Subchondral pre-solidified chitosan/blood implants elicit reproducible early osteochondral wound-repair responses including neutrophil and stromal cell chemotaxis, bone resorption and repair, enhanced repair tissue integration and delayed matrix deposition
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In this study we evaluated a novel approach to guide the bone marrow-driven articular cartilage repair response in skeletally aged rabbits. We hypothesized that dispersed chitosan particles implanted close to the bone marrow degrade in situ in a molecular mass-dependent manner, and attract more stromal cells to the site in aged rabbits compared to the blood clot in untreated controls.
Three microdrill hole defects, 1.4 mm diameter and 2 mm deep, were created in both knee trochlea of 30 month-old New Zealand White rabbits. Each of 3 isotonic chitosan solutions (150, 40, 10 kDa, 80% degree of deaceylation, with fluorescent chitosan tracer) was mixed with autologous rabbit whole blood, clotted with Tissue Factor to form cylindrical implants, and press-fit in drill holes in the left knee while contralateral holes received Tissue Factor or no treatment. At day 1 or day 21 post-operative, defects were analyzed by micro-computed tomography, histomorphometry and stereology for bone and soft tissue repair.
All 3 implants filled the top of defects at day 1 and were partly degraded in situ at 21 days post-operative. All implants attracted neutrophils, osteoclasts and abundant bone marrow-derived stromal cells, stimulated bone resorption followed by new woven bone repair (bone remodeling) and promoted repair tissue-bone integration. 150 kDa chitosan implant was less degraded, and elicited more apoptotic neutrophils and bone resorption than 10 kDa chitosan implant. Drilled controls elicited a poorly integrated fibrous or fibrocartilaginous tissue.
Pre-solidified implants elicit stromal cells and vigorous bone plate remodeling through a phase involving neutrophil chemotaxis. Pre-solidified chitosan implants are tunable by molecular mass, and could be beneficial for augmented marrow stimulation therapy if the recruited stromal cells can progress to bone and cartilage repair.
KeywordsCartilage repair Bone marrow Chitosan Osteoclast Neutrophil Collagen Marrow stimulation Bone remodeling Mesenchymal stromal cell Micro-computed tomography
Degree of deacetylation
Number-average molecular weight
Rhodamine B isothiocyanate
Recombinant human Factor VIIa
Ethylene diamine tetraacetic acid
- col I
Collagen type I
- col II
Collagen type II
Tartrate- resistant Acidic Phosphatase
Receptor activator of NF-κB ligand
Monocyte chemoattractant protein 1 IL-8/CXCL8
Marrow stimulation is a cartilage repair technique in which bone channels are created at the base of the debrided cartilage lesion, to permit migration of bone marrow-derived repair cells into the lesion. Marrow stimulation techniques most often elicit fibrous or fibrocartilaginous tissue  that breaks down with time, with a documented ~25% failure rate at 5 years post-operative . Therefore, implants that elicit a more hyaline repair tissue quality from marrow stimulation defects are currently under intense research.
In designing new treatments to regenerate articular cartilage, biomaterials that do not need to be seeded with cultured cells have the advantage of being clinically practical and cost-efficient. However, to be effective, biomaterial-only implants must be able to guide mesenchymal stem cells with chondrogenic potential from the bone marrow to above the osteochondral junction and into the cartilage lesion. Biomaterials have previously been successfully implanted into osteochondral defects, but reproducible long-term clinical benefits have yet to be demonstrated. A tubular implant composed of electrospun poly(D,L-lactide-co-glycolide) (PLG) inserted in large (5 mm wide, 5 mm deep) osteochondral defects in a rabbit model generated good cartilage repair in most defects at 24 weeks post-operative . Subchondral implants made of PLG copolymer, calcium sulfate, polyglycolide fibers and surfactant have demonstrated clinical benefit, with complete pain alleviation and resumption of functional activity after 24 months of continued rehabilitation in a case study ; although other studies reported that PLG persists and inhibits subchondral bone regeneration 6 to 12 months post-operative [5, 6]. In a rabbit model, filling the drill hole with a chemically cross-linked chitosan hydrogel was previously shown to block cell infiltration and bone repair . Altogether, these data suggest that the porosity and degradation kinetics of biomaterials implanted in subchondral bone are key elements in the induction of reproducible osteochondral repair.
