Electrical signals have been applied towards the repair of articular tissues in the laboratory and clinical settings for over seventy years. We focus on healing of the meniscus, a tissue essential to knee function with limited innate repair potential, which has been largely unexplored in the context of electrical stimulation. Here we demonstrate for the first time that electrical stimulation enhances meniscus cell migration and integrative tissue repair. We optimize pulsatile direct current electrical stimulation parameters on cells at the micro-scale, and apply these to healing of full-thickness defects in explants at the macro-scale. We report increased expression of the adenosine A2b receptor in meniscus cells after stimulation at the micro- and macro-scale, and propose a role for A2bR in meniscus electrotransduction. Taken together, these findings advance our understanding of the effects of electrical signals and their mechanisms of action, and contribute to developing electrotherapeutic strategies for meniscus repair.
Electric fields are known to guide the development and regeneration of many tissues, including cartilage1,2,3. However, the exact roles of electrical signals in regulating the biosynthetic activity and homeostasis of articular tissues remain elusive, although preclinical and clinical studies have demonstrated superior healing following their application4,5,6. The meniscus is of particular interest, as knee arthroscopy for meniscus intervention is the most performed procedure by orthopaedic surgeons7. In the past, the entire meniscus was routinely removed by total meniscectomy, but long-term outcomes have since demonstrated that the incidence and severity of osteoarthritis is proportional to the amount of tissue removed8. Moreover, the extent of intrinsic repair after surgery is largely determined by the location of the injury: while meniscus tears in the vascularized, outer tissue region can undergo repair, those in the avascular inner region, similar to cartilage, do not heal, and the damaged tissue must instead be removed9. Therefore, general wisdom in orthopaedics has been that vascularity is necessary for healing, and the regional variation that exists within the meniscus has led to novel approaches to overcome the limited treatment options for injuries in the inner region.
The biochemical composition of the meniscus also varies by region, with predominantly type I collagen in the more fibrous outer region, and a mixture of types I and II collagen in the more cartilaginous inner region10. The bulk of the remaining extracellular matrix (ECM) is composed of negatively charged glycosaminoglycans (GAGs)11, which hydrate the tissue, contribute to its compressive properties, and also allow for electrical activity12. After meniscus injury, increases in GAG levels in the synovial fluid peak early, and persist out to four years after injury13. The synovial environment after injury also has elevated levels of IL-1 and TNF-α14,15,16, which act in concert to increase the production of nitric oxide (NO), prostaglandin E2 (PGE2), and matrix metalloproteinases (MMPs), increase the release of GAGs, and decrease the synthesis of collagen in the meniscus17,18,19. The full-thickness defect model in explants has been employed extensively in the study of meniscus repair in the presence of IL-1 and TNF-α, demonstrating dose-dependent decreases in integration strength and tissue repair over sustained supplementation20, and long-term potentiation of effects even after acute exposure21. The application of dynamic loading on meniscus explants in the presence of IL-1 was found in turn to combat the cytokine's inflammatory effects on integrative repair22.
The endogenous electrical potentials during physiological loading of articular cartilage have been studied using theoretical23,24,25 and experimental26,27,28 models, and these native electrical signals have been implicated in transducing mechanical signals to cells within tissues26,29,30. A variety of electrical stimulation modalities investigated in 2-D and 3-D models of cartilage in vitro and cartilage repair in vivo4,5,6 were shown to significantly increase cell proliferation31,32 and GAG synthesis33,34, upregulate the expression of ECM genes35, and reduce the production of inflammatory mediators such as IL-1 and MMPs36. However, questions remain as to how electrical signals influence cells and propagate their effects. The adenosine receptors have been implicated in the electrotransduction of pulsed electromagnetic fields in cartilage37,38. Stimulation of the high-affinity A2a and low-affinity A2b adenosine receptors resulted in elevated cyclic AMP39 and subsequent activation of anti-inflammatory pathways via protein kinase A and EPAC, which in turn lead to the suppression of NO and PGE240 and downstream feedback inhibition of TNF-α and IL-1β41. We therefore hypothesized that electrical stimulation will enhance repair of the meniscus and control the inflammatory events underlying tissue degradation.
