Literature DB >> 30243515

Recognizing the Molecular Multifunctionality and Interactome of TIMP-1.

Barbara Grünwald1, Benjamin Schoeps2, Achim Krüger3.   

Abstract

Tissue inhibitor of metalloproteinase 1 (TIMP-1) is a major player in preserving tissue integrity and has recently also emerged as a decisive factor in several human pathologies. This appreciation has prompted this review addressing the largely underestimated complexity of the functions executed by TIMP-1 and their mechanistic basis. In fact, the versatile impact of TIMP-1 on cellular functions stems from its two-domain structure harboring metalloproteinase-inhibitory and cytokine-like signaling activities. This feature leads to functional interactions with numerous and distinct enzymatic and cell-surface proteins that initiate an exceptionally broad range of downstream effects. We propose here that this multifunctionality and the remarkably large interactome explain the diverse biological consequences of TIMP-1 expression in health and disease.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  natural protease inhibitor; protein multifunctionality; proteolytic networks

Mesh:

Substances:

Year:  2018        PMID: 30243515     DOI: 10.1016/j.tcb.2018.08.006

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  29 in total

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10.  Matrix metalloproteinase-9 (MMP-9) and tissue inhibitor of metalloproteinases 1 (TIMP-1) are localized in the nucleus of retinal Müller glial cells and modulated by cytokines and oxidative stress.

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