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1From the Department of Ophthalmology, University of Erlangen-Nürnberg, Erlangen, Germany; and the 2University Department of Ophthalmology, AHEPA Hospital, Thessaloniki, Greece.
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Abstract |
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METHODS. Aqueous humor and serum samples were collected from 100 patients with PEX syndrome, PEX glaucoma (PEXG), POAG, and cataract, respectively. Levels of MMP-1, -2, -3, -7, -9, and -12 and TIMP-1 and -2 were determined by zymography, Western blot analysis, and specific immunoassays. Activity assay kits were used to quantitate levels of endogenously activated MMP-2 and -9.
RESULTS. MMP-2, -3, -7, -9, and -12 and TIMP-1 and -2 were identified in human aqueous humor samples from all groups of patients with a six to sevenfold molar excess of TIMPs over MMPs. Whereas serum samples showed no significant differences, total MMP-2 and -3 and TIMP-1 and -2 were detected at significantly higher concentrations in aqueous samples from PEX eyes with and without glaucoma compared with cataractous eyes. MMP-2 and -3 and TIMP-1 were also detected in higher, but not significantly different, amounts in aqueous samples of POAG eyes. However, levels of endogenously activated MMP-2 were significantly decreased in both PEX and POAG samples. The ratio of MMP-2 to its principal inhibitor TIMP-2 was balanced in cataract samples, but was decreased in samples from patients with PEXG, resulting in an excess of TIMP-2 over MMP-2.
CONCLUSIONS. The findings suggest that complex changes in the local MMP-TIMP balance and reduced MMP activity in aqueous humor may promote the abnormal matrix accumulation characteristic of PEX syndrome and may be causally involved in the pathogenesis of both PEX glaucoma and POAG.
Similarly, an excessive accumulation of extracellular material in the juxtacanalicular tissue of the meshwork has been postulated to cause an increased outflow resistance in eyes with primary open-angle glaucoma (POAG),10 11 and an impaired trabecular meshwork matrix turnover, which is critical to the regulation and maintenance of aqueous humor outflow, has been implicated in the development of POAG.12 13
Extracellular matrix turnover is mediated by matrix metalloproteinases (MMPs), a large family of endopeptidases with variable substrate spectra,14 15 the presence of which has been described in human aqueous humor.16 17 18 19 20 However, no quantitative studies of aqueous levels of MMPs and TIMPs have appeared in the literature. The activity of these enzymes is regulated in part by specific endogenous inhibitors, the tissue inhibitors of metalloproteinases (TIMPs). Dysregulated expression of MMPs and TIMPs has been implicated in many disease processes accompanied by abnormal matrix production, such as fibrotic disorders,21 22 23 and a variety of other disease states. In the eye, abnormal expression of MMPs has been implicated, among many other disorders, in proliferative vitreoretinopathy,24 25 26 secondary cataract formation,27 and the pathogenesis of pterygia.28 29 Therefore, MMPs and TIMPs are likely candidates to be involved in the abnormal extracellular matrix metabolism characteristic of PEX syndrome/glaucoma (PEXG) and POAG.
The purpose of this study was to analyze members of the main MMP families—interstitial collagenases (MMP-1), gelatinases (MMP-2 and -9), stromelysins (MMP-3), matrilysins (MMP-7), and metalloelastase (MMP-12)—and their endogenous inhibitors (TIMP-1 and -2) in aqueous humor and serum of patients with PEX syndrome, PEXG or POAG and in control patients with cataract to determine the potential role of MMPs and TIMPs in the pathogenesis of PEX syndrome, PEX glaucoma, and POAG. We performed Western blot analysis, substrate gel electrophoresis (zymography), activity assays, and enzyme-linked immunosorbent assays, with specific monoclonal antibodies used to determine the presence, activity, and quantitative differences of MMPs and TIMPs in the samples. Our data suggest that complex changes in the local MMP-TIMP balance and reduced MMP-2 activity in the aqueous humor may promote the abnormal matrix accumulation characteristic of PEX syndrome and may be causally involved in the pathogenesis of both PEXG and POAG.