Given the wealth of background information on electrical stimulation, inflammation, and adenosine receptor signaling in cartilage repair, it may come as a surprise that very little published information exists in the context of the meniscus. Only recently, meniscus cells from the outer region were found to migrate more quickly in 2-D culture than inner cells, in the presence of static direct current (DC) fields42. However, electrical stimulation studies have demonstrated a disparity in migration behavior between 2-D and more physiologically relevant 3-D environments43. Moreover, pulsatile electric fields (EFs) are already used in the clinical setting for related conditions44,45. At this time, the effects of applied EFs on meniscus cells and subsequent development of novel repair strategies are only beginning to be understood. We investigated the effects of pulsatile direct current electric field stimulation on meniscus cell migration in a micropatterned 3-D hydrogel system. Our micro-scale system also enabled study of the paracrine signaling between meniscus and vascular endothelial cells, in concert with electrical stimulation. Electric fields are known to induce VEGF receptor signaling in endothelial cells46, so we expected that patterns of meniscus cell migration that result from the differences in intrinsic vascularity within the tissue will be further enhanced by interactions between electric fields and endothelial cells. Moreover, little is known about the signal transduction pathways that respond to electrical stimuli in meniscus cells. Screening and optimization of stimulation parameters at the micro-scale enabled us to identify potential pathways involved in electrotransduction. By translating from the micro- to the macro-scale, we established stimulation regimes that enhanced integrative repair of full-thickness defects in meniscus, and demonstrated promising therapeutic effects of electrical stimulation on meniscus healing.
Electrical stimulation has differential effects on meniscus cell migration
Electrical stimulation of the meniscus was investigated using three distinctly different yet related experimental model systems in which inner and outer meniscus cells or explants were subjected to pulsatile direct current electrical stimulation: (a) micropatterned three-dimensional hydrogels with encapsulated inner or outer meniscus cells, (b) micropatterned 3-D hydrogels with spatially distributed meniscus and endothelial cells, and (c) a macroscopic in vitro model of meniscus healing (Fig. 1). When cultured in the micropatterned 3-D hydrogel system, meniscus cells migrated over six days of culture, with the stimulated cells demonstrating enhanced migration relative to non-stimulated control cells (Fig. 2a). Notably, both inner and outer meniscus cells exhibited similar increases in migration with applied electrical signals at 3 V/cm, 1 Hz, 2 ms pulse duration (Fig. 2b), despite the variation in repair response between their respective tissue regions. When injected charge, or the total amount of charge delivered during one stimulus pulse, was maintained at a constant field strength of 3 V/cm, further increases in cell migration were gained as the frequency of stimulation increased to 10 Hz and the pulse duration decreased to 0.2 ms (Fig. 2c). The combinations of 3 V/cm, 0.1 Hz, 20 ms pulse duration, and 3 V/cm, 100 Hz, 0.02 ms pulse duration were also tested, but the longer pulse duration associated with 0.1 Hz led to a more rounded, quiescent cell appearance rather than the spread-out, migrating cell phenotype seen at the channel edge. The increase in frequency to 100 Hz did not markedly improve the migration behavior of inner or outer meniscus cells, likely a result of too brief of a refractory period for cells to fully respond to subsequent stimulation pulses.
No apparent difference in positive BrdU staining, indicative of cellular proliferation, was apparent between the inner and outer cells, with and without stimulation (Fig. 2d), suggesting that differences in cell motility over six days of culture were not the result of proliferation only. Finally, type I collagen, a key ECM component throughout the meniscus, exhibited trends of elevated gene expression in both inner and outer cells when the frequency of electrical stimulation was increased while maintaining constant injected charge (Fig. 2e).
Cooperative action of electrical stimulation and endothelial cells on meniscus cell migration
Co-culture with human umbilical vein endothelial cells (HUVECs) was investigated in the context of regional variation in healing between the inner and outer meniscus. Notably, HUVECs further potentiated the effects of electrical stimulation on meniscus cell migration (Fig. S1). Stimulating HUVECs alone in the hydrogel system led to increased expression of EDN1, PDGFA, and PDGFB genes (Fig. 3a), which encode key angiogenic factors (endothelin-1, PDGF-A, B) that modulate the behaviors of chondrocytes47 and meniscus cells48, suggesting a dual role of electrical stimulation in upregulating angiogenic factors that specifically enhance meniscus cell migration, in addition to promoting cell migration in general. Although meniscus cells alone exhibited greater migration in response to the 3 V/cm, 10 Hz, 0.2 ms pulse duration regime, meniscus cell migration in co-culture with HUVECs at 10 Hz stimulation was not significantly greater than without HUVECs at 10 Hz, but was significantly greater than in non-stimulated meniscus cells with HUVECs (Fig. 3b). The cooperative action of stimulation and co-culture was observed in the 3 V/cm, 1 Hz, 2 ms pulse duration regime (Fig. 3b), suggesting that frequency-dependent interactions between chemical and electrical stimuli require optimization for collaborative effects. In this system, the expression of angiogenic factors by HUVECs was upregulated dramatically with stimulation at 1 Hz as compared to non-stimulated controls, whereas the effect of increasing frequency from 1 to 10 Hz was much smaller (Fig. 3a). These findings may account for the positive trends seen in meniscus cell migration with co-culture at 1 Hz stimulation that were not apparent at 10 Hz.
