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CD147 expression in peritoneal injury

Authors :
M. Dominik Alscher
Rudolf P. Wüthrich
Joerg Latus
Jin Chen
Stephan Segerer
Harald Seeger
Ilka Edenhofer
Daniel Kitterer
Dagmar Biegger
University of Zurich
Segerer, Stephan
Source :
Clinical and Experimental Nephrology. 21:1097-1104
Publication Year :
2017
Publisher :
Springer Science and Business Media LLC, 2017.

Abstract

Peritoneal injury is an important cause of technical failure of long-term peritoneal dialysis (PD). Encapsulating peritoneal sclerosis (EPS) is a severe complication of long-term PD with potentially life threatening consequences. CD147 is a glycoprotein with diverse functions including modulation of extracellular matrix via induction of matrix metalloproteinases, cell adhesion, and regulation of immune reactions. We hypothesized that CD 147 plays a role in the peritoneal cavity. In this retrospective study, we localized CD147 by immunohistochemistry in peritoneal biopsies from uremic patients not on PD (n = 8), on PD without signs of EPS (n = 7), and in biopsies in patients with the diagnosis of EPS (n = 7). Double immunofluorescence was used to co-localize α-smooth-muscle actin (α-SMA) and CD147 in selected biopsies from each group. Expression was scored semi-quantitatively. In biopsies from uremic controls, CD147 was prominently expressed in mesothelial cells, focally between fat cells and by some perivascular cells. In patients on PD, a similar distribution was present (although mesothelium was rarely conserved), with some focal accentuation. In EPS, layers of fibroblastic cells were positive for CD147. EPS biopsies demonstrated a significantly higher score in a blinded evaluation, compared to uremic patients. Cells expressing CD147 were α-SMA positive myofibroblasts as demonstrated by double immunofluorescence. Mean CD147 scores did not differ between patients with different transporter status. This is the first study demonstrating CD147 on a major part of fibroblastic cells in EPS. Future studies need to address the role of these cells in this severe complication of long-term PD.

Details

ISSN :
14377799 and 13421751
Volume :
21
Database :
OpenAIRE
Journal :
Clinical and Experimental Nephrology
Accession number :
edsair.doi.dedup.....c4f42574284a5efae11a732ed27e3823
Full Text :
https://doi.org/10.1007/s10157-017-1390-0