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Methods |
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Informed consent to aqueous humor and serum donation was obtained from the patients, and the research was in compliance with the tenets of the Declaration of Helsinki for experiments involving human tissue.
Protein Determination
Total aqueous protein concentrations were determined in aliquots (2 µL) of all aqueous humor samples, by using the Bradford assay reagent (Sigma-Aldrich; St. Louis, MO), with bovine serum albumin used as a standard.
SDS-PAGE Zymography
Proteolytic activities were detected in sodium dodecyl sulfate (SDS)-polyacrylamide gels (5%–15%) copolymerized with 1 mg/mL porcine skin type A gelatin (Sigma-Aldrich) as substrate for MMP-2 (gelatinase A) and MMP-9 (gelatinase B) or 1 mg/mL bovine milk casein (Sigma-Aldrich) as substrate for MMP-3 (stromelysin) and serine proteinases.30 Briefly, aliquots of aqueous humor (2 µg protein for gelatin zymography, 5 µg for casein zymography) and serum samples (20 µg protein for gelatin zymography, 50 µg for casein zymography) from all groups of patients were incubated in equal volumes of nonreducing sample buffer (10 mM Tris containing 1.5% [wt/vol] SDS, 10% [vol/vol] glycerol, and 2.5 µg/mL bromophenol blue) for 30 minutes at 37°C. After electrophoresis, the gels were washed two times in 2.5% (wt/vol) Triton X-100, and incubated in 50 mM Tris/HCl (pH 7.4) containing 150 mM NaCl, 10 mM CaCl2, 2 µM ZnSO4, and 0.005% polyoxyethylene-23-lauryl-ether for 24 (gelatin) or 72 (casein) hours at 37°C. After staining with 0.1% (wt/vol) Coomassie blue (Coomassie Brilliant Blue R 250; Sigma-Aldrich) in 30% (vol/vol) methanol and 5% (vol/vol) acetic acid for 1 hour and destaining in 20% (vol/vol) ethanol and 5% (vol/vol) acetic acid, the proteolytic activities were detected as clear bands on a stained background. Molecular weight standards and trypsin (5 ng, bovine pancreas, Sigma-Aldrich) as a positive control were run in parallel. In some gelatinase experiments, one of the metalloproteinase inhibitors, EDTA (10 mM, Sigma-Aldrich) was included in the 2.5% Triton X-100 solution and in the substrate buffer. The zymograms from three similar experiments were subjected to densitometric analysis. Semiquantitative analysis of the bands was performed with NIH Image (ImageJ ver. 1.25s; http://rsb.info.nih.gov/ij/; produced by Wayne Rasband and provided in the public domain by the National Institutes of Health, Bethesda, MD).
Western Blot Analysis
To determine protein levels of the various MMPs and TIMPs, aliquots (100 µg protein) of aqueous humor, which was concentrated by acetone precipitation, and unconcentrated serum samples were electrophoresed on 12% SDS-PAGE gels under reducing conditions, after normalization for total protein concentration, and electrophoretically transferred onto nitrocellulose membranes with a semidry blotting unit. After the membranes were blocked with 1% normal goat serum in PBS/0.1% Tween-20 for 12 hours, they were incubated in mouse monoclonal anti-human MMP (MMP-1, -2, -3, -7, -9, and -12) and TIMP (TIMP-1 and -2) antibodies (Oncogene, Boston, MA) diluted 1:500 in PBS/0.05% Tween-20 for 1 hour at room temperature or overnight at 4°C. Immunodetection was performed with a goat anti-mouse IgG-alkaline phosphatase conjugate (Oncogene) diluted 1:1000 in PBS/0.05% Tween-20 and nitroblue tetrazolium salt (NBT) and 5-bromo-4-chloro-3-indolyl phosphate (BCIP) as a substrate.
