Bovine NP tissue (1.5 to 2.5 g) was isolated from caudal discs (3 discs per tail) of cattle aged less than 18 months from a local abattoir (Humphreys and Sons, Chelmsford, Essex, UK). Tails from 15 animals were used for all experiments. The tissue was diced and incubated on rollers in Dulbecco Modified Eagle Medium (DMEM)/F12 supplemented with penicillin/streptomycin (5%), ascorbic acid (2.5 µg/mL), amphoceterin B (5%), FCS (20%), collagenase type XI (0.8 mg/mL) and DNAse I (2.6 units/mL) for 16 h at 37 °C. The cell suspension was filtered through a 70 µM cell strainer, centrifuged at 2,000 rpm for 5 min and resuspended in media. Cells were subsequently expanded in monolayer culture in DMEM/F12 + 10% FCS until 80% confluent.

Confluent NP cells (Passage 1) were detached with 0.2% trypsin and 0.1% EDTA and counted on a hemocytometer using the trypan blue exclusion assay. Viable NP cells were seeded into 3% agarose type VII (low gelling temperature agarose) or 4% agarose type IX (ultra-low temperature gelling agarose) at 4 million cells/mL, using well-established methods, as previously described [25,26]. The agarose concentration and type were chosen based on previous observations [25,26]. To review briefly, the cells were resuspended in medium at a cell concentration of 8 × 10⁶ cells/mL and added to an equal volume of molten 6% (w/v) agarose type VII or 8% (w/v) agarose type IX in Earle Balanced Salt Solutions (EBSS) to yield a final cell concentration of 4 × 10⁶ cells/mL in 3% (w/v) agarose type VII or 4% agarose type XI (Sigma-Aldrich, Poole, UK). This is equivalent to approximately 400,000 cells per construct. The chondrocyte/agarose suspension was transferred into a sterile stainless steel mold, containing holes 5 mm in diameter and 5 mm in height and allowed to gel at 4 °C for 20 min. NP/agarose constructs were equilibrated in culture in DMEM/F12 + 10% FCS for up to 72 h to enable re-differentiation prior to further cell culture or mechanical loading experiments. The NP/agarose constructs were subsequently cultured for 48 h either under free-swelling conditions or when subjected to dynamic compression (15%, 1 Hz frequency). At the end of the culture period, constructs and media samples were stored at −20 °C prior to biochemical analysis or examined for mechanical testing. In addition, cell viability was assessed using calcein AM (5 µM) and ethidium homodimer (5 µM) by fluorescence microscopy (Invitrogen, Paisley, UK), as previously described [25].

In separate experiments, equilibrated NP/agarose constructs (3%, type VII) were cultured for a further 48 h under free-swelling conditions in the presence and absence of 0.1, 1 and 10 ng/mL TGFβ₃ (Cambrex Bioscience, Wokingham, Berkshire). At the end of the experiment, constructs and media samples were stored at −20 °C prior to biochemical analysis.

In separate experiments, the combined effects of TGFβ and dynamic compression on protein synthesis and gene expression were examined in NP/agarose constructs (3%, type VII) cultured for 6 and 48 h. The bioreactor system has been extensively described previously [25,26]. To review briefly, equilibrated constructs were transferred into individual wells of a 24-well culture plate (Costar, High Wycombe, UK) and mounted within the bioreactor. One milliliter of media supplemented with either 0 or 10 ng mL⁻¹ TGFβ were introduced into each well. Two separate compression regimens were applied to constructs in a dynamic manner at a strain amplitude of 15% and a frequency of 1 Hz:

1.5 h compression with a 22.5 h unstrained period repeated 2 × (1.5 h/22.5 h^×2);

1.5 h compression with a 4.5 h unstrained period repeated 8 × (1.5 h/4.5 h^×8).

Control constructs were maintained in an unstrained state within the bioreactor system and cultured for the same time period. At the end of the culture period, the constructs and corresponding media were immediately stored at −70 °C prior to analysis.