It was previously shown that hybrid chitosan/blood implants solidified in situ over the surface of microfracture or microdrill defects elicit a more hyaline repair compared to marrow stimulation alone [8, 9]. The chitosan used to generate these implants was biodegradable with ~80% degree of deacetylation (DDA) and a molecular weight of ~100-250 kDa. The mechanisms of action were shown in a rabbit model to implicate the sequential attraction of neutrophils, osteoclasts and blood vessels, along with enhanced subchondral bone remodeling, repair tissue integration and delayed chondrogenesis in repairing microdrill holes [9, 10, 11, 12]. The cartilage repair response, however, was attenuated in aged rabbits , which parallels the reduced efficacy of marrow stimulation therapies in patients over 40 years old [13, 14]. A new approach is thus needed to reproducibly elicit hyaline repair in older patients treated by microfracture. Rabbits are widely used as an in vivo cartilage repair model, which provides an abundant base of literature for data comparison, and the use of aged rabbits in a cartilage repair model could be useful in translating new implants for augmented microfracture to treatments for older subjects.
We hypothesized that chitosan/blood implants placed directly in the marrow stimulation subchondral bone channel of skeletally aged rabbits could attract more bone marrow stromal cells than drilled control defects. We also hypothesized that subchondral chitosan/blood implants would be cleared with kinetics similar to a blood clot and, compared to drilled control defects, would attract more wound repair cells (neutrophils and marrow-derived stromal cells) in a molecular weight-dependent manner. Implants were delivered to drilled subchondral defects to avoid bone compaction and osteocyte death induced by microfracture . In addition, our study was designed to track tissue reactions of three implant formulations with distinct chitosan molecular weight in 3 drill holes per knee trochlea. The generation of three structurally distinct fluorescent chitosan tracers with the same rhodamine derivatization level (1 tag per 200 monomers)  is an innovation that permitted comparative monitoring of the chitosan particle fate after 1-day and 3-weeks of in vivo repair. This formulation screening experiment will thus allow the identification of the optimal chitosan molecular weight to be used for subchondral implantation in subsequent studies.
Three osteochondral drill holes were created bilaterally in the knee trochlea of 30-month old New Zealand White rabbits. In one knee, the 3 holes were press-fit with 3 distinct pre-solidified chitosan-NaCl/blood implants containing chitosan (either high, low or ultra-low molecular weight, inserted in the proximal, middle, and distal holes, respectively). The 3 drill holes created in the contralateral control trochlea were left to bleed as surgical controls or each drill hole treated with the same dose of Tissue Factor used to pre-solidify the chitosan/blood implants. Individual drill holes (30 total holes) and associated repair tissues were analyzed after 1 day (N=1 rabbits) or 21 days (N=4 rabbits) post-operatively by micro-computed tomography to analyze residual bone defect size, and by histology and histomorphometry to assess implant residency, cell recruitment, matrix deposition, evidence of new bone formation, and repair tissue integration.
Materials and chitosan characterization
Chitosans and chitosan solutions used in this study
High (150K) Powder*
High (150K) Solution**
0.50% mol/mol RITC/chi
Low (40K) Powder*
Low (40K) Solution**
0.52% mol/mol RITC/chi
Ultralow (10K) Powder*
Ultralow (10K) Solution**
0.58% mol/mol RITC/chi
Recombinant human Tissue Factor with phospholipids (Innovin®, Dade-Behring, Cedarlane, Mississauga, ON, Canada) was reconstituted with 2 mL water for injection (Abbott Laboratories, Dallas, TX, USA) at 5-times the normal recommended concentration and stored at 4°C. Microman M100 tips and microman pipettors were from Gilson, Inc. (Middleton, MI, USA). Recombinant human Factor VIIa (rhFVIIa, Novo Nordisk, Copenhagen, Denmark) was reconstituted at 500 μg/mL in water for injection and stored as aliquots at −80°C.
