Abstract

MATERIALS AND METHODS

RESULTS

To determine whether sex-specific differences are inherent in the corneal reparative response during an acute and self-resolving epithelial injury, age-matched female and male Balb/c mice were wounded by complete mechanical removal of the corneal epithelium up to the limbus border. Corneas of male mice consistently healed faster than corneas of female mice (Fig. 1A, B). At 2 and 3 d after epithelial injury, 80 and 100% of the males (n=5) had achieved full epithelial wound healing, compared to 0% at d 2 and 50% at d 3 for females (n=5, P=0.001). By d 7, both male and female corneas were 100% reepithelialized. Histology (Fig. 1C) demonstrated that the normal corneal epithelial layer in the uninjured healthy cornea of males and females contains 5–7 cell layers, while this normal epithelium is only partially restored at 7 d postinjury (2–3 cell layers). More important, the stroma of healed corneas in both male and female mice contained significant numbers of remnant leukocytes from the acute inflammatory response. A pattern of increased H&E straining in the cornea at 7 d postinjury potentially indicates more infiltrating cells in males than in females. The most abundant infiltrating cells in the injured cornea are PMN cells. Quantification by MPO assay (Fig. 2) clearly indicates that there are no sex-specific differences in corneal PMN cell content at 7 d postinjury. The identity of all H&E-staining cells in the cornea cannot be determined by H&E staining and cell morphology alone. Cells in the tissue section may include dendritic cells, γδ T cells, and macrophages, and their potential role in the sex-specific difference in epithelial wound healing are of interest but remain to be defined.

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Figure 1.

Corneal epithelial wound healing is delayed in female mice. Corneas of age-matched Balb/c male and female mice were injured by complete epithelial abrasion. In the reinjury group, the regenerated epithelium was removed at 7 d after initial epithelial injury. Wound healing was quantified via flourescein stain at 1–4 d after initial injury and 2 d after reinjury. A) Wound healing is expressed as percentage of corneas with complete epithelial wound closure. Significant differences were assessed by Fisher's exact test (n=5). *P < 0.05 vs. males. B) Representative images of male and female fluorescein-stained eyes at 2 d after initial injury and 2 d after reinjury. C) Representative H&E images of 5-μm cross sections of uninjured corneas and healed corneas at 7 d after injury.

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Figure 2.

Attenuated PMN cell response to recurrent epithelial injury in females. Corneas from male and female mice were harvested at indicated time points postinjury, and tissue MPO activity was quantified (n=5–8). MPO activity is expressed as PMN cells/cornea based on calibration curves that were established with isolated peritoneal PMN cells. *P < 0.05 vs. males.

A key feature of corneal inflammatory diseases such as dry eye syndrome is recurrent epithelial injury. To assess whether sex-specific differences in wound healing persist during recurrent epithelial injury, the regenerated corneal epithelium was reabraded at 7 d postinjury. Despite reinjury of the healing epithelium and inflamed cornea, the second injury induced a rapid and accelerated wound-healing response, with 88% of male mice achieving full epithelial wound closure by d 2. In sharp contrast, only 48% of females achieved full epithelial wound closure at 2 d after reinjury (P=0.026). These findings provide the first evidence for a sex-specific difference in the rate of epithelial wound healing in corneas of female mice.

Inflammation is intimately linked to wound healing. In the corneal reparative response to acute epithelial abrasion injury, PMN cell infiltration is an essential and beneficial factor that drives corneal reepithelialization (31, 42–44). Hence, we next assessed whether sex-specific differences in wound healing correlate with a difference in levels of recruited PMN cells in male and female corneas. Despite a marked difference in epithelial wound closure at 2 d postinjury, corneal PMN cell content did not differ in injured corneas of males and females, nor was PMN cell resolution delayed in the reepithelialized cornea at d 7 (Fig. 2). However, epithelial reinjury induced markedly amplified recruitment of PMN cells to the cornea at 2 d after a second abrasion when directly compared to the initial abrasion injury. Specifically, a second epithelial abrasion induced >7.6-fold increase in the male PMN cell response (302,800±46,284 cells/cornea) than was observed with the initial 2-d epithelial injury (39,920±13,541 cells/cornea). Amplified inflammation in response to a recurrent epithelial injury also revealed a marked sex-specific difference, as females had an average of 166,443 fewer PMNs per cornea (55% lower response) when directly compared to age-matched males (Fig. 2). This finding correlates with a significant delay in full wound closure in females (36% females with full wound closure vs. 88% males with full wound closure, Fig. 1A). These results provide strong evidence for a specific intrinsic difference in the corneal inflammatory-reparative response of male and female mice.

