- Open Access
Macrophage metalloelastase (MMP-12) deficiency does not alter bleomycin-induced pulmonary fibrosis in mice
© Manoury et al; licensee BioMed Central Ltd. 2006
- Received: 30 August 2005
- Accepted: 22 February 2006
- Published: 22 February 2006
Pulmonary fibrosis is characterized by excessive deposition of extracellular matrix in the interstitium resulting in respiratory failure. The role of remodeling mediators such as metalloproteinases (MMPs) and their inhibitors (TIMPs) in the fibrogenic process remains misunderstood. In particular, macrophage metalloelastase, also identified as MMP-12, is known to be involved in remodeling processes under pathological conditions. However, MMP-12 involvement in pulmonary fibrosis is unknown. Here we investigated fibrotic response to bleomycin in MMP-12 deficient mice.
Materials and methods
C57BL/6 mice, Balb/c mice and MMP-12 -/- mice with a C57BL/6 background received 0.3 mg bleomycin by intranasal administration. 14 days after, mice were anesthetized and underwent either bronchoalveolear lavage (BAL) or lung removal. Collagen deposition in lung tissue was determined by Sircol™ collagen assay, MMP activity in BAL fluid was analyzed by zymography, and other mediators were quantified in BAL fluid by ELISA. Real time PCR was performed to assess gene expression in lung removed one or 14 days after bleomycin administration. Student t test or Mann & Whitney tests were used when appropriate for statistical analysis.
The development of pulmonary fibrosis in "fibrosis prone" (C57BL/6) mice was associated with prominent MMP-12 expression in lung, whereas MMP-12 expression was weak in lung tissue of "fibrosis resistant" (Balb/c) mice. MMP-12 mRNA was not detected in MMP-12 -/- mice, in conformity with their genotype. Bleomycin elicited macrophage accumulation in BAL of MMP-12 -/- and wild type (WT) mice, and MMP-12 deficiency had no significant effect on BAL cells composition. Collagen content of lung was increased similarly in MMP-12 -/- and WT mice 14 days after bleomycin administration. Bleomycin elicit a raise of TGF-β protein, MMP-2 and TIMP-1 protein and mRNA in BAL fluids and lung respectively, and no significant difference was observed between MMP-12 -/- and WT mice considering those parameters.
The present study shows that MMP-12 deficiency has no significant effect on bleomycin-induced fibrosis.
- Wild Type Mouse
- Idiopathic Pulmonary Fibrosis
- Pulmonary Fibrosis
- Control Wild Type Mouse
Extracellular matrix (ECM) remodelling is a key factor of numerous interstitial lung diseases. Airway remodelling-associated disorders of ECM can be illustrated by different pathological situations including emphysema and pulmonary fibrosis. In the first, progressive proteolytic ECM degradation is prevailing, whereas in the latter excessive matrix deposition occurs. Both phenomena are hypothesized to result partially from an imbalance of ECM homeostasis and protease – antiprotease activity [1, 2] which is partially regulated by potent fibrogenic growth factors such as TGF-β [3, 4].
Metalloproteinases (MMPs) are a family of zinc-binding endopeptidases which proteolytic activity is involved in normal and pathological ECM turnover. MMPs activity is regulated by their natural tissue inhibitors, TIMPs. MMPs have been implicated in lung pathological conditions, including fibrosis , emphysema  and asthma . Matrilysin (MMP-7) was shown to have great importance in idiopathic pulmonary fibrosis and found to be dramatically involved in bleomycin-induced pulmonary fibrosis in mice . Also, gelatinase-A (MMP-2) seems to be a good marker of tissue remodelling. It is localized in the area of fibroproliferation and basal membrane disruption  and shows intense activity in experimental models of pulmonary fibrosis [9–11]. Hence, TIMP-1 has been increasingly associated with pulmonary fibrosis [8, 9, 12, 13]. It has been suggested that abnormal alteration of MMPs/TIMPs balance could lead to disruption of lung tissue, and/or accumulation of extracellular matrix without adequate repair, leading to impairment of lung function [2, 3, 8].