Implant optimization and rabbit surgical model
All procedures involving animals, including a specific protocol for experimental procedures with aged rabbits, were approved by institutional ethics review boards. For in vitro optimization studies, isotonic chitosan solutions [1.6% w/v chitosan-150 mM NaCl or 1.6% w/v chitosan-100 mM disodium β-glycerol phosphate (GP)] were made from distinct 2% w/v chitosan solutions and laced with 0.05% w/v RITC-chitosan of matching molecular mass (Table 1). Formulations were mixed with rabbit peripheral whole blood from anesthetised rabbits at a 1:3 or 1:6 v/v chitosan:blood ratio in flat-bottom 2.0 mL cryovials containing three sterile 0.39 g surgical steel mixing beads (Salem Specialty Ball Company, Canton, CT, USA), and shaken manually for 10 seconds. Liquid mixtures were solidified in glass tubes with an inner diameter of 2.0 mm at 37°C for 30 minutes or at room temperature for 5 to 30 minutes in plastic syringes or microman tips with the tapered end cut off using rhFVIIa or Tissue Factor to accelerate coagulation. The macroscopic properties of the solidified implants (shape, elasticity, serum extruded) were determined visually and by manual assessment. The distribution of fluorescent chitosan particles in implants pre-solidified in glass tubes was documented by epifluorescence microscopy. Implants with 1:6 v/v ratio chitosan-NaCl/blood were selected for further analysis in vivo based on a more rapid coagulation than chitosan-GP/blood, and homogeneous dispersion of chitosan particles.
Five skeletally aged New Zealand White rabbits (2.5 years old, 3 male, 2 female, mean 4.68±0.44 kg, Charles River, St-Constant, QC, Canada), were housed individually in cages at controlled room temperature and light cycle with ad libitum standard commercial rabbit chow and municipal tap water available, and acclimatized for at least 2 weeks prior to surgery. The rabbits were anaesthetized with ketamine-xylazine-buprenorphine, had their knees shaved and disinfected and were kept under anaesthesia with 3% isoflurane/8% oxygen. Small bilateral arthrotomies were used to generate three osteochondral drill holes to 2 mm target depth in each femoral trochlea using a 1.4 mm diameter round drill burr (Fine Sciences Tools, Foster City, CA, USA) and a hand-held high speed drill under irrigation with Ringer’s Lactated Saline. For each rabbit, 3 mixtures were generated in distinct flat-bottom cryovials as described above, using 125 μL of 150K, 40K or 10K chitosan solution (1.6% w/v chitosan/150 mM NaCl solution), 12.5 μL 5 mg/mL RITC-chitosan of matching molecular mass (see Table 1) and 0.75 mL aseptic rabbit peripheral arterial liquid whole blood. 15 μL of the liquid implant mixture was drawn into a M100 sterile microman tip with the tapered end cut off. 3 μL of Tissue Factor was deposited in a sterile petri dish and then drawn into the same tip by back-screwing the microman pipettor to stimulate coagulation and thus solidify the implant inside the plastic microman tip (5 minutes at room temperature). Solid implants were extruded onto a sterile petri with labels, then each was press-fit into the 3 drill holes of the left knee (150K proximal, 40K middle, and 10K distal hole), while right knee control drill holes were left to bleed (N=2) or treated with 3 μL of Tissue Factor (3 μL per hole, N=2). Knees were closed in three layers using prolene 5–0 sutures, and buprenorphine was administered post-operatively twice a day for at least 3 days. Macroscopic appearance of the knees and incisions, body weight and signs of both pain and anorexia were monitored daily from the surgery to the necropsy to assess the health of the rabbits. There were no signs of knee infection at necropsy. After 1 day (N=1) or 21 days (N=4) post-surgery, the rabbits were euthanized under ketamine-xylazine anesthesia by IV injection of sodium pentobarbital and the femoral ends were retrieved and fixed in 4% paraformaldehyde/100mM cacodylate, pH 7.4. Fixed femur ends were placed trochlea face-down in buffered saline in a petri to acquire macroscopic fluorescent images of the defects with an inverted epifluorescent microscope, digital camera and calibrated histomorphometric software with a controlled image acquisition time (Northern Eclipse, Empix, Missisauga, ON, Canada).
