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The effect of synthetic cannabinoids and their combination with TGF-β3 on wound healing of cell cultured human bone cell monolayers and 3D models. The role of synthetic cannabinoid HU308 and HU308/TGF-β3 combinations on cellular adhesion, proliferation, wound healing, nitric oxide, MMP-2 and ECM protein regulation of MG-63 osteoblast monolayers and 3D modelsGenedy, Mohamed A. January 2013 (has links)
Despite the ongoing political debate regarding the legality of medical marijuana, clinical
investigations of the therapeutic use of cannabinoids are now more prevalent than at any
time in history. Cannabinoids have been shown to have analgesic, anti-spasmodic, anticonvulsant,
anti-tremor, anti-psychotic, anti-inflammatory, anti-oxidant, anti-emetic and
appetite-stimulant properties. There are mainly two well-known cannabinoid receptors,
CB1 and CB2, located in the central (CB1) and peripheral (CB2) nervous systems as well
as the immune system. More recently, endocannabinoids (ligands) and their receptors
have also been found in the skeleton which appear as the main body system and
physiologically regulated by CB2.
This study aimed to examine the effect of both CB1 and CB2 receptor stimulation on
wound closure response of MG-63 osteoblast bone cell monolayers using different
treatments with cannabinoid such as Winn55,212-2, URB602 and HU308. Also, cell
adhesion, cell proliferation and cell length was investigated. The study also aimed to
examine the effect of HU308 treatments in combination with TGF-β3 (transforming
growth factor beta -3) on wound healing, cell adhesion and extracellular matrix up
regulation (collagen type I, fibronectin and protien S-100A6) as well as other biological
factors such as secretion of matrix metalloproteinase (MMP-2) and nitric oxide (NO).
Finally, this study investigated HU308/TGF-β3 combination treatment on the regulation
of extracellular matrix (collagen type I, fibronectin and protien S-100A6) in a 3D
multilayer system of MG-63 osteoblast bone cells.
Wound healing assays of MG-63 monolayers revealed accelerated wound repair as well
as increased cell proliferation mainly regulated through CB2 receptors, and that
treatments with HU308 and HU308/TGF-β3 achieved minimum closure timings
compared with control groups (P<0.05). Our finding suggested that proliferation rate
with 500nM HU308 was significantly higher than control and TGF-β3/HU308
combination groups (P<0.05). Interestingly, percentage of wound remained open after
15 hours for combination groups was 17.6%±1.32 whereas treatment with 500nM
HU308 had 20%±2.25 indicating that the combination groups took the lead throughout wound healing. It was also observed that bridge formation in all treatment groups was
taking place between 15 to 20 hour periods whereas within control treatments bridge
formation started to take place after 25 hours.
Cell surface attachment was examined via the trypsinization assay in which the time
taken to trypsinize cells from the surface provided a means of assessing the strength of
attachment. The results indicated that higher concentrations of HU308 (2μM), induced
significant force of cell attachment compared with control and concentrations of 500nM
and 1μM (P<0.05). However, groups treated with TGF-β3 and combination
HU308/TGF-β3 indicated reduced cell surface attachment compared with control
groups, indicating enhanced cell migration.
Immunofluorescence staining as well as Elisa based semi-quantification technique
indicated that both collagen type I and fibronectin were unregulated using higher
concentrations of HU308 with decreased cell proliferation compared to lower
concentrations. Nevertheless, protein S-100A6 was up-regulated in treatments with
HU308, TGF-β3 and their combination HU308/TGF-β3 (P<0.05), indicating the
positive role of these treatments in promoting cell differentiation. MMP-2 levels in the
current study were also shown to be concentration-dependent, i.e. higher concentrations
of HU308 significantly reduced MMP-2 secretion leading to decreased cell migration,
while HU308/TGF-β3 combination treatment increased MMP-2 levels, indicating an
increase in cell migration. The current study also examined levels of nitric oxide
synthesis in relation to different treatments with HU308, TGF-β3 and HU308/TGF-β3
combination. It was found that nitric oxide up-regulation influences rate of MG-63
osteoblast wound healing in a concentration dependent manner.
Lastly, UpCell culture dishes proved to have efficacy in obtaining a multilayer model of
MG-63 osteoblast system in-vitro through changes in cell morphology. It was also
found that treatments with HU308, TGF-β3 and HU308/TGF-β3 combination
influenced collagen type I, fibronecton and protein S-100A6 secretion. These findings
supported the earlier Elisa based semi-quantification results obtained for monolayer
cultures.
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15-HYDROXYPROSTAGLANDIN DEHYDROGENASE IS A TGF-beta INDUCED SUPPRESSOR OF HUMAN COLORECTAL CANCERYan, Min January 2005 (has links)
No description available.
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The Roles of a LIM Domain Protein, Hic-5/ARA55, in TGF-β Signaling in Prostate Cancer CellsWang, Hui 06 October 2008 (has links)
No description available.
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Activin A Reduces Brain Injury After StrokeMukerji, Shibani Sharon 10 January 2009 (has links)
No description available.
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Transforming Growth Factor-Beta (TGFΒ)-Mediated Post-Transcriptional Regulation of Epithelial-Mesenchymal Transdifferentiation (EMT)Chaudhury, Arindam 06 April 2010 (has links)
No description available.
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Controlled Delivery of TGF-β1 from PLGA NanoparticlesVaidya, Pratik K. 14 December 2012 (has links)
No description available.
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Molecular Mechanism of Fibrosis and Central Role of Cardiotonic Steroids in Uremic CardiomyopathyElkareh, Jihad Victor 18 June 2008 (has links)
No description available.
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Characterization and Quantitation of Collagen-I Oxidation in TGF-β Stimulated Fibroblast CultureUddin, Muhammad Erfan 25 May 2017 (has links)
No description available.
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THE FUNCTION OF XPACE4 AND Vg1 DURING EARLY <i>XENOPUS</i> EMBRYOGENESISTUNCA, BILGE 03 April 2006 (has links)
No description available.
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The role and regulation of FoxI1e in <i>Xenopus ectoderm</i> formationMir, Adnan 08 October 2007 (has links)
No description available.
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