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The effect of WIN55, 212-2 on protein S100, matrix metalloproteinase-2 and nitric oxide expression of chondrocyte monolayer
Abdeldayum, Ali I.A. ; ; Sefat, Farshid ; Genedy, Mohamed A. ; Abdul Jamil, M.M. ; Javid, F.
Abdeldayum, Ali I.A.
Sefat, Farshid
Genedy, Mohamed A.
Abdul Jamil, M.M.
Javid, F.
Publication Date
2017-01
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© 2017 M Youseffi. This work is licensed under a Creative Commons Attribution 4.0 International License. http://creativecommons.org/licenses/by/4.0/
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2017-01-03
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Abstract
Studies have been conducted to highlight the anti-inflammatory and immunosuppressive properties of
synthetic cannabinoids as well as their potential for cartilage repair. Various wound healing techniques can be
used to investigate the mechanisms of chondrocyte repair in monolayers or three dimensional tissues constructs.
In this work the effect of WIN55, 212-2 (WIN-2) on nitric oxide (NO) and matrix metalloproteinase-2 (MMP-2)
expressed by wounded chondrocyte monolayers was investigated. Moreover, expression of collagen type-I and
type-II, fibronectin and S100 proteins were detected using immunofluorescence and quantitatively verified using
ELISA based techniques following treatment with 1 μM and 2 μM of WIN-2. Treating chondrocytes with 1 μM
of WIN-2 significantly increased expression of collagen type-II, fibronectin and S100, and significantly reduced
collagen type-I expressions as compared to the control groups. On the other hand, both concentrations of WIN-2
significantly reduced the expression of the inflammation markers NO and MMP-2 in a dose dependent manner.
These findings highlight the potential use of the synthetic cannabinoids for improving cartilage healing properties
as well as acting as an anti-inflammatory agent which could be used to enhance tissue engineering protocols
aimed at cartilage repair.
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Citation
Abdeldayum A, Youseffi M, Sefat F et al (2017) The effect of WIN55, 212-2 on protein S100, matrix metalloproteinase-2 and nitric oxide expression of chondrocyte monolayer. SM Journal of Biomedical Engineering. 3(1): 1011.
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