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Part 2: Cellular and Molecular Biology of the Peritoneum and Peritoneal Dialysis |
Department of Medicine, University of Hong Kong, Hong Kong SAR, PR China
Correspondence to: S. Yung, Department of Medicine, University of Hong Kong, Queen Mary Hospital, Pok Fu Lam Road, Hong Kong SAR, PR China. ssyyung{at}hkucc.hku.hk
Background: Preservation of the structural and
functional integrity of the peritoneum is essential to maintain the dialytic
efficacy of the peritoneal membrane. Although much improvement has been made
to peritoneal dialysis (PD) fluids, they remain bioincompatible, and together
with peritonitis, they continue to induce peritoneal inflammation and
fibrosis.
Method: This article reviews the putative factors that
mediate mesothelial cell inflammation during PD, and the mechanisms by which
mesothelial cells attempt to regulate and resolve peritoneal
inflammation.
Results: The mesothelium is the first line of defense
to foreign particles and chemicals in the peritoneal cavity. Constant exposure
of the mesothelium to the bioincompatible constituents of PD solutions results
in denudation of the mesothelium and loss of the peritoneal cavity's
protective layer. Detached mesothelial cells in PD solutions have the capacity
to replenish the mesothelial layer through their ability to migrate and attach
to areas of denudation. Mesothelial cells synthesize a plethora of growth
factors, matrix proteins, and proteoglycans that aid in the reparative process
and regulate the formation of chemotactic gradients that are essential for
infiltration of leukocytes to sites of injury.
Conclusions: Far from being bystanders in peritoneal
function, mesothelial cells have been shown to play a dynamic role in
peritoneal homeostasis and immunoregulation. Studies have highlighted the
potential use of mesothelial cells in gene therapy and cell transplantation,
both of which may provide novel therapeutic strategies for the preservation of
the peritoneum during PD.
KEY WORDS: Mesothelial cells; inflammation; cytokines; epithelial-to-mesenchymal transdifferentiation; hyaluronan; proteoglycans.
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