Macrophage metalloelastase, also identified as MMP-12, has been previously described as a key factor of pathological progressive proteolytic destruction of ECM. Indeed, MMP-12 has been reported to be essential in tissue remodelling associated with emphysema in mice exposed to cigarette smoke . In addition, an increased expression of MMP-12 in macrophages from patients with COPD was recently reported . MMP-12 has potent ECM remodelling properties due to its specific elastolytic activity, but may also participate to the inflammatory process through the activation of TNF-alpha . Moreover, MMP-12 presents potent direct pro-inflammatory properties including the ability to induce neutrophil influx, cytokine and chemokine production . MMP-12 seems to be involved in numerous models of acute lung inflammation [16, 18–20]. Although the role of MMP-12 in animal models of emphysema is well documented, its involvement in pulmonary fibrosis remains unclear. We therefore investigated the involvement of MMP-12 in the development of bleomycin-induced pulmonary fibrosis. Firstly, we investigated differential MMP-12 expression in lungs of "fibrosis prone" (C57BL/6) mice and in "fibrosis resistant" (Balb/c) mice [12, 21] after bleomycin administration. Secondly, we compared the inflammatory and fibrotic responses of MMP-12 null mice with those of their wild type C57BL/6 littermates.
Seven-week-old Balb/c and C57BL/6 male mice were purchased from CERJ (Le Genest Saint Isle, France) and quarantined for 1 week before experiments. MMP-12 -/- mice were obtained from Charles River laboratories following a transfer from Washington University  and rederivation on C57BL/6 background. C57BL/6 mice were used as wild type (WT) control mice. They were housed under controlled and ethical conditions that complied with the Interdisciplinary Principles and Guidelines for the Use of Animals in Research, Marketing and Education, New York Academy of Sciences' Ad Hoc Committee on Animal Research.
The following materials were used: bleomycin sulfate from Bellon Laboratories (Montrouge, France); gelatin, Triton X-100, Coomassie Brilliant Blue, Tween 20 solution, and trypan blue from Sigma (St Louis, MO, USA) ; pepsin was from Fluka (Buchs, Switzerland) ; May-Grünwald and Giemsa stains from RAL (Paris, France); sodium pentobarbital from Sanofi Santé Animale (Libourne, France); etomidate (Hypnomidate®, 2 mg/mL) from Janssen-Cilag (Issy-les-Moulineaux, France); acrylamide, sodium dodecyl sulfate (SDS), Tris, and BSA from Eurobio (Les Ulis, France); ELISA kits for TGF-β and TIMP-1 detection were from R&D Systems (Minneapolis, MN, USA); isopentane from Prolabo (Fontenay-sous-Bois, France); a low-range weight marker for SDS-PAGE from Biorad (Munich, Germany).
Pulmonary fibrosis was induced by intranasal (i.n.) instillation, as previously described [5, 22]. Each mouse was administered 0.3 mg bleomycin dissolved in 0.9% NaCl solution. Control mice received saline vehicle only. One day or 14 days after i.n. administration, mice were quickly anesthetized by an i.p. injection of sodium pentobarbital (60 mg/kg) and underwent either bronchoalveolar lavage (BAL) or lung removal. These samples were stored at -80°C until further analysis.
Bronchoalveolar lavage and preparation of tissue homogenates
Mice were anesthetized with an i.p. administration (20 mL/kg) of sodium pentobarbital 0.6%. Bronchoalveolar lavage (BAL) fluids were obtained by washing the airways 10 times with 0.5 mL of 0.9% NaCl solution at 37°C with a 1 mL syringe. The BAL fluid was centrifugated (600 g for 10 min, 4°C), and the supernatant of the first two fractions (1 mL) divided into aliquots and frozen at -80°C until analysis. The cell pellets were then pooled with the last fractions. Total cells were counted with a Coulter Z2® (particle counter and size distribution analyzer, Beckman Coulter). Red blood cells were eliminated by adding 3 mL of distilled water for 30 seconds and then 1 mL of KCl 0.6 M onto the pellets. After centrifugation (600 g for 10 min, 4°C), supernatant was eliminated and the cells were suspended in 1 mL of PBS. They were then cytospun at 700 rpm for 10 minutes (Cytospin 3®, Thermo Shandon, Ltd, Astmoor, United Kingdom) and stained with the May-Grünwald Giemsa method. Differential cell counts of 200 cells used standard morphological criteria.