Estrogen has been shown to regulate and promote cutaneous wound healing in rodent models (5, 45), which may explain reported differences in healing abilities between sexes and between postmenopausal and premenopausal females (1, 2, 4). The role of estrogen in ocular reparative responses is unknown, even though estrogen is present in the tear film (46) and its biosynthetic enzyme (aromatase) and receptors (ERα and ERβ) are expressed in the cornea (refs. 47, 48; see Fig. 5A). To assess the in vivo action of estrogen on epithelial wound healing, we treated male mice topically with 17β-estradiol throughout the wound-healing response. The action of estradiol on the inflammatory-reparative response was assessed at 2 d after reinjury, as this time point exhibits marked sex-specific differences in both epithelial wound healing and the PMN cell response to injury. Treatment of males with estradiol recapitulated the female phenotype of delayed corneal reepithelialization and attenuated PMN cell recruitment (Fig. 3). Specifically, topical estradiol reduced the number of mice that achieved complete reepithelialization by 56% (Fig. 3A, B), which correlated with a 71% reduction (Fig. 3C) in the amplified PMN cell infiltration that is a consequence of recurrent epithelial injury.

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Figure 3.

Estradiol treatment induces a female-specific wound-healing and PMN cell response in male mice. Eyes of male mice were treated topically with 17β-estradiol (1 μM, 5 μl drop/eye, t.i.d.) or saline alone from d 0 to 9, and full wound closure was quantified at 2 d after epithelial reinjury. A) Percentage of eyes in each group with full epithelial wound closure (Fisher's exact test, n=5). B) Representative fluorescein-stained corneas at 2 d after reinjury. C) Estradiol regulation of the amplified PMN response to reinjury. Corneas were harvested at 2 d after reinjury, and MPO activity was quantified. MPO activity is expressed as number of PMN cells/cornea (n=5–8). *P < 0.05 vs. saline group.

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Figure 5.

Estradiol regulates epithelial wound healing and LXA₄ formation. A) HCE monolayers were treated with estradiol (1 pM) for 24 h. Cells were harvested, and 5-LOX and 15-LOX mRNA expression was quantified by qPCR (n=6). B) Epithelial LXA₄ formation. HCE cells were treated with estradiol (1 pM) or pure medium for 24 h, cells were activated with calcium ionophore for 15 min, and medium was collected for LC/MS/MS quantification of endogenous LXA₄ formation (n=6). C) In vitro epithelial wound healing. Confluent cells were incubated with or without LXA₄ (1 nM) in the presence or absence of estradiol (1 pM) for 24 h prior to scratch wounding. Wound healing was assessed at 8 h postinjury and is expressed as percentage area healed (n=5). D) Representative image of epithelium at 8 h after scratch injury. Lines indicate initial wound area. *P < 0.05 vs. control; ^#P < 0.05 vs. estradiol treatment.

Corneal epithelial cells have a critical function in defending the ocular surface while also expressing high levels of 15-LOX, a key enzyme for the formation of LXA₄ and regulator of epithelial wound healing in the cornea (31, 49, 50). Hence, we next assessed whether 15-LOX (Alox15) expression in male and female corneas exhibits sex-specific differences 2 d after epithelial reinjury. The average mRNA level of 15-LOX was lower in the cornea of females (Fig. 4A). However, this difference did not reach statistical significance, which is likely due to the presence of distinct 15-LOX-expressing leukocyte populations in the stroma of the healing cornea. To focus on the sex-specific differences in epithelial 15-LOX expression, we isolated corneal epithelial sheets 2 d after reinjury from both male and female mice. qPCR analysis demonstrated a significant 47% lower expression of 15-LOX in the regenerated epithelium of females when directly compared to males (Fig. 4B). Topical treatment of male eyes with estradiol throughout the wound-healing response reduced the expression of 15-LOX in the regenerated male epithelium to levels measured in the epithelium of females. These findings provide the first evidence for sex-specific differences in the expression of corneal epithelial 15-LOX and for the ability of estrogens to down-regulate intrinsic epithelial 15-LOX expression.