Micro-computed tomography (Micro-CT)
Femur ends were trimmed of their condyles using a low-speed isomet saw and scanned on a 180° axis using a SkyScan1172 high-resolution desktop X-ray microtomograph (Skyscan, Kontich, Belgium) set to an image size of 2000 X 1048 pixels at pixel size resolution of 9.8 μm, 2-frame averaging and at 80 kV with an aluminum-copper filter. The data sets were reconstructed in a 3D model using the NRecon software (Skyscan, Kontich, Belgium) with smoothing = 2, ring artifact correction = 4, beam hardening correction = 30%, object bigger than field of view = ON, output range = 0.00 to 0.05. The reconstructed files were blinded by a third party. Using the DataViewer software (Skyscan, Kontich, Belgium), each drill hole was re-positioned so that the y-axis ran vertically through the hole depth. The correct vertical alignment was then confirmed by two readers and the repositioned dataset was cropped into a new file. The top of each hole represented the osteochondral junction, visualized in corresponding histological sections as the tidemark of the calcified cartilage layer, and was defined as the most superficial image slice on the aligned reconstructed scans on which the bone completely surrounded the residual drill hole edges. The bottom of the hole was defined as the deepest axial slice that contained non-mineralized tissue, while a constant and dense bone zone could be observed at the base of the hole on both sagittal and coronal planes. The hole depth was calculated as the number of 2-D slices between the top and the bottom of the hole and multiplied by the pixel size (9.8 μm per slice). The residual hole cross-sectional area (mm2) was quantified at the top of the hole and at three different depths (0.5 mm, 1.0 mm and 1.5 mm) from the top of the hole using a polygon tool (CTAn software, Skyscan, Kontich, Belgium) to draw a 2D region of interest in the axial plane that circumscribed the non-mineralized hole edge (Additional file 1: Figure S1A). The signal inside the region of interest was then processed using an inverted 70–0 grayscale threshold to exclude mineralized tissue and include the non-mineralized drill hole cross-sectional area (Additional file 1: Figure S1B, C), which was then computed by the CTAn software.
Histoprocessing, histostaining and immunohistochemistry
Femoral ends were decalcified at 4°C in 10% (w/v) ethylene diamine tetraacetic acid (EDTA)/0.1% (w/v) paraformaldehyde/phosphate buffered saline pH 7.2. 25 serial sagittal cryosections of 10 μm thickness were collected at the medial edge and through the middle of the 3 drill holes with CryoJane tape (Instrumedics, St Louis, MO, USA). Images of sections containing residual RITC-chitosan particles were generated with unstained and unmounted cryosections, by merging a 1.25x epifluorescence image with a low-intensity bright field image of the same field. Residual chitosan implant was measured by semiquantitative threshold analysis of red fluorescent particles in 1.25x fluorescent images acquired at a constant 400 ms exposure. Soft tissue in each hole was cropped into a new image, thresholded to a fixed value, and the total fluorescent area per hole was obtained in distinct sections from the edge and middle of the holes and the values averaged (N=4). Northern Eclipse software was used (Empix, Mississauga, ON, Canada). Cryosections were stained with Safranin O-fast green-iron hematoxylin, or immunostained for collagen type I (col I) and collagen type II (col II), following previously described methods , using anti-human collagen type I antibody I-8H5 (MP Biomedicals, Solon, OH, USA) at 10 μg/mL, anti-human collagen type II hybridoma supernatant II6B3 (DSHB, Iowa City, IA, USA) diluted 1:10 and biotinylated goat anti-mouse secondary antibody (B-7151; Sigma-Aldrich, Oakville, ON, Canada) at 11 μg/mL. Specificity was confirmed by the absence of immunostaining by isotype-specific mouse antisera or primary antibody omission.