Zymographic analysis of MMPs
Since some MMPs can degrade gelatin, zymographic techniques were used to detect MMPs in BAL. In non reducing conditions and in the presence of SDS, as previously described , aliquots of BAL fluid or lung homogenate underwent electrophoresis onto a 6% acrylamide stacking gel /10% acrylamide separating gel containing 1 mg/mL gelatin. After electrophoresis, gels were washed twice with 2.5% Triton X-100, rinsed with water, and incubated overnight at 37°C in 50 mM Tris, 5 mM CaCl2, 2 μM ZnCl2, pH = 8. The gels were stained with Coomassie Brilliant Blue in a solution of 25% ethanol-10% acetic acid in water and rinsed in an identical solution. Gelatinase activity appeared as clear bands against blue background. We used recombinant protein molecular weight markers (20 kDa-214 kDa) to estimate the molecular weights of the gelatinolytic bands. Relative enzyme amounts were quantified by measuring the intensity of the bands with a densitometric analyzer (Bio-Profile, Vilber-Lourmat, Marne la Vallée, France). Results were expressed as a percentage of the band of migration of one control BAL sample loaded onto each gel. This sample was used as an internal standard to allow further comparisons between gels.
Determination of TGF-β-1 and TIMP-1 in BAL
The amounts of total TGF-β-1 and TIMP-1 were determined with ELISA methods, performed according to the manufacturer's recommendations. Assay sensitivity was 15 pg/mL for TGF-β-1 and 31 pg/mL for TIMP-1. As ELISA protocol called for processing samples in 0.6N HCl before the assay, both TGF-β-1 latent and active forms were measured at the same time.
In vivo expression of α1(I) collagen, Mmp-12, Mmp-2, and Timp-1 mRNA in lungs
Genes and primers for real time PCR.
Sense Primer (5' to 3')
Reverse Primer (5' to 3')
For quantification of collagen in lung tissue, mice were sacrificed fourteen days after BLM administration. Lungs were freshly removed and frozen in isopentane using liquid nitrogen. Frozen lungs were ground to a fine powder with a mortar and pestle, weighed, and homogenized in acetic acid 0.5 M containing pepsin (2.7 U/mL) pH = 7.4. Total soluble collagens were extracted overnight at room temperature by using 5 mg/ml pepsin (2.7 U/mL) in 0.5 M acetic acid and measured by the Sircol™ collagen assay (Biocolor Ltd, Newtonabbey, UK).
Expression of the results and statistical analysis
Results were expressed as means ± SEM. Normality of data distribution was determined using the Kolmogorov-Smirnov normality test. The groups were compared according to treatment and strain by using either student t test or nonparametric Mann-Withney Rank Sum Test, when data distribution was respectively normal or not. For each analysis, P values under 0.05 were considered to be statistically significant, unless another range is specified.
In vivo expression of MMP-12 mRNA in lung tissue of Balb/c and C57BL/6 mice
In vivo expression of MMP-12 mRNA in lung tissue of MMP-12 -/- and WT mice
MMP-12 mRNA was not detected in lung of MMP-12 -/- mice, confirming the genotype of the mice used for the study. In contrast, MMP-12 was detected in control WT mice, and was increased after bleomycin administration (50 fold increase).
Cell composition of bronchoalveolar lavage (BAL) fluids of MMP-12 -/- and WT mice
Total and differential cell counts of BAL fluid from MMP-12 -/- and WT mice 14 days after intranasal administration of bleomycin (BLM) or saline vehicle (Control). Results are presented as the mean (.103 cells) ± SEM. n: number of mice. a: P < 0.05, b: P < 0.01, c: P < 0.001 compared with control mice exposed to saline solution only.