Using the 1 Hz stimulation regime, gene expression profiles of the meniscus cells were further investigated to elucidate how stimulation and co-culture cooperate to enhance migration. As seen in cultures of meniscus cells with electrical stimulation alone, both inner and outer cells showed increases in COL1A2 expression in response to combined stimulation at 1 Hz and co-culture with HUVECs (Fig. 3c). Although inner and outer meniscus cells demonstrated similar migration behavior in co-culture with HUVECs, they do so in response to different angiogenic factors secreted by endothelial cells, as seen at the gene expression level. Both types of cells responded to stimulation in co-culture with HUVECs by increased expression of EDNRA, encoding endothelin receptor type A (Fig. 3c). However, outer cells responded to the secretion of PDGF isoforms by HUVECs with increased expression of PDGFRA and PDGFRB, encoding PDGF receptors α and β, while no such changes were detected for inner cells. These results demonstrate that electrical stimulation and endothelial cells collaborate to activate meniscus cell receptors at the gene expression level, suggesting potential synergy between the biophysical and biochemical stimuli.
Electrical stimulation enhanced integrative repair of meniscus explants
Using a macroscopic in vitro model of meniscus healing, translation of the micro-scale findings to the macro-scale revealed a significant increase in the integration strength of full-thickness defects in explants stimulated at 3 V/cm, 10 Hz, 0.2 ms pulse duration, after six weeks of culture (Fig. 4a). Stimulation at 1 Hz, 2 ms pulse duration initially corresponded to decreases in integration strength over the first four weeks of culture, but surpassed control conditions without stimulation by day 42, albeit to a lesser extent than stimulation at 10 Hz. The underlying basis for the enhanced integration strength of defects in explants stimulated at 10 Hz was further explored by assaying for biochemical content and visualizing the distribution of cells and ECM within the tissue. The overall biochemical content of explants without stimulation decreased throughout six weeks of culture, consistent with previous studies of explant stability in long-term culture, in the absence of growth factor supplementation49,50 (Fig. 4b). However, the GAG and OHP content of explants stimulated at 10 Hz was not significantly different than at day 0, in comparison to explants without stimulation, which were significantly lower than initial values (Fig. 4b). In general, stimulation led to significant upward trends in DNA and OHP content of explants after six weeks of culture, as compared to explants without stimulation (Fig. 4b).
Histological evaluation revealed that the defect interface appeared more closely apposed in explants stimulated at 10 Hz than in control explants (Fig. 4c). Specifically, newly synthesized matrix was observed at the interface, containing sulfated GAGs and collagens, as evidenced by Alcian blue and Picrosirius red staining, respectively. BrdU labeling was performed to assess the effects of electrical stimulation on cell proliferation, yielding more BrdU-positive cells at the interface of stimulated explants, and indicating a moderate role of electrical stimulation in triggering cell proliferation in explants over long-term culture. Taken together, these data suggest that in addition to tissue repair, electrical stimulation acts to maintain cells and overall ECM composition, and prevent explant degradation in vitro.
Anti-inflammatory effects of electrical stimulation on meniscus explants
Evaluation of the components from media collected throughout six weeks of culture revealed increases in endogenous TNF-α and IL-1β production by explants without stimulation, compared to those receiving stimulation at 3 V/cm, 10 Hz, 0.2 ms pulse duration, particularly within the first four weeks (Fig. S2a, b). The elevated cytokine levels in explants without stimulation corresponded with changes in NO production (Fig. S2c), MMP activity (Fig. S2d), and GAG release (Fig. S2e), which were typical of catabolic degradation: in comparison to stimulated explants, greater NO production, MMP activity, and GAG release were detected in explants without stimulation, suggestive of an anti-inflammatory, anti-catabolic, and stabilizing effect of electrical stimulation in long-term culture in vitro. These changes in explants without stimulation occurred early in culture, within the first three weeks, but their biochemical composition continued to decrease for the remainder of the culture period.
Adenosine A2b receptor plays a role in meniscus electrotransduction
Adenosine receptors in meniscus were identified by gene expression analysis of migrating cells, with and without stimulation at 3 V/cm, 10 Hz, 0.2 ms pulse duration. In hydrogel-encapsulated cells, the expression of ADORA1, ADORA2A, and ADORA3, encoding the adenosine A1, A2a, and A3 receptors, respectively, was minimal at day 0 (2−ΔCT ≪ 10−4; n = 4) and at day 6 after culture, with and without stimulation (2−ΔCT ≪ 10−5; n = 4), but ADORA2B encoding A2bR was upregulated in meniscus cells with electrical stimulation at 3 V/cm, 10 Hz, 0.2 ms, as well as 3 V/cm, 1 Hz, 0.2 ms pulse duration (Fig. 5a). Translation to the protein level was evident through immunofluorescence staining of migrating meniscus cells at day 6, against A2bR and DAPI for nuclei (Fig. 5b). Cells receiving stimulation demonstrated strong, positive staining for A2bR, while cells without stimulation exhibited little or none, suggesting that the applied electrical signals may activate A2bR directly.