Quantitative histomorphometry was carried out on calibrated 40x digitally scanned slides and Northern Eclipse V8.0 software (Empix Imaging, Inc., Mississauga, ON, Canada). Percent tissue stained for GAG, col I or col II was obtained by thresholding, and dividing by the total soft repair tissue area per drill hole. Histomorphometry of cross-sectional area (mm2) occupied by 4 granulation tissue types was carried out by selective cropping and threshold analysis of tissues from digital images of col I-immunostained sections (middle and edge of the holes), using the following criteria: (1) Apoptotic tissues contained mainly cells with fragmented nuclei, nuclear debris, and few cells with intact nuclei, (2) Neutrophil-rich tissues contained neutrophils with lobed or round nuclei, few stromal cells and low levels of apoptotic cells and nuclear debris, (3) Neutrophil+stromal tissues contained abundant neutrophils and stromal cells with an elongated fibroblast-like cell shape, (4) Stromal tissues were devoid of neutrophils and contained abundant stromal cells. Unbiased quantitative stereology for neutrophil and stromal cell density was carried out on a representative 40x image from each of the 4 tissue types in each treated defect (N=4, middle of the hole), over which a 20 x 20 μm grid, with 108 total points (Ptotal), was randomly placed. All neutrophils or stromal cells touching the grid intersections were counted (Vv = ΣPcell type/ΣPtotal). A 100x picture of an apoptotic cell and a viable neutrophil were also taken. Repair tissue integration with the bone plate was analyzed in Safranin O, col I and col II-stained sections by calibrated histomorphometry. Line measures along the drill hole side-walls determined the distance between the osteochondral junction, as extrapolated from the tidemark in flanking cartilage-bone, and the closest subchondral repair tissue that was integrated to calcified cartilage or bone. Integration/detachment was measured on both sides of each hole and the mean value was retained. Cryosections were enzymatically stained with tartrate- resistant acidic phosphatase (TRAP) to reveal osteoclasts as previously described  and counterstained in methyl green (Vector Laboratories, Burlingame, CA, USA). TRAP-stained sections were digitally scanned at 40x. All large TRAP-positive cells adhering or adjacent to bone with a rounded cell shape were defined as osteoclasts  and were quantified in three different depths from the defect surface: projected tidemark-0.5 mm, 0.5 mm-1.0 mm and 1.0 mm-1.5mm, on both sides of each hole. The GAG, col I and col II-positive areas, as well as the osteoclast quantification, were performed by two independent blinded readers with consistent inter-reader results. Cryosections were also stained with Gomori Trichrome solution using 0.6% (w/v) Chromotrope 2R (C-3143, Sigma, Oakville, Ontario, Canada), 0.3% (w/v) Fast Green and 0.6% phosphotungstic acid (P-4006, Sigma, Oakville, Ontario, Canada).
The General Linear Model (GLM, Statistica version 9.0, StatSoft, Tulsa, OK, USA) with Fisher LSD post hoc analysis to analyze univariate effects was used to test the effect of chitosan molecular mass (150K, 40K, 10K) and defect position (proximal, mid, distal) after 21 days on chitosan residency, percent GAG-positive area, percent col I-positive area, percent col II-positive area, percent apoptotic, neutrophil-rich, neutrophil+stromal and stromal repair tissue area, neutrophil and stromal cell volume density, detached repair tissue, number of osteoclasts in three depth ranges, residual hole area at the top of the hole and at three depths and residual hole depth (N=4). Significance was set at p<0.05.