Enzyme Immunoassays of MMPs and TIMPs
The total (pro, active, and complexed forms) concentrations of MMP-1 (interstitial collagenase), -2 (gelatinase A), -3 (stromelysin), -7 (matrilysin), and -9 (gelatinase B) and the total (free and complexed) concentrations of TIMP-1 and -2 were assessed in aqueous humor and serum with commercially available sandwich enzyme immunoassay kits (Biotrak; Amersham Biosciences, Piscataway, NJ). To increase sensitivities, additional enzyme-immunoassays were applied for the detection of MMP-3 with another commercially available assay kit (Quantikine; R&D Systems, Minneapolis, MN) and MMP-9 with a designed ultrasensitive enzyme immunoassay, as previously described, for the detection of MMP-9 in human cerebrospinal fluid.31 Activity assay systems (Biotrak; Amersham Biosciences) were used to quantitate either the endogenously active levels of free MMP-2 and -9 or the total levels (active and pro forms) of free MMP-2 and -9 not complexed to TIMPs. Aqueous samples from the same patients were used to measure the total and active concentrations of both MMP-2 and -9 and the total concentrations of TIMP-1 and -2. Aqueous samples from different patients had to be used to quantitate MMP-1, -3, and -7. Assays were performed in duplicate according to the manufacturer’s instructions. The characteristics of the assays used are indicated in Table 1 .
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Zymography of Aqueous Humor and Serum
Substrate gel electrophoresis (zymography) was performed to detect gelatinolytic and caseinolytic activities of MMPs in aqueous humor and serum samples from patients with cataract, POAG, PEX syndrome, or PEXG. Ten aqueous humor samples and five serum samples were analyzed in each group. By means of SDS-mediated dissociation of MMP-TIMP complexes, this method detects both activated forms and latent pro forms of gelatinase A (MMP-2), gelatinase B (MMP-9), and stromelysin (MMP-3), because SDS in the gel and sample buffer activates the pro enzymes without a change in molecular weight.
Zymography of gelatin-containing gels showed one major band of gelatinolytic activity at a molecular mass of 70 to 72 kDa, consistent with the molecular mass of the pro form of MMP-2 in aqueous humor samples from all patients (Fig. 1A) ; there was, however, a distinct increase in the amount of gelatinolytic activity in PEX samples compared with control samples as assessed by densitometric analysis (Fig. 1B) . Minor bands were also apparent at molecular masses of 66 kDa consistent with an activated form of MMP-2 and 120 kDa, probably corresponding to MMP-TIMP complexes that were not completely dissociated by the SDS treatment. The 66-kDa band was present in the aqueous humor of patients with cataract, but was either absent or markedly weaker in the POAG and PEX groups. The 120-kDa band was more prominent in the PEX samples assessed by densitometric analysis.
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The casein-containing gels incubated for an extended period of 72 hours showed caseinolytic activities at molecular masses of 80 to 84 kDa and 66 to 68 kDa in the serum samples only, but no activities in the aqueous humor samples (Fig. 2) .
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Western blot analysis identified immunoreactive bands at 72 and 66 kDa corresponding to latent and active MMP-2, at 54 and 22 kDa corresponding to latent and active MMP-12, at 28.5 kDa corresponding to TIMP-1, and at 22 or 24 kDa corresponding to TIMP-2 in aqueous humor and serum samples from patients with PEX and control patients (Fig. 3) . Relative band intensities of MMP-2 and -12 and TIMP-1 and -2 appeared higher in PEX aqueous than in control aqueous. Weak bands at 28 and 59 kDa characteristic of MMP-3 were observed in some serum but not in the aqueous samples. Distinct protein bands characteristic of MMP-1, -7, and -9 were not detected in any of the aqueous or serum samples.
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MMP-2 was detected in considerable amounts in aqueous humor samples from all groups of patients and ranged from 18.6 to 232.4 ng/mL. Despite this high interindividual variability, the total level of MMP-2 (pro enzymes and complexed forms) was significantly increased in aqueous humor of patients with PEX syndrome without and with glaucoma (P < 0.0001, significant after BC) compared with control patients with cataract. In patients with POAG, the difference (P < 0.01) was no longer significant after BC (Fig. 4A) . The increase in MMP-2 in relation to total aqueous protein levels amounted to 8% in POAG, 50% in PEX syndrome, and 35% in PEXG samples compared with cataract samples and was only significant in the PEX groups. The free, not the complexed pro form of MMP-2, ranging from 1.5 to 63.7 ng/mL and representing 22% to 24% of the total amount in the aqueous humor, was markedly increased in patients with PEX syndrome or PEXG (P < 0.01, not significant after BC), but not in patients with POAG. The levels of intrinsically active MMP-2 decreased significantly from 1.5% of the total amount in the cataract group to 0.3% to 0.4% of the total amount in both the POAG and the PEX groups (P < 0.001, significant after BC). Serum levels of total, pro, and active MMP-2 showed no significant differences between the groups.