RNA was isolated from NP cells cultured in agarose using protocols described in the QIAquick ^℘ Spin gel extraction and RNeasy ^℘ kits, as previously described (Qiagen,West Sussex, UK) [27]. Following manufacturer’s instructions, Ambion’s DNA-free DNase treatment and removal reagents were used to eliminate any contaminating DNA from the RNA sample (Ambion Applied Biosystems, Warrington, UK). RNA was quantified on the Nanodrop ND-1000 spectrophotometer (LabTech, East Sussex, UK) and reverse transcribed (200 ng) in a 20 µL reaction volume using the manufacturer-supplied oligo (dT) primers. Minus reverse transcriptase (NoRT) control reactions were prepared for each sample by omitting the Stratascript℘ reverse transcriptase. Real-time quantitative PCR assays coupled with molecular beacon probes were performed in 25 µL reaction mixtures containing 1 µL cDNA, 12.5 µL Brilliant ^℘ QRT-PCR Master Mix, primer pairs and probes listed in Table 1 and nuclease free PCR grade water to 25 µL (Sigma Genosys, Cambridge, UK). Each sample was run in duplicate on the 96-well thermal system of the M × 3000P quantitative PCR instrument (Stratagene, Amsterdam, the Netherland).

Thermocycling conditions comprised of an initial polymerase activation step at 95 °C for 3 min, followed by denaturation of 35 cycles at 95 °C for 30 s, annealing at 55 °C for 1 min and extension at 72 °C for 1 min. PCR efficiencies for optimal primer pair and probe concentrations were derived from standard curves (n = 3) by preparing a ten-fold serial dilution of cDNA from a sample which represented the untreated control at time zero conditions. The real-time PCR efficiencies (E) of amplification for each target was defined according to the relationship, E = 10^[−1/slope]. The R² value of the standard curve exceeded 0.9998 and revealed efficiency values between 0.99 and 1.01.

Fluorescence data was collected during the annealing stage of amplification and data was analyzed on the MxPro℘ qPCR software (version 3, Stratagene). Baselines and thresholds were automatically set by the RG-3000℘ qPCR software and used after manual inspection. The cycle threshold (C_t) value for each duplicate reaction was expressed as the mean value and the results were exported into Microsoft Excel for further analysis. Relative quantification of aggrecan and collagen type II signals were accomplished by normalizing each target to the reference gene, GAPDH and to the calibrator sample by a comparative C_t approach. For each sample, the ratio of target ∆Ct and reference ∆Ct was calculated, as previously described [27,28]. In addition, the C_t values for GAPDH remained stable with no changes detected under all culture conditions, suggesting its suitability as a reference gene.

The production of nitrite was determined in media samples and assayed spectrophotometrically at 540 nm using the Griess reaction. sGAG content was measured in media and constructs digested overnight at 37 °C with 10 U mL⁻¹ agarase followed by 1 h at 60 °C with 2.8 U mL⁻¹ papain (both Sigma Chemical Co., Poole, UK) using the DMMB assay [25,26]. Total DNA content which remained stable throughout the culture conditions was assayed using the Hoescht dye 33258 in agarase/papain digests.

NP/agarose constructs were tested in unconfined compression with a mechanical test system (MTS Bionix 100, Billingshirt, UK) using stainless steel platens which were larger compared with the 5 mm diameter constructs. Samples were initially subjected to a 0.02 N tare load followed by a strain rate of 0.05% strain/s up to a maximum strain of 15%. This constant strain was maintained while the constructs relaxed until an equilibrium stress was reached. From the stress-strain response a tangent modulus was estimated, while an equilibrium modulus was calculated following stress relaxation [29].

Forfree-swelling experiments, data represent the mean and SEM values of 12 replicates from three separate experiments. For the mechanical loading experiments, data represent the mean and SEM values of 15 replicates from four separate experiments. Statistical analysis was performed by a two-way analysis of variance (ANOVA) and the multiple post hoc Bonferroni-corrected t-tests to compare differences between the various treatment groups. In all cases, a level of 5% was considered statistically significant (p

The effect of culturing NP cells in constructs of different agarose types and concentrations on protein synthesis and the resulting mechanical properties are illustrated in Figure 1. GAG synthesis was significantly enhanced over the 48 h culture period (pp 30,31]. In particular, long term culture of NP cells in agarose constructs increased cell proliferation and GAG synthesis and enhanced gene expression of aggrecan and collagen type II [32,33]. In addition, 3D cultures of NP cells were previously described in alginate beads or in fibrin/hylauronan and were shown to maintain cell phenotype and matrix synthesis [32,34,35,36]. Accordingly, subsequent experiments were limited to examining the effect of mechanical conditioning of NP cells cultured in 3% agarose type VII.

