Abstract

PurposeHyaluronic acid plays an essential role in water retention of the intervertebral disc (IVD) and thus provides flexibility and shock absorbance in the spine. Hyaluronic acid gets degraded by hyaluronidases (HYALs), and some of the resulting fragments were previously shown to induce an inflammatory and catabolic response in human IVD cells. However, no data currently exist on the expression and activity of HYALs in IVD health and disease.MethodsGene expression, protein expression and activity of HYALs were determined in human IVD biopsies with different degrees of degeneration (n = 50 total). Furthermore, freshly isolated human IVD cells (n = 23 total) were stimulated with IL-1β, TNF-α or H2O2, followed by analysis of HYAL-1, HYAL-2 and HYAL-3 gene expression.ResultsGene expression of HYAL-1 and protein expression of HYAL-2 significantly increased in moderate/severe disc samples when compared to samples with no or low IVD degeneration. HYAL activity was not significantly increased due to high donor–donor variation, but seemed overall higher in the moderate/severe group. An inflammatory environment, as seen during IVD disease, did not affect HYAL-1, HYAL-2 or HYAL-3 expression, whereas exposure to oxidative stress (100 µM H2O2) upregulated HYAL-2 expression relative to untreated controls.ConclusionAlthough HYAL-1, HYAL-2 and HYAL-3 are all expressed in the IVD, HYAL-2 seems to have the highest pathophysiological relevance. Nonetheless, further studies will be needed to comprehensively elucidate its significance and to determine its potential as a therapeutic target.Graphic abstractThese slides can be retrieved under Electronic Supplementary Material.

Highlights

  • Glycosaminoglycans (GAGs), which are major components of the extracellular matrix (ECM) of numerous connective tissues, including the intervertebral disc (IVD), are a family of negatively charged heteropolysaccharides

  • The G1 domain at the N-terminal end of aggrecan interacts with hyaluronic acid (HA) and link protein and provides the hydrated gel structure seen in healthy IVDs, in the nucleus pulposus (NP) [1, 2]

  • Gene expression of HYAL-1, HYAL-2 and HYAL-3 in human disc tissue was analyzed in relation to the degeneration grade

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Summary

Introduction

Glycosaminoglycans (GAGs), which are major components of the extracellular matrix (ECM) of numerous connective tissues, including the intervertebral disc (IVD), are a family of negatively charged heteropolysaccharides. Chondroitin sulfate and keratan sulfate as the IVD-typical GAGs bind to an extended protein core, resulting in the brush-like proteoglycan (PG) named aggrecan. The G1 domain at the N-terminal end of aggrecan interacts with hyaluronic acid (HA) and link protein and provides the hydrated gel structure seen in healthy IVDs, in the nucleus pulposus (NP) [1, 2]. Ample evidence has been provided over the past decades for the degradation of aggrecan with IVD degeneration. Changes in spatial distribution and disaccharide sulphation patterns of GAGs are commonly observed during IVD aging and degeneration [8,9,10]

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