579 ± 92
561 ± 79
13 ± 10
0 ± 0
6 ± 6
547 ± 92
540 ± 94
2 ± 2
0 ± 0
4 ± 4
2204 ± 284c
1783 ± 210c
285 ± 78b
55 ± 19b
81 ± 33b
1352 ± 355a
1152 ± 255a
104 ± 62b
19 ± 17
76 ± 55
Quantification of collagen deposition in lung tissue of MMP-12 -/- and WT mice
TGF-β and TIMP-1 levels in BAL fluids of MMP-12 -/- and WT mice
Metalloproteinase activity in BAL fluids of of MMP-12 -/- and WT mice
Mmp-2 and Timp-1 gene mRNA analysis by real time PCR in MMP-12 -/- and WT mice
Bleomycin induced Mmp-2 mRNA expression in both WT and MMP-12 -/- mice (respectively 1.6 fold and 2.8 fold) (figure 5A). Basal level was higher in WT mice compared to MMP-12 -/-.
Timp-1 mRNA was induced by bleomycin in MMP-12 -/- (7.3 fold), and WT (4.1 fold), (figure 5B).
The present study showed that MMP-12 -/- mice developed pulmonary fibrosis in a similar intensity to WT mice and the level of TIMP-1 protein and Timp-1 mRNA is similar in both strains.
Metalloproteinases have been described to be involved in the remodelling process and ECM turn over in several respiratory diseases associated with inflammation, including pulmonary fibrosis . Indeed, it has been previously reported that a broad range MMP inhibitor, batimastat, prevented bleomycin-induced pulmonary fibrosis in mice . In addition, several studies focussing on specific members of MMP family have been providing information about their relative importance in the process. In particular, the involvement of gelatinases (MMP-2 and MMP-9) has been described in human and in in vivo experimental animal models [5, 23]. However, MMP-9 null mice were not protected from extensive collagen deposition following bleomycin administration, but did not develop small airway fibrosis .
MMP-12, also known as macrophage metalloelastase, and neutrophil elastase (NE) are two major elastases involved in lung inflammation and remodelling. Moreover, NE null mice have already been described to be resistant to bleomycin-induced pulmonary fibrosis . In contrast, the role of MMP-12 in the development of fibrosis is relatively unknown.
In a first set of experiments, we investigated MMP-12 mRNA level in lung of Balb/c and C57BL/6 after bleomycin administration. Indeed, C57BL/6 mice are known to be "fibrosis prone" strain, whereas Balb/c mice are described as resistant to the development of pulmonary fibrosis [12, 21]. In conformity with this, the preliminary hydroxyproline level measurement revealed that C57BL/6 mice developed important collagen accumulation 14 days after 0.1 mg bleomycin administration, whereas no raise of collagen level was observed in lung of Balb/c mice . Here, we show that MMP-12 mRNA level in lung tissue was increased in C57BL/6 mice at day1 and day14, whereas a slight raise of MMP-12 mRNA was detected only at day14 in Balb/c. We confirm here that bleomycin elicits MMP-12 mRNA induction in lung tissue of WT mice, as previously described by Swiderski et al. . Moreover, as MMP-12 mRNA level is associated with strain-dependent susceptibility to develop bleomycin-induced pulmonary fibrosis, MMP-12 seems to be a relevant candidate for the determination of a pivotal proteolytic element in the development of pulmonary fibrosis. Hence, we investigated the effect of MMP-12 deficiency in bleomycin-induced fibrosis model which hitherto has not been related.
In the present study, we observed that MMP-12 -/- mice responded to bleomycin administration by an increase of collagen content in lung tissue, which is the hallmark of pulmonary fibrosis. This raise did not differ significantly from observations in WT mice, suggesting that MMP-12 is not necessary for the development of bleomycin-induced pulmonary fibrosis. Similarly, Lanone et al.  observed in IL-13-induced injury in mice that MMP-12 deficiency did not alter subepithelial fibrosis following inducible IL-13 transgene expression. Consistent with their genotype, MMP-12 -/- mice did not demonstrate MMP-12 expression.
It is interesting to observe that all mRNA level in MMP-12 -/- mice are lower than in wild type under basal conditions, although all mRNA were all extracted and reverse transcribed during the same run. However, such differences are not observed at the protein level regarding either collagen, MMP-2 nor TIMP-1, suggesting that a strong post-traductional regulation of gene expression occurs.