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Figure 4.

Regenerated corneal epithelium has sex-specific 15-LOX expression that is induced by estradiol. A) Whole corneas were isolated from male and female mice at 2 d after reinjury, and 15-LOX mRNA expression was quantified by qPCR (P=0.14, n=4). B) Corneal epithelial sheets were isolated from corneas at 2 d after reinjury, and 15-LOX mRNA expression was quantified by qPCR in male and female mice (n=3–4). C) Male mice were treated topically with saline alone or 17β-estradiol (1 μM, t.i.d., 5 μl drop/eye) from d 0 to 9, epithelial sheets were isolated at 2 d after reinjury, and 15-LOX expression was quantified by qPCR (n=3–4). *P < 0.05.

To assess the direct action of estrogen on epithelial wound healing and functional expression of the LXA₄ circuit, we used HCE cells in an established in vitro scratch-injury model. Uninjured confluent human epithelial monolayers, like mouse corneal epithelial cells (31), functionally express both 5-LOX and 15-LOX, as evidenced by mRNA expression (Fig. 5A) and generate LXA₄ (16.7±3.3 pg/ml) following calcium ionophore activation (Fig. 5B). Activation of epithelial cells with a low concentration of estradiol (1 pM) significantly reduced expression of 15-LOX and 5-LOX by 47 and 38% (Fig. 5A), respectively, after 24 h. More importantly, estradiol inhibited endogenous LXA₄ formation by ionophore-activated epithelial cells by 64% (Fig. 5B). A defined scratch injury to the epithelial monolayer results in rapid reepithelialization of the denuded area. At 8 h after injury, 30.4 ± 2.1% of the wound area was reepithelialized (Fig. 5C, D). Activation of epithelial cells with a low concentration of LXA₄ (1 nM) at 24 h prior to the epithelial injury significantly increased epithelial wound healing by 31%, which is consistent with our previous findings that topical LXA₄ in mice increases the rate of epithelial wound healing in injured corneas at 24 h and 48 h after injury (31). In sharp contrast, treatment with estradiol (1 pM) at 24 h prior to injury reduced the normal rate of epithelial wound healing by 93%, to 2.4 ± 0.3% (Fig. 5C, D). LXA₄ could rescue epithelial cells from the estradiol effect, as the wound-healing rate of epithelial monolayers treated with a combined dose of estradiol and LXA₄ at 24 h prior to injury was not significantly different from untreated cells (Fig. 5C, D). These results indicate that estradiol down-regulates biosynthetic pathways for LXA₄ formation in epithelial cells and that this inhibition directly correlates with impaired epithelial wound healing.

The bioactions of estradiol are primarily mediated by two nuclear hormone receptors, namely ERα and ERβ. Both of these receptors are expressed in immortalized HCE cell lines (Fig. 6C) and mouse and human corneas (15, 47, 51). qPCR analysis of gene expression in freshly isolated corneal epithelial sheets demonstrated that murine expression of both ERα and ERβ is markedly higher in females than in males (Fig. 6A). Based on relative RNA expression, ERα is the most abundant ER in the corneal epithelium; its RNA expression levels are ~5 fold higher than ERβ in both sexes. The wound-healing response in female epithelium markedly upregulated the expression ratio of ERβ:ERα from 0.21 ± 0.07 to 1.43 ± 0.65 at 2 d after reinjury (Fig. 6B). Hence, corneal injury in females results in sex-specific up-regulation of epithelial ERβ, which is of interest as each ER regulates distinct but yet to be defined gene cassettes (3, 52). Estradiol (1 pM) significantly up-regulates both ERα and ERβ expression (Fig. 6C) in HCE cells within 24 h, suggesting a feed-forward loop for the action of estradiol in these cells.

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Figure 6.

Corneal inflammatory-reparative response regulates epithelial ERα and ERβ expression. A) Corneas from uninjured male and female mice were removed, and epithelial sheets were isolated for qPCR analysis of ERα and ERβ mRNA expression (n=5). B) Expression ratio of ERβ to ERα. Epithelial sheets were collected from uninjured corneas and corneas at 2 d after reinjury, and relative expression of ERβ:ERα was assessed by qPCR (n=5). C) Estradiol regulation of ERα and ERβ. HCE cells were treated with estradiol (1 pM) or medium control (CT) for 24 h, and expression of ERα and ERβ was quantified by qPCR (n=5). *P < 0.05 vs. males or control; ^#P<0.05 vs. uninjured group.

