PDI 2009 ISDP LAC
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Perit Dial Int 27(6): 625-633 2007
© 2007 International Society for Peritoneal Dialysis
This Article
Right arrow Full Text (PDF)
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Nishino, T.
Right arrow Articles by Devuyst, O.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nishino, T.
Right arrow Articles by Devuyst, O.

TECHNOLOGICAL ADVANCES IN PERITONEAL DIALYSIS RESEARCH

TRANSGENIC MOUSE MODELS

Tomoya Nishino1, Jie Ni2 and Olivier Devuyst1

Division of Nephrology,1 Université catholique de Louvain Medical School, Brussels, Belgium; Division of Nephrology,2 First Affiliated Hospital of Harbin Medical University, Harbin, China

Correspondence to: O. Devuyst, Division of Nephrology, UCL Medical School, 10 Avenue Hippocrate, B-1200 Brussels, Belgium. devuyst{at}nefr.ucl.ac.be

The development of peritoneal dialysis has been paralleled by a growing interest in establishing suitable experimental models to better understand the functional and structural processes operating in the peritoneal membrane. Thus far, most investigations have been performed in rat and rabbit models, with mechanistic insights essentially based on intervention studies using pharmacological agents, blocking antibodies, or transient expression systems. Since the body size of a species is no longer a limiting factor in the performance of in vivo studies related to peritoneal dialysis, it has been considered that mice, particularly once they have been genetically modified, could provide an attractive tool to investigate the molecular mechanisms operating in the peritoneal membrane. The purpose of this review is to illustrate how investigators in peritoneal dialysis research, catching up with other fields of biomedical research, are increasingly taking advantage of mouse models to provide direct evidence of basic mechanisms involved in the major complications of peritoneal dialysis.

KEY WORDS: Transport; inflammation; peritonitis; RAGE; AGE; peritoneum; knock-out mice.

Received 10 June 2007; accepted 30 July 2007.




This article has been cited by other articles:


Home page
Nephrol Dial TransplantHome page
O. Devuyst and E. Goffin
Water and solute transport in peritoneal dialysis: models and clinical applications
Nephrol. Dial. Transplant., July 1, 2008; 23(7): 2120 - 2123.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Multimed Inc. logo
Copyright © 2007 by Multimed Inc.