In vitro pre-solidified chitosan/blood implant optimization
In vivo implant residency, repair responses and tissue characterization
Initial defects by quantitative micro-CT analysis had a uniform ~1.6 mm diameter and 2.3 mm deep shape (N=6, Figure 9B-C). All implants induced bone resorption, which lead to tear drop-shaped bone defects at 3 weeks post-operative, as opposed to no appreciable change in control defect dimensions (Figure 9B-C). Compared to initial and control defects, all treated defects showed a ~2-fold increase in hole area at the calcified cartilage/bone plate (p<0.001), and ~3-fold wider hole area at deeper levels (p<0.001 vs controls, Figure 9B). By micro-CT, high molecular weight chitosan induced a particularly strong bone resorption at 0.5mm and 1.5mm depths (p<0.05, 150K vs 40K hole area, Figure 9B), which was consistent with histomorphometry measures in collagen type I-stained sections showing a larger area of granulation tissue in 150K-treated defects than in both 40K and 10K-treated defects after 21 days (p<0.05, data not shown). Micro-CT analysis of hole depth also showed that middle control bone defects were significantly shallower than the 40K-treated middle hole (p<0.05, Figure 9C).
This study demonstrated that subchondral chitosan implants sequentially draw neutrophils and undifferentiated bone marrow-derived stromal cells into drilled bone defects, which was accompanied by osteoclast formation and bone remodeling. Neutrophil attraction and bone resorption increased in proportion to higher chitosan molecular mass. After 3 weeks of repair, all chitosan implants induced neutrophil chemotaxis, stromal cell recruitment, delayed extracellular matrix deposition, and enhanced osteoclast-driven subchondral bone remodeling. Although both subchondral bone resorption and the synthesis of new woven bone were observed, the resorption was definitively stronger during the first three weeks of repair, as evidenced by the larger size of the treated holes compared to acute defects. At day 21, osteoclast recruitment below the bone plate was similar in both treated and control defects, which suggests a shift towards woven bone repair in treated defects after 21 days (Figure 10). Our data confirm the hypothesis that subchondral chitosan implants attract more bone marrow stromal cells than control defects in a time-delayed manner. Our data do not support the hypothesis that the implants are cleared with similar kinetics as the blood clot, given that chitosan particles still persisted at 3 weeks in the drill holes.
Biodegradable chitosan is known to elicit neutrophils via a leukotriene B4-sensitive pathway, while promoting an anti-inflammatory phenotype as chitosan-stimulated neutrophils release neither superoxide nor myeloperoxidase . Previous chitosan-induced cartilage repair studies in rabbits have documented neutrophil chemotaxis at 21 days that is associated with a delay in matrix deposition, as observed in the current study [9, 26]. The benefits of delayed matrix deposition after three weeks was also demonstrated in defects treated with PLG subchondral implants in rabbits, although implant clearance was not specifically reported and evidence of neutrophil or osteoclast attraction was not shown [3, 27]. Most importantly, in a separate study, 10K pre-solidified chitosan-NaCl/blood implants elicited hyaline-like cartilage repair tissue and delayed callus formation compared to drill-only defects after 2.5 months in skeletally aged rabbits . The more potent wound repair response to subchondral chitosan implants may therefore be the key to eliciting therapeutic marrow-stimulation repair tissues in aged subjects.