To assess the in vivo action of ERα and ERβ, we treated male mouse eyes topically with selective and established receptor agonists (1 μM, 5 μl drop, t.i.d.) throughout the duration of the inflammatory-reparative response. The therapeutic dose was selected based on a clinical trial in menopausal women that used an ophthalmic topical dose of 1 μM estradiol (40). DPN was used as an ERβ-specific agonist, which has a 70-fold higher binding affinity for ERβ, and PPT was used as an ERα-specific agonist, which has a 410-fold higher binding affinity for ERα. Topical treatment with both DPN and PPT reduced PMN content at 2 d after reinjury by 58–62% in male mice, effectively inducing a female PMN response to recurrent epithelial injury (Fig. 7A). Reduced PMN infiltration correlated with a >50% reduction in the rate of full wound healing in the ERβ treatment group (Fig. 7B). Even though a trend was found, the ERα agonist PPT did not significantly delay full reepthelialization of the corneal wound, which suggests that the epithelial and leukocyte-targeted actions of estrogen are receptor specific.

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Figure 7.

ER-specific regulation of the PMN cell response, wound healing, and 15-LOX/LXA₄ circuit. A) ER regulation of PMN cell recruitment. Male mice were treated topically with PPT, DPN, or saline alone (1 μM, 5 μl t.i.d., d 0–9) and were compared to females. Corneal PMN cell content at 2 d after reinjury was measured by quantifying MPO activity (n=4). B) ERβ regulation of epithelial wound healing. Wound closure was assessed at 2 d after reinjury in males treated topically with PPT, DPN, or saline alone (n=4). C) ERβ regulation of epithelial wound healing in vitro. HCE cells were incubated with 1 pM estradiol, PPT, or DPN 24 h prior to scratch wounding. Wound area was quantified by image analysis at 8 h postinjury. (n=4–5). D) Expression of the LXA₄ circuit. Male mice were treated topically with saline, PPT, or DPN, and mRNA expression of 15-LOX, 5-LOX, and LXA₄ receptors (ALX1, ALX2) was quantified by qPCR in the isolated epithelial sheets (n=5). E) ER regulation of LXA₄ in the leukocyte-rich stroma. Corneas were isolated from saline-, PPT-, or DPN-treated male mice at 2 d after reinjury; the corneal epithelium was removed, and the leukocyte-rich stroma was activated with calcium ionophore. Released LXA₄ in the medium was quantified by LC/MS/MS (n=5). *P < 0.05 vs. saline or control.

To assess direct epithelial action of the ER agonists, we employed the in vitro epithelial injury model. Consistent with experiments in Fig. 3, estradiol abrogated reepithelialization of denuded area (94% inhibition, Fig. 7C). The epithelial action of estradiol was selectively mediated by ERβ, as DPN reduced wound healing from 33 ± 6 to 3 ± 1%. In contrast, the ERα selective agonist PPT did not affect the epithelial wound-healing rate (Fig. 7C). Next, we assessed the selective in vivo action of ERα and ERβ on the intrinsic expression of the 15-LOX/ALX circuit in the regenerated corneal epithelium. Eyes were treated topically with DPN, PPT or saline throughout the initial wound-healing response (d 0–7) and the recurrent epithelial injury (d 7–9). Expression of 5-LOX in the regenerated epithelial sheets was not affected by treatment with either ER agonist. In contrast, ERβ activation during the in vivo reparative response reduced 15-LOX expression in the regenerated epithelium by 63%, while the ERα agonist PPT did not change epithelial 15-LOX expression. This finding indicates that estradiol's ability to markedly reduce epithelial 15-LOX expression (Figs. 4B and ​and55B) and endogenous LXA₄ formation (Fig. 5C) is selectively mediated by the epithelial ERβ receptor. The expression levels of the two mouse LXA₄ receptors, ALX1 and ALX2, showed trends for reduced expression following topical treatment with either ERα or ERβ agonist, but this difference did not reach significance (ANOVA, P>0.05, n=5) due to variability in the saline treatment group (Fig. 7D). Functional expression of the LXA₄ circuit in the cornea depends on LXA₄ formation, which is driven by both epithelial cells and leukocytes during inflammatory responses. Hence, we next assessed whether the leukocyte-rich stroma 2 d after epithelial reinjury could generate LXA₄ in the absence of epithelial cells and whether ERα and/or ERβ receptors regulate leukocyte-dependent LXA₄ formation. On activation with calcium ionophore, the isolated leukocyte-rich stroma generated significant levels of LXA₄ (43±4 pg/cornea, n=4). More importantly, endogenous LXA₄ formation was significantly impaired in mice treated with either the ERα (PPT, 65% inhibition, 15±1 pg/cornea) or ERβ (DPN, 52% inhibition, 21±6 pg/cornea) selective agonist.

