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Am J Respir Cell Mol Biol. 2006 September; 35(3): 306–313. Published online 2006 April 6. doi: 10.1165/rcmb.2005-0443OC. | PMCID: PMC2643283 |
Extracellular Matrix Remodeling by Dynamic Strain in a Three-Dimensional Tissue-Engineered Human Airway Wall Model Melanie M. Choe, Peter H. S. Sporn, and Melody A. Swartz Department of Biomedical Engineering, Northwestern University, Evanston; Division of Pulmonary and Critical Care Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois; and Institute of Bioengineering, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland Received December 3, 2005; Accepted March 31, 2006. Airway wall remodeling is a hallmark of asthma, characterized by subepithelial thickening and extracellular matrix (ECM) remodeling. Mechanical stress due to hyperresponsive smooth muscle cells may contribute to this remodeling, but its relevance in a three-dimensional environment (where the ECM plays an important role in modulating stresses felt by cells) is unclear. To characterize the effects of dynamic compression in ECM remodeling in a physiologically relevant three-dimensional environment, a tissue-engineered human airway wall model with differentiated bronchial epithelial cells atop a collagen gel containing lung fibroblasts was used. Lateral compressive strain of 10 or 30% at 1 or 60 cycles per hour was applied using a novel straining device. ECM remodeling was assessed by immunohistochemistry and zymography. Dynamic strain, particularly at the lower magnitude, induced airway wall remodeling, as indicated by increased deposition of types III and IV collagen and increased secretion of matrix metalloproteinase-2 and -9. These changes paralleled increased myofibroblast differentiation and were fibroblast-dependent. Furthermore, the spatial pattern of type III collagen deposition correlated with that of myofibroblasts; both were concentrated near the epithelium and decreased diffusely away from the surface, indicating some epithelial control of the remodeling response. Thus, in a physiologically relevant three-dimensional model of the bronchial wall, dynamic compressive strain induced tissue remodeling that mimics many features of remodeling seen in asthma, in the absence of inflammation and dependent on epithelial–fibroblast signaling. Keywords: asthma, collagen, fibrosis, in vitro, myofibroblast Remodeling of the airway wall in asthma is characterized by thickening of the subepithelial lamina reticularis, increase in smooth muscle mass, fibroblast hyperplasia, mucus hypersecretion, edema, and angiogenesis ( 1– 6). The subepithelial fibrosis that is often part of this remodeling is further characterized by the differentiation of fibroblasts to myofibroblasts, which are more contractile than fibroblasts and are likely to contribute to the alignment and stiffening of the airway matrix by secretion of types I, III, and V collagen ( 7– 14). In addition, matrix metalloproteinases (MMPs) and their inhibitors (tissue inhibitors of metalloproteinases [TIMPs]), particularly MMP-2 and -9 and TIMP-1, are also increased in the airways in asthma, as they are key players in extracellular matrix (ECM) remodeling ( 15, 16). Evidence from clinical studies supports the concept that airway remodeling contributes to irreversible airflow obstruction and loss of pulmonary function over time in patients with chronic asthma ( 17, 18). The complex interplay of factors contributing to airway wall remodeling, which includes inflammatory and mechanical factors, is not well understood. Immune cells recruited to the inflamed airways release cytokines such as RANTES (CCL5), IL-13, TGF-β 1, and cysteinyl leukotrienes C4, D4, and E4 ( 19– 21) that can stimulate epithelial cells, fibroblasts, and smooth muscle cells (SMCs). In asthma, the increase in SMC mass and hyperresponsiveness can result in amplified bronchoconstriction ( 22– 25), which is associated with compressive stresses on the epithelial cells and fibroblasts ( 26, 27). These mechanical forces may then further contribute to airway remodeling ( 28, 29); for example, static compressive stress on epithelial cells can alter the expression of TGF-β 1, endothelin-1 (ET-1), early growth response-1 (Egr-1), epidermal growth factor receptor (EGFR) ligands, and fibronectin ( 30– 33) (likely via an autocrine ligand signaling mechanism ( 34)), which may, in turn, activate fibroblasts to secrete matrix remodeling proteins ( 32). However, it is difficult to interpret the relevance of such stresses on matrix remodeling in the absence of a truly three-dimensional environment, where the ECM can ( 1) regulate cell–cell signaling by binding cytokines like RANTES ( 35) and growth factors like TGF-β 1 ( 36); ( 2) buffer mechanical stress via local heterogeneity in matrix properties ( 37); and ( 3) itself signal cells with soluble ECM fragments liberated during matrix remodeling. Indeed, such environmental factors may act to either augment or decrease the remodeling response by coordinating the various cell responses to stress ( 32). In addition, two-way cell–cell communication is critical for mediating overall remodeling responses, since fibroblasts and epithelial cells may each sense stress differently and play different roles in matrix remodeling. Clearly, the three-dimensional ECM is critical to modulating a stress environment to its resident cells, and thus the role of mechanical stress in airway wall remodeling cannot be definitively determined without a three-dimensional tissue environment. In this study, we evaluate the effects of dynamic strain on matrix remodeling in a physiologically relevant three-dimensional tissue engineered human airway wall model. Several research groups, including our own, have recently demonstrated the advantages of three-dimensional airway co-culture models that provide an ECM and organization of a cellular community over traditional (two-dimensional, single-cell) culture models for recapitulating physiologic and pathophysiologic behavior ( 38– 41). Our model here additionally mimics the mechanical function of the smooth muscle cells by incorporating lateral and dynamic compression to the three-dimensional culture system over a long-term period. We examine the effects of this mechanical strain on the airway wall with a focus on cell–cell and cell–matrix interactions. The results show that strain magnitudes of 10% and 30%, at frequencies of 1 and 60 cph, elicit selective responses in matrix remodeling that can be partly understood by the spatial deposition of ECM proteins with respect to cellular locations. In summary, we demonstrate that dynamic compression in our tissue engineered airway wall model can contribute to tissue remodeling similar to that seen in diseases such as asthma. Cell Culture IMR-90 human fetal lung fibroblasts (HLF; ATCC, Manassas, VA) were used at passage 14–16 and cultured in α-MEM supplemented with 10% fetal bovine serum (Gibco BRL, Grand Island, NY) and 1% penicillin/streptomycin (Sigma, St. Louis, MO). Normal human bronchial epithelial cells (HBEC; Clonetics, Walkersville, MD) were expanded in bronchial epithelial growth medium (BEGM; Clonetics) supplemented with 50 nM retinoic acid (Sigma) and used at passage 3. Detailed methods of culturing HLFs and HBECs and their characterization in three-dimensional collagen gels have been previously discussed ( 39). After cell expansion, each strain device ( see below) was filled with a mixture of 5 × 10 5 cells/ml HLFs suspended in 2.5 mg/ml type I collagen isolated from rat tail tendon. The surface was then coated with an additional thin layer of acellular 2.5 mg/ml collagen before culture in media consisting of BEGM:DMEM (Gibco BRL) in a ratio of 1:1. After 2–4 h, HBECs were seeded on the surface at 2.5 × 10 5 cells/cm 2 (although some models were cultured without HBECs for fibroblast-only controls). The system was cultured in submersion for 7 d to allow HBECs to reach confluence, and in air–liquid interface (ALI) for another 7 d to allow differentiation of HBECs. Strain Model and Characterization We designed a dynamic strain culturing device () in which cells could be cultured to their differentiated state and then exposed to various amplitudes and frequencies of lateral dynamic strain to mimic the mechanical environment in constricting airway walls. The design included a strain applicator made of a Teflon frame, porous polyethylene (PE) ends to anchor the gel (both from Small Parts Inc., Miami Lakes, FL), and polyether sponge side linings threaded with 1-mm-diameter elastic bands for elastic recoil, with inner well dimensions of 40 × 10 × 5 mm (). To support the tissue culture in ALI, a porous polycarbonate filter with 8-μm pores (Osmonics, Kent, WA) was attached to the bottom of the well with silicone glue. Static controls were cultured in devices that were identical, except that they had half the inner dimensions (to conserve cells). To assemble the straining device, the sponge sides were fully extended to the length of the frame and clamped in place. Then collagen and cells were introduced to the model. After culture for 7 days submerged followed by 7 days in ALI in this expanded state, 10% or 30% compressive strain was imposed in the lateral direction at frequencies of 1 or 60 cph for a period of 48 h. This was achieved by releasing the clamp and applying strain (where compression was achieved by recoil of the elastic bands) via a computer-controlled, motor-driven mechanical arm (). The strain was applied in step fashion; that is, 1 cph consisted of ~ 30 min of compressive strain followed by 30 min without strain, and 60 cph consisted of 26 s of 10% compressive strain or 19 s of 30% strain followed by the same respective time without strain. In all cases, a ramping velocity of 1 mm/s (2.5% of original length per second) was used. Equivalent static controls were cultured in parallel with each experimental run. These magnitudes of strain were chosen according to published reports of ASM shortening in normal and asthmatic airways ( 24), and the frequencies were chosen as possible low and high bounds for frequency of ASM hyperactive episodes over a 48-h period. The local distribution of strain within the three-dimensional matrix was determined in separate experiments using 10-μm-diameter fluorescent polystyrene microbeads (Molecular Probes, Eugene, OR), suspended at 250,000 beads/ml in the fibroblast-embedded collagen, at well-distributed points along the length of the gel before epithelial cell seeding. After the culturing protocol outlined in the previous section, strain was applied for a period of 24 h and three-dimensional images were obtained using confocal microscopy. Strain was estimated for discrete bead clusters in the direction of strain application by taking the change in distance in any two of these clusters (i.e., pre-strain distance minus strained distance) and dividing by their pre-strained distance. A total of three to six measurements were made throughout each gel ( n ![[gt-or-equal, slanted]](/corehtml/pmc/pmcents/ges.gif) 7 for each strain level). In addition, the relative distribution of strain at different depths within the gel was determined by measuring the microbead density in four contiguous regions beneath the epithelium, each 88 μm in height ( n = 3–6); this was assessed both before and after 24 h strain application of 10% or 30% strain at 1 cph for direct comparison between pre-strained and post-strained conditions. Immunofluorescence Ten-micrometer sections from paraffin-embedded samples, taken along the direction of applied strain, were stained with antibodies against human type III collagen (Oncogene, Boston, MA), type IV collagen (MP Biomedicals, Aurora, OH), fibronectin (Transduction Laboratories, Lexington, KY), and α-smooth muscle actin (α-SMA) (clone 1A4; Sigma). Standard immunostaining protocols were used, with 10% host serum (Dako, Glostrup, Denmark) of the secondary antibody used as a pre-staining block, biotinylated secondaries (Dako), and avidin-conjugated fluorescein for detection with DAPI-containing mounting medium (both from Vector Laboratories, Burlingame, CA). The relative amounts and spatial distributions of matrix proteins were analyzed using Metamorph software (Molecular Devices Corp., Downington, PA), and α-SMA expression was quantified by determining the percentage of nuclei with corresponding cytoplasmic staining for α-SMA. Protease Analysis Along with matrix deposition, increases in matrix metalloproteinases (MMPs) were examined after 48 h of strain application. For spatial distribution of MMP activity, in situ zymography was performed on cryosections ( 42). Briefly, unfixed thin cryosections were incubated in fluorescein-conjugated DQ-collagen type I (Molecular Probes) overnight in a dark humidified chamber at room temperature. Upon digestion or cleavage of the DQ-collagen substrate, the resulting fluorophore was excited at 495 nm and captured using an epifluorescence microscope. Additionally, MMP-2 and -9 released into the media were detected with gel zymography. Media collected at the end of experiments were run on gelatin-containing zymogram gels (BioRad, Hercules, CA), a substrate for many MMPs, including MMP-2 and -9, in a standard vertical mini-electrophoresis cell. The gels were then renatured for 30 min at room temperature, developed overnight at 37°C, counterstained in 0.5 wt% Coomassie blue, and destained (all solutions from BioRad). Pictures were captured using Kodak DC290 (Kodak, New Haven, CT), and band intensities analyzed with ImageJ (NIH, Bethesda, MD). Statistical Analysis Results are expressed as mean and standard error of at least eight samples per condition. Mean (± SEM) values were compared using one-way ANOVA with Tukey post hoc analysis, and considered significant for P values < 0.05. Model Characterization With an applied lateral strain of 10% and 30%, the local strain within the collagen gel, as measured by microbead displacements, translated to 11.6 ± 1.4% and 38.7 ± 7.6%, respectively (). They were significantly different from each other (using a t test) but there was no significant difference between measured and applied strains. No relationship between bead position and measured strain could be detected, implying uniform strain throughout the gel. Epithelial differentiation and cellular organization in the airway wall model were consistent with our previous findings in a similar unstrained model, which we adapted for the current study ( 39). We observed tightly packed and ciliated epithelial cells after 10 d of ALI () that were active in synthesizing mucins (). The cells were well organized, with a pseudostratified layer of epithelial cells on the apical surface, and individual fibroblasts spread sparsely throughout the matrix below (). These features replicate the anatomic relationships of HBECs and HLFs in the airway in vivo, and therefore establish the physiologic relevance of our tissue-engineered airway wall model. ECM Protein Deposition ECM proteins that are typically seen in remodeled airways include types III and IV collagen and fibronectin (). We found that in our tissue engineered airway wall model, deposition of type III collagen increased with all levels of dynamic strain, except 30% strain at 60 cph, which, interestingly, was the highest strain and frequency applied. For type IV collagen, we saw similar trends in that the lower magnitude (10%) was more effective at increasing ECM deposition than the higher magnitude of strain. In contrast, fibronectin deposition was decreased with all levels of strain compared with static controls. None of these ECM proteins were detected in acellular samples (data not shown), indicating that they were all cell-derived. We also saw qualitative differences in the deposition patterns of these proteins between strained and static samples (). While type III collagen in the static control was expressed uniformly throughout the matrix and in layers aligned parallel to the surface (), strained samples showed higher levels just beneath the epithelium with a decreasing gradient away from the surface (). In contrast, type IV collagen appeared as punctate strands extended in the horizontal direction and localized around the fibroblasts (). Furthermore, an increased amount of type IV collagen was deposited just beneath the epithelium in strained samples (), although the spatial gradient in expression was not as pronounced as that seen for type III collagen (). Finally, fibronectin distribution was similar to that of type IV collagen, with obvious staining of the basement membrane (), but no differences were detected in the spatial distribution of fibronectin in any of the conditions. Quantitative analyses of ECM immunofluorescent stainings confirmed that types III and IV collagen () were significantly increased with strain at all levels except the highest strain conditions (30% at 60 cph for type III collagen and 30% at both frequencies for type IV collagen). In addition, fibronectin was decreased by dynamic strain at all levels (). To assess the relevance of epithelial signaling in fibroblast remodeling of these proteins, fibroblast-only experiments were performed at the 10%, 1 cph condition. We found that strain did significantly upregulate type III collagen in fibroblast-only cultures (), although the levels of total protein were much lower at both unstrained and strained conditions than in all co-culture conditions. In contrast, type IV collagen was not significantly affected by strain in fibroblast-only cultures (). Finally, fibronectin remodeling was similar in fibroblast-only compared with co-culture conditions (). Thus, these data indicate that epithelial signaling (1) dominates the strain-induced remodeling response of type IV collagen, (2) strongly affects the strain-induced increase of type III collagen, and (3) does not affect strain-induced remodeling of fibronectin, which appears to be solely controlled by fibroblasts alone. Protease Secretion ECM degradation by metalloproteinases is an important component of tissue remodeling. We therefore examined the spatial distribution of collagenolytic activity in cryosections of the airway wall model by in situ zymography and specifically assessed the activity of MMP-2 and -9 secreted into culture medium by electrophoresis and gelatin zymography (). Representative in situ zymograms, comparing static versus strained (10% at 60 cph) samples, are shown in . Collagenolytic activity in the epithelium and around fibroblasts was increased by mechanical strain. Interestingly, collagenolytic activity beneath the epithelium was distributed in a horizontal orientation, similar to that of the fibroblasts themselves. Gelatin zymography was performed on conditioned medium after each experiment (), and bands were detected at 62, 72, and 92 kD, corresponding to the active form of MMP-2 and latent forms of MMP-2 and -9, respectively. In fibroblast-only cultures, only active and latent forms of MMP-2 were present. Quantification of the band intensities verified that these MMP levels were increased with all levels of strain, with MMP-9 being the most strain-sensitive (). We also verified that the increased levels of MMPs were not simply due to their release from the interstitial space under a one time compression of 50%, which gave similar results as unstrained samples (data not shown). Myofibroblast Differentiation Fibroblast-to-myofibroblast differentiation is an important contributor to airway wall remodeling ( 43). Myofibroblasts are characterized by expression of α-SMA, which is associated with the contractile phenotype of these cells and may contribute to airway narrowing by an increased capacity for ECM protein synthesis ( 12). We found that 10% strain increased myofibroblast differentiation (quantified by number of α-SMA–positive cells) compared with static controls (). Interestingly, this effect was not seen with 30% strain. Thus, like type IV collagen deposition, increased myofibroblast differentiation was only seen in low-strain samples. Spatial Distribution of Remodeling As noted in and , the deposition of types III and IV collagen and myofibroblast differentiation were concentrated just beneath the epithelium and decreased with increasing distance from the epithelium. To quantify this spatial distribution, the sections were divided into four contiguous regions, each of 88 μm in depth, beneath the epithelium (). This revealed that the density in the number of myofibroblasts (), as well as the intensity of type III collagen staining (), was significantly greater just beneath the epithelium than in any other region of the tissue. Furthermore, although this increase near the epithelium was seen in both static and strained co-culture samples, the gradient was amplified by strain: over 50% more expression of myofibroblasts and type III collagen was found in region I than the other regions for 10% strain (in the case of myofibroblasts) and all levels of strain except the highest strain rate (in the case of type III collagen) in co-cultures. This highlights the importance of epithelial–fibroblast communication in remodeling. We note that these spatial gradients were not due to nonuniform strain distribution at different depths within the gel. The inset graph in shows the difference in microbead density before and after strain, normalized to respective region I for direct comparison, which shows no significant differences among the four regions, implying a uniform distribution of strain. In fibroblast-alone systems, while 10% strain at 1 cph resulted in an overall increase of myofibroblast expression in all regions, no gradient in expression was observed for both myofibroblast and type III collagen, indicating a role for epithelial–fibroblast signaling in strain-induced remodeling in the co-culture system. Similar results were found by analyzing regional intensities for type IV collagen expression (data not shown). Thus, strain-induced matrix production was largely controlled by signals from the epithelium as evidenced by increased remodeling near (and below) the epithelium, where myofibroblasts were found in abundance. As the importance of the microenvironment in governing cell responses has been demonstrated in numerous examples, three-dimensional tissue models are proving to be invaluable to studying cell and tissue physiology and pathophysiology ( 44, 45). As such, there is a growing appreciation for the importance of the biophysical environment, with appropriate mechanical cues, in both making the three-dimensional models more physiologic and also in studying the roles of such cues in pathophysiology ( 37). Our results, using a physiologically relevant three-dimensional tissue model of the human airway wall, demonstrate the importance of mechanical stress in airway wall remodeling and the importance of epithelial–fibroblast crosstalk in such remodeling. Our in vitro tissue model showed physiologically relevant cell organization and function: it has a pseudostratified epithelium with both ciliated and mucus-producing cells, and under baseline culturing conditions secreted basement membrane beneath the epithelium and type III collagen and fibronectin, among other matrix proteins, within the tissue. SMCs were absent in our model, which is important to consider in interpreting overall remodeling response, since they can also secrete molecular regulators