2013 Volume No 26 – pages 107-119
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Title: Best Paper NASS 2013: Link-N can stimulate proteoglycan synthesis in the degenerated human intervertebral discs |
Author: R Gawri, J Antoniou, J Ouellet, W Awwad, T Steffen, P Roughley, L Haglund, F Mwale |
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Address: Lady Davis Institute for Medical Research, Sir Mortimer B. Davis – Jewish General Hospital, 3755 Chemin Cote Ste Catherine, Montréal, H3T 1E2 Canada |
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E-mail: fmwale at ldi.jgh.mcgill.ca |
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Key Words: Human intervertebral disc degeneration; regeneration; tissue engineering; organ culture; proteoglycans; bioactive peptides; Link-N; biological repair. |
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Publication date: September 11th 2013 |
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Abstract: Intervertebral disc (IVD) degeneration is the most common cause of back pain. Presently there is no medical treatment, leaving surgery as the only offered option. Here we evaluate the potential of Link-N to promote extracellular matrix regeneration in human IVDs. Human disc cells cultured in alginate and intact human discs were exposed to a combination of Link-N and 35SO4 in the presence or absence of interleukin (IL)-1, and the effect on proteoglycan synthesis was evaluated. In addition, message levels of aggrecan, matrix metalloproteinase (MMP)-3, MMP-13, a Disintegrin And Metalloproteinase with Thrombospondin Motifs (ADAMTS)-4 and ADAMTS-5 were evaluated in alginate cultures. Human disc cells responded in a dose dependent manner with maximal proteoglycan synthesis at 1 µg/mL Link-N. Link-N treatment also induced proteoglycan synthesis in intact human discs, and a prolonged effect was found up to one week after Link-N treatment. Message levels of proteinases were decreased by Link-N in the presence of IL-1. Thus, Link-N can promote proteoglycan synthesis and deplete proteinase expression in adult human discs. Link-N could therefore be a promising candidate for biologically-induced disc repair, and could provide an alternative to surgical intervention for early stage disc degeneration. |
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Article download: Pages
107-119 (PDF file) |
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