Although wound healing benefits from an early influx of neutrophils, failure to clear apoptotic neutrophils can cause impaired tissue repair [29, 30], which could render the subchondral chitosan implant reactions problematic when scaling-up the implant to enhance marrow stimulation in patients. Efferocytosis, the uptake of apoptotic cells by macrophages , is a natural process in the resolution of inflammation. The low levels of apoptotic tissue in 10K and 40K-treated defects, as opposed to 150K-treated defects, suggest efficient efferocytosis by local macrophages that prevents triggering a foreign body response. The lower levels of residual apoptotic cells in the defects treated with low molecular weight chitosan (Figure 7B) correlate with sparse resident chitosan particles in the current study and a more rapid cell-based clearance of the smaller chitosan polymer chains, as previously documented . Efferocytotic macrophages also secrete transforming growth factor-β [33, 34], a key cytokine in wound healing , as well as the anti-inflammatory factor interleukin-10 , which further emphasizes the importance of proper neutrophil clearance in scaffold-guided osteochondral repair. While the areas in all defects that were characterized by high levels of neutrophils (viable or apoptotic) contained few stromal cells and no collagen type I, they were directly bordered by tissues rich with stromal cells (Vvstromal = 0.17), at levels similar to that previously reported at 3 weeks post-operative in microdrill defects overlayed with chitosan-GP/blood implant (Vvstromal = ~0.15) . Stromal cells were thus recruited to the periphery of treated defects but only following timely neutrophil clearance; the sustained but more controlled neutrophil response for 40K and 10K implants therefore predicts a more therapeutic response at a later period in the rabbit model. This prediction is consistent with the outcome of a separate mid-term study in skeletally aged rabbits, in which 10K pre-solidified chitosan-NaCl/blood implants elicited a more hyaline repair tissue compared to 40K implant and untreated control drill holes .
Enhanced bone resorption correlated with the accumulation of neutrophils in treated defects compared to controls. The larger soft tissue area in 150K-treated defects also supports a relationship between prior neutrophil recruitment (i.e., apoptotic neutrophils present at 3 weeks in 150K-treated defects) and prior osteoclast activity. Receptor activator of NF-κB ligand (RANKL) induces the differentiation of osteoclast precursors [38, 39]. In synovial fluid-derived neutrophils from patients with rheumatoid arthritis, as well as in blood-derived neutrophils stimulated with lipopolysaccharide and granulocyte macrophage colony-stimulating factor, RANKL is expressed and mediates bone resorption and osteoclastogenesis in vitro. RANKL is also chemotactic for human monocytes [41, 42]. Additionally, monocyte chemoattractant protein 1 (MCP-1/CCL2) and interleukin-8 (IL-8/CXCL8), are released from leukocytes within chitosan/blood clots and whole blood clots . At the wound site, these chemokines could continue to be released from extravasated neutrophils  and endothelial cells through neutrophil mediators such as proteinase-3 [44, 45]. In other studies, these chemokines stimulated osteoclast differentiation of human bone marrow mononuclear cells  and rat osteoclast precursor cells . The local release of RANKL, MCP-1/CCL2 and IL-8/CXCL8 could thus polarize elicited macrophages to differentiate into osteoclasts in the drill hole. Interestingly, MCP-1/CCL2 could also have a role in neutrophil clearance, as it enhances efferocytosis . Osteoclast formation promoted by “topical” chitosan-blood implants solidified over drill holes was previously tied to bone remodeling and improved repair tissue integration , as well as a more hyaline repair tissue at 8 weeks post-operative [9, 11]. Osteoclast recruitment is also closely related to angiogenesis [49, 50] and osteoclast conditioned media has a chemotactic effect on mesenchymal stem cells . Osteoclast-dependant bone resorption could therefore enhance migration of mesenchymal stem cells to the bone plate region, which could be a key event in the cartilage repair properties of chitosan that is indirectly related to neutrophil recruitment. Stem cell recruitment could hold an especially important role in the treatment of cartilage defects in older patients who tend to be especially susceptible to microfracture failure [13, 14]. Altogether, data in this study shows that pre-solidified chitosan-NaCl/blood implants can elicit osteoclasts to the subchondral bone plate, most probably through a neutrophil recruitment phase, and that molecular weight of the polymer can be used to adjust the potency of the bone remodeling response.
