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Dry eye is a common disease that develops as a result of alteration of tear fluid, leading to osmotic stress and a perturbed epithelial barrier. Matrix metalloproteinase-9 (MMP-9) may be important in dry eye disease, as its genetic knockout conferred resistance to the epithelial disruption. We show that extracellular matrix metalloproteinase inducer (EMMPRIN; also termed CD147), an inducer of MMP expression, participates in the pathogenesis of dry eye through MMP-mediated cleavage of occludin, an important component of tight junctions. EMMPRIN expression was increased on the ocular surface of dry eye patients and correlated with those of MMP-9. High osmolarity in cell culture, mimicking dry eye conditions, increased both EMMPRIN and MMP-9 and resulted in the disruption of epithelial junctions through the cleavage of occludin. Exogenously added recombinant EMMPRIN had similar effects that were abrogated in the presence of the MMP inhibitor marimastat. Membrane occludin immunostaining was markedly increased in the apical corneal epithelium of both EMMPRIN and MMP-9 knock-out mice. Furthermore, an inverse correlation between EMMPRIN and occludin membrane staining was consistently observed both in vitro and in vivo as a function of corneal epithelial cells differentiation. These data suggest a possible role of EMMPRIN in regulating the amount of occludin at the cell surface in homeostasis beyond pathological situations such as dry eye disease, and EMMPRIN may be essential for the formation and maintenance of organized epithelial structure.
Epithelial cells interact to form a polarized tissue that acts as a protective barrier against infection and environmental stress while allowing exchange of molecules with the extracellular surroundings. Such a continuous permeability barrier functions through the formation of tight junctions that mediate adhesion between adjacent epithelial cells.
Tight junctions are composed of transmembrane proteins, including occludin, claudin, and a number of peripheral membrane structural proteins, such as zonula occludens (ZO), and are associated with a variety of regulatory proteins.
This can be caused by decreased tear production or increased tear evaporation. The resultant high osmolarity in the tear film leads to disruption in the intercellular connections and is considered to be a key factor in the pathogenesis of dry eye syndrome.
EMMPRIN was first identified in tumor cells, where it is particularly enriched. However, it is also expressed in nontumoral tissues, in particular in normal epithelia such as skin, lung, or cornea, and may be implicated in numerous physiological and pathological systems where proteolysis occurs. EMMPRIN has been shown to induce the expression of a variety of MMPs, including MMP-9, without an effect on their physiological inhibitors, TIMP-1 and TIMP-2, thereby increasing the net proteolytic potential.
In this study, we demonstrate a role for EMMPRIN in the disruption of the epithelial integrity observed in dry eye syndrome, an excellent model for studying epithelial barrier function. Increased EMMPRIN expression by high osmolarity resulted in an MMP-9–mediated loss of cell surface occludin and cell–cell contact. The decrease in EMMPRIN levels in dry eye patients after treatment and improvement of clinical symptoms further supports the role of EMMPRIN in the function of the epithelial barrier in vivo. Moreover, the inverse distribution of EMMPRIN and occludin observed as a function of differentiation of epithelial cells, both in culture and in the stratified corneal epithelium in vivo, suggests that the regulation of occludin by EMMPRIN represents a novel physiological function.
Materials and Methods
Antibodies and Chemicals
Antibodies and chemicals used in this study were as follows: anti-EMMPRIN mAb: anti-CD147, clone HIM6 (Becton Dickinson France, Le Pont de Claix, France); anti-occludin pAb: anti-occludin N-term (Invitrogen, Cergy Pontoise, France); anti-GAPDH: clone 6C5 (Applied Biosystems, Courtabouef, France); horseradish-peroxidase–conjugated anti-mouse antibody (Jackson Immuno Research, Immunotech, Marseille, France); anti-mouse IgG Alexa 488 and anti-rabbit IgG Alexa 594 (Invitrogen); Marimastat (British Biotechnology, Oxford, UK); BM Chemi-luminescence Western Blotting Substrate (POD) and DAPI (Roche Diagnostics, Meylan, France); and Protease Inhibitor Cocktail Set V EDTA-free (Calbiochem, VWR International, Strasbourg, France).
