Extracellular matrix remodelling proteases in acute appendicitis and their impact on appendiceal perforation

• Abstract Background Appendicitis is associated with varying degradation of extracellular matrix involved in tissue injury. The principal aim of this study was to investigate whether immunoreactive techniques could illustrate the course and severity of appendicitis and separate the different inflammatory grades, phlegmonous, gangrenous and perforated appendicitis, from each other and from uninflamed appendix. This could lead to early identification of patients with appendicitis that have or are at risk of a perforation, thereby improving their treatment and outcome. Materials and Methods In Papers I-II, tissue biopsies were taken from 40 appendectomized patients. Ten patients who had a hemicolectomy served as controls. In Paper III, proteolysis from tissue biopsies at and adjacent to the perforation was studied in 15 patients operated on for perforated appendicitis. In Paper IV, plasma samples taken prior to surgery and 4 weeks postoperatively and biopsies from the appendix were taken in 57 patients operated on for suspected appendicitis. Protein levels of matrix metalloproteinase (MMP) -1, -2, -3, -9 and tissue inhibitor of metalloproteinase (TIMP-1) (Papers I, III and IV), urokinase plasminogen activator (uPA) and plasminogen activator inhibitor type 1 (PAI-1) (Papers II, III and IV) were determined by ELISA and localised by immunohistochemistry. Results MMP-9 was the most abundant protease in all groups of appendicitis compared with controls. The expression of MMP-1 and PAI-1 was significantly higher in perforated appendicitis compared with phlegmonous appendicitis and controls while MMP-2 showed an opposite pattern. uPA was twice as high in all groups of appendicitis compared with controls while no differences were found in MMP-3 and TIMP-1 expression between the groups. Immunohistochemically a scattered distribution of MMP-9 and TIMP-1 was demonstrated in the appendiceal wall in gangrenous and perforated appendicitis. When investigating the proteases in relation to the sites of perforation, MMP-9 and PAI-1 were found to be highest at the perforation sites while MMP-1 was higher close to them and MMP-2 decreased gradually away from them. No difference was seen in TIMP-1 and uPA. The individual differences in plasma for TIMP-1 were higher in patients with perforated appendicitis than in them who had phlegmonous and gangrenous appendicitis. Conclusions ECM remodelling proteases and anti-proteases could be demonstrated in appendicitis. A local imbalance between MMP-9 and TIMP-1 in combination with an over-expression of PAI-1 participated in the ECM degradation, leading to tissue injury in appendiceal perforation. TIMP-1 in plasma could be an inflammatory diagnostic marker for patients with appendicitis and at risk for perforation. Keywords; Appendicitis, Perforation, Extracellular matrix, MMP-9, TIMP-1, uPA, PAI-1

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kirurgi (hsv//swe)

MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Surgery (hsv//eng)

Nyckelord

appendicitis

perforation

extracellular matrix

MMP-9

TIMP-1

uPA

PAI-1

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