecules. Notably, MMP-9 signaling was shown to be indispensable for long-term memory formation that requires synaptic remodeling. The core regulators of the dynamic reorganization of the actin cytoskeleton and cell adhesion are the Rho family of GTPases. These proteins have been implicated in the control of a wide range of cellular processes occurring in brain physiology and pathology. Here, we discuss the contribution of Rho GTPases to MMP-9-dependent signaling pathways in the brain. We also describe how the regulation of Rho GTPases by post-translational modifications (PTMs) can influence these processes.

Indexed as

Neuronal PlasticityActinsAnimalsBrainBrain-Derived Neurotrophic FactorCD56 AntigenCell AdhesionCell Adhesion MoleculesCell Adhesion Molecules, NeuronalCentral Nervous SystemDystroglycansExtracellular MatrixHumansHyaluronan ReceptorsIntercellular Signaling Peptides and ProteinsMatrix Metalloproteinase 9ActinsBDNF protein, humanBrain-Derived Neurotrophic FactorCD44 protein, humanCD56 AntigenCell Adhesion MoleculesCell Adhesion Molecules, Neuronalcollapsin response mediator protein-2DystroglycansEPHB2 protein, humanHyaluronan ReceptorsICAM5 protein, humanIntercellular Signaling Peptides and ProteinsMatrix Metalloproteinase 9MMP9 protein, humanNCAM1 protein, humanNerve Tissue Proteinsneuroligin 1Receptor, EphB2rho GTP-Binding Proteinsextracellular matrixMMP-9post-translational modificationssmall Rho GTPasessynaptic plasticity

Identifiers

PMID33467671
PMCPMC7830260
OpenAlexW3120940421

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.