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      Brain Extracellular Matrix in Neurodegeneration

      review-article
      1 , 1
      Brain Pathology (Zurich, Switzerland)
      Blackwell Publishing Ltd
      ECM, neurodegeneration, CNS

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          Abstract

          The role of extracellular matrix (ECM) in neurological development, function and degeneration has evolved from a simplistic physical adhesion to a system of intricate cellular signaling. While most cells require ECM adhesion to survive, it is now clear that differentiated function is intimately dependent upon cellular interaction with the ECM. Therefore, it is not surprising that the ECM is increasingly found to be involved in the enigmatic process of neurodegeneration. Descriptive studies of human neurodegenerative disorders and experimental studies of animal models of neurodegeneration have begun to define potential mechanisms of ECM disruption that can lead to synaptic and neuronal loss.

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          Most cited references90

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          Matrix metalloproteinases.

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            Of extracellular matrix, scaffolds, and signaling: tissue architecture regulates development, homeostasis, and cancer.

            The microenvironment influences gene expression so that the behavior of a cell is largely determined by its interactions with the extracellular matrix, neighboring cells, and soluble local and systemic cues. We describe the essential roles of context and organ structure in directing mammary gland development and differentiated function and in determining the response to oncogenic insults, including mutations. We expand on the concept of "dynamic reciprocity" to present an integrated view of development, cancer, and aging and posit that genes are like the keys on a piano: Although they are essential, it is the context that makes the music.
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              Chemokine and cytokine processing by matrix metalloproteinases and its effect on leukocyte migration and inflammation.

              The action of matrix metalloproteinases (MMPs) was originally believed to be restricted to degradation of the extracellular matrix; however, in recent years, it has become evident that these proteases can modify many nonmatrix substrates, such as cytokines and chemokines. The use of MMP-deficient animals has revealed that these proteases can indeed influence the progression of various inflammatory processes. This review aims to provide the reader with a concise overview of these novel MMP functions in relation to leukocyte migration.
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                Author and article information

                Journal
                Brain Pathol
                Brain Pathol
                10.1111/(ISSN)1750-3639
                BPA
                Brain Pathology (Zurich, Switzerland)
                Blackwell Publishing Ltd (Oxford, UK )
                1015-6305
                1750-3639
                25 July 2008
                October 2009
                : 19
                : 4 ( doiID: 10.1111/bpa.2009.19.issue-4 )
                : 573-585
                Affiliations
                [ 1 ]Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pa.
                Author notes
                [*]Clayton A. Wiley, MD, PhD, Presbyterian University Hospital, Neuropathology Division, 200 Lothrop St. Pittsburgh, PA 15213 (E‐mail: claytonwiley1@ 123456mac.com )
                Article
                BPA195
                10.1111/j.1750-3639.2008.00195.x
                2742568
                18662234
                f6118bec-b504-47af-bdba-2622b19e2307
                © 2008 The Authors. Journal Compilation © 2008 International Society of Neuropathology

                This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

                History
                : 18 February 2008
                : 27 May 2008
                Page count
                links-crossref: 0, links-pubmed: 0, Figures: 3, Tables: 2, Equations: 0, References: 100, Pages: 13, Words: 10795
                Categories
                Review Article
                Custom metadata
                2.0
                October 2009
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.0 mode:remove_FC converted:15.04.2020

                Pathology
                ecm,neurodegeneration,cns
                Pathology
                ecm, neurodegeneration, cns

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