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   <subfield code="a">Development of an intact intervertebral disc organ culture system in which degeneration can be induced as a prelude to studying repair potential</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Bernice Jim, Thomas Steffen, Janet Moir, Peter Roughley, Lisbet Haglund]</subfield>
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   <subfield code="a">The present work describes a novel bovine disc organ culture system with long-term maintenance of cell viability, in which degenerative changes can be induced as a prelude to studying repair. Discs were isolated with three different techniques: without endplates (NEP), with bony endplates (BEP) and with intact cartilage endplates (CEP). Swelling, deformation, and cell viability were evaluated in unloaded cultures. Degeneration was induced by a single trypsin injection into the center of the disc and the effect on cell viability and matrix degradation was followed. Trypsin-treated discs were exposed to TGFβ to evaluate the potential to study repair in this system. NEP isolated discs showed &gt;75% maintained cell viability for up to 10days but were severely deformed, BEP discs on the other hand maintained morphology but failed to retain cell viability having only 27% viable cells after 10days. In CEP discs, both cell viability and morphology were maintained for at least 4weeks where &gt;75% of the cells were still viable. To mimic proteoglycan loss during disc degeneration, a single trypsin injection was administered to the center of the disc. This resulted in 60% loss of aggrecan, after 7days, without affecting cell viability. When TGFβ was injected to validate that the system can be used to study a repair response following injection of a bio-active substance, proteoglycan synthesis nearly doubled compared to baseline synthesis. Trypsin-treated bovine CEP discs therefore provide a model system for studying repair of the degenerate disc, as morphology, cell viability and responsiveness to bio-active substances were maintained.</subfield>
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   <subfield code="u">Orthopaedic Research Laboratory, McGill University, 687 Pine Avenue West, Room L4.70, H3A 1A1, Montreal, QC, Canada</subfield>
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   <subfield code="t">European Spine Journal</subfield>
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