MMP-12 is known to be a prominent protease produced by activated alveolar macrophage [1, 30]. We observed a marked accumulation of macrophages in BAL of WT mice 14 days after bleomycin administration. Taken together, these data could mean than bleomycin induces infiltration and activation of macrophages in respiratory tract, alveolar spaces and interstitium, leading to prominent expression of MMP-12 in lung. Therefore MMP-12 does not seem to be implicated in the fibrosis genesis, but may be an indicator of macrophage activation and recruitment following bleomycin administration.
In contrast, several studies reported that MMP-12 was necessary for accumulation of macrophages in the airways, and associated with alveolar enlargement and emphysematous lesions after cigarette smoke exposure  or inducible IL-13 transgene expression . Hence, Nénan et al.  recently demonstrated that instillation of recombinant catalytic domain of human MMP-12 to mice induced inflammation with important and stable macrophage recruitment in airways. Parks and Shapiro  suggested that MMP-12 may actually be involved in leucocyte recruitment and activation. Indeed, it has been shown that proteolytically generated elastin fragments mediate monocyte chemotaxis . However, in our model, BAL total cell count and macrophage accumulation were not significantly altered by MMP-12 deficiency at day14. This may suggest that, at that time point, macrophage accumulation is monitored by other mediators than MMP-12.
Taken together these results suggest that bleomycin-induced fibrosis and associated inflammation involve different mechanisms from MMP-12 dependent pathways. Several hypothesis suggest that crucial components of fibrogenic process are due to remodelling disorders involving growth factors such as TGF-β  and a non degrading microenvironment created by a "shield" of protease inhibitors, including TIMP-1 [2, 8]. TGF-β has been demonstrated to be a prominent fibrogenic mediator in many organs, including lung [32, 33]. Moreover, TGF-β presents a pivotal situation by regulating global lung tissue remodelling. Indeed, mice lacking integrin αvβ6 (integrin αvβ6 null mice) fail to activate TGF-β and develop an age-related emphysema, which is MMP-12-dependent . MMP-12 in lung has been described to be down regulated by TGF-β signalling pathway [3, 4]. In our experimental model of pulmonary fibrosis, TGF-β-1 protein was induced similarly in both MMP-12 -/- and WT mice. In accordance with our results, Lanone et al.  did not report alteration of total TGF-β in BAL fluid of MMP-12 -/- mice after IL-13 transgene expression. Interestingly, in WT mice, bleomycin elicits both MMP-12 and TGF-β increase. Therefore further investigations are required in order to explain why MMP-12 expression coexists with high TGF-β level.
Growing evidence tends to establish TIMP-1 as a major fibrogenic effector in lung. Indeed, upon fibrogenic stimuli, a large amount of TIMP-1 in the remodelling tissue is supposed to participate to the creation of a non degrading environment, leading to alteration of protease/anti-protease balance, extracellular matrix accumulation, and tissue fibrosis [2, 8]. Moreover, TIMP-1 has been designated as a key factor to explain strain-dependent susceptibility to develop fibrogenic response to transfer of active TGF-β in lung of mice . We previously observed that TIMP-1 expression and protein were importantly increased by bleomycin administration. We and others had previously reported such an induction in lung of C57BL/6 mice after bleomycin administration [5, 10, 13, 27]. According to our results, MMP-12 deficiency does not seem to be involved in TIMP-1 regulation and this would be consistent with the development of pulmonary fibrosis in MMP-12 -/- mice.
Gelatinases MMP-9 and MMP-2 have been observed in various lung injury models [10, 18, 27], and in pulmonary fibroses in humans [8, 34]. Studying the present study, we detected pro-MMP-2 and MMP-2 activities in BAL. Here, MMP-2 protein and mRNA levels were both increased at day14 after bleomycin administration, in a similar extent in MMP-12 -/- and WT mice. This result does not appear consistent with the hypothesis that IL-13-induced MMP-2 increase was mediated at least partially by a MMP-12-dependent pathway . Therefore, even though Th2 cytokine IL-13 has been involved in bleomycin-induced pulmonary fibrosis , IL-13-induced injury model seems to follow different pathways, including different participation of MMP-12. Moreover, IL-13-induced injury is associated with airspace enlargement, which is not observed in bleomycin-induced lung injury.