Cells and Tissues
SV40-immortalized human corneal epithelial cells (Dr. Kaoru Araki-Sasaki, Riken Cell Bank, Saitama, Japan) were cultured in Dulbecco's modified Eagle's medium and Ham's nutrient mixture F12 (1:1) culture medium (Invitrogen), supplemented with 1% (v/v) antibiotic/antimycotic solution, 2 mmol/L l-glutamine, 5 μg/mL insulin, 10 ng/mL human epidermal growth factor (SHEM medium) and 10% (v/v) fetal calf serum (FCS; PAA Laboratories, Les Mureaux, France). For immunohistochemistry studies in mice corneas, eyes were dissected from wild type (WT), EMMPRIN and MMP-9 knock-out (KO) mice
and were embedded in optimal cutting temperature (OCT) compound (VWR International) before sectioning and immunostaining for occludin and EMMPRIN.
Corneal epithelial cells were cultured in SHEM medium containing 10% serum and complemented with 2.5 mmol/L CaCl2. When cells reached approximately 90% confluence, culture medium was replaced with fresh SHEM medium with added 2.5 mmol/L CaCl2 but not containing serum, and 0, 70, or 90 mmol/L NaCl was then added to increase the osmolarity (corresponding to 312, 450, or 500 mOsM, respectively). Cells were incubated for 24 hours before protein extraction and conditioned medium collection. To study epithelial cell differentiation in vitro, cells were cultured in SHEM medium with or without added calcium.
Measurements of Transepithelial Electrical Resistance
Corneal epithelial cells were seeded in the upper chambers of a Transwell tissue culture plates (Costar, 12-mm diameter, 0.4-μm pore size, Corning Life Sciences, VWR) in SHEM medium containing 10% FCS and allowed to reach confluence. Cells were then cultured for a further 2 days in SHEM medium containing 2% FCS and 2.5 mmol/L CaCl2, after which the transepithelial electrical resistance (TER) was measured with an epithelial voltohmmeter (Evom, World Precision Instruments, Sarasota, FL). When TER reached 100 Ω cm2 or greater, cells were treated with either 90 mmol/L NaCl or 10 μg/mL recEMMRPIN for 24 hours, and measurements were repeated.
Expression and Purification of Recombinant EMMPRIN
Soluble recombinant EMMPRIN (recEMMPRIN), consisting of the extracellular domain of human EMMPRIN, was generated after truncation of its transmembrane and cytoplasmic parts at Leu200 by PCR-directed mutagenesis and cloning into pcDNA3 vector. This was transfected to CHO cells, and positive clones with stable expression of soluble recombinant EMMPRIN were identified by Western blot. CHO-conditioned medium was purified first on a Concanavalin A-sepharose column (GE Health Care, Velisy, France) equilibrated and washed with 0.5 mol/L NaCl in 20 mmol/L Tris-HCl, pH 7.4. Elution was carried out with 0.2 mol/L methyl-α-d-mannopyranoside (Sigma-Aldrich, St. Quentin Fallavier, France). Eluted fraction was dialyzed against 0.1 mol/L NaCl in 20 mmol/L Tris-HCl, pH 7.4, and then applied to a 1-mL Mono Q 5/50 column (GE Health Care) at 0.5 mL/min previously equilibrated with 0.1 mol/L NaCl in 20 mmol/L Tris-HCl, pH 7.4. The column was washed using the same buffer until the A280 dropped to < 1% of its maximum. Protein bound to the column were eluted with a linear gradient of NaCl increasing from 0.1 mol/L to 1 mol/L in 20 mmol/L Tris-HCl, pH 7.4, buffer. Purity of EMMPRIN in each chromatographic step was evaluated by sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE) and confirmed by Western blot.