At the macro-scale level, cells in stimulated explants also stained positively for A2bR, whereas those not receiving stimulation appeared negative (Fig. 5c), lending further evidence to the potential relationship between electrical signals and activation of the adenosine A2b receptors in meniscus. Moreover, the consistency in protein expression from the micro- to macro-scale continues to support the use of micro-scale systems for evaluation of a broad range of electrical stimulation regimes, in order to identify the optimal parameters to apply at the macro-scale tissue level.
Electrical stimulation is a versatile treatment modality that has yet to be fully explored in the context of injuries to the meniscus, in which negatively charged glycosaminoglycans form the basis for endogenous electrical activity26,29,30. We demonstrate that pulsatile direct current electric fields enhance meniscus cell migration in a micropatterned hydrogel system, and the integrative repair of meniscus defects in an in vitro explant model of meniscus healing. Notably, the responses of meniscus cells from the inner and outer regions were comparable, suggesting that the meniscus cells from both regions can be induced to migrate and promote healing by external electrical signals.
In our 3-D systems, electrical stimulation alone induced similar migration behavior in cells isolated from both the inner and outer regions, whereas previous studies have shown that outer cells migrate more quickly than inner cells during 2-D galvanotaxis42. This disparity in observation may arise in part from the use of distinct cell populations within the meniscus between the two studies: cells isolated by tissue explant outgrowth in culture in the present study, versus cells isolated by release from tissue matrix via digestion in the galvanotaxis studies42. The inner and outer meniscus cells used in our study were previously characterized as a population capable of differentiating along multiple lineages, and may represent tissue-specific stem cells contributing to endogenous repair51. These cells, by nature of their isolation via tissue outgrowth, exhibit a predisposition for migration, which may also account for the level of motility observed in cells, even in the absence of electrical stimulation. As such, an enriched population of these cells after passaging may have led to a more robust response to exogenous electrical stimuli than a mixed population obtained by digestion in previous studies. In addition, the applied electric fields in the current study were perpendicular to the direction of cell migration, but no bias in polarity of movement was observed, in contrast to the cathodal migration of meniscus cells during 2-D galvanotaxis42. However, the observed behavior is consistent with studies of human fibroblasts on 3-D collagen gels in static DC fields, in which preferred movement occurred perpendicular to the axis of stimulation, but not towards a specific pole43.
The fibrin hydrogel used in the micropatterned system represented a simple three-dimensional environment to observe meniscus cell migration phenomena. However, it does not begin to replicate the dense tissue matrix found in the native meniscus. Therefore, it was particularly encouraging to discover that the parameters optimized at the hydrogel level were applicable at the tissue level, inducing the migration of endogenous repair cells to the defect interface. However, migration at the tissue level also necessarily requires remodeling of the dense surrounding matrix to enable movement, which involves the interplay and balance of pro-inflammatory cytokines and MMPs, and anti-inflammatory and anabolic factors. After meniscus injury, experimentally induced or clinically occurring, this balance is tilted in favor of pro-inflammatory, catabolic events, necessitating examination into interventions that can re-initiate synthesis of key ECM components. It has been previously reported that meniscus explants lose their biochemical properties, specifically, DNA49 and GAG49,50 content, over time in culture. In this study, a similar loss in DNA and GAG content was seen in explants without stimulation over six weeks, and in addition, we observed a significant loss of collagen content. Interestingly, the explants receiving the optimal stimulation regime maintained their biochemical composition, suggesting a stabilizing effect of electrical stimulation, moving the balance away from the destructive aspect of remodeling towards the constructive side. By applying the findings on the cellular micro-scale to the tissue macro-scale, an additional benefit of electrical stimulation was revealed, that it may counteract the natural degradation of explant tissue in vitro, in addition to mediating cell migration.