In conclusion, we demonstrated that MMP-12 does not appear to be involved in the fibrogenic pathway of bleomycin-induced lung injury. MMP-12 deficiency did not influence the bleomycin-induced raise of neither TGF-beta-1 nor TIMP-1 in lung, which are described as important pro-fibrogenic effectors. Moreover, in this model, MMP-12 deficiency has no influence on macrophages accumulation in lung. Accordingly to the protease/antiprotease imbalance hypothesis, accumulation of extracellular matrix may be due by dysfunction of other proteases than MMP-12.
This study is supported by a research grant from Conseil Régional de Bretagne, France, (ref # 20044797), and a collaboration project INSERM/FIOCRUZ cooperation. The authors are thankful to I. Derrien for her assistance.
- Barnes PJ, Shapiro SD, Pauwels RA: Chronic obstructive pulmonary disease: molecular and cellular mechanisms. Eur Respir J. 2003, 22: 672-688.PubMedView ArticleGoogle Scholar
- Gauldie J, Kolb M, Sime PJ: A new direction in the pathogenesis of idiopathic pulmonary fibrosis?. Respir Res. 2002, 3: 1-10.1186/rr158.PubMedPubMed CentralView ArticleGoogle Scholar
- Bonniaud P, Kolb M, Galt T, Robertson J, Robbins C, Stampfli M, Lavery C, Margetts PJ, Roberts AB, Gauldie J: Smad3 null mice develop airspace enlargement and are resistant to TGF-beta-mediated pulmonary fibrosis. J Immunol. 2004, 173: 2099-2108.PubMedView ArticleGoogle Scholar
- Morris DG, Huang X, Kaminski N, Wang Y, Shapiro SD, Dolganov G, Glick A, Sheppard D: Loss of integrin alpha(v)beta6-mediated TGF-beta activation causes Mmp12-dependent emphysema. Nature. 2003, 422: 169-173. 10.1038/nature01413.PubMedView ArticleGoogle Scholar
- Corbel M, Caulet-Maugendre S, Germain N, Molet S, Lagente V, Boichot E: Inhibition of bleomycin-induced pulmonary fibrosis in mice by the matrix metalloproteinase inhibitor batimastat. J Pathol. 2001, 193: 538-545. 10.1002/path.826.PubMedView ArticleGoogle Scholar
- Kelly EA, Jarjour NN: Role of matrix metalloproteinases in asthma. Curr Opin Pulm Med. 2003, 9: 28-33. 10.1097/00063198-200301000-00005.PubMedView ArticleGoogle Scholar
- Zuo F, Kaminski N, Eugui E, Allard J, Yakhini Z, Ben Dor A, Lollini L, Morris D, Kim Y, DeLustro B, Sheppard D, Pardo A, Selman M, Heller RA: Gene expression analysis reveals matrilysin as a key regulator of pulmonary fibrosis in mice and humans. Proc Natl Acad Sci U S A. 2002, 99: 6292-6297. 10.1073/pnas.092134099.PubMedPubMed CentralView ArticleGoogle Scholar
- Selman M, Ruiz V, Cabrera S, Segura L, Ramirez R, Barrios R, Pardo A: TIMP-1, -2, -3, and -4 in idiopathic pulmonary fibrosis. A prevailing nondegradative lung microenvironment?. Am J Physiol Lung Cell Mol Physiol. 2000, 279: L562-L574.PubMedGoogle Scholar
- Manoury B, I. G, S. CM, Lagente V, Boichot E: Differences in the pulmonary fibrogenic and inflammatory responses after intranasal administration of bleomycin to C57BL/6J and BALB/c mice. 2003, In: International conference of the American thoracic society: 2003; Seattle (USA): A349-Google Scholar
- Manoury B, Nenan S, Leclerc O, Guenon I, Boichot E, Planquois JM, Bertrand CP, Lagente V: The absence of reactive oxygen species production protects mice against bleomycin-induced pulmonary fibrosis. Respir Res. 2005, 6: 11-10.1186/1465-9921-6-11.PubMedPubMed CentralView ArticleGoogle Scholar