Triton X-114 Extraction of Membrane Proteins
After treatment with recEMMPRIN, cells were washed and lysed with ice-cold 2% Triton X-114 in Tris-buffered saline (TBS; 50 mmol/L Tris-HCl, pH 7.4, and 150 mmol/L NaCl). After centrifugation of the lysate at 10,000 g for 10 minutes to remove the Triton-insoluble material, the supernatant was partitioned into detergent (lower) and aqueous (upper) phases by incubation at 37°C for 1 minute, followed by centrifugation at 1000 g for 5 minutes. After protein determination of the aqueous phase, fractions of the detergent phase containing identical protein amounts were assayed by Western blotting.
Membranes were immunoblotted with either anti-EMMPRIN mAb or occludin pAb overnight at 4°C or with anti-GAPDH mAb for 1 hour at room temperature, followed by enhanced chemiluminescence detection of bound primary antibodies as previously described.
Data were normalized to the β2 microglobulin (b2m) housekeeping gene transcripts.
Small Interfering RNA Transfection
Two different EMMPRIN siRNA (Ambion, Applied Biosystems) or scramble siRNA (BLOCK-iT fluorescent oligo, Invitrogen) were transfected into cells using oligofectamine transfection reagent in Opti-MEM I (Invitrogen), as described previously.
Cells were then incubated for 18 hours in SHEM medium with 10% FCS and for a further 24 hours in serum-free SHEM medium with or without NaCl addition before analysis.
Confocal Immunohistochemistry and Immunocytochemistry
Cryostat sections (8-μm) were prepared from frozen WT and KO cornea and immunostained after fixation in chilled acetone for 10 minutes, re-hydratation in PBS (Invitrogen), and incubation in blocking solution (3% BSA in PBS) for 30 minutes. For immunocytochemistry, cells were seeded on glass slides, cultured for 2 to 3 days in the presence of 10% FCS, and treated as indicated in Figure 2, Figure 3, Figure 4, Figure 5. Slides were then washed and fixed in 4% paraformaldehyde/DMEM (v/v). Section or cell slides were then incubated for 1 hour with either anti-EMMPRIN mAb or anti-occludin pAb and then for 30 minutes with affinity-purified secondary antibodies (donkey anti-mouse and/or anti-goat IgG, Alexa 488 and 594, respectively). The slides were mounted and examined with a laser scanning confocal microscope (Leica Lasertechnik, Heidelberg, Germany). In negative controls, the primary antibody was substituted with PBS.
Patients and Clinical Data
Conjunctival impression cytology specimens were obtained from 15 patients with dry eye syndrome before and after treatment with unpreserved artificial tears (Larmabak, Laboratoire Thea, Clermont-Ferrand, France). The study was conducted in compliance with the Declaration of Helsinki, Scotland amendment, 2000. All patients received specific explanations on impression cytology principles and the study aims and gave informed consent for the procedure and subsequent use of conjunctival specimens. Patients' characteristics are as follows: median age, 53 years (range, 43 to 71 years), sex ratio, 1:1; all Caucasian/white. No statistically significant modification in either Schirmer test or tear break-up time were observed after 6 weeks treatment. The Schirmer test value was 5.3 mm (± 2.3) before and 5.9 mm (± 3.0) after treatment and tear film break-up time 4.5 seconds (± 2.3) before and 4.8 seconds (± 3.1) after treatment. Eight of 15 patients reported improved symptoms, seven of 15 reported unchanged symptoms, and none were worse after treatment, P = 0.265 by paired t-test. Specimens were collected in the superior bulbar conjunctiva by using 0.20-μm polyether sulfone filters (Supor Membranes, Gelman Sciences, Ann Arbor, MI) after instillation of 1 drop of 0.4% oxybuprocain. Membranes were later placed in RNA (Sigma-Aldrich) and stored at −20°C before quantitative RT-PCR analysis.
