Skip Navigation



NDT Advance Access published online on April 8, 2008

Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfn127
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
23/9/2925    most recent
gfn127v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
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 Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Dihazi, H.
Right arrow Articles by Mueller, G. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dihazi, H.
Right arrow Articles by Mueller, G. A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author [2008]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org



Protein adsorption during LDL-apheresis: proteomic analysis

Hassan Dihazi1,*, Michael J. Koziolek1,*, Tanja Söllner1, Elke Kahler2, Reinhard Klingel3, Rieke Neuhoff1, Frank Strutz1 and Gerhard A. Mueller1

1 Department of Nephrology and Rheumatology 2 Department of Medical Statistics, Georg-August-University Goettingen 3 Apheresis Research Institute, Cologne, Germany

Correspondence and offprint requests to: M. Koziolek, Department of Nephrology and Rheumatology, Georg-August University Göttingen, Robert-Koch-Strasse 40, D-37075 Göttingen, Germany. Tel: +049-551-396331; Fax: +049-551-398906; E-mail: mkoziolek{at}med.uni-goettingen.de



  Abstract

Background. The aim of our study was to investigate the clearance of functional proteins by different low-density lipoprotein-apheresis (LDL-A) methods with the help of proteomic analyses.

Methods. Proteins were eluated from the different LDL-A columns and investigated with 2D electrophoresis combined with mass spectrometry methods. In parallel, we quantified the plasma protein loss from patients treated with double-filtration plasmapheresis (DFPP; n = 9), direct adsorption of lipoproteins (DALI; n = 5) or heparin-induced extracorporeal LDL precipitation (HELP; n = 7) with routine laboratory methods and western blots.

Results. Proteomic analyses of the column-bound proteins revealed a column-type-dependent loss with the highest number of protein spots in DALI-treated patients (1001 ± 36), followed by HELP (881 ± 25) and DFPP (535 ± 20). More than 70 functional proteins were identified. These proteins are involved in the coagulation pathway (e.g. kininogen1) and have adhesive (e.g. fibronectin), rheological (e.g. fibrinogen) and immunological/inflammatory properties (e.g. complement components). Quantification with western blot analyses demonstrated a significant depletion (P < 0.01) of these proteins comparing serum samples before and after the column with a systemic lowering in patients’ serum.

Conclusions. These data reveal strong interaction between column and serum proteins during LDL-A. The clearance of proteins with adhesive, rheological, and inflammatory characteristics may have beneficial effects on microcirculation and reduce chronic inflammation but may also concomitantly induce side effects such as an increased bleeding risk.

Keywords: atherosclerosis; chronic inflammation; LDL-apheresis; microcirculation; rheology


* Contributed equally to this paper.

Received for publication: 12.11.07
Accepted in revised form: 15. 2.08


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.