The effect of two distinct dynamic compression regimens on NP protein synthesis is illustrated in Figure 3. In both cases, nitrite levels were significantly reduced by dynamic compression in NP/agarose constructs (pp 16,37]. In addition, a single load for 30 min or daily for four weeks increased anabolic gene expression in human NP cells cultured in collagen gels [38,39]. Conversely, compression applied at high frequencies (>3 Hz) and magnitude (>1 MPa) for extended periods (>48 h) reduced matrix synthesis and increased gene expression of catabolic factors, such as nitric oxide (NO), matrix metalloproteinase-3 (MMP-3), matrix metalloproteinase-13 (MMP-13) and a disintegrin and metalloproteinase with thrombospondin motifs-4 (ADAMTS-4) [16,37]. The deleterious effects were shown to cause cell death and were similar to murine studies in which static compression was applied at high magnitudes (>1 MPa) for 6 hours [16,37].

In a separate study, stimulation by static compression for one week was associated with degenerative changes involving cell death, decreased aggrecan and collagen type II expression and elevated protease gene expression in murine disc tails [40,41,42,43]. Interestingly, these effects were not found at low magnitudes of static compression (

The autocrine and paracrine production of growth factors is considered to be a major regulatory mechanism in IVD tissues [5]. We therefore examined the effect of TGFβ on protein synthesis in NP/agarose constructs. The presence of TGFβ significantly increased GAG synthesis and inhibits nitrite release in a dose-dependent manner (Figure 4). These data are in agreement with previous studies which showed dose-dependent upregulation of proteoglycan synthesis and gene expression of aggrecan and collagen type II by TGFβ in the agarose or alginate model [10,32]. At 1 ng/mL, TGFβ increased cell proliferation and proteoglycan synthesis in canine NP cells and the response was further increased with 20% FCS [8]. In rodent organ culture, TGFβ (5 ng/mL) maintained phenotype and proteoglycan synthesis when cultured in insulin-transferrin-selenium (ITS) containing media with 20% FCS [47]. At 10 ng/mL, NP cells cultured in collagen or hylauronan scaffolds with TGFβ results in the production of several types of proteoglycans and collagens [48]. However, matrix integrity could not be maintained during long term culture, highlighting the importance of choosing an optimal environment for TGFβ stimulation in 3D models. Furthermore, the expression of TGFβ and the TGFβ Type II receptor (TGFβRII) were found to be low in human herniated IVDs. In rat and murine models, TGFβ and its receptors were shown to decrease with age [49,50]. These findings support the potential of TGFβ in promoting matrix synthesis and maintaining tissue integrity and imply its absence may be a risk factor for IVD degeneration.

The combined effect of TGFβ and dynamic compression on protein synthesis and gene expression in NP/agarose constructs are presented in Figures 5 and 6, respectively. Stimulation by TGFβ and dynamic compression significantly enhanced GAG synthesis and reduced nitrite levels in NP/agarose constructs (both pFigure 5). In addition, TGFβ and dynamic compression significantly induced gene expression of aggrecan and collagen type II in a time-dependent manner (all pFigure 6). This is the first study to show an additive effect of TGFβ and dynamic compression on protein synthesis and gene expression in NP/agarose constructs. The combined effect of growth factors and mechanical loading on IVD metabolism is not known. Moreover, previous studies demonstrate enhanced chondrogenesis with TGFβ and dynamic compression resulting in anabolic gene expression in human mesenchymal progenitor cells cultured in monolayer or alginate [51,52,53]. It is possible that other growth factors such as GDF-5 or IGF-1 could initiate differentiation of MSCs to an IVD phenotype during physiological dynamic loading. However, the anabolic response will be dependent on the exposure time to growth factors and whether loading was applied during early or late stage cultures [54].