Data are represented as mean ± SEM. The Wilcoxon test was used to analyze the significance of the change in EMMPRIN and MMP-9 (between groups) on treatment. The Spearman rank correlation was used to evaluate the association between the differences in mRNA levels in EMMPRIN and MMP-9 normalized to the reference gene b2m on treatment in a 15 patients' samples. The Student test was used to analyze the significance of the change in EMMPRIN and MMP-9 mRNA or protein levels after cell treatment.
Correlation between EMMPRIN and MMP-9 Levels in Dry Eye Patients
MMP-9 RNA was previously reported to be increased in tears of dry eye patients
and was suggested to be directly associated with the disruption of epithelial barrier function. To assess the potential role of EMMPRIN in MMP-9 increase, conjunctival impression cytology was performed in 15 patients diagnosed with dry eye syndrome before treatment and 1 month after treatment, with preservative-free physiological saline solution. This treatment is known to reduce osmolarity and to improve symptoms.
A statistically significant reduction in both MMP-9 and EMMPRIN mRNA levels (Wilcoxon test, P = 0.0026 and P = 0.0014, respectively) was observed after treatment (Figure 1). The reduction in EMMPRIN mRNA was correlated with that of MMP-9 (P < 0.05, Spearman rank correlation coefficient = 0.6393, df = 13), suggesting that the increase of MMP-9 in dry eye patients may be a consequence of EMMPRIN increase.
Recombinant EMMPRIN Induces MMP-9 in Human Corneal Epithelial Cells: Consequences in Epithelial Barrier Function
To explore the possible role of EMMPRIN in the disruption of the epithelial barrier observed in dry eye patients, we looked at the effect of exogenously added recombinant EMMPRIN (recEMMPRIN) on the expression of MMP-9 and on the tight junction component occludin in cultured corneal epithelial cells.
Gelatin zymography of the conditioned medium obtained from corneal epithelial cells treated with exogenously added recEMMPRIN (10 μg/mL) demonstrated an increase in MMP-9 production (Figure 2A). This was associated with a decrease in occludin protein levels as shown by Western blot of cell lysates (Figure 2A). Similarly, a decrease in the cell surface expression of occludin was observed by confocal immunohistochemistry after recEMMPRIN treatment (Figure 2B). The co-addition of the MMPs inhibitor marimastat (10 μmol/L) with recEMMPRIN abrogated EMMPRIN's effect on occludin surface expression (Figure 2B,). This suggests that MMP activity is necessary for the EMMPRIN-mediated occludin disappearance and hence the disruption of epithelial cell–cell junctions.
High Osmolarity Increases EMMPRIN Expression in Human Corneal Epithelial Cells and Is Associated with an Increase in MMP-9 and a Loss of Epithelial Cell–Cell Junctions
The question of the possible role of EMMPRIN in dry eye was addressed using high osmolarity in culture, a commonly used cellular model which mimics the pathogenesis of dry eye.
Normal osmolarity of culture medium, 312 mOsM, was switched to hyperosmolar media, 450 and 500 mOsM, by adding, respectively, 70 and 90 mmol/L NaCl. Although tear hyperosmolarity in patients with dry eye rarely reaches 360 mOsM, most in vitro studies of hyperosmolarity use higher levels (400 to 600 mOsM) to demonstrate response.
Figure 3 shows that the addition of 90 mmol/L NaCl to corneal epithelial cells had the greatest effect in increasing EMMPRIN expression at both the protein and RNA levels (Figure 3, A and C). Although a smaller increase was observed with 70 mmol/L NaCl, no effect could be discerned at the lower concentrations (30 and 50 mmol/L NaCl; not shown).