DISCUSSION

To the best of our knowledge, this study provides the first findings demonstrating a sex-specific difference in ocular reparative-inflammatory responses. The clinical relevance of our findings in mice is underscored by results from a post hoc analysis of a trial of 120 patients that received treatment for fungal corneal ulcers (53). The analysis demonstrated sex-specific differences in the clinical outcome of corneal ulcers. Specifically, reepithelialization of corneal wounds was significantly delayed in female patients, suggesting worse prognoses for ocular surface wound healing in women. Even though sex-specific prevalence and incidence of ocular diseases are carefully tracked, no studies have reported sex-specific differences in ocular surface wound healing or the clinical outcome of ocular inflammatory or immune events. Ocular diseases are not triggered by single events but likely by the recurrent dysregulation of intrinsic circuits essential for executing routine tissue maintenance, wound-healing, and innate or adaptive immune responses. Sex-specific differences in the dynamic execution of routine epithelial wound healing in the cornea identifies a potential factor in the etiology of ocular surfaces diseases in females, as recurrent epithelial injury is a hallmark of dry eye syndrome. Wound healing and inflammation are fundamental and intimately linked responses. Hence, delays in wound healing may contribute to shifting healthy ocular inflammation during the reparative response to disease causing inflammation and adaptive immune responses if epithelial injury is recurrent or in the context of other stress factors, such as deficient tear film, infection, or hypoxia.

Our results demonstrate that recurrent epithelial injury, which resulted in greatly amplified PMN cell infiltration into the stroma, correlated with accelerated reepithelialization. Furthermore, the magnitude of the increased PMN cell response to recurrent epithelial injury was markedly reduced in female mice (>50%) compared to males, which correlated with a significant delay in wound closure in females. These findings seem counterintuitive based on epidermal wound-healing studies that indicate that PMN cells in general impair wound healing. However, it is important to recognize that a unique feature of corneal epithelial wound-healing responses to self-resolving and minor epithelial injuries is the requirement of inflammation, PMN cell infiltration into the stroma, and platelet activation at the vascular border (31, 42–44, 54). Reduced PMN cell infiltration directly correlates with delayed reepithelialization of corneal wounds that normally heal within 2–5 d. This unique privileged injury response dictates that redundant circuits are in place to tightly control the precarious activation and recruitment of beneficial PMN cells and is highly evolved in the delicate visual axis (32). Consistent with the beneficial role of PMN cells in mild and self-resolving corneal injury responses, we have demonstrated previously that genetic disruption of the protective LXA₄ biosynthetic pathway decreases, while topical treatment with LXA₄ significantly increases, PMN cell content in the cornea, which correlates with decreased or increased epithelial wound healing, respectively (31). In sharp contrast, LXA₄ in chronic or severe corneal injury responses (29, 30) or in every other reported severe inflammatory model (27) inhibits PMN cell infiltration. This in vivo attenuation of PMN cell content in inflamed tissues by LXA₄ is likely indirectly mediated by decreased expression of chemotactic gradients and increased phagocytosis by macrophages. Results from the rapidly self-resolving epithelial injury model point toward a novel injury-specific and PMN cell-targeted bioaction of LXA₄ that is the subject of future studies.

Sex-specific differences in corneal PMN cell content were observed only after recurrent epithelial injury, while the rate of wound closure was delayed in females both in the initial and recurrent reparative response. This finding suggests that both epithelial and leukocyte responses to injury exhibit sex-specific differences. The notion of sex-specific regulation of epithelial and leukocyte function in the cornea is indirectly supported by the expression of distinct ERs in these cell types (1, 3, 51) and the presence of estrogen and estrogen biosynthetic enzymes in the cornea (46, 48).