Total MMP-3 was detected in minimal amounts in the aqueous humor of all patients, ranging from 0.15 to 3.86 ng/mL. The differences in the POAG (P < 0.05) and both PEX groups (PEX syndrome P < 0.01; PEXG P < 0.0001) compared with the cataract group showed statistical significance after BC in the PEXG group only (Fig. 4B) . When the MMP-3 increase was expressed relative to aqueous protein concentrations (POAG: 21%, PEX syndrome: 92%, PEXG: 127% compared with cataract concentrations), a statistical significance was established for the PEX groups only. Serum levels of MMP-3 showed no significant differences between the groups.
MMP-7 was detected in minimal amounts in part of the aqueous samples of all groups but showed no significant differences (data not shown). Serum samples could not be assessed with the assay used.
Levels of total, pro form, and active MMP-9 were below detection limits (600 and 125 pg/mL) of the commercially available assay kits in most aqueous humor samples from all groups of patients. However, minimal amounts of MMP-9 in the range of 15 to 55 pg/mL were detected in the aqueous humor samples of all groups of patients by using the ultrasensitive enzyme immunoassay with a detection limit of 10 pg/mL.31 Significant differences between the groups were not observed, however. Serum levels of total, pro, and active MMP-9 were markedly lower in patients with POAG and PEXG (P < 0.01, not significant after BC) than in patients with cataract.
Both TIMP-1 and -2 were detected in considerable amounts in aqueous humor samples from PEX and control eyes. The total amount of TIMP-1 generally ranged from 210.8 to 1803.8 ng/mL and that of TIMP-2 from 44.3 to 205.0 ng/mL. Aqueous TIMP-1 was in six- to eightfold molar excess over TIMP-2 in all groups of patients. A significant increase in aqueous TIMP-1 (Fig. 4C) and -2 (Fig. 4D) levels was measured in both PEX groups compared with the cataract and the POAG groups (P < 0.0001, significant after BC). The difference was more pronounced in eyes with PEXG than in eyes with PEX syndrome only. TIMP-1 levels were also increased in aqueous samples of patients with POAG compared with patients with cataract, but the difference was not statistically significant. Expressing the TIMP increase relative to aqueous protein concentrations, both TIMP-1 (PEX syndrome and PEXG: 52%) and TIMP-2 levels (PEX syndrome: 23%, PEXG: 52%) in PEX samples were still significantly different from cataract control samples. Serum levels of TIMP-1 were elevated in patients with PEX, with and without glaucoma, compared with patients with cataract and POAG, but the difference did not reach statistical significance.
The ratio of total MMP-2 to activated MMP-2 increased in POAG and PEX aqueous samples compared with cataract samples by means of a reduction of the active portion (Table 3) . The ratio of total MMP-2 to total TIMP-2 was balanced in cataract aqueous samples, but increased in POAG and PEX syndrome samples, with a slight excess of MMP-2 over TIMP-2; however, in PEXG samples, the ratio decreased in favor of TIMP-2 (Table 3) . In contrast, serum samples showed a marked surplus of MMP-2 over TIMP-2. In aqueous humor, the combined molarity of the two inhibitors was six- to sevenfold greater than the combined enzyme molarity in all groups of patients, but this surplus of specific inhibitors was again not evident in the serum (Table 3) .
