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PMID: 30797944 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Distinct degenerative phenotype of articular cartilage from knees with meniscus tear compared to knees with osteoarthritis.

Osteoarthritis and cartilage ·Vol. 27 ·No. 6 ·2019-00-00 ·页码 945-955

Rai MF, Tycksen ED, Cai L, Yu J, Wright RW, Brophy RH

Abstract

To compare the transcriptome of articular cartilage from knees with meniscus tears to knees with end-stage osteoarthritis (OA). Articular cartilage was collected from the non-weight bearing medial intercondylar notch of knees undergoing arthroscopic partial meniscectomy (APM; N = 10, 49.7 ± 10.8 years, 50% females) for isolated medial meniscus tears and knees undergoing total knee arthroplasty (TKA; N = 10, 66.0 ± 7.6 years, 70% females) due to end-stage OA. Ribonucleic acid (RNA) preparation was subjected to SurePrint G3 human 8 × 60K RNA microarrays to probe differentially expressed transcripts followed by computational exploration of underlying biological processes. Real-time polymerase chain reaction amplification was performed on selected transcripts to validate microarray data. We observed that 81 transcripts were significantly differentially expressed (45 elevated, 36 repressed) between APM and TKA samples (≥ 2 fold) at a false discovery rate of ≤ 0.05. Among these, CFD, CSN1S1, TSPAN11, CSF1R and CD14 were elevated in the TKA group, while CHI3L2, HILPDA, COL3A1, COL27A1 and FGF2 were highly expressed in APM group. A few long intergenic non-coding RNAs (lincRNAs), small nuclear RNAs (snoRNAs) and antisense RNAs were also differentially expressed between the two groups. Transcripts up-regulated in TKA cartilage were enriched for protein localization and activation, chemical stimulus, immune response, and toll-like receptor signaling pathway. Transcripts up-regulated in APM cartilage were enriched for mesenchymal cell apoptosis, epithelial morphogenesis, canonical glycolysis, extracellular matrix organization, cartilage development, and glucose catabolic process. This study suggests that APM and TKA cartilage express distinct sets of OA transcripts. The gene profile in cartilage from TKA knees represents an end-stage OA whereas in APM knees it is clearly earlier in the degenerative process.

Keywords
Extracellular matrix organization Immune response Knee arthroplasty Microarrays Partial meniscectomy lincRNAs
MeSH 主题词
Adult Aged Arthroplasty, Replacement, Knee Cartilage, Articular/metabolism Case-Control Studies Caseins/genetics Chitinases/genetics Collagen Type III/genetics Complement Factor D/genetics Female Fibrillar Collagens/genetics Fibroblast Growth Factor 2/genetics Gene Expression Profiling Humans Lipopolysaccharide Receptors/genetics Male Meniscectomy Middle Aged Neoplasm Proteins/genetics Osteoarthritis, Knee/genetics,surgery Phenotype RNA/metabolism RNA, Antisense/metabolism RNA, Long Noncoding/metabolism RNA, Messenger/metabolism RNA, Small Nuclear/metabolism Real-Time Polymerase Chain Reaction Receptors, Granulocyte-Macrophage Colony-Stimulating Factor/genetics Tetraspanins/genetics Tibial Meniscus Injuries/genetics,surgery
化学物质
COL27A1 protein, human COL3A1 protein, human CSF1R protein, human Caseins Collagen Type III Fibrillar Collagens HILPDA protein, human Lipopolysaccharide Receptors Neoplasm Proteins RNA, Antisense RNA, Long Noncoding RNA, Messenger RNA, Small Nuclear Receptors, Granulocyte-Macrophage Colony-Stimulating Factor TSPAN11 protein, human Tetraspanins Fibroblast Growth Factor 2 RNA CHI3L2 protein, human Chitinases CFD protein, human Complement Factor D
作者与单位
共 6 位作者,点击展开单位 / ORCID
Rai M F
Department of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: [email protected].
Tycksen E D
Genome Technology Access Center, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: [email protected].
Cai L
Department of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: [email protected].
Yu J
Genome Technology Access Center, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: [email protected].
Wright R W
Department of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: [email protected].
Brophy R H
Department of Orthopaedic Surgery, Musculoskeletal Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: [email protected].
Article Info
Journal
Osteoarthritis and cartilage
Abbr.
Osteoarthritis Cartilage
ISSN
1522-9653
Published
2019-00-00
电子出版
2019-00-21
页码
945-955
Language
English
Country/Region
England
NLM ID
9305697
基金资助
NIAMS NIH HHS · R00 AR064837 · United States
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