In order to understand the basis of the in vitro degradation, the concentration of pro-inflammatory cytokines, TNF-α and IL-1β, were measured in the media collected during explant culture. The fetal bovine serum used in culture medium contained baseline amounts of both cytokines, but it is notable that statistically significant differences existed between the levels of TNF-α and IL-1β in explant culture media, with and without stimulation, in the absence of exogenous supplementation of either cytokine or other pro-inflammatory mediators. In clinical observation, synovial fluid from patients who underwent arthroscopy for a meniscus tear contained between 35–85 pg/mL TNF-α, and 90–125 pg/mL IL-1β52. The level of TNF-α detected in this system was well above what was found in a pathological state of meniscus injury, but within the working range of exogenous supplementation in other studies of meniscus repair20. In contrast, IL-1β was below both pathologic levels and the range used in other meniscus studies53. IL-1α levels were not measured in this study, but are relevant due to the differences in relative potency of IL-1α and β in porcine meniscus explants54. Moreover, the effects of TNF-α and IL-1 were not independent, and interplay between the two cytokines in activating pro-inflammatory pathways has been documented14,15,16,17,18,19. The lower levels of TNF-α and IL-1β in explants receiving the optimal stimulation regime suggest inhibitory effects of electrical stimulation on their production. In contrast, increases in these cytokines were observed in explants without stimulation, with corresponding increases in NO production, MMP activity, and subsequent GAG loss in media. These two observations correlate with previous findings demonstrating that inhibition of MMPs can significantly reduce GAG loss in culture50. The loss of explant stability in the absence of electrical stimulation, particularly in the first half of the culture period, corresponds with the observation that meniscus injury disrupts tissue homeostasis and initiates a series of events furthering degradation8,55,56,57.
The migration and anti-inflammatory responses elicited by electrical stimulation occur via the activation of membrane receptors on meniscus cells. It has been previously postulated that electromagnetic fields can serve as first messengers in signaling towards tissue repair58. Based upon the findings in this study, a new model of electrotransduction in meniscus could be proposed: after meniscus injury, TNF-α and IL-1 levels are elevated, progressing toward further tissue degradation (Fig. 6a). Within this environment, the application of pulsatile DC electrical stimulation selectively activates the adenosine A2b receptor, producing the second messenger cAMP, which triggers anti-inflammatory pathways that reduce NO production, MMP activity, and GAG release, and inhibit the initial pro-inflammatory cytokines (Fig. 6b).
The physiological role of low-affinity A2bR has been less characterized than the high-affinity A2aR, which has been studied extensively for anti-inflammatory activity in the context of osteoarthritis and rheumatoid arthritis59,60,61. However, activation of the A2bR, leading to elevated cAMP, has been shown to inhibit MMP-1 production in fibroblast-like synoviocytes from RA patients62, and in this study, we report for the first time in meniscus, among the class of adenosine receptors, the increased expression of A2bR following electrical stimulation at both the micro- and macro-scale. In order to fully elucidate the role of A2bR in meniscus electrotransduction, further experiments using receptor agonists and antagonists must be tested in meniscus defect models, with the addition of exogenous sources of pro-inflammatory cytokines to the system, and measurement of changes in adenylyl cyclase and cAMP levels. To this end, our micro-scale system for meniscus cell migration will allow for blocking or knock-down of the adenosine A2b receptor by antagonists or gene silencing, in order to verify the integral role of A2bR via short-term experiments, and subsequent application at the macro-scale in long-term culture of explants, for confirmation at the tissue level. Moreover, cells and explants in this study were derived from juvenile bovine meniscus, requiring future studies using adult or even osteoarthritic tissue to confirm and extend findings. While growth factors were not supplemented to medium in this system, the addition of TGF-β3 alone49 or TGF-β1 in the presence of IL-163 has been shown to significantly enhance meniscus repair, meriting the further study of any potential synergy between electrical and chemical stimuli. However, it should be noted that the reparative and protective effects of electrical stimulation alone, as shown in this study, are more immediately translatable to the clinic, without the need for in vivo delivery of growth factors. Moreover, the integration strength of explants stimulated at the optimal regime is among the highest reported in literature for this model of meniscal repair, even in the absence of exogenous growth factors20,21,22,49,63,64.
