2010
DOI: 10.2217/thy.10.72
|View full text |Cite
|
Sign up to set email alerts
|

Synovium in the pathophysiology of osteoarthritis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
14
0

Year Published

2015
2015
2023
2023

Publication Types

Select...
6
1

Relationship

1
6

Authors

Journals

citations
Cited by 10 publications
(14 citation statements)
references
References 34 publications
0
14
0
Order By: Relevance
“…Production of IL-6 in disease-affected joint tissue is a response from IL-1β and TNF-α [8]. IL-1β is mostly produced by synovial macrophages and chondrocytes in the OA joint [9]. The synovial intimal cells, termed synoviocytes, are believed to be responsible for the production of synovial fluid components, for absorption from the joint cavity, and for blood/synovial fluid exchanges.…”
Section: Discussionmentioning
confidence: 99%
See 2 more Smart Citations
“…Production of IL-6 in disease-affected joint tissue is a response from IL-1β and TNF-α [8]. IL-1β is mostly produced by synovial macrophages and chondrocytes in the OA joint [9]. The synovial intimal cells, termed synoviocytes, are believed to be responsible for the production of synovial fluid components, for absorption from the joint cavity, and for blood/synovial fluid exchanges.…”
Section: Discussionmentioning
confidence: 99%
“…Interlukin-1β (IL-1β) is considered as one of the most important and most influential cytokines in its involvement in the OA pathogenesis. IL-1β is mostly produced by synovial macrophages and chondrocytes in the OA joint [9]. These cytokines can induce inflammatory reactions and catabolic influences independently [8].…”
Section: Interleukin 1βmentioning
confidence: 99%
See 1 more Smart Citation
“…TIMP-1 is a protective mediator and appears to be exceptionally high in OA in synovial fluid. TIMP-1 and TIMP-2 are both present in the SM of OA [13], [14], [15]. The expression of mRNA from TIMP by chondrocytes in OA cartilage is higher than TIMP by normal cartilage chondrocytes.…”
Section: Pathogenesismentioning
confidence: 92%
“…These cytokines also increase the expression of inflammatory mediators and the activity of several proteolytic enzymes such as MMPs and aggrecanase that play a role in degrading joint cartilage [10], [13], [20], [21], [22]. Molecules included in pro-inflammatory cytokines include IL-1β (IL-1β), TNFα, IL-6, IL-15, IL-17, and IL-18 [7], [13], [14], [16], [23] ( Figure 1).…”
Section: Pathogenesismentioning
confidence: 99%