Gelatin zymography analysis of serum-free conditioned medium of corneal epithelial cells only shows single bands of MMP-9 and MMP-2 with no detectable additional bands of the active gelatinases. However, the mere detection of the MMP-9 protein in biological samples is generally considered to represent the existence of MMP-9–mediated proteolysis. The MMP-9 band increased in the presence of increasing NaCl concentrations, parallel to the increase in EMMPRIN (Figure 3B). MMP-9 RNA levels were also significantly increased in both 70 mmol/L and 90 mmol/L NaCl (Figure 3D). No effect of high osmolarity could be observed on either TIMP-1 or TIMP-2 production by reverse zymography (data not shown).
The increased EMMPRIN level after exposure to higher osmolarity was also shown by confocal immunohistochemistry (Figure 3E, red). Conversely, the strong occludin staining observed at the intercellular junctions of untreated corneal epithelial cells decreased in the hyperosmolar-treated cells (Figure 3E, green). This was associated with increased intercellular spaces observed by bright field microscopic observations when cells were incubated with 90 mmol/L NaCl (Figure 3E, BF), confirming the disruptive effect of high osmolarity on the epithelial cell barrier. TER measurements confirm this change in epithelial permeability. TER of 122 ± 12 Ω cm2 was observed for an untreated monolayer of epithelial cells that dropped to 75 ± 13 Ω cm2 with 90 mmol/L NaCl treatment and to 86 ± 7 Ω cm2 with 10 μg/mL of recEMMPRIN treatment (all values represent the mean ± SD of two experiments conducted in triplicate).
EMMPRIN Inhibition Suppresses MMP-9 Induction by High Osmolarity and Restores Occludin Membranous Expression
EMMPRIN siRNA transfection of corneal epithelial cells abrogated high osmolarity-mediated induction of both EMMPRIN and MMP-9 levels, as shown by Western blot and gelatin zymography, respectively, as compared with the scrambled control siRNA transfected cells (Figure 4A). Similar results were obtained using two different EMMPRIN siRNA. Furthermore, double-labeled immunocytochemistry showed that the inhibition of EMMPRIN by siRNA also restored membrane occludin staining in high-osmolarity conditions (Figure 4B). Of note, a detailed examination of the immunostaining images revealed that areas of higher EMMPRIN staining corresponded to low occludin membranous staining (arrows), underscoring a dissociation of the surface expression of the two molecules within the same cell. We reasoned, therefore, that a regulation mechanism may exist between EMMPRIN and occludin expression, even under homeostasis conditions.
Dissociation of EMMPRIN and Occludin Membranous Expression during Epithelial Cell Differentiation/Stratification in Vitro and in Vivo
We have previously shown that EMMPRIN levels are highest in the basal layers of the corneal epithelium, gradually decreasing from basal to the superficial cells.
This prompted us to look whether the role of EMMPRIN in regulating occludin in dry eye conditions can exist under physiological conditions.
We first looked for a differential expression of EMMPRIN and occludin during calcium mediated epithelial cell differentiation in vitro. Modulation of calcium concentration in the culture medium is commonly used to study epithelial cell differentiation and stratification. Figure 5 shows that increasing calcium concentrations was followed by a decrease in membranous EMMPRIN expression and an increase in that of occludin, supporting the possible role of EMMPRIN in the modulation of occludin membranous expression in corneal epithelial cells.