The contribution of growth factors was explored at the micro-scale through the co-culture of endothelial cells, as a model of clinical methods that increase the vascular response to the inner region65,66, which does not naturally undergo repair. Although up to 30% of the meniscus is vascularized in adults67, and endothelial cells from the meniscus have been isolated and cultured68, the exact percentage of endothelial cells in the tissue remains unknown. However, endothelial cells may potentiate their effects via paracrine signaling, and these angiogenic factors can be supplemented in avascular tissues where they and endothelial cells are natively absent, such as in the inner region of the meniscus. Here we report that the combination of biophysical and biochemical stimuli via EFs and co-culture with HUVECs cooperatively enhanced the migration of meniscus cells in a 3-D environment. Despite the variation in vascularity of their respective tissue regions, inner and outer cells demonstrated trends of increased migration in the presence of both stimuli as compared to either stimulus alone. The cooperative effects of electrical signals and HUVECs appeared to result from the direct effects of electrical signals on HUVECs, which have been shown to regulate HUVEC behavior46, and in our system, upregulated the gene expression of angiogenic factors such as endothelin-1 and PDGF isoforms, previously shown to act on chondrocytes47 and meniscus cells48. Curiously, we observed a regional variation in expression of endothelin and PDGF receptors by meniscus cells in co-culture with HUVECs, which is now the focus of ongoing studies to examine the differential paracrine mechanisms of endothelial cells on the meniscus. Specifically, we will investigate if direct interactions between meniscus and endothelial cells are necessary, or if paracrine factors secreted by endothelial cells are sufficient to induce migration behavior in outer cells, which natively co-exist with vasculature, versus inner cells, which do not. The differential expression of PDGF receptor genes in outer versus inner cells in co-culture with HUVECs may arise from the presence of endothelial cells in one region versus the other, a disparity that was further amplified by electrical signals. However, the upregulation of ETAR gene expression in cells of both regions with co-culture suggests that ET-1 signaling is involved in the vascular response of the outer region for healing. Moreover, the limited healing potential of the inner region could be enhanced if ET-1 is supplemented to the avascular tissue, which does not receive these signals natively in the absence of endothelial cells. If these differential paracrine mechanisms of HUVECs on cells from the inner and outer regions are validated in future studies, by applying conditioned medium or specific angiogenic factors, we not only gain a further understanding of the variation in repair response between the two regions, but we also identify the angiogenic factors that are natively absent in the inner region, but can be supplemented in order to promote healing.
In addition, we found that the coordinated action of EFs and HUVECs on meniscus cell migration was more apparent using a different set of stimulation parameters than for EFs alone. This observation, as well as the variation in migration response seen during initial optimization of parameters for meniscus cells only, is in line with previous theories that a window exists in which productive electrical stimulation occurs33, and parameters must be optimized for all relevant cell types within the system. Moreover, although the co-culture studies were performed at one fixed channel-to-channel distance, the system can be easily modified to vary this distance by simply changing the design of the micropattern, in order to identify a length scale over which paracrine signaling occurs. Although it was not tested in this study, the interaction of electrical stimulation and endothelial cells is pertinent at the tissue level as well, with implications for clinical and adjuvant therapies. However, in vitro models of meniscus repair cannot fully replicate the regional variation in vascular environment within the tissue and its influence on healing64. Experimentation in an animal model is the most suitable next step towards validation of electrical stimulation as a modality for treatment of meniscus injury.
In summary, the effects of pulsatile electric field stimulation on meniscus repair were demonstrated for the first time. Optimization of electrical stimulation regimes for cell migration was achieved at the micro-scale with short-term experiments, and then applied at the macro-scale towards significant integrative repair of full-thickness defects in meniscus explants. In situ stimulation of explants revealed another role of electric fields in modulating inflammation and reducing tissue degradation. The dual functions of electrical stimulation in meniscus support its use in the clinical setting, after surgical intervention, to recruit cells for tissue repair and to prevent the matrix degradation that leads to osteoarthritis. Future establishment of therapeutic strategies, by testing stimulation regimes and translating to macro-scale tissue repair, has the potential to overcome current limitations in meniscus healing.
Juvenile bovine meniscus cells were isolated from the inner and outer regions as previously described51. Briefly, the menisci of calves were obtained from a commercial source (Green Village Packing Company), dissected within 36 h of slaughter, and sectioned into inner (2/3) and outer (1/3) regions. The tissue was then minced into 1–2 mm3 pieces, and plated on tissue culture plates in basal medium consisting of high glucose DMEM, 1× antibiotic-antimycotic, 10% FBS, and 50 μg/mL ascorbate 2-phosphate. Over 2–3 weeks, cells migrated out of the tissue pieces, and were expanded to passage 2.
Human umbilical vein endothelial cells (HUVECs) were isolated from fresh umbilical cords of term delivery, collected according to an active IRB at Columbia University (IRB-AAAC4839)69. According to the protocol, tissue samples were fully deidentified and there was no patient information available to the investigators. Umbilical cords were rinsed with PBS, and the umbilical vein lumen was infused with a 2.5% trypsin solution and clamped at both ends. Enzymatic digestion occurred at 37°C for 15 min, and the resulting cell digest was collected by rinsing the vein with PBS and centrifugation at 300 × g for 5 min. The cell pellet was resuspended on 25 cm2 tissue culture flasks in endothelial growth medium (EGM-2, Lonza), and expanded to passage 5.
Juvenile bovine meniscus explants were harvested from the central tissue region using sterile 4 mm Ø biopsy punches, and cut to 1.5 mm height using a custom microtome device. A 1.5 mm Ø central core was punched and immediately replaced into the explant ring to simulate a full-thickness defect. Explants were cultured for 3 days in basal medium prior to the start of each experiment.
Cell migration assay
The micropatterned three-dimensional hydrogel system used in cell migration studies was previously established for the study of human mesenchymal stem cells and HUVECs in co-culture69. Briefly, the poly(dimethylsiloxane) (PDMS; 9:1 elastomer:curing agent; Sylgard 184 silicone elastomer kit, Dow Corning) micropattern consisted of two parallel channels (1 cm length, 1000 μm width, 200 μm height, channel-to-channel distance: 2000 μm; Fig. 1b). Prior to cell encapsulation, the PDMS surface was blocked using a 5% solution of FBS in sterile distilled water.
In single channel studies (Fig. 1a), inner or outer meniscus cells were encapsulated at 3.5 × 106 cells/mL each in 1.8% fibrin (bovine fibrinogen, MP Biomedicals; thrombin from bovine plasma, Sigma-Aldrich) and printed into single channels on plastic slides. The cell-fibrin suspension was allowed to polymerize for 15 min, before removal of the PDMS mold and encapsulation in an additional layer of 1.8% fibrin to permit cell migration. In co-culture studies (Fig. 1b), inner or outer meniscus cells and HUVECs were encapsulated at 3.5 × 106 cells/mL each in 1.8% fibrin, printed into two parallel channels on plastic slides, and covered by another layer of 1.8% fibrin. Single channels of inner or outer meniscus cells served as controls. Cultures were maintained in EGM-2 over 6 days after encapsulation, and migration was monitored by bright field imaging at days 0 and 6, using an Olympus IX81 microscope with an IX2-UCB digital camera and Metamorph software.
Electrical stimulation of cells
After 3 days of pre-culture without stimulation, the cells were transferred into custom bioreactors with carbon electrodes (Ladd Research Industries) spaced 2.5 cm apart (Fig. 1a)70. Bioreactors were connected by platinum wire to an electrical stimulator (Grass Technologies) generating continuous pulses of 7.5 V, corresponding to a field strength of 3 V/cm, and various frequency and pulse duration combinations (0.1, 1, 10 Hz and 2 ms pulse duration; 10 Hz and 0.2 ms pulse duration) for 3 days. Bioreactors not connected to the stimulator served as controls (0 V).
Electrical stimulation of explants
After 3 days of pre-culture, explants were stimulated in a custom bioreactor (Fig. 1c), consisting of a 5 × 6 array outfitted with carbon electrodes that were spaced 1 cm apart, and connected directly to a stimulator generating pulses of 3 V, corresponding to a field strength of 3 V/cm, and either 1 Hz and 2 ms pulse duration or 10 Hz and 0.2 ms pulse duration. Each row was independently stimulated, with six wells per row receiving the same stimulation regime. Rows not connected to the stimulator served as controls (0 V). Explants were stimulated four days a week over six weeks of culture in basal medium, with media collection at each change, and sample collection for mechanical integration testing, biochemical assays, and histological and immunofluorescence staining at biweekly time points.
Evaluation of meniscus cell migration
Bright field images were processed using a custom MATLAB program71 to track cell migration. Briefly, the program applied the Sobel edge detection algorithm and eliminated small regions of isolated, single meniscus cells. Each image was evenly subdivided into regions corresponding to ~1580 μm of the channel length, for which average channel-to-channel distances were calculated.
The total RNA of meniscus cells or HUVECs after six days of culture was extracted by TRIzol reagent (Invitrogen) and reverse transcribed (High Capacity cDNA Reverse Transcription Kit, Applied Biosystems). Meniscus cells and HUVECs were also collected at day 0 prior to encapsulation and processed to facilitate fold change analysis (2−ΔΔCT). Real-time PCR was performed on an Applied Biosystems StepOnePlus Real-Time PCR System using Fast SYBR Green Master Mix (Invitrogen), custom bovine primers for COL1A2, EDNRA, PDGFRA, PDGFRB, ADORA1, ADORA2A, ADORA2B, ADORA3, and GAPDH, and custom human primers for EDN1, PDGFA, PDGFB, and GAPDH.
Mechanical integration testing of explants
The integration of full-thickness defects in explants was tested with a custom device consisting of a 1.33 mm Ø indenter in series with a 50 g load cell, placed above a cup with a 2 mm Ø hole. Prior to testing, the height of each sample was measured using a digital caliper. The indenter was displaced at a ramp rate of 0.3% of the sample height per second, until the central core was pushed fully through the outer ring. Integration strength was calculated as the ratio of the peak force to the surface area of contact between the central core and outer ring. After testing, samples were collected for further biochemical analysis.
