- Open Access
Systemic administration of mesenchymal stem cells combined with parathyroid hormone therapy synergistically regenerates multiple rib fractures
Stem Cell Research & Therapy volume 8, Article number: 51 (2017)
A devastating condition that leads to trauma-related morbidity, multiple rib fractures, remain a serious unmet clinical need. Systemic administration of mesenchymal stem cells (MSCs) has been shown to regenerate various tissues. We hypothesized that parathyroid hormone (PTH) therapy would enhance MSC homing and differentiation, ultimately leading to bone formation that would bridge rib fractures.
The combination of human MSCs (hMSCs) and a clinically relevant PTH dose was studied using immunosuppressed rats. Segmental defects were created in animals’ fifth and sixth ribs. The rats were divided into four groups: a negative control group, in which animals received vehicle alone; the PTH-only group, in which animals received daily subcutaneous injections of 4 μg/kg teriparatide, a pharmaceutical derivative of PTH; the hMSC-only group, in which each animal received five injections of 2 × 106 hMSCs; and the hMSC + PTH group, in which animals received both treatments. Longitudinal in vivo monitoring of bone formation was performed biweekly using micro-computed tomography (μCT), followed by histological analysis.
Fluorescently-dyed hMSCs were counted using confocal microscopy imaging of histological samples harvested 8 weeks after surgery. PTH significantly augmented the number of hMSCs that homed to the fracture site. Immunofluorescence of osteogenic markers, osteocalcin and bone sialoprotein, showed that PTH induced cell differentiation in both exogenously administered cells and resident cells. μCT scans revealed a significant increase in bone volume only in the hMSC + PTH group, beginning by the 4th week after surgery. Eight weeks after surgery, 35% of ribs in the hMSC + PTH group had complete bone bridging, whereas there was complete bridging in only 6.25% of ribs (one rib) in the PTH-only group and in none of the ribs in the other groups. Based on the μCT scans, biomechanical analysis using the micro-finite element method demonstrated that the healed ribs were stiffer than intact ribs in torsion, compression, and bending simulations, as expected when examining bone callus composed of woven bone.
Administration of both hMSCs and PTH worked synergistically in rib fracture healing, suggesting this approach may pave the way to treat multiple rib fractures as well as additional fractures in various anatomical sites.
Affecting 350,000–400,000 patients each year in the United States, rib fractures occur in 10–15% of patients who sustain blunt trauma and are associated with morbidity and mortality rates in up to 25% of these patients . Common complications are respiratory failure due to lung contusions and impaired mechanical properties as well as severe pain originating from the fractured rib. Patients rate their pain on average as 9.2 on a 1–10 scale and may not be able to return to work for at least 8.5 weeks . Even after they return to daily activities, 67% of patients have reported prolonged disability and pain . In patients suffering the most severe complications, poor mechanical ventilation leads to pneumonia, which is a frequent cause of death . The risk of rib fracture increases with age. One study found the incidence of rib fractures among elderly men to be 3.5 per 1000, with 24% of all fractures occurring in osteoporotic men . Another study showed that 56% of patients older than 60 years who died of chest injury suffered no injury worse than a rib fracture .
Currently, the gold-standard of treatment is pain management, because pain limits one’s ability to cough and breathe deeply, resulting in sputum retention, atelectasis, and reduced functional residual capacity . These factors can ultimately result in decreased lung compliance, ventilation-perfusion mismatch, hypoxemia, and respiratory distress. Fixation of fractured ribs is controversial, because surgical intervention entails prolonged mechanical ventilation and hospitalization . Other than fixation, however, there is no available treatment aimed at facilitating rib fracture healing. Therefore, multiple rib fractures are serious and constitute a significant unmet clinical need.
Few new ideas have emerged in the biomedical field about how to accelerate bone repair in fractured ribs. Graeber et al. proposed harvesting autografts from a contralateral rib to treat flail chest; they reported improved healing in injured ribs but no healing in donor ribs 30 days after surgery . Santana-Rodriguez and colleagues suggested using ultrasound pulses to facilitate healing in rib fractures, but these researchers reported a nonsignificant increase in bone volume when animals were treated using optimal parameters . None of the osteogenic genes examined in that study was found to be overexpressed, and accordingly none of the treated fractures was reported as healed. Ishihara et al. examined direct gene therapy via an adenoviral vector and indirect gene therapy in which transduced cells were employed to introduce bone morphogenetic protein (BMP) to the injury site. The results, achieved using an equine model of drilled holes in the rib, were encouraging . However, drilled defect models do not realistically represent the human condition of rib fracture. Adenovirus-mediated gene therapy does carry a promise: researchers found that the Coxsackievirus and adenovirus receptor are specifically expressed in immature osteoblasts residing in fractured ribs and not in healthy intact ribs .
