|
|
||||||||
Bench Science |
Division of General Internal Medicine and Nephrology1 and Division of Gastroenterology, Hepatology and Endocrinology,2 Department of Internal Medicine; Division of Pathology,3 Department of Diagnostic Medicine; Division of General Surgery,4 Department of Surgery, Robert-Bosch Krankenhaus, Stuttgart; Fachbereich Nephrologie,5 Deutsche Klinik für Diagnostik, Wiesbaden, Germany
Correspondence to: D.M. Alscher, Robert-Bosch Krankenhaus, Auerbachstrasse 110, D-70376 Stuttgart, Germany. dominik.alscher{at}rbk.de
Background: Local defense mechanisms are important for
the integrity of the peritoneum, but few details are known about the
expression patterns of antimicrobial proteins such as human defensin in normal
and damaged peritoneum.
Methods: Part A: The expression of different defensins
in normal (n = 12), inflamed (n = 5), and metastatic
peritoneum (n = 4) and in cultured human peritoneal mesothelial cells
was analyzed using mRNA and immunohistochemistry. Part B: Using
immunohistochemistry the expression of different defensins was analyzed in
different subgroups: healthy controls (n = 25), patients with chronic
appendicitis (n = 25) or acute appendicitis (n = 10), and
end-stage renal disease patients (n = 25, with 15 on peritoneal
dialysis).
Results: Part A: Human neutrophil peptides (HNP) 1 and
3 and human ß-defensins (HBD) 1 to 3 mRNA were detected in peritoneal
specimens. In addition, HNP1,3, HBD1, HBD2, and HBD3 proteins were detected
using immunohistochemistry. Part B: HBD1 showed a constitutive expression in
mesothelium, while HBD2 and HNP1,3 were associated with inflammation.
Decreased expressions of HNP1,3 were observed in end-stage renal disease
patients and in patients on peritoneal dialysis.
Conclusions: For the first time, the expression
patterns of defensins in normal and damaged peritoneum have been described.
The reduced expression of some defensins in end-stage renal disease is of
potential clinical interest against the background of the frequent infective
complications seen in peritoneal dialysis.
KEY WORDS: Innate immunity; defensins; peritonitis; infective complications; local defense; mesothelium.
Received 22 March 2007; accepted 17 July 2007.
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |