Roles of Matrix Metalloproteinases and Their Natural Inhibitors in Metabolism: Insights into Health and Disease.

Int J Mol Sci

Institut de Génétique et de Biologie Moléculaire et Cellulaire Illkirch, 67400 Illkirch-Graffenstaden, France.

Published: June 2023

AI Article Synopsis

  • Matrix metalloproteinases (MMPs) are zinc-dependent enzymes that play a role in breaking down proteins and are classified into six main types.
  • Their activity is regulated by tissue inhibitors of metalloproteinases (TIMPs), and MMPs are involved in various biological processes, both during development and in adulthood.
  • Recent research has begun to explore their specific roles in metabolism and metabolic diseases, focusing on how MMPs affect adipose tissue and contribute to conditions like obesity, fatty liver disease, and type 2 diabetes.

Article Abstract

Matrix metalloproteinases (MMPs) are a family of zinc-activated peptidases that can be classified into six major classes, including gelatinases, collagenases, stromelysins, matrilysins, membrane type metalloproteinases, and other unclassified MMPs. The activity of MMPs is regulated by natural inhibitors called tissue inhibitors of metalloproteinases (TIMPs). MMPs are involved in a wide range of biological processes, both in normal physiological conditions and pathological states. While some of these functions occur during development, others occur in postnatal life. Although the roles of several MMPs have been extensively studied in cancer and inflammation, their function in metabolism and metabolic diseases have only recently begun to be uncovered, particularly over the last two decades. This review aims to summarize the current knowledge regarding the metabolic roles of metalloproteinases in physiology, with a strong emphasis on adipose tissue homeostasis, and to highlight the consequences of impaired or exacerbated MMP actions in the development of metabolic disorders such as obesity, fatty liver disease, and type 2 diabetes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341707PMC
http://dx.doi.org/10.3390/ijms241310649DOI Listing

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