Systemically administered mesenchymal stem cells (MSCs) preferentially migrate to sites of injury within the body in various experimental disease models, including myocardial infraction, brain injury, and lung fibrosis models . It has been shown that MSCs home to bones when transplanted into children with severe osteogenesis imperfecta, even in those without recent fractures; this results in denser bone formation and reduced fracture frequency . MSCs can be introduced back into the donor as an autologous graft or used as allogeneic cells to treat other recipients. Since allogeneic MSCs can be preserved as an “off-the-shelf” product and do not require a separate cell isolation phase for each patient, their use is considered advantageous for the clinical setting. Indeed, allogeneic MSCs are being evaluated as a systemic treatment option in a large number of clinical trials. To date, systematic administration of MSCs—autologous or allogeneic—has not yet been investigated for the treatment of rib fractures.
Teriparatide, the 1–34 portion of parathyroid hormone (PTH), has been approved by the US FDA for use as an anabolic agent in the treatment of adults with severe osteoporosis, who are at high risk for fractures. In humans, the anabolic effects of teriparatide manifest as increases in skeletal mass, markers of bone formation and resorption, and bone strength. Preclinical studies also support the potential for PTH as a treatment for bone fractures, demonstrating PTH-improved quality of the fracture callus, increased bone mineral content and density, and accelerated endochondral ossification . Randomized controlled trials aimed at assessing the effect of PTH on fracture healing are ongoing . The PTH anabolic effect stems from its ability to induce the osteoblast transcription factors Osterix (Osx) and Runt-related transcription factor 2 (Runx2) in MSCs . Furthermore, MSCs in treated mice have been shown to progress through accelerated osteoblast maturation and on to accelerated fracture healing concomitant with increased Osx expression in fracture calluses. Other studies have demonstrated that PTH stimulates MSC recruitment to bone by inducing C-X-C motif chemokine type 12/stromal cell-derived factor 1 (CXCL12/SDF1) expression in osteoblasts [18, 19]. However, researchers in these preclinical studies used extremely high doses of PTH (approximately 140 times the dose allowed in humans).
We previously studied a combined approach in which we used intravenous (IV) injections of human MSCs (hMSCs) and teriparatide therapy to regenerate vertebral compression fractures using osteoporotic rat and healthy pig models . We showed that teriparatide not only enhanced hMSC homing to vertebral defects by inducing key mediators of MSC migration, but also promoted the terminal differentiation of exogenously delivered cells toward the osteogenic lineage. This dual approach synergistically yielded superior bone formation and fracture repair, compared to each treatment alone, in both animal models. Importantly, the systemically administered hMSCs were undetectable in major organs such as the brain, bone marrow, liver, lung, and spleen 12 weeks after injection. These results of treating vertebral compression fractures using the cell-and-PTH approach are encouraging, although one should bear in mind the unique clinical challenge of multiple rib fractures. The main hurdle preventing a more rapid and effective rib fracture repair is the continual movements and shear forces applied to ribs that inhibit callus formation . In fact, the tensile forces affecting rib fractures are of such magnitude that researchers found in animal studies that the diminished callus that forms is enriched with myofibroblast-like cells . In the present study we hypothesized that systemic administration of hMSCs combined with PTH treatment would enhance cell migration to fractured ribs and induce osteogenic differentiation, which will ultimately lead to effective fracture repair compared to the use of each treatment alone.
Human MSC isolation, expansion, and labeling
Cell preparation was performed in a manner previously described . Briefly, human bone marrow (Lonza, Walkersville, MD, USA) was washed with phosphate-buffered saline (PBS), layered on lymphocyte separation medium, and centrifuged at 900 g for 30 min at 30 °C without a break. Mononuclear cells were collected, washed with PBS, and plated at a density of 2 × 105 cells/cm2 in media supplemented with 10% fetal bovine serum (FBS, Invitrogen, Carlsbad, CA, USA), in 5% CO2/95% air at 37 °C. The cells were cultured until they reached the fifth passage and then were prestained with a lypophilic fluorescent dye (Vybrant-CM-DiI, Invitrogen) prior to in vivo injection.
Multiple rib defect surgery
All procedures described in this study were approved by the Cedars-Sinai Medical Center’s Institutional Animal Care and Use Committee (Request No. 5684). The animals were treated in strict adherence to NIH guidelines. Thirty-six 12-week-old female athymic rats (Crl:NIH-Foxn1rnu) were purchased from Charles River Laboratories (Wilmington, MA, USA). The animals were anesthetized by intraperitoneal injections of ketamine/dexmedetomidine, after which they received intubation and mechanical ventilation (Model 683 small animal respirator, Harvard Apparatus, Holliston, MA, USA), to establish positive pressure respiration. Each animal was placed in the lateral position, and the chest area was shaved and disinfected using iodine and chlorhexidine (Fig. 1a). A 2-cm-long incision was made along the lateral aspect of the thorax through the skin, subcutaneous tissue, and the latissimus dorsi muscle, exposing the rib cage (Fig. 1b–d). A 5-mm-long segment was excised from the bony portion of the fifth rib, avoiding damaging the rib’s cartilaginous portion (Fig. 1e). Next the periosteum was removed and the intercostal muscles were sutured using a 5-0 Vicryl suture. A defect was created in the sixth rib in a similar manner (Fig. 1f). The muscular layer and skin were then sutured separately (Fig. 1g, h), and the animal was removed from mechanical ventilation and anesthesia. After the procedure, each rat was randomly assigned to one of the following experimental groups (eight to ten rats per group): (1)the negative control group, in which animals were given only vehicle (PBS); (2) the hMSC-only group, in which each animal received separate IV injections of 2 × 106 hMSCs on days 3, 7, 10, 14, and 17 after surgery; (3) the PTH-only group, in which animals received daily subcutaneous injections of PTH (4 μg/kg body weight/day; Teriparatide, Forteo, Eli Lilly, Indianapolis, IN, USA) for 17 days beginning on day 3; and (4) the hMSC + PTH group, in which animals received the combined therapy of hMSCs and PTH (Fig. 1i).
