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Published on: July 19, 2018
Activation of matrix metalloproteinase-2 causes peritoneal injury during peritoneal dialysis in rats
Ichiro Hirahara1, Yumi Ogawa, Eiji Kusano
1Terumo, R and D Center, Kanagawa, Japan. Ichirou_Hirahara@terumo.co.jp
Background:
Sclerosing peritonitis (SP) and encapsulating peritoneal sclerosis (EPS) are serious complications of continuous ambulatory peritoneal dialysis. Although we have shown previously that matrix metalloproteinase-2 (MMP-2) is increased in peritoneal injury leading to SP/EPS, most of the MMP-2 in the dialysate drained from the peritoneal cavity was the latent form that was lacking activity. In the present study, we investigated whether MMP-2 causes peritoneal injury.
Methods:
To create an animal model of peritoneal injury, we administered intraperitoneally chlorhexidine gluconate to rats. Dialysate drained from these rats was analysed by gelatin zymography and MMP-2 activity was analysed by an in situ film zymography method. In vitro myofibroblasts were cultured in collagen three-dimensional culture and then MMP-2 in conditioned medium from the culture was analysed by gelatin zymography.
Results:
Zymographic analysis revealed that latent form MMP-2 levels were high in the dialysate from peritoneal injury rats, whereas the active form was barely detectable. MMP-2 activity in the peritoneal tissue of the peritoneal injury rats was strongly detected by in situ film zymography. In vitro myofibroblasts were promoted to produce MMP-2 and to activate MMP-2 in collagen three-dimensional culture.
Conclusions:
In the present model, most of the MMP-2 was in the latent form, but activation of MMP-2 was promoted in the peritoneum during peritoneal injury. Activated MMP-2 may be associated with the progression of peritoneal injury.
Insights
Matrix metalloproteinase-2 (MMP-2) activation in the peritoneum may drive peritoneal injury, a complication of dialysis. While latent MMP-2 is common, its active form is present in injured tissue, suggesting a role in disease progression.
Area of Science:
- Nephrology
- Biochemistry
- Cell Biology
Background:
- Sclerosing peritonitis (SP) and encapsulating peritoneal sclerosis (EPS) are severe complications of continuous ambulatory peritoneal dialysis.
- Previous studies indicated elevated matrix metalloproteinase-2 (MMP-2) in peritoneal injury, but mostly in its inactive, latent form.
Purpose of the Study:
- To investigate the role of matrix metalloproteinase-2 (MMP-2) in causing peritoneal injury.
- To determine if MMP-2 activation occurs within the peritoneum during injury.
Main Methods:
- An animal model of peritoneal injury was established using chlorhexidine gluconate in rats.
- MMP-2 levels and activity in dialysate and peritoneal tissue were analyzed using gelatin zymography and in situ film zymography.
- In vitro studies cultured myofibroblasts in a collagen 3D matrix to assess MMP-2 production and activation.
Main Results:
- High levels of latent MMP-2 were found in dialysate from injured rats, with minimal active form detected.
- In situ zymography confirmed significant MMP-2 activity within the peritoneal tissue of injured rats.
- Myofibroblasts in a 3D collagen culture promoted both MMP-2 production and activation.
Conclusions:
- Despite predominantly latent MMP-2 in dialysate, peritoneal injury involves MMP-2 activation within the peritoneum.
- Activated MMP-2 is implicated in the progression of peritoneal injury, a serious dialysis complication.
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