The stratified epithelium of the cornea represents an in vivo model of differentiation, as the basal layers are known to contain the undifferentiated or “stem” cells, whereas the terminally differentiated epithelial cells reside in the apical surface. The potential role of EMMPRIN in the regulation of occludin expression in epithelial stratification in vivo was also examined on corneas obtained from wild-type (WT) and knock-out (KO) mice for EMMPRIN. Corneas from MMP-9 KO mice were examined in parallel to evaluate the role for the MMP-9 inducing activity of EMMPRIN in epithelial physiology. Occludin immunostaining in cornea sections from these mice is shown in Figure 6A. The most noticeable difference can be observed in the apical epithelium, where a more pronounced occludin membrane staining in the form of thick lines is seen in both EMMPRIN and MMP-9 KO mice while being hardly noticeable in the WT mice. Double immunostaining of wild-type corneas visualized with confocal microscopy confirmed the inverse relationship between EMMPRIN and occludin membrane expression throughout the epithelium (Figure 6B). EMMPRIN staining was highest in the basal epithelial cells and gradually decreased toward the superficial cells (Figure 6B, red). By contrast, although occludin staining was detectable throughout the epithelium, membranous occludin was observed only in the most superficial layer in the form of dots or short thin lines, whereas occludin staining, which was also observed in the deeper layers, appeared to be mainly cytoplasmic (Figure 6B, green). In EMMPRIN KO mice, the absence of EMMPRIN was associated with a marked increased occludin membrane staining in the apical layers, appearing as much longer and thicker lines that covered more cell membrane area. An increase in occludin staining was observed in the MMP-9 KO mice that was similar to that in the EMMPRIN KO epithelium, further suggesting that the regulation of MMP-9 may be behind the EMMPRIN-mediated effect on occludin in corneal epithelium. However, the implication of other proteases induced by EMMPRIN during differentiation cannot be excluded. Altogether, these results support the role of EMMPRIN in mediating occludin membranous expression at least partially via MMP-9.
The barrier function of the epithelium is critical for the maintenance and regulation of its permeability characteristics, and depends on the integrity of the tight junctions. By cleaving occludin, MMP-9 has been shown to be able to disrupt the corneal epithelial barrier and to contribute to the pathogenesis of dry eye syndrome.
However, the factors responsible for the up-regulation of MMP-9 in this pathological condition are not fully understood.
Our work presented here suggests that EMMPRIN, by inducing MMP-9, is an important actor in the regulation of epithelium integrity, both in corneal physiology and in dry eye disease through its action on cell surface occludin. This was demonstrated both by the exogenous addition of recombinant EMMPRIN to cultured epithelial cells and by the increased endogenous expression of EMMPRIN in these cells by high osmolarity, conditions used to mimic the dry eye situation in vitro. These treatments resulted in an MMP-9 increase and a concomitant disappearance of occludin. The fact that the MMP inhibitor marimastat protected occludin from EMMPRIN's effect suggests that the loss of occludin from epithelial cell surface involved an MMP-dependent cleavage. Our findings thus describe a new role for EMMPRIN as a regulator of tight junction structure and integrity through its MMP-inducing function. Furthermore, the increase in MMP-9 levels observed in vivo in the ocular surface of dry eye patients was correlated with EMMPRIN levels, and both were markedly decreased after treatment, supporting the role of EMMPRIN behind the MMP increase.
We have previously shown that EMMPRIN expression in the normal cornea and skin presented a gradient with high levels in the basal undifferentiated epithelial cells which decrease toward the superficial layers of the more differentiated cells.
The fact that occludin, on the contrary, is known to be localized in the apical layers of the stratified epithelium led us to hypothesize that this inverse distribution observed in the normal epithelium may also result from an EMMPRIN-mediated decrease in occludin. This possibility, implying a role for EMMPRIN in the regulation of the epithelial barrier under physiological conditions, was questioned both in vitro and in vivo. We first used an in vitro model of epithelial cell differentiation through the modulation of calcium concentrations.
On differentiation/stratification, the typical membranous staining of EMMPRIN was markedly reduced and only diffusely localized in the cytoplasm, concomitantly with the appearance of clear membranous occludin staining. This striking inverse correlation, which was repeatedly observed between EMMPRIN decreased expression and the appearance of membranous occludin, thus evokes a more general pattern of regulation beyond pathological situations such as in dry eye disease.