Longitudinal micro-computed tomography (μCT) imaging of bone formation
The ribs were evaluated using a cone-beam in vivo μCT imaging system (vivaCT 40; Scanco Medical, Brüttisellen, Switzerland). To analyze healing, the animals were imaged on day 1 and again 2, 4, 6, and 8 weeks after generation of the bone defect. Microtomographic slices were acquired using an X-ray tube with a 55-kVp potential and an intensity of 145 μA, and reconstructed at a voxel size of 35 μm. Histomorphometric three-dimensional (3D) evaluation was performed following definition of a volume of interest (VOI) that included the bony defect margins as well as the area from which the bone was resected; a constrained 3D Gaussian filter (σ = 0.8, support = 1) was used to partly suppress the VOI noise. The bone tissue was segmented from marrow and soft tissue by using a global thresholding procedure in which 200 mgHa/cm3 was determined to be the threshold as it matched the histological rib morphology. For each rib, the defect margins were located on day 1 scans and aligned to a standard position ; a cylindrical VOI (5.25 mm in diameter, 7 mm in height) was defined for 3D histomorphometric evaluation. The anatomical match obtained by the registration procedure allowed us to apply the predefined VOI of day 1 to all remaining time points. Bone volume density was used to assess new bone formation. In addition, the percentage of completely gapped ribs was calculated for each group.
Biomechanical analysis of ribs
Micro-finite element (μFE) analysis was used to compare the biomechanical characteristics of healed ribs to intact ribs when subjected to compression, torsion along the rib axis, and bending of the healed segment in two perpendicular planes. For each healed rib (revealed by μCT scanning), a consecutive rib from the same animal was chosen as a control. Each rib was aligned to the standard position as described above, and regions of low, medium, and high mineralization were defined by threshold as 200 mgHa/cm3, 500 mgHa/cm3, and 800 mgHa/cm3, respectively. Each voxel was converted into an equally shaped brick element for the μFE model. The low, medium, and high areas of mineralization were assigned a Young modulus of 50 MPa, 5 GPa, and 15 GPa, respectively. In all cases, these boundary conditions were applied by prescribing displacements of the nodes at the top and bottom surfaces in such a way that a longitudinal compressive strain of 1% or an angular rotation at the long ends of 0.01 radians results. Stiffness was then calculated as the ratio of the reaction force over the applied displacement (compression, N/mm) , or the ratio of the reaction moment over the applied angular rotation (torsional, x bending, and y bending, Nmm/rad) . Analysis was done by Scanco Medical, Zurich, Switzerland.
Histological analysis and immunofluorescence imaging
Histological analysis was performed on rat ribs that had been retrieved 8 weeks postoperatively (the endpoint of the experiment). The ribs were sectioned along the longitudinal axis, preserved using paraformaldehyde, and embedded in paraffin. Five-micrometer slices were sectioned, deparaffinized, and stained using hematoxylin and eosin (H&E) for a morphological analysis, as previously described . For immunofluorescence staining, the tissues were deparaffinized, and the antigens were retrieved by incubation in preheated Target Retrieval Solution (Dako, Carpinteria, CA, USA) for 45 min at 37 °C. Nonspecific antigens were blocked by applying serum-free blocking solution (Dako). Tissue slides were stained with primary antibodies against human bone sialoprotein (BSP) and osteocalcin (Oc) to examine osteogenic differentiation and with Stromal cell-Derived Factor 1 (SDF1), C-X-C motif receptor type 4 (CXCR4), epidermal-like growth factor receptor (EGFR), and amphiregulin (Amp) antibodies to determine the mechanism of MSC migration. These primary antibodies were applied to the slides and incubated at 4 °C overnight, after which they were washed off using PBS. Then the slides were incubated with secondary antibodies (Additional file 1: Table S1) for 1 hour at room temperature; these antibodies were also washed off with PBS. The slides were stained with 1 μg/ml 4′,6-diamidino-2-phenylindole dihydrochloride (DAPI) for 5 min in the dark, after which they were finally washed three times with PBS. VectaMount mounting medium (Vector Laboratories, Burlingame, CA, USA) was applied to the tissue. Tissue samples on the slides were imaged using a four-channel confocal Laser Scanning Microscope 780 (Zeiss, Pleasanton, CA, USA) with × 20 magnification, z-stacking, and 5 × 5 tile scanning. For zoom-in images, a single z-stacked image was generated. All samples were scanned using the same gain and exposure settings. In addition, DiI-positive cells in five fields of × 40 magnification were automatically counted using ImageJ software.