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Discussion |
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These enzymes are synthesized and secreted as inactive proenzymes and are activated by proteolytic cleavage of a polypeptide from the molecule. MMPs are tightly regulated at the levels of transcription, secretion, and proteolytic activation of their precursors.14 15 In addition, MMP activities are further controlled by unspecific plasma- and specific tissue-derived inhibitors, such as 
-macroglobulins and TIMPs, which prevent accidental activation by complex formation.32 Four TIMPs have been described to date that have the capacity to inhibit all active MMPs. TIMP-1 controls most MMPs, in particular MMP-1, whereas TIMP-2 is the major inhibitor of MMP-2.33
MMPs have been implicated in normal matrix remodeling processes—for example, in embryonic development, morphogenesis, tissue homeostasis, and wound healing. Abnormal expression of MMPs and TIMPs or disturbances in the proteolytic balance between MMPs and TIMPs has been associated with a number of pathologic conditions including inflammatory diseases, cancer, cardiovascular disease, neurologic disease, and fibrotic conditions.34 In the eye, MMPs and TIMPs have been implicated in inflammatory and fibrotic conditions, including vitreoretinal disorders.24 25 26
MMPs and TIMPs in Human Aqueous Humor
The presence of MMPs and their inhibitors has been previously reported in human aqueous humor, by using zymographic and immunoblot techniques.16 17 18 19 20 Whereas MMP-2 (gelatinase A) activity has been consistently detected as a major constituent of normal aqueous humor samples,17 19 20 MMP-9 (gelatinase B) activity has been variably identified in patients with cataract17 18 or uveitis.18 20 In addition, other investigators have identified MMP-1 and -3 and TIMP-1 with considerable interindividual variations.16 18 However, no quantitative studies of aqueous levels of MMPs and TIMPs have been performed.
The present study demonstrates the concentrations of a broad spectrum of MMPs and TIMPs in aqueous humor of patients with cataract, POAG, PEX syndrome, or PEXG, and establishes significant quantitative differences between the groups, despite considerable interindividual variations in levels of MMP and TIMP. The use of zymography, immunoblots, specific immunoassays, and activity assays allowed the determination of the presence, activity, and quantitative concentrations of MMPs and TIMPs in individual samples. We found that aqueous humor from all groups of patients contains relatively high quantities of pro-MMP-2, TIMP-1, and TIMP-2 with a six- to eightfold molar excess of TIMP-1 over -2, and only low amounts of MMP-3, -7, and -9, which were not detectable by zymography or Western blot analysis. Moderate amounts of latent and active MMP-12 were additionally detected by Western blot analysis only. The presence of MMP-7 and -12 and TIMP-2 has not been previously reported in human aqueous humor. MMP-1, however, was not identified in any of the samples, which may be due to the low sensitivity (1.7 ng/mL) of the assay used. Whereas MMP-9 was also below the detection limit of the commercially available assay kits, it was detected in minimal amounts with a designed ultrasensitive immunoassay confirming the results obtained for cerebrospinal fluid of normal human subjects.31 The free form, not the complexed pro form, of MMP-2 contributed to 22% to 24% of the total amount of MMP-2. Intrinsically active MMP-2 was measured in minimal amounts, forming 0.3% to 1.5% of the total amount.
The high levels of TIMPs and the six- to sevenfold stoichiometric excess of TIMPs over MMPs in aqueous humor point to a predominant role of these specific inhibitors in the protection against accidental activation of MMPs in the absence of large amounts of unspecific serum-derived inhibitors. The ratio between MMP-2 and TIMP-2 was roughly balanced, however, suggesting generation of MMP-2/TIMP-2 complexes. Any disturbances of this delicate balance within the anterior compartment of the eye should influence cell biological activities. In contrast, the surplus of MMPs over TIMPs in serum samples indicates a role for unspecific inhibitors such as -macroglobulins in addition to TIMPs in regulating circulatory MMP activities.