In vivo studies using EMMPRIN KO mice revealed that when EMMPRIN is absent in the corneal epithelium, cell surface occludin, which is normally limited to the superficial layer, has shown both an increase in level of expression, appearing as thicker and longer lines on the membrane, and a localization in deeper epithelial layers. A similar occludin distribution was observed in the corneal epithelium of MMP-9 KO mice, further supporting an MMP-dependent action of EMMPRIN in the regulation of occludin cellular expression and localization in the stratified epithelium. Interestingly, Pflugfelder et al. demonstrated that MMP-9 KO were more resistant to superficial epithelial cell desquamation under desiccating stress conditions,
possibly owing to the increased membranous occludin at this localization. The normal gradient in EMMPRIN expression, decreasing from the basal to the apical epithelial layers, may thus represent a possible protection mechanism allowing occludin membranous expression at the corneal apical surface and the maintenance of tight junction integrity in physiological conditions. However, proteolysis induced through EMMPRIN action may not be the only mechanism involved in the physiological regulation of occludin expression in the epithelium, as the lack of EMMPRIN or MMP-9 does not abolish the occludin gradient. Other mechanisms, such as regulation of gene expression or membrane trafficking, may also contribute to the formation of the occludin gradient.
Although the role of MMP-9 in the pathogenesis of dry eye through occludin cleavage has already been suggested, its role in the physiological expression of occludin remains to be determined. MMP-9 has been reported both in the apical and in the basal surface of the epithelium, depending on whether the protein, RNA, or activity was evaluated. Although constitutive protein expression of MMP-9 has been reported in the superficial layers of normal cornea, which greatly increased when challenged with desiccating stress,
suggesting that MMP-9 is produced essentially by the basal cells where EMMPRIN is localized. A growing body of evidence has indicated that cancer progression is associated with decreased tight junctions, and the loss of occludin is generally correlated with tumor development.
Prognostic impact of extracellular matrix metalloprotease inducer: immunohistochemical analyses of colorectal tumors and immunocytochemical screening of disseminated tumor cells in bone marrow from patients with gastrointestinal cancer.
In view of our results presented here, it is tempting to speculate that EMMPRIN induction during tumor progression may lead to an MMP-dependent cleavage of occludin and may decrease cell contact, thus promoting invasion. However, whether other factors beside MMPs contribute to the inverse relationship between EMMPRIN and occludin in cancer cells remains to be investigated. We have recently shown that EMMPRIN increases hypoxia-inducible factors (HIF 1 and 2) in both endothelial cells and in melanoma tumor cells.
thus representing an additional potential mechanism for the regulation of occludin by EMMPRIN in cancer cells.
On the basis of the results obtained in this study, the following scenario may be postulated on the possible events that follow increased tear osmolarity. The increased EMMPRIN expression induces MMPs, including MMP-9, which then cleaves occludin and disrupts the tight junctions. The released MMPs may favor the shedding of EMMPRIN from the epithelial cell surface.
can then further induce both EMMPRIN and MMP production, creating a perpetuating loop that contributes to the disruption of the epithelial barrier and aggravates disease severity. Our ongoing studies investigate the possible use of EMMPRIN as a biological marker for dry eye severity.
By controlling occludin levels on the epithelial surface, EMMPRIN may play a crucial role in the formation and maintenance of organized epithelial structures. The identification of this new molecular mechanism underlying disruption of tight junctions will facilitate the development of novel treatments for diseases in which tight junction barriers are compromised.
We thank Patricia Zadigu and Celine Narayanane for valuable technical help.
Tight junction transmembrane protein claudin subtype expression and distribution in human corneal and conjunctival epithelium.
Prognostic impact of extracellular matrix metalloprotease inducer: immunohistochemical analyses of colorectal tumors and immunocytochemical screening of disseminated tumor cells in bone marrow from patients with gastrointestinal cancer.
In the article entitled, “Distinct Expression Profiles of p63 Variants during Urothelial Development and Bladder Cancer Progression” (Volume 178, pages 1350–1360, of the March 2011 issue of The American Journal of Pathology), the third author's name was listed incorrectly. The correct name is Tian Huai Shen.