4.6 Review

Granzyme B in injury, inflammation, and repair

Journal

TRENDS IN MOLECULAR MEDICINE
Volume 18, Issue 12, Pages 732-741

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.molmed.2012.09.009

Keywords

granzyme B; extracellular matrix; wound healing; aging; skin; inflammation

Funding

  1. Canadian Institutes of Health Research (CIHR)
  2. CIHR Skin Research Training Centre
  3. Natural Sciences and Engineering Research Council of Canada

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Fragile skin and susceptibility to skin tearing are major problems among the elderly and can be complicated further by impaired wound healing. Non-healing wounds fail to progress through the normal stages of healing and enter a state of chronic inflammation featuring increased proteolytic activity. Increased expression of the serine protease granzyme B is observed during prolonged inflammation and is implicated in the pathogenesis of several chronic inflammatory diseases. Although its role in cytotoxic lymphocyte-mediated apoptosis is well established, granzyme B can also degrade extracellular matrix proteins and alter inflammation if present in the extracellular milieu. The present review focuses on the emerging evidence for the involvement of granzyme B in chronic inflammation, impaired wound healing, and age-related skin fragility.

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