Aqueous levels of MMPs and TIMPs showed significant differences between patients with PEX syndrome, PEXG, or POAG compared with individuals with cataract, with the differences being more pronounced in the PEX samples than in the POAG samples. Aqueous samples from patients with PEX syndrome and PEXG showed a highly significant increase of total MMP-2, total MMP-3, and TIMP-1 and -2 compared with samples from patients with cataract. MMP and TIMP levels were approximately twofold those in the cataract samples. These differences were confirmed by immunoassays, Western blot analysis, and zymography with densitometric analysis, and were still significant when the MMP and TIMP levels were compared with total aqueous protein levels. An additional increase of aqueous MMP-12 in PEX samples was suggested by semiquantitative Western blot analysis. In aqueous samples from patients with POAG, total levels of MMP-2 and -3 and TIMP-1 were also increased, compared with levels in patients with cataract, but the differences were no longer significant after BC. Despite the total increase, the activated form of MMP-2 was significantly decreased in both PEX and POAG samples, as demonstrated by zymography and activity assays and the ratio of the total to activated MMP-2 increased from 66.6 in cataract samples to 333.3 in PEX samples and 250.0 in POAG samples. The ratio of total MMP-2 and its principal inhibitor TIMP-2 was balanced in normal cataract samples, but was increased in PEX syndrome and POAG samples and decreased in PEXG samples, resulting in a stoichiometric excess of TIMP-2 over MMP-2.
In contrast, serum levels of MMPs and TIMPs did not show any significant differences between the groups, apart from markedly decreased MMP-9 levels in patients with PEX or POAG. Serum levels of TIMP-1 were increased in PEX compared with cataract samples, but the difference was also not statistically significant.
Functional Significance of MMPs and TIMPs in Human Aqueous Humor
Normal tissue homeostasis requires a balanced interaction of MMPs and TIMPs, and the ratio of enzyme to inhibitor is normally 1:1. Any disturbance in the balance may result in excessive or insufficient matrix degradation and matrix accumulation. An excess of proteases over inhibitors or an excessive MMP activity is associated with abnormal matrix degradation, as seen in inflammatory diseases.20 26 In contrast, an excess of inhibitors over proteases or reduced MMP activity may lead to abnormal matrix accumulation, as observed in chronic fibrotic disorders and scarring.22 23 35 In fibrotic liver disease, for example, expression of MMP-1 is downregulated, whereas expression of MMP-2 and TIMP-1 and -2 is generally enhanced.21 22 23 Similar findings have been reported in patients with scleroderma36 and in hypertrophic scar tissue.35 37 Significantly higher levels of TIMP-1 and MMP-2 have also been found in the vitreous of patients with proliferative vitreoretinopathy.25 38 However, evaluation of the biological significance and functional proteolytic activity of MMPs requires data on endogenously active rather than total protein levels and on MMP-to-TIMP ratios as well.
The MMPs and TIMPs present in the aqueous humor may participate in the remodeling of the extracellular matrix in tissues bordering the ocular chambers. In ocular tissues, a role for MMPs and TIMPs has been suggested in trabecular meshwork matrix turnover, which is critical to the regulation and maintenance of aqueous humor outflow and has been implicated in the pathogenesis of POAG.12 13 In both POAG and PEXG, accumulation of abnormal extracellular material in the trabecular meshwork, either in the form of plaque material or PEX material, may be responsible for increased outflow resistance and chronic elevation of pressure.8 9 10 11 The decreased aqueous levels of endogenous MMP-2 activity may contribute to the abnormal matrix accumulation found in the juxtacanalicular meshwork of POAG eyes.10 11 Conflicting results have been reported by a previous study, demonstrating increased MMP-2 (gelatinase-A) activity in aqueous humor from patients with POAG by means of zymography only.19
In eyes with PEX syndrome and PEXG, the excess de novo production of various extracellular matrix components results in a progressive accumulation of an abnormal fibrillar material in most anterior segment tissues, including the juxtacanalicular region of the trabecular meshwork.1 2 8 9 The findings of this study suggest that both the reduced levels of activated MMP-2 and the significantly increased concentrations of TIMP-1 and -2 leading to a stoichiometric excess of TIMP-2 over MMP-2 in aqueous humor from PEXG eyes are causally related to inappropriate matrix degradation and progressive matrix accumulation. A decreased degradability of PEX material from increased cross-linking processes preventing access of proteases or MMP activators may further play a role. Although the differences were generally more pronounced in patients with PEXG, they were also evident in patients with PEX syndrome only, arguing against a decisive influence of previous laser treatment or glaucoma medication on aqueous MMP and TIMP levels.