of airway wall remodeling and fibroblast differentiation ( 23, 25). However, their mechanical function was simulated by inducing lateral dynamic strain with a custom-made strain device. It has been reported in computational models of airway mechanics in asthma that 40% shortening of the airway smooth muscle (ASM) can result in almost total occlusion of the airway ( 26), while in others, 30% shortening may translate to a > 15-fold increase in pulmonary resistance in asthmatic versus normal airways ( 46, 47). In additionally, isolated human bronchial smooth muscle cells from individuals with asthma were found to contract to a greater extent—more than 10% in length—compared with cells from normal subjects ( 24). In light of these results, we chose 10% and 30% as representative strain magnitudes of ASM shortening. In addition to strain magnitude, the duration and frequency of ASM contraction were important parameters to consider. While it is difficult to generalize the transient behavior of smooth muscle contraction, several studies have shown with isolated human bronchial ASM cells ( 24) and canine muscle strips ( 48) that 75% of their contractions are completed within 1.5–4 s. The time we imposed for contraction was ~ 4 s for 10% strain and ~ 12 s for 30% strain. In addition, frequency may also be an important factor in remodeling, but the duration of ASM hyperactivity can vary dramatically for individuals with asthma with variation in severity; thus it is difficult again to generalize the relevant frequencies to use for in vitro simulations. We chose 1 and 60 cph as possible low and high frequencies of ASM contraction over a 48-h period. Therefore, with these parameters, we attempted to represent reasonably relevant values of strain that may contribute to ECM remodeling. In our three-dimensional model, strain influenced cell–matrix and cell–cell interactions to change the architecture and organization of the ECM in the absence of inflammation. The deposition of types III and IV collagen was concentrated near the epithelium and decreased away from the epithelium, which was not observed in fibroblast-only conditions. The epithelium may play an important role as a source of profibrotic mediators such as TGF-β 1 leading to matrix remodeling ( 8, 10). Furthermore, the spatial gradient in ECM protein deposition was amplified under all strain conditions compared with static controls (, data not shown for type IV collagen), suggesting that epithelial–fibroblast communication, possibly aided by convection of secreted mediators, may act to facilitate the spatial deposition of these ECM proteins. While this study examined only a few ECM proteins, our results correlate with remodeling characteristics seen in the human airways. In individuals with asthma, the subepithelial layer of the airway wall is thickened and enriched with types III and IV collagen, as well as type V collagen, fibronectin, and tenascin ( 1, 49, 50). Consistent with such pathologic remodeling, we observed deposition of types III and IV collagen concentrated in the subepithelial region and amplified with dynamic strain in our model. Interestingly, we found that strain decreased fibronectin deposition, indicating differential regulation of various ECM proteins in response to mechanical strain. In addition to HBECs and HLFs, myofibroblasts may have contributed to collagen production in our system. Myofibroblasts are commonly found in the thickened subepithelial collagen layer of the asthmatic airway wall ( 7, 14), and in the lungs of patients with pulmonary fibrosis ( 43). They play an important part in remodeling by matrix contraction ( 12, 51) and synthesis of types I and III collagen ( 52). In our system, myofibroblasts were found in increased numbers just beneath the epithelium, in the same spatial distribution as type III collagen under conditions of mechanical strain (). These results suggest that myofibroblasts were likely an important cellular source of collagen synthesis in response to mechanical strain. In conclusion, we have shown that mechanical strain in a tissue engineered three-dimensional co-culture model of the airway wall can be an important determinant of ECM remodeling, as indicated by deposition/secretion of ECM proteins and MMPs, and by differentiation of myofibroblasts. In our three-dimensional airway wall model, we found lateral compressive strain on airway cells resulted in upregulation of types III and IV collagen and increased levels of secreted MMP-2 and -9, but downregulation of fibronectin. In addition, type III collagen was spatially correlated with myofibroblast differentiation. 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