GraphPad Prism 5.0b software (GraphPad Prism, San Diego, CA, USA) was used to analyze the data. The results are presented as means ± SE (* p ≤ 0.05; ** p ≤ 0.01; *** p ≤ 0.001; **** p ≤ 0.0001; ns = not significant). The longitudinal data analysis was conducted using a one-way ANOVA or a two-way ANOVA with repeated measures and the Bonferroni post-test. To assess significance, p < 0.05 was considered statistically significant.
PTH enhances hMSC migration to the rib fracture
We were able to quantify the homing of exogenously delivered hMSCs to the fracture site by histological analysis, thanks to pre-labeling of the cells with the lipophilic fluorescent dye DiI. The animals were sacrificed 8 weeks after surgery and histological processing was performed. Significantly more DiI-stained cells were counted in ribs of animals given both hMSCs and PTH than in animals given hMSCs only (Fig. 2a): 15 DiI-positive cells per × 40 field compared to 5 DiI-positive cells, respectively. When we looked exclusively at DAPI-positive cells in all groups, we calculated the percentages of DiI-positive cells to be on average 12% in the hMSC + PTH group and only 2.5% in the hMSC group—no more than the percentages of DiI-positive cells among DAPI-positive cells found in the other groups, which had not been given any cells at all (i.e. background staining). Next we examined activation of the stromal cell-derived factor 1 (SDF1)/C-X-C chemokine receptor type 4 (CXCR4) axis, a critical pathway of MSC recruitment in the fracture-healing process (Fig. 2b) [26, 27]. We found ample immunostaining of both SDF1 and CXCR4 in the hMSC + PTH group and, only in that group, in the area of new bone formation. An alternative pathway of MSC mobilization that is induced by PTH treatment is the pathway of amphiregulin, an epidermal growth factor (EGF)-like ligand that is secreted from injured tissue and signals through the epidermal growth factor receptor (EGFR) in homing cells . We found prominent staining of amphiregulin in both groups of animals that received PTH therapy (Fig. 2b). In the hMSC + PTH group, we found EGFR staining co-localized with DiI staining, signifying systemically administered hMSCs (Fig. 2b).
PTH therapy induced osteogenic differentiation in hMSCs in vivo
We stained tissue sections with primary antibodies against two well-established markers of osteogenesis, bone sialoprotein (BSP) and human osteocalcin (Oc) , to detect osteogenic differentiation in injected hMSCs (Fig. 3). Our results showed that, indeed, PTH induced osteogenic differentiation in systemically injected hMSCs (Fig. 3). In the negative control group and in the hMSC-only group there was scarce staining of osteogenic markers, whereas in the PTH-only group some Oc staining was present. In the hMSC + PTH group, we observed ample Oc and BSP staining. Both markers were found in DiI-positive cells, and Oc was detected in many non–DiI-positive cells as well.
Systemic administration of both hMSCs and PTH induces superior healing of rib fractures
To assess bone formation induced by the combined cell-and-PTH approach, we performed μCT biweekly. Two weeks after the multiple rib fractures were induced, qualitative μCT analysis demonstrated prominent bone formation stemming from the bone stumps in the animals given PTH-alone and MSC + PTH treatment (Fig. 4a). Two weeks later, the newly formed bone was resorbed in the PTH-only group, while bone calluses bridging the defects were observed in several animals given MSC + PTH. By the 6th and the 8th week after surgery, these bone calluses remodeled so that intramedullary soft tissue could be discerned from mature cortexes. By the latter time point, limited bone regeneration beyond the defect margins was clearly demonstrated in all other experimental groups. Quantitative analysis demonstrated the formation of significantly more bone volume in the hMSC + PTH group beginning in the 4th week (Fig. 4b); this continued to be the case until the end of the experiment, 8 weeks after surgery. In all experimental groups, other than the hMSC-only group, we observed insignificant increases in bone volume in the 2nd week. By the 4th week, bone volumes in the negative control group (which received vehicle only) and PTH-only group returned to the levels of bone volume measured a day after the defects had been created. At the same time point there was twice as much bone volume in the hMSC + PTH group. The percentages of healed ribs in all groups were calculated based on careful examinations of 2D and 3D μCT reconstructions (Fig. 4c); in the negative control and hMSC-only groups no ribs healed. In the PTH-only group we found bone bridging in one rib (1/16 ribs, 6.25%), while in the hMSC + PTH group we found bone bridging in 7 of 20 (35%). Interestingly, fractured ribs that displayed no bone bridging or near bone bridging by the 4th week did not achieve bridging at any later time point (data not shown). In the hMSC + PTH group, histological analysis using H&E staining confirmed bone bridging and revealed a trabecular structure of woven bone filled with vital bone marrow (Fig. 5). In the other experimental groups, particularly in the hMSC-only and negative control groups, we detected fibrotic tissue between the defect margins.