- Ruiz V, Ordonez RM, Berumen J, Ramirez R, Uhal B, Becerril C, Pardo A, Selman M: Unbalanced collagenases/TIMP-1 expression and epithelial apoptosis in experimental lung fibrosis. Am J Physiol Lung Cell Mol Physiol. 2003, 285: L1026-L1036.PubMedView ArticleGoogle Scholar
- Kolb M, Bonniaud P, Galt T, Sime PJ, Kelly MM, Margetts PJ, Gauldie J: Differences in the fibrogenic response after transfer of active transforming growth factor-beta1 gene to lungs of "fibrosis-prone" and "fibrosis-resistant" mouse strains. Am J Respir Cell Mol Biol. 2002, 27: 141-150.PubMedView ArticleGoogle Scholar
- Madtes DK, Elston AL, Kaback LA, Clark JG: Selective induction of tissue inhibitor of metalloproteinase-1 in bleomycin-induced pulmonary fibrosis. Am J Respir Cell Mol Biol. 2001, 24: 599-607.PubMedView ArticleGoogle Scholar
- Hautamaki RD, Kobayashi DK, Senior RM, Shapiro SD: Requirement for macrophage elastase for cigarette smoke-induced emphysema in mice. Science. 1997, 277: 2002-2004. 10.1126/science.277.5334.2002.PubMedView ArticleGoogle Scholar
- Molet S, Belleguic C, Lena H, Germain N, Bertrand CP, Shapiro SD, Planquois JM, Delaval P, Lagente V: Increase in macrophage elastase (MMP-12) in lungs from patients with chronic obstructive pulmonary disease. Inflamm Res. 2005, 54: 31-36. 10.1007/s00011-004-1319-4.PubMedView ArticleGoogle Scholar
- Churg A, Wang RD, Tai H, Wang X, Xie C, Wright JL: Tumor necrosis factor-alpha drives 70% of cigarette smoke-induced emphysema in the mouse. Am J Respir Crit Care Med. 2004, 170: 492-498. 10.1164/rccm.200404-511OC.PubMedView ArticleGoogle Scholar
- Nenan S, Planquois JM, Berna P, De MI, Hitier S, Shapiro SD, Boichot E, Lagente V, Bertrand CP: Analysis of the inflammatory response induced by rhMMP-12 catalytic domain instilled in mouse airways. Int Immunopharmacol. 2005, 5: 511-524. 10.1016/j.intimp.2004.10.011.PubMedView ArticleGoogle Scholar
- Lanone S, Zheng T, Zhu Z, Liu W, Lee CG, Ma B, Chen Q, Homer RJ, Wang J, Rabach LA, Rabach ME, Shipley JM, Shapiro SD, Senior RM, Elias JA: Overlapping and enzyme-specific contributions of matrix metalloproteinases-9 and -12 in IL-13-induced inflammation and remodeling. J Clin Invest. 2002, 110: 463-474. 10.1172/JCI200214136.PubMedPubMed CentralView ArticleGoogle Scholar
- Warner RL, Lukacs NW, Shapiro SD, Bhagarvathula N, Nerusu KC, Varani J, Johnson KJ: Role of metalloelastase in a model of allergic lung responses induced by cockroach allergen. Am J Pathol. 2004, 165: 1921-1930.PubMedPubMed CentralView ArticleGoogle Scholar
- Warner RL, Lewis CS, Beltran L, Younkin EM, Varani J, Johnson KJ: The role of metalloelastase in immune complex-induced acute lung injury. Am J Pathol. 2001, 158: 2139-2144.PubMedPubMed CentralView ArticleGoogle Scholar
- Schrier DJ, Kunkel RG, Phan SH: The role of strain variation in murine bleomycin-induced pulmonary fibrosis. Am Rev Respir Dis. 1983, 127: 63-66.PubMedView ArticleGoogle Scholar
- Shipley JM, Wesselschmidt RL, Kobayashi DK, Ley TJ, Shapiro SD: Metalloelastase is required for macrophage-mediated proteolysis and matrix invasion in mice. Proc Natl Acad Sci U S A. 1996, 93: 3942-3946. 10.1073/pnas.93.9.3942.PubMedPubMed CentralView ArticleGoogle Scholar