Biochemical analysis of explants and media
The biochemical composition of explants was evaluated for DNA, sulfated GAG, and OHP content. Briefly, samples were lyophilized for 24 h and digested at 60°C for 16 h in a papain solution containing 125 μg/mL papain (Sigma-Aldrich), 50 mmol phosphate buffer (pH 6.5), and 2 mmol N-acetyl cysteine (Sigma-Aldrich). DNA content of the sample digests was obtained using the PicoGreen dsDNA quantitation kit (Invitrogen), according to manufacturer's protocol. Sulfated GAG content was measured using the 1,9-dimethylmethylene blue dye-binding (DMMB) assay72. Hydroxyproline (OHP) content was quantified by a modified acid hydrolysis assay73. Media collected at each change was assayed for TNF-α, IL-1β, and NO production, MMP activity, and GAG release using the DMMB assay. Briefly, TNF-α and IL-1β production were quantified directly on media samples using the bovine TNF-α (GenWay Biotech) and IL-1β (Thermo Fisher Scientific) ELISA kits, respectively. Prior to NO analysis, media samples were filtered through Vivaspin 500 units (10,000 MWCO PES filters, Sartorius), and total NO production in media samples was determined by quantification of nitrate and nitrite, according to manufacturer's protocol (nitrate/nitrite colorimetric assay kit, Cayman Chemical Company). The activity of MMP-1, -2, -3, -9, -13, and -14 was assessed via cleavage of a fluorescent peptide substrate (PEPDAB008, BioZyme), adapted from a previously published protocol53. Media samples were incubated in either 2.5 mM p-aminophenylmercuric acetate (APMA; pH 7.0–7.5) in assay buffer (200 mM NaCl, 50 mM Tris, 5 mM CaCl2, 10 μM ZnSO4, 0.01% Brij 35, pH 7.5) or in assay buffer alone at 37°C for 5 h. Samples were then diluted twofold with assay buffer containing 20 μM substrate at 37°C for 2 h, and measured at 485 nm excitation and 530 nm emission. Total MMP activity was calculated as the difference in fluorescence readings between samples incubated with and without APMA.
5-bromo-2-deoxyuridine labeling of cells and explants
At the endpoint of both migration and integration studies, samples were labeled with 5-bromo-2-deoxyuridine (BrdU, Invitrogen) to assess cellular proliferation. Single channel studies of meniscus cells were incubated with BrdU labeling reagent (1:50) at 37°C for 4 h, and explants (1:50) at 37°C overnight. Samples were then fixed for further histological processing.
Histological and immunofluorescence staining of cells and explants
Cell migration samples were fixed in a graded series of formaldehyde from 1% to 4% for 10 min each, and maintained in PBS at 4°C until preparation for staining. Briefly, samples were blocked and permeabilized with agitation in PBS containing 5% BSA and 0.1% Triton X-100 at 25°C for 1 h, and incubated at 4°C overnight with the primary antibody (rabbit anti-adenosine A2b receptor antibody, 50 μg/mL, Millipore) in PBS with 5% BSA. After 3 washes of 30 min each in PBS at 25°C with agitation, samples were incubated at 4°C overnight with Alexa Fluor® 555 goat anti-rabbit IgG (1:200, Invitrogen) and DAPI (1:200, Invitrogen), followed by 3 additional washes. Alternatively, samples were directly incubated after blocking and permeabilization with DAPI and mouse anti-BrdU antibody (Alexa Fluor® 488 conjugate, 1:50, Invitrogen).
Explants were fixed in 4% formaldehyde at 4°C overnight and embedded in 2% low-melting-temperature agarose. All samples were dehydrated in a graded series of ethanol, embedded in paraffin, and sectioned to 8 μm thickness. Sections were stained with hematoxylin and eosin (H&E) for nuclei and cytoplasmic elements, respectively, Alcian blue (pH 1.0) for sulfated GAGs, and Picrosirius red for collagens. For immunofluorescence staining of A2bR in paraffin-embedded samples, antigen retrieval was performed with 10 mM citrate buffer (pH 6.0). Blocking in PBS with 5% BSA, and primary and secondary antibody incubations in PBS with 5% BSA were completed, as previously described. Immunohistochemical staining of BrdU was conducted, according to manufacturer's protocol (BrdU staining kit, Invitrogen). Stained hydrogels and explants were imaged with an Olympus FSX100 microscope.
For cell migration studies, 1-way ANOVA with Tukey post tests or post tests for linear trend were performed with Prism (α = 0.05). For integration studies, 2-way ANOVA with Bonferroni post tests and 1-way ANOVA with post tests for linear trend were also performed with Prism. All data are presented as mean ± SEM.
We gratefully acknowledge NIH support of this work (grants EB002520, EB015888, DE016525, and AR061988). We also thank George Eng for his assistance with the micropatterned system, endothelial cell isolation, and bioreactor design; Kara Spiller for endothelial cell isolation; Keith Yeager for custom device design; Nina Tandon for bioreactor design; and Quentin Jallerat for his contribution to figures.
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