Healed ribs are stiffer than intact ribs
To evaluate the quality of rib healing beyond the mere finding of gap bridging, we performed virtual biomechanical testing using a micro-finite element method analysis (μFE). For this purpose, we converted each μCT voxel into a brick element and used multiple thresholds—200, 500, and 800 mgHa/cm3—to realistically mimic levels of strain on the bone (Fig. 6a). The healed rib stiffness with respect to compression was similar to that of intact ribs, about 1000 N/mm (Fig. 6b). Stiffness in response to torsion was significantly higher in the healed rib group: 90 Nmm/rad compared to 30 Nmm/rad. When we measured stiffness in response to bending on the x-axis, upward towards the consecutive rib in the plane of the chest wall, healed ribs yielded a measurement of 200 Nmm/rad compared to 90 mgHa/cm3 in intact ribs. Bending along the y-axis outwardly (or inwardly towards the lungs) yielded a significant change in stiffness: 150 Nmm/rad in healed ribs compared to 30 mg Ha/cm3 in intact ribs.
Systemic administration of MSCs has been proposed to facilitate regeneration of various injured tissues including the myocardium , spinal cord , and the brain , in which the involvement of the SDF1/CXCR4 axis has been demonstrated . These reports are in accordance with our findings (Fig. 2b), and also with a previously published study on bone regeneration . Intravenous administration is the most common approach to the circulatory system, and the main hurdle is that injected cells must pass through the lungs prior to their distribution throughout the body . Several methods have been proposed to enhance MSC migration to targeted organs, including magnetic guidance of cells pre-labeled with super-paramagnetic iron oxide nanoparticles [36, 37], coating cells with vascular cell adhesion molecule antibodies , and also the use of a synthetic peptide-mimetic ligand (which has a high affinity for activated α4β1 integrin on the surface of MSCs) conjugated to a bisphosphonate in order to target MSCs to the osteoblast surface .
The optimal targeting strategy will use a device or a drug that enhances both MSC targeting and differentiation to achieve fracture healing. PTH, the only anabolic treatment for osteoporosis in postmenopausal women that is approved by the FDA , has been found in both animal and clinical research to enhance fracture healing . PTH treatment increases SDF-1 mRNA levels near epiphyseal plates while significantly decreasing serum SDF-1 levels, creating a gradient that possibly enhances cell engraftment . As mentioned above, we have demonstrated that PTH promotes exogenous MSC homing to vertebral fractures in models of osteoporotic rats and healthy pigs by activation of the SDF1/CXCR4 and amphiregulin/EGFR axes . PTH therapy induced expression of Oc and BSP, which led to complete regeneration of injured vertebrae that was more significant than any treatment alone.
Given those findings, we decided to examine the ability of the combined cell-and-PTH approach to regenerate multiple rib fractures in a rat model. In the present study, we addressed the clinical need of multiple rib fracture regeneration. Our results demonstrate that migration of systemically administered hMSCs to the fractured rib is enhanced by intermittent PTH treatment via activation of two parallel pathways: SDF1/CXCR4 and amphiregulin/EFGR (Fig. 2). Interestingly, we observed a population of CXCR4-positive cells in the ribs of animals that were given PTH treatment alone. Endogenous CXCR4-expressing cells were not observed in the vertebral model in which we used osteoporotic ovariectomized rats , which can be explained by the report that ovariectomized rats have diminished MSC population in bone marrow available to respond to PTH signaling . We showed that PTH therapy induces stem cell differentiation (Fig. 3), which leads to greater bone formation and a higher rate of bone bridging across the defect when the combined hMSC-PTH therapy is given (Figs. 4 and 5).
While some exogenously administrated DiI-positive cells were found to express osteocalcin and bone sialoprotein under PTH induction, representing osteogenic differentiation, many non-DiI host cells were found to express these osteogenic markers in the MSC + PTH group. The enhanced recruitment and differentiation of resident cells that was not observed when only cells were administrated and only scarcely observed when PTH was given alone, can be explained by MSC paracrine effects, which play a central role in response to injury ; specifically, by exosomal signaling that has been shown to play a key role in bone marrow MSC differentiation  and in fracture healing .
Lastly, we demonstrated that using this combined therapy, healed ribs are stiffer than intact ribs when subjected to torsion and bending along the plane perpendicular to the chest wall (Fig. 6). This last point is of importance to the patient, because stiffer ribs are less likely to move and cause pain while breathing or coughing . The stiffness is typical to bone repaired by stem cell therapy, and the ribs are expected to remodel over time evolving to be less dense, allowing some elasticity [24, 47]. Interestingly, simple fracture repair involves formation of a bone callus which is softer than native bone and does not remodel to a less stiff bone [48, 49], though Manjubala et al. reported that the bone callus reaches its maximum stiffness 6 weeks after fracture and becomes softer after 9 weeks . Taken together, the predicted stiffness of the rib bone callous may be attributed to the artificial biological enhancement of fracture repair by MSC and PTH, and an interesting future research would be the examination of repaired rib biomechanics over time.