- Corbel M, Belleguic C, Boichot E, Lagente V: Involvement of gelatinases (MMP-2 and MMP-9) in the development of airway inflammation and pulmonary fibrosis. Cell Biol Toxicol. 2002, 18: 51-61. 10.1023/A:1014471213371.PubMedView ArticleGoogle Scholar
- Primer 3 [http://frodo.wi.mit.edu/]. 2000, [http://frodo.wi.mit.edu/]
- Shibata Y, Zsengeller Z, Otake K, Palaniyar N, Trapnell BC: Alveolar macrophage deficiency in osteopetrotic mice deficient in macrophage colony-stimulating factor is spontaneously corrected with age and associated with matrix metalloproteinase expression and emphysema. Blood. 2001, 98: 2845-2852. 10.1182/blood.V98.9.2845.PubMedView ArticleGoogle Scholar
- Itoh T, Ikeda T, Gomi H, Nakao S, Suzuki T, Itohara S: Unaltered secretion of beta-amyloid precursor protein in gelatinase A (matrix metalloproteinase 2)-deficient mice. J Biol Chem. 1997, 272: 22389-22392. 10.1074/jbc.272.36.22389.PubMedView ArticleGoogle Scholar
- Swiderski RE, Dencoff JE, Floerchinger CS, Shapiro SD, Hunninghake GW: Differential expression of extracellular matrix remodeling genes in a murine model of bleomycin-induced pulmonary fibrosis. Am J Pathol. 1998, 152: 821-828.PubMedPubMed CentralGoogle Scholar
- Betsuyaku T, Fukuda Y, Parks WC, Shipley JM, Senior RM: Gelatinase B is required for alveolar bronchiolization after intratracheal bleomycin. Am J Pathol. 2000, 157: 525-535.PubMedPubMed CentralView ArticleGoogle Scholar
- Dunsmore SE, Roes J, Chua FJ, Segal AW, Mutsaers SE, Laurent GJ: Evidence that neutrophil elastase-deficient mice are resistant to bleomycin-induced fibrosis. Chest. 2001, 120: 35S-36S. 10.1378/chest.120.1_suppl.S35.PubMedView ArticleGoogle Scholar
- Parks WC, Shapiro SD: Matrix metalloproteinases in lung biology. Respir Res. 2001, 2: 10-19. 10.1186/rr33.PubMedPubMed CentralView ArticleGoogle Scholar
- Senior RM, Griffin GL, Mecham RP: Chemotactic activity of elastin-derived peptides. J Clin Invest. 1980, 66: 859-862.PubMedPubMed CentralView ArticleGoogle Scholar
- Coker RK, Laurent GJ, Jeffery PK, du Bois RM, Black CM, McAnulty RJ: Localisation of transforming growth factor beta1 and beta3 mRNA transcripts in normal and fibrotic human lung. Thorax. 2001, 56: 549-556. 10.1136/thorax.56.7.549.PubMedPubMed CentralView ArticleGoogle Scholar
- Sime PJ, Xing Z, Graham FL, Csaky KG, Gauldie J: Adenovector-mediated gene transfer of active transforming growth factor-beta1 induces prolonged severe fibrosis in rat lung. J Clin Invest. 1997, 100: 768-776.PubMedPubMed CentralView ArticleGoogle Scholar
- Fukuda Y, Ishizaki M, Kudoh S, Kitaichi M, Yamanaka N: Localization of matrix metalloproteinases-1, -2, and -9 and tissue inhibitor of metalloproteinase-2 in interstitial lung diseases. Lab Invest. 1998, 78: 687-698.PubMedGoogle Scholar
- Belperio JA, Dy M, Burdick MD, Xue YY, Li K, Elias JA, Keane MP: Interaction of IL-13 and C10 in the pathogenesis of bleomycin-induced pulmonary fibrosis. Am J Respir Cell Mol Biol. 2002, 27: 419-427.PubMedView ArticleGoogle Scholar
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