2008
DOI: 10.1097/jsa.0b013e31818d56b3
|View full text |Cite
|
Sign up to set email alerts
|

Emerging Technologies and Fourth Generation Issues in Cartilage Repair

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
41
0
5

Year Published

2010
2010
2024
2024

Publication Types

Select...
5
3

Relationship

0
8

Authors

Journals

citations
Cited by 70 publications
(46 citation statements)
references
References 100 publications
0
41
0
5
Order By: Relevance
“…Moreover, ADMSCs show chondrogenic potential, with the ability to maintain the differentiated chondrocyte phenotype for a long time both in vivo and in vitro (Erickson et al, 2002), and exhibit a strong capacity to form chondrocytes (Kessler et al, 2008). In the current study, the number of chondrocytes in the control and vector groups was lower than that in the hBMP-7 group, suggesting that the differentiation of ADMSCs induced by BMP-7 toward chondrocytes was effective.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, ADMSCs show chondrogenic potential, with the ability to maintain the differentiated chondrocyte phenotype for a long time both in vivo and in vitro (Erickson et al, 2002), and exhibit a strong capacity to form chondrocytes (Kessler et al, 2008). In the current study, the number of chondrocytes in the control and vector groups was lower than that in the hBMP-7 group, suggesting that the differentiation of ADMSCs induced by BMP-7 toward chondrocytes was effective.…”
Section: Discussionmentioning
confidence: 99%
“…17,18 Hydrogels have a high water content that creates a protective environment which mimics native cartilage. 19 They allow the addition of growth factors and cell signaling molecules that can diffuse freely. 20 The addition of bone morphogenetic peptide-7 (BMP-7) has been shown to improve the repair histology when used in addition to microfracture.…”
Section: Microfracturementioning
confidence: 99%
“…These findings clearly suggest a correlation between a change of biomechanical properties following injury and the development of OA; however, the exact mechanisms are yet to be elucidated. OA is a chronic disease that leads to slow degradation of articular cartilage and pathological changes to the synovium as well as other connective tissues in the joint [135]. Symptoms attributed to OA involve debilitating pain in affected joints and impaired mobility [136].…”
Section: Osteoarthritismentioning
confidence: 99%
“…With the advancement of OA, pro-inflammatory cytokines including interleukin-1 and -6 (IL-1, IL-6), as well as tumour necrosis factor-α (TNF-α) cause an up-regulation of catabolic pathways in chondrocytes [135]. These cytokines play a key role in OA through activation of matrix-degrading aggrecanases ("A Disintegrin and Metalloproteinase with Thrombospondin motifs", or ADAMTS) and MMPs, as well as nitric oxide signalling pathways [141].…”
Section: Osteoarthritismentioning
confidence: 99%
See 1 more Smart Citation