We initially performed a pilot study in which we used a single-point fracture that had been created by tweaking the rat rib with a bone cutter. These fractures healed by the 4th week in all experimental groups, regardless of the given treatment (data not shown). We concluded that the single-point fracture does not realistically mimic the clinical event, in which rib fractures heal only after a prolonged time, and thus we switched to a segmental defect model. We excised 5-mm-long segments from the fifth and sixth ribs, and noted that a day later, the gap was about 1–2 mm long, which may be attributed to collapse of the chest wall (Fig. 4a). We also noted that although the defect margins were not aligned at that time point, 8 weeks later they were in all animals, even when bridging did not occur. Future studies of these interesting phenomena may explain how bone bridging is achieved in a continual moving environment. In two animals, bone formed between the fifth and sixth ribs’ dorsal margins and between the fifth and sixth ribs’ ventral margins, from which we can infer that there is some paracrine signaling (data not shown). One limitation of our model is that we had to resect the periosteum, as it is known to induce spontaneous healing in a 5-mm segmental rib defect ; which does not truly mimic the clinical condition. Another limitation is the fact that our treatment protocol yielded a union rate of 35% (Fig. 4c), which although higher than any union rate obtained using other strategies reported above, is not optimal and necessitates refinement of the protocol. Optimization of PTH dosing and cell administration is central to this purpose. A PTH dosage of 4–40 μg/kg per day is generally used in rodent studies [52, 53]; the FDA-approved PTH dose for human patients is 20 mg/day, which in rats is approximately equivalent to 0.3–0.5 μg/kg/d. Higher doses do not necessarily lead to improved results, and looking at the rat vertebral fracture model we found that the 0.4 μg/kg dose yields a faster increase in bone density, suggesting that human dosing is preferable . The ideal systemic cell administration protocol would include a single systemic injection for the sake of patient comfort. Kean et al. have demonstrated the efficiency of intra-arterial MSC injection, which represents a promising future direction . Another approach to enhance cell homing would be intra-cardiac administration, that may lead to tenfold more cells arriving to the defect site .
To evaluate the true impact of our proposed approach on patient recuperation, future studies of the cell-and-PTH treatment’s effect on pain and respiration should be performed. The rodent model we describe allows the use of relatively easy and accurate methods to study these key parameters. For example, respiration dynamics can be quantified by using whole body plethysmography, and any pain experienced by the rats can be evaluated using well-established behavioral tests such as the rotating rod and open field tests.
Intermittent PTH treatment has promoted the migration of systemically administrated hMSCs and induced osteogenic differentiation, leading to rib fracture repair and gap bridging. The success of the cell-and-PTH approach could lead to a novel stem cell therapy for life-endangering ribs fractures, and may prove beneficial for other clinical indications such as craniofacial and carpal fractures.
C-X-C motif chemokine type 12, also known as stromal cell-derived factor 1 (SDF1)
C-X-C motif receptor type 4
Epidermal-like growth factor receptor
Fetal bovine serum
Hematoxylin and eosin
Human mesenchymal stem cell
Runt-related transcription factor 2
Stromal cell-derived factor 1, also known as C-X-C motif chemokine type 12 (CXCL12)
Volume of interest
Micro-finite element (method)
Pressley CM, Fry WR, Philp AS, et al. Predicting outcome of patients with chest wall injury. Am J Surg. 2012;204:910–3. discussion 913–4.
Majercik S, Cannon Q, Granger SR, et al. Long-term patient outcomes after surgical stabilization of rib fractures. Am J Surg. 2014;208:88–92.
Fabricant L, Ham B, Mullins R, et al. Prolonged pain and disability are common after rib fractures. Am J Surg. 2013;205:511–5. discussion 515–6.
Brasel KJ, Guse CE, Layde P, et al. Rib fractures: relationship with pneumonia and mortality. Crit Care Med. 2006;34:1642–6.
Barrett-Connor E, Nielson CM, Orwoll E, et al. Epidemiology of rib fractures in older men: Osteoporotic Fractures in Men (MrOS) prospective cohort study. BMJ. 2010;340:c1069.
Kent R, Woods W, Bostrom O. Fatality risk and the presence of rib fractures. Ann Adv Automot Med. 2008;52:73–82.
Karmakar MK, Ho AM. Acute pain management of patients with multiple fractured ribs. J Trauma. 2003;54:615–25.
Nirula R, Diaz Jr JJ, Trunkey DD, et al. Rib fracture repair: indications, technical issues, and future directions. World J Surg. 2009;33:14–22.
Graeber GM, Cohen DJ, Patrick DH, et al. Rib fracture healing in experimental flail chest. J Trauma. 1985;25:903–8.
Santana-Rodriguez N, Clavo B, Fernandez-Perez L, et al. Pulsed ultrasounds accelerate healing of rib fractures in an experimental animal model: an effective new thoracic therapy? J Thorac Cardiovasc Surg. 2011;141:1253–8.
Ishihara A, Zekas LJ, Weisbrode SE, et al. Comparative efficacy of dermal fibroblast-mediated and direct adenoviral bone morphogenetic protein-2 gene therapy for bone regeneration in an equine rib model. Gene Ther. 2010;17:733–44.
