Differential Proteome of Articular Chondrocytes From Patients with Osteoarthritis |
| Raquel Rollín 1,2, Pilar Tornero 1, Fernando Marco 2, Emilio Camafeita 3, Enrique Calvo 3,
Luis López-Durán 2, Juan Ángel Jover 1, Juan Antonio López3, José Ramón Lamas 1,
Benjamín Fernández-Gutiérrez 1* |
| 1Servicio de Reumatología, Hospital Clínico San Carlos, Madrid |
| 2Servicio de Cirugía Ortopédica y Traumatología, Hospital Clínico San Carlos, Madrid |
| 3Unidad de Proteómica, CNIC, Madrid |
| *Corresponding author: |
Benjamín Fernández-Gutiérrez. Servicio de Reumatología,
Hospital Clínico San Carlos, C/ Profesor Martín Lagos s/n, 28040 Madrid, Spain,
Phone/Fax:34-91-3303615
E-mail:bfernandez.hcsc@salud.madrid.org |
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| Received July 11, 2008; Accepted August 03, 2008; Published August 14, 2008 |
| Citation: Raquel R, Pilar T, Fernando M, Emilio C, Enrique C, etal. (2008) Differential Proteome of Articular Chondrocytes
From Patients with Osteoarthritis. J Proteomics Bioinform 1: 267-280. doi:10.4172/jpb.1000034 |
| Copyright: ©2008 Raquel R, etal. This is an open-access article distributed under the terms of the Creative Commons
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original
author and source are credited. |
| Abstract |
Cartilage damage is a major problem in osteoarthritis (OA). To gain insight into the pathogenesis of OA, we
have analyzed the differential proteome of articular chondrocytes from these patients. Protein extracts were
prepared from cultured chondrocytes from 6 patients with end-stage OA and 6 normal donors and were analyzed
by 2D-DIGE. Differentially expressed proteins were identified by mass spectrometry (MS). Significant differential
expression was observed for 27 proteins, with 14 underexpressed and 13 overexpressed chondrocyte OA
proteins. Of special interest was the identification of destrin, cofilins, gelsolin, annexin A2, glycolytic enzymes,
chaperones, cathepsin D, proteasome beta 9 subunit isoform 2 proprotein and proteasome activator hPA28
subunit beta. The altered expression of these proteins is consistent with events such as cytoskeleton binding,
protein disruption, apoptosis, and glycolysis, demonstrating the ability of the 2D-DIGE/MS platform to identify
proteins with altered expression in chondrocytes from patients with end-stage OA. The identification of these
proteins may open new lines of research for this disease. |
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