Unique glycosignature for intervertebral disc and articular cartilage cells and tissues in immaturity and maturity

• Published in: Scientific reports Vol. 6; no. 1; p. 23062
• Main Authors: Collin, E C, Kilcoyne, M, White, S J, Grad, S, Alini, M, Joshi, L, Pandit, A S
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 11.03.2016
• Subjects: Animals; Annulus Fibrosus - growth & development; Annulus Fibrosus - metabolism; Antibodies; Cartilage (articular); Cartilage, Articular - growth & development; Cartilage, Articular - metabolism; Chondrocytes; Chondrocytes - metabolism; Chondroitin sulfate; Chondroitin Sulfates - isolation & purification; Chondroitin Sulfates - metabolism; Chromatography, High Pressure Liquid; High-performance liquid chromatography; Humans; Intervertebral Disc - growth & development; Intervertebral Disc - metabolism; Intervertebral discs; Lectins; Maturity; Nucleus pulposus; Nucleus Pulposus - growth & development; Nucleus Pulposus - metabolism; Sheep - growth & development; Sheep - metabolism; Sulfate
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep23062

In this study, on/off markers for intervertebral disc (IVD) and articular cartilage (AC) cells (chondrocytes) and distinct glycoprofiles of cell and tissue-types were identified from immaturity to maturity. Three and eleven month-old ovine IVD and AC tissues were histochemically profiled with a panel of lectins and antibodies. Relationships between tissue and cell types were analysed by hierarchical clustering. Chondroitin sulfate (CS) composition of annulus fibrosus (AF), nucleus pulposus (NP) and AC tissues was determined by HPLC analysis. Clear on/off cell type markers were identified, which enabled the discrimination of chondrocytes, AF and NP cells. AF and NP cells were distinguishable using MAA, SNA-I, SBA and WFA lectins, which bound to both NP cells and chondrocytes but not AF cells. Chondrocytes were distinguished from NP and AF cells with a specific binding of LTA and PNA lectins to chondrocytes. Each tissue showed a unique CS composition with a distinct switch in sulfation pattern in AF and NP tissues upon disc maturity while cartilage maintained the same sulfation pattern over time. In conclusion, distinct glycoprofiles for cell and tissue-types across age groups were identified in addition to altered CS composition and sulfation patterns for tissue types upon maturity.