Ito T, Tokunaga K, Maruyama H, et al. Coxsackievirus and adenovirus receptor (CAR)-positive immature osteoblasts as targets of adenovirus-mediated gene transfer for fracture healing. Gene Ther. 2003;10:1623–8.
Chamberlain G, Fox J, Ashton B, et al. Concise review: mesenchymal stem cells: their phenotype, differentiation capacity, immunological features, and potential for homing. Stem Cells. 2007;25:2739–49.
Horwitz EM, Gordon PL, Koo WKK, et al. Isolated allogeneic bone marrow-derived mesenchymal cells engraft and stimulate growth in children with osteogenesis imperfecta: Implications for cell therapy of bone. Proc Natl Acad Sci U S A. 2002;99:8932–7.
Alkhiary YM, Gerstenfeld LC, Krall E, et al. Enhancement of experimental fracture-healing by systemic administration of recombinant human parathyroid hormone (PTH 1-34). J Bone Joint Surg. 2005;87-A:731–41.
Chesser T, Fox R, Harding K, et al. The administration of intermittent parathyroid hormone affects functional recovery from pertrochanteric fractured neck of femur: a protocol for a prospective mixed method pilot study with randomisation of treatment allocation and blinded assessment (FRACTT). BMJ Open. 2014;4:e004389.
Kaback LA, do Soung Y, Naik A, et al. Teriparatide (1-34 human PTH) regulation of osterix during fracture repair. J Cell Biochem. 2008;105:219–26.
Jung Y, Wang J, Schneider A, et al. Regulation of SDF-1 (CXCL12) production by osteoblasts; a possible mechanism for stem cell homing. Bone. 2006;38:497–508.
Calvi LM, Adams GB, Weibrecht KW, et al. Osteoblastic cells regulate the haematopoietic stem cell niche. Nature. 2003;425(6960):841-6.
Sheyn D, Shapiro G, Tawackoli W, et al. PTH induces systemically administered mesenchymal stem cells to migrate to and regenerate spine injuries. Mol Ther. 2016;24:318–30.
Elkins J, Marsh JL, Lujan T, et al. Motion predicts clinical callus formation: construct-specific finite element analysis of supracondylar femoral fractures. J Bone Joint Surg Am. 2016;98:276–84.
McDonald SJ, Dooley PC, McDonald AC, et al. Transient expression of myofibroblast-like cells in rat rib fracture callus. Acta Orthop. 2012;83:93–8.
Kallai I, Mizrahi O, Tawackoli W, et al. Microcomputed tomography-based structural analysis of various bone tissue regeneration models. Nat Protoc. 2011;6:105–10.
Kallai I, van Lenthe GH, Ruffoni D, et al. Quantitative, structural, and image-based mechanical analysis of nonunion fracture repaired by genetically engineered mesenchymal stem cells. J Biomech. 2010;43:2315–20.
Shefelbine SJ, Simon U, Claes L, et al. Prediction of fracture callus mechanical properties using micro-CT images and voxel-based finite element analysis. Bone. 2005;36:480–8.
Kitaori T, Ito H, Schwarz EM, et al. Stromal cell-derived factor 1/CXCR4 signaling is critical for the recruitment of mesenchymal stem cells to the fracture site during skeletal repair in a mouse model. Arthritis Rheum. 2009;60:813–23.
Shi M, Li J, Liao L, et al. Regulation of CXCR4 expression in human mesenchymal stem cells by cytokine treatment: role in homing efficiency in NOD/SCID mice. Haematologica. 2007;92:897–904.
Zhu J, Siclari VA, Liu F, et al. Amphiregulin-EGFR signaling mediates the migration of bone marrow mesenchymal progenitors toward PTH-stimulated osteoblasts and osteocytes. PLoS One. 2012;7:e50099.
Marsell R, Einhorn TA. The biology of fracture healing. Injury. 2011;42:551–5.
Barbash IM, Chouraqui P, Baron J, et al. Systemic delivery of bone marrow-derived mesenchymal stem cells to the infarcted myocardium: feasibility, cell migration, and body distribution. Circulation. 2003;108:863–8.
Osaka M, Honmou O, Murakami T, et al. Intravenous administration of mesenchymal stem cells derived from bone marrow after contusive spinal cord injury improves functional outcome. Brain Res. 2010;1343:226–35.
Lu D, Mahmood A, Wang L, et al. Adult bone marrow stromal cells administered intravenously to rats after traumatic brain injury migrate into brain and improve neurological outcome. Neuroreport. 2001;12:559–63.
Wang Y, Deng Y, Zhou GQ. SDF-1alpha/CXCR4-mediated migration of systemically transplanted bone marrow stromal cells towards ischemic brain lesion in a rat model. Brain Res. 2008;1195:104–12.
Kumar S, Wan C, Ramaswamy G, et al. Mesenchymal stem cells expressing osteogenic and angiogenic factors synergistically enhance bone formation in a mouse model of segmental bone defect. Mol Ther. 2010;18:1026–34.
Kean TJ, Lin P, Caplan AI, et al. MSCs: delivery routes and engraftment, cell-targeting strategies, and immune modulation. Stem Cells Int. 2013;2013:732742.
