Analysis of pressure ulcer wound fluid using two-dimensional electrophoresis

被引:25
作者
Wyffels, Jennifer T. [1 ]
Fries, Kristin M. [1 ]
Randall, Jason S.
Ha, Daniel S. [2 ]
Lodwig, Christa A.
Brogan, Michael S. [3 ]
Shero, Marlene
Edsberg, Laura E.
机构
[1] Daemen Coll, Nat & Hlth Sci Res Ctr, Ctr Wound Healing Res, Dept Chem, Amherst, NY 14226 USA
[2] Millersville Univ Pennsylvania, Dept Biol, Millersville, PA 17551 USA
[3] Daemen Coll, Nat & Hlth Sci Res Ctr, Ctr Wound Healing Res, Phys Therapy Dept, Amherst, NY 14226 USA
关键词
2D-PAGE; Chronic wound; Pressure ulcer; Proteomics; S100A9; Wound healing; HUMAN CEREBROSPINAL-FLUID; MASS-SPECTROMETRY; HUMAN SKIN; PROTEOMICS; FIBROBLASTS;
D O I
10.1111/j.1742-481X.2010.00672.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The incidence rate of pressure ulcers in the USA ranges from 0.4% to 38% in acute care settings and from 2.2% to 23.9% in long-term care settings, and their treatment costs are in the billions of dollars yearly. The proteome of wound fluid may contain early indicators or biomarkers associated with healing in pressure ulcers that would enable treatment regimes to be optimised for each individual. Wound fluid was collected from the interior and periphery of 19 chronic pressure ulcers at 15 time points during 42 days for an analysis of protein expression. Proteins were fractionated using two-dimensional polyacrylamide gel electrophoresis. A comparison of the spot distributions indicates a biochemical difference between the interior and the periphery of wounds. Pressure ulcers that healed show a greater number of spots for interior and peripheral locations combined over time when compared with wounds that did not heal. Using this technique, protein S100A9 was identified as a potential biomarker of wound healing. The identification of differences within the proteome of healing versus non healing pressure ulcers could have great significance in the use of current treatments, as well as the development of new therapeutic interventions.
引用
收藏
页码:236 / 248
页数:13
相关论文
共 20 条
[1]  
Chen GA, 2005, INFORMATICS IN PROTEOMICS, P227
[2]  
CHOJNACKI C, 2007, LANGENBECK ARCH SURG, V392, P831
[3]   Proteomics as a tool for clinically relevant biomarker discovery and validation [J].
Duncan, MW ;
Hunsucker, SW .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2005, 230 (11) :808-817
[4]   Fibroblasts facilitate re-epithelialization in wounded human skin equivalents [J].
El Ghalbzouri, A ;
Hensbergen, P ;
Gibbs, S ;
Kempenaar, J ;
van der Schors, R ;
Ponec, M .
LABORATORY INVESTIGATION, 2004, 84 (01) :102-112
[5]   Development of an enhanced proteomic method to detect prognostic and diagnostic markers of healing in chronic wound fluid [J].
Fernandez, M. L. ;
Broadbent, J. A. ;
Shooter, G. K. ;
Malda, J. ;
Upton, Z. .
BRITISH JOURNAL OF DERMATOLOGY, 2008, 158 (02) :281-290
[6]   Broad-based proteomic strategies: a practical guide to proteomics and functional screening [J].
Graham, DRM ;
Elliott, ST ;
Van Eyk, JE .
JOURNAL OF PHYSIOLOGY-LONDON, 2005, 563 (01) :1-9
[7]   Optimised two-dimensional electrophoresis procedures for the protein characterisation of structural tissues [J].
Hopkinson, A ;
McIntosh, RS ;
Layfield, R ;
Keyte, J ;
Dua, HS ;
Tighe, PJ .
PROTEOMICS, 2005, 5 (07) :1967-1979
[8]  
Jaynes CD, 2003, ACUTE CARE PERSPECT, V12, P11
[9]   Proteomic analysis of suction blister fluid isolated from human skin [J].
Macdonald, N ;
Cumberbatch, M ;
Singh, M ;
Moggs, JG ;
Orphanides, G ;
Dearman, RJ ;
Griffiths, CEM ;
Kimber, I .
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2006, 31 (03) :445-448
[10]  
Mehta AI, 2003, DIS MARKERS, V19, P1