Sex-Specific Differences in Extracellular Vesicle Protein Cargo in Synovial Fluid of Patients with Osteoarthritis.

cartilage degeneration exosomes gender mass spectrometry

Journal

Life (Basel, Switzerland)
ISSN: 2075-1729
Titre abrégé: Life (Basel)
Pays: Switzerland
ID NLM: 101580444

Informations de publication

Date de publication:
10 Dec 2020
Historique:
received: 30 10 2020
revised: 02 12 2020
accepted: 03 12 2020
entrez: 16 12 2020
pubmed: 17 12 2020
medline: 17 12 2020
Statut: epublish

Résumé

Women are at a significantly higher risk of developing osteoarthritis (OA) compared to males. The pathogenesis of osteoarthritis (OA) in women is poorly understood. Extracellular vesicles (EVs) have been shown to play an essential role in numerous signaling processes during the pathogenesis of age-related diseases via paracrine signaling. Molecular profiling of the synovial fluid-derived EVs cargo in women may help in the discovery of novel biomarkers and therapeutics for the treatment of OA in women. Previously, we reported that synovial fluid-derived EV miRNA cargo differs in a sex-specific manner. This study aims to characterize synovial fluid-derived EV protein cargo in OA patients. Our data showed sex-specific EVs protein content in OA. We found haptoglobin, orosomucoid, and ceruloplasmin significantly up-regulated, whereas apolipoprotein down-regulated in female OA EVs. In males, we discovered β-2-glycoprotein, and complement component 5 proteins significantly up-regulated and Spt-Ada-Gcn5 acetyltransferase (SAGA)-associated factor 29 down-regulated in male OA EVs. Database for Annotation, Visualization, and Integrated Discovery (DAVID) and QuickGO analysis revealed OA-specific protein involvement in several biological, molecular, and cellular pathways, specifically in inflammatory processes. In conclusion, synovial fluid EV protein content is altered in a sex-specific manner with OA, explaining the increased prevalence and severity of OA in women.

Identifiants

pubmed: 33321751
pii: life10120337
doi: 10.3390/life10120337
pmc: PMC7763294
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Ravindra Kolhe (R)

Department of Pathology, Augusta University, Augusta, GA 30912, USA.

Virgenal Owens (V)

Department of Orthopaedic Surgery, Augusta University, Augusta, GA 30912, USA.
Department of Orthopaedic Surgery, Carolinas Medical Center, Charlotte, NC 28203, USA.

Ashok Sharma (A)

Center for Biotechnology and Genomic Medicine, Augusta University, Augusta, GA 30912, USA.

Tae Jin Lee (TJ)

Center for Biotechnology and Genomic Medicine, Augusta University, Augusta, GA 30912, USA.

Wenbo Zhi (W)

Center for Biotechnology and Genomic Medicine, Augusta University, Augusta, GA 30912, USA.

Umar Ghilzai (U)

Department of Orthopaedic Surgery, Augusta University, Augusta, GA 30912, USA.

Ashis K Mondal (AK)

Department of Pathology, Augusta University, Augusta, GA 30912, USA.

Yutao Liu (Y)

Cell Biology and Anatomy, Augusta University, Augusta, GA 30912, USA.

Carlos M Isales (CM)

Department of Pathology, Augusta University, Augusta, GA 30912, USA.
Department of Medicine, Augusta University, Augusta, GA 30912, USA.
Institute of Healthy Aging, Augusta University, Augusta, GA 30912, USA.

Mark W Hamrick (MW)

Department of Pathology, Augusta University, Augusta, GA 30912, USA.
Cell Biology and Anatomy, Augusta University, Augusta, GA 30912, USA.
Institute of Healthy Aging, Augusta University, Augusta, GA 30912, USA.

Monte Hunter (M)

Department of Orthopaedic Surgery, Augusta University, Augusta, GA 30912, USA.

Sadanand Fulzele (S)

Department of Pathology, Augusta University, Augusta, GA 30912, USA.
Cell Biology and Anatomy, Augusta University, Augusta, GA 30912, USA.
Department of Medicine, Augusta University, Augusta, GA 30912, USA.
Institute of Healthy Aging, Augusta University, Augusta, GA 30912, USA.

Classifications MeSH