Vanecek V, Zablotskii V, Forostyak S, et al. Highly efficient magnetic targeting of mesenchymal stem cells in spinal cord injury. Int J Nanomedicine. 2012;7:3719–30.
Yanai A, Hafeli UO, Metcalfe AL, et al. Focused magnetic stem cell targeting to the retina using superparamagnetic iron oxide nanoparticles. Cell Transplant. 2012;21:1137–48.
Ko IK, Kim BG, Awadallah A, et al. Targeting improves MSC treatment of inflammatory bowel disease. Mol Ther. 2010;18:1365–72.
Yao W, Guan M, Jia J, et al. Reversing bone loss by directing mesenchymal stem cells to bone. Stem Cells. 2013;31:2003–14.
Neer RM, Arnaud CD, Zanchetta JR, et al. Effect of parathyroid hormone (1-34) on fractures and bone mineral density in postmenopausal women with osteoporosis. N Engl J Med. 2001;344:1434–41.
Einhorn TA, Gerstenfeld LC. Fracture healing: mechanisms and interventions. Nat Rev Rheumatol. 2015;11:45–54.
Tewari D, Khan MP, Sagar N, et al. Ovariectomized rats with established osteopenia have diminished mesenchymal stem cells in the bone marrow and impaired homing, osteoinduction and bone regeneration at the fracture site. Stem Cell Rev. 2015;11:309–21.
Caplan AI, Correa D. The MSC: an injury drugstore. Cell Stem Cell. 2011;9:11–5.
Zhang J, Liu X, Li H, et al. Exosomes/tricalcium phosphate combination scaffolds can enhance bone regeneration by activating the PI3K/Akt signaling pathway. Stem Cell Res Ther. 2016;7:136.
Furuta T, Miyaki S, Ishitobi H, et al. Mesenchymal stem cell-derived exosomes promote fracture healing in a mouse model. Stem Cells Transl Med. 2016;5:1620–30.
Campbell N, Conaglen P, Martin K, et al. Surgical stabilization of rib fractures using Inion OTPS wraps--techniques and quality of life follow-up. J Trauma. 2009;67:596–601.
Morgan EF, Mason ZD, Chien KB, et al. Micro-computed tomography assessment of fracture healing: relationships among callus structure, composition, and mechanical function. Bone. 2009;44:335–44.
Currey JD. The many adaptations of bone. J Biomech. 2003;36:1487–95.
Wehner T, Steiner M, Ignatius A, et al. Prediction of the time course of callus stiffness as a function of mechanical parameters in experimental rat fracture healing studies--a numerical study. PLoS One. 2014;9:e115695.
Manjubala I, Liu Y, Epari DR, et al. Spatial and temporal variations of mechanical properties and mineral content of the external callus during bone healing. Bone. 2009;45:185–92.
Tripuraneni N, Srour MK, Funnell JW, et al. A surgical procedure for resecting the mouse rib: a model for large-scale long bone repair. J Vis Exp. 2015;(95):52375.
Dhillon RS, Xie C, Tyler W, et al. PTH-enhanced structural allograft healing is associated with decreased angiopoietin-2-mediated arteriogenesis, mast cell accumulation, and fibrosis. J Bone Miner Res. 2013;28:586–97.
Komatsu DE, Brune KA, Liu H, et al. Longitudinal in vivo analysis of the region-specific efficacy of parathyroid hormone in a rat cortical defect model. Endocrinology. 2009;150:1570–9.
Liu S, Zhou J, Zhang X, et al. Strategies to optimize adult stem cell therapy for tissue regeneration. Int J Mol Sci. 2016;17(6). doi:10.3390/ijms1.7060982.
The authors would like to thank Marissa K. Srour for her help with the surgical model and Sagi Pelled for assistance with microCT data analysis.
The research was supported by grants from California Institute for Regenerative Medicine (CIRM) (TR2-01780) and National Institutes of Health (NIH) (R01DE019902)
Availability of data and materials
The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.
DCY, DS, EJL, DG, ZG and GP contributed to the study concepts. DCY, DS, MB, SD-M, WT, and EJL performed small animal surgical procedures. DCY, MB, YS, EY, AS, MA, AY, and XD performed μCT imaging and data analysis. DS, SD-M and SB-D were responsible for vector production, cell preparation, tissue staining, and microscopy. DCY, EJL, DG, ZG, and GP wrote the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
All procedures described in this study were approved by the Cedars-Sinai Medical Center’s Institutional Animal Care and Use Committee (Protocol No. 5684). The animals were treated in strict adherence to NIH guidelines.
Zulma Gazit and Gadi Pelled are co- senior authors.
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Cohn Yakubovich, D., Sheyn, D., Bez, M. et al. Systemic administration of mesenchymal stem cells combined with parathyroid hormone therapy synergistically regenerates multiple rib fractures. Stem Cell Res Ther 8, 51 (2017) doi:10.1186/s13287-017-0502-9
- Systemic stem cell administration
- Parathyroid hormone
- Rib fracture