Development of chitosan-blood implants pre-solidified ex vivo provides a novel strategy for delivering specific dosages of low molecular weight chitosan (10K and 40K) with low viscosity  to marrow stimulation defects. Tissue Factor generated rapid implants which projects to be more convenient in a clinical setting, although Innovin® is not currently available as a pharmaceutical-grade reagent. Clinical use of Innovin® in dental sinus bone-augmentation procedures has been documented . In this study, no apparent differences were observed between control defects left to bleed or administered with TF, although in a sheep model, subchondral TF implants were found to elicit sporadic bone plate resorption [Bell et al., unpublished data]. Future studies are needed to address the role of subchondral hemostasis and polymer clearance in marrow stimulation repair.
Chitosan-NaCl/blood pre-solidified subchondral implants elicited highly reproducible and distinct biological responses compared to controls. The statistically significant responses to implant compared to the controls is quite remarkable considering the low number of rabbits used (N=4). In the context of formulation screening, the current study also permitted the observation of greater neutrophil chemotaxis and bone resorption associated with slower clearance of 150K implants compared to 10K and 40K. These observations suggest that subchondral high molecular weight chitosan implants are at risk for the development of cysts at longer timepoints in the rabbit model, while low molecular weight chitosan implants have a greater potential for eliciting a delayed and improved osteochondral repair. The use of only one rabbit at day 1 was sufficient to document acute implant residency (Figures 2–3), and to document very uniform initial defect dimensions (Figure 9B-C), but did not permit any statistical comparison with day 21 defects. It is possible that proximo-distal effects on repair were present, as only the proximal holes showed fibroplasias in the deeper marrow. Such acute alterations in the deep marrow are likely to be transient given that adipocyte conversion in trabecular bone marrow is seen after 3 to 6 months post-operative below rabbit drilled defects [54, 55]. The close proximity of the 3 drill holes in one trochlea may have biased the molecular mass-dependant repair reaction to the implants by those in the adjacent hole, although the study still permitted the observation of molecular weight-specific clearance and induction of neutrophil chemotaxis and bone resorption. These data have led us to change the model for mid-term repair responses by using only two drill holes per trochlea and further investigating the use of low molecular weight chitosan.
This study has demonstrated that pre-solidified TF-chitosan-NaCl/blood implants can be successfully retained in microdrill holes, become partly cleared, and elicit neutrophils followed by bone marrow-derived stromal cells at 21 days in a skeletally aged rabbit model of cartilage repair. Three chitosan implant formulations reproducibly elicited neutrophils which guided osteoclasts to the bone plate, delayed deposition of collagen and glycosaminoglycan, induced subchondral bone resorption and repair and improved integration of the repair tissue with the subchondral bone. In contrast, in control defects, osteoclasts did not migrate to the bone plate, bone remodeling was limited to new woven bone at the base of the hole and stromal cells that migrated into the control drill holes promptly differentiated into chondrocytes and fibroblasts (col I-rich fibrocartilage). This study also showed that the level of neutrophil chemotaxis and osteoclast resorption was proportional to chitosan molecular weight. The successful characterization of the early, molecular weight-specific repair responses to osteochondral implants in aged rabbits constitutes a foundation for the elucidation of the molecular and cellular mechanisms of chitosan-guided neutrophil, stromal cell and osteoclast recruitment to marrow stimulation defects, as well as the further investigation of the cartilage repair properties of these implants at longer timepoints.
We gratefully acknowledge Geneviève Picard for histology contributions, Julie Tremblay for Quality Assurance, Myriam Lamarre for chitosan labeling, and Vincent Darras for chitosan molecular mass analyses. This work was funded by operating grants Natural Sciences and Engineering Research Council (NSERC, STPGP 365025), and Canadian Institutes of Health Research (CIHR, 185810-BME). Salary support was from the Fonds de Recherche Québec (FRSQ, CDH, FQRNT, JGM), the Canadian Arthritis Network (AH, TDS) and BioSyntech Inc. (now Piramal Healthcare Canada Inc., JS). Data in this paper were generated towards the M.Sc. thesis of CHLF (École Polytechnique), and were presented in part at the International Cartilage Repair Society (2010, Sitges, Spain) and the Orthopaedic Research Society (2012, San Francisco, USA).
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