Increased deposition of matrix components may provide a signal for increased MMP synthesis. Therefore, the significantly increased levels of total (i.e., biologically inactive) MMP-2 and -3 in PEX samples cannot be causally related to pathogenesis, and upregulation of total MMPs is more likely to be a consequence of matrix remodeling and accumulation than a cause. However, the enzymes are obviously not activated, and an appropriate matrix turnover is compromised.
Source and Regulation of MMPs and TIMPs in Human Aqueous Humor
The origin of MMPs in normal aqueous humor is not known, but they may be produced by surrounding cells and tissues, such as the corneal endothelium or the trabecular meshwork.39 40 The elevated levels of MMPs and TIMPs present in the aqueous humor of PEX and POAG eyes may be produced by anterior segment tissues or may be derived from breakdown of the blood–aqueous barrier, which is a consistent feature of at least eyes with PEX syndrome.41 Correspondingly, significantly increased protein concentrations were measured in the aqueous humor of PEX eyes in this study. Correlation of enzyme and inhibitor levels with total aqueous protein concentration, which is a marker of barrier breakdown, suggests a passive influx from the blood rather than local synthesis.
Total aqueous protein concentration appeared to correlate with total MMP-2 in all groups except patients with PEX syndrome, and with MMP-3 and TIMP-1 in patients with PEXG only. TIMP-2 did not correlate with protein concentration at all. Despite significantly increased protein levels, patients with PEX syndrome did not show any correlation between protein concentration and any of the enzymes or inhibitors studied. These findings support the active upregulated production of MMPs and TIMPs by anterior segment tissues rather than passive derivatives from the circulation. Regardless of the source, altered aqueous levels of any of these factors may have potentially adverse pathologic effects.
MMPs and TIMPs are regulated at the transcriptional level by various growth factors and cytokines (e.g., TGF-ß).42 TGF-ß1, in particular, has been shown to downregulate the expression of MMP-1 and -3, and to upregulate the expression of MMP-2 and TIMP-1 and -322 26 43 ; however, the repressive effects of TGF-ß1 on MMP mRNA expression were not apparent in aged cells.43 The combined effect is to prevent the destruction of the newly formed matrix and explains why elevated levels of TGF-ß are associated with fibrosis within the eye44 and elsewhere in the body. The increased levels of TGF-ß1 and TGF-ß2 in the aqueous humor of PEX45 46 and POAG eyes, respectively,47 may be involved in the upregulation and increased levels of MMPs and TIMPs in these patients. Reduced oxygen tension, as measured in the aqueous humor of PEX eyes48 may be another regulatory factor, because the TIMP-1 promoter contains a hypoxia response element.49
In conclusion, the findings of this study suggest that complex changes in the local MMP-TIMP balance and reduced MMP activity in the aqueous humor may promote the abnormal matrix accumulation characteristic of PEX syndrome and may be causally involved in the pathogenesis of both PEXG and POAG. As the importance of MMP-TIMP involvement, in particular in PEX syndrome and PEXG, becomes increasingly apparent, these enzymes and inhibitors may become targets for pharmacotherapeutic intervention.
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Footnotes |
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Submitted for publication April 12, 2002; revised September 5 and October 2, 2002; accepted October 15, 2002.
Commercial relationships policy: F (AGPK); N (all others).
The publication costs of this article were defrayed in part by page charge payment. This article must therefore be marked "advertisement" in accordance with 18 U.S.C. 
1734 solely to indicate this fact.
Corresponding author: Ursula Schlötzer-Schrehardt, Department of Ophthalmology, University of Erlangen-Nürnberg, Schwabachanlage 6, D-91054 Erlangen, Germany; ursula.schloetzer{at}augen.imed.uni-erlangen.de.
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G G Koliakos, A G P Konstas, U Schlotzer-Schrehardt, G Hollo, D Mitova, D Kovatchev, S Maloutas, and N Georgiadis Endothelin-1 concentration is increased in the aqueous humour of patients with exfoliation syndrome Br. J. Ophthalmol., April 1, 2004; 88(4): 523 - 527. [Abstract] [Full Text] [PDF]
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