4.6 Review

Multifunctional intracellular matrix metalloproteinases: implications in disease

Journal

FEBS JOURNAL
Volume 288, Issue 24, Pages 7162-7182

Publisher

WILEY
DOI: 10.1111/febs.15701

Keywords

cancer; cardiovascular disease; cytosol; inflammation; matrix metalloproteinase; mitochondria; nucleus; proteolysis; sarcomere

Funding

  1. Canadian Institutes of Health Research [143299]
  2. SUNY startup fund [910252-50]
  3. Alberta Innovates Graduate Student Scholarship
  4. Heart and Stroke Foundation of Canada

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Matrix metalloproteinases (MMPs) are a family of zinc-dependent endopeptidases that were initially discovered as proteases targeting extracellular proteins. However, recent research has revealed their crucial intracellular roles in various pathological conditions, including cardiovascular renal disorders, inflammation, and malignancy. In addition to MMP-2, at least eleven other MMPs have been identified to function intracellularly, highlighting the importance of understanding their roles in cellular processes and potential as therapeutic targets.
Matrix metalloproteinases (MMPs) are zinc-dependent endopeptidases that were first discovered as proteases, which target and cleave extracellular proteins. During the past 20 years, however, intracellular roles of MMPs were uncovered and research on this new aspect of their biology expanded. MMP-2 is the first of this protease family to be reported to play a crucial intracellular role where it cleaves several sarcomeric proteins inside cardiac myocytes during oxidative stress-induced injury. Beyond MMP-2, currently at least eleven other MMPs are known to function intracellularly including MMP-1, MMP-3, MMP-7, MMP-8, MMP-9, MMP-10, MMP-11, MMP-12, MMP-14, MMP-23 and MMP-26. These intracellular MMPs are localized to different compartments inside the cell including the cytosol, sarcomere, mitochondria, and the nucleus. Intracellular MMPs contribute to the pathogenesis of various diseases. Cardiovascular renal disorders, inflammation, and malignancy are some examples. They also exert antiviral and bactericidal effects. Interestingly, MMPs can act intracellularly through both protease-dependent and protease-independent mechanisms. In this review, we will highlight the intracellular mechanisms of MMPs activation, their numerous subcellular locales, substrates, and roles in different pathological conditions. We will also discuss the future direction of MMP research and the necessity to exploit the knowledge of their intracellular targets and actions for the design of targeted inhibitors.

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