17β-Estradiol, the most prominent human estrogen, induced a female phenotype of wound healing in corneas of male mice that was mirrored by concomitant decrease in the PMN cell response to recurrent epithelial injury and expression of epithelial 15-LOX. These data provide evidence that topical estradiol is sufficient to induce a female reparative-inflammatory response in male mice and provides further evidence for the critical role of PMN and epithelial cell 15-LOX in acute wound-healing responses. The fact that estradiol at concentrations as low as 1 pM delayed wound healing in monolayers of HCE cells demonstrates that estradiol has direct and physiologically relevant epithelial actions. More important, estradiol significantly reduced the constitutive expression of 5-LOX and 15-LOX in HCE cells. These two LOX enzymes are required for the formation of LXA₄ in the cornea and are expressed in mouse and HCE cells (21, 31). LXA₄ alone could increase the rate of epithelial wound healing in vitro, which is consistent with previous studies that have demonstrated that LXA₄ and 15-LOX promote epithelial wound healing in vivo (30, 31) and that the EGF mediates its epithelial effects in part through LXA₄ (49). Epithelial cells that were treated with LXA₄ and estradiol retained normal wound-healing responses. This add-back experiment provides strong evidence that estradiol's actions on epithelial proliferation and migration are mediated in part by inhibition of the constitutive LXA₄ biosynthetic pathway in corneal epithelial cells. A recent study (55) demonstrated that LXA₄ can bind to ERα and can regulate estradiol-targeted gene expression in endometrial epithelial cells. Bioactions of estradiol and LXA₄ are likely distinct for tissue-specific epithelial cell types. However, regulation of estradiol-targeted genes offers a potential mechanism for the ability of LXA₄ to retain normal wound healing in estrogen-treated epithelial cells. Expression of 15-LOX is markedly lower in the regenerated epithelium of female mice, and topical estradiol reduces expression of 15-LOX in male to the levels measured in the corneal epithelium of females. The mechanism for estrogen regulation of 15-LOX or 5-LOX expression remains to be defined. Gene regulation by ERs is complicated and is often not via response elements in the promoter region of a target gene (3, 52). Taken together, these multiple lines of in vivo and in vitro evidence link the sex-specific differences in the corneal reparative-inflammatory response to regulation of the intrinsic epithelial LXA₄ biosynthetic pathway.

Estrogens regulate expression of distinct gene targets by two nuclear hormone receptors, ERα and ERβ (1, 3, 52). The expression of both receptors in the cornea and corneal epithelium has been established in both males and females (6, 47, 51), though expression of both receptors is markedly higher in females (Fig. 5). Our results demonstrate for the first time that epithelial expression of ERs is regulated by the corneal inflammatory-reparative response, as the receptor expression ratio shifts from predominantly ERα in the resident epithelium to ERβ in the regenerated epithelium. ERβ is of particular interest, as this receptor has been linked to many of estrogen's immune regulatory functions (4). Activation of either ERα or ERβ in the cornea resulted in reduced PMN cell infiltration in response to epithelial reinjury. By contrast, only ERβ activation significantly delayed epithelial wound healing in vivo in mice and in vitro in HCE cells. These findings identify ERβ as the specific receptor that mediates estradiol's epithelial-targeted bioactions and indicate that, by either direct or indirect actions, both ERβ and ERα can regulate PMN cell recruitment to the injured cornea. Consistent with ERβ-specific regulation of epithelial wound healing, only ERβ markedly down-regulated expression of 15-LOX in the regenerated epithelium of reinjured corneas. Neither ERα nor ERβ altered the expression of 5-LOX in the regenerated epithelium. This finding is in contrast to estradiol's ability to markedly reduce constitutive 5-LOX expression in vitro in HCE cells. These differences are likely due to distinct differences between cultured human epithelial cells and in vivo regenerated mouse epithelium, as well as multiple tissue-specific factors that regulate 5-LOX expression in vivo in the inflamed cornea. Epithelial reinjury induces profound up-regulation of PMN cell migration into the stroma that correlates with rapid epithelial wound healing. Even though the corneal epithelium expresses low levels of functional 5-LOX, the predominant source of 5-LOX activity in the inflamed cornea are leukocytes, especially PMN cells and macrophages. Consistent with the ability of both ERα and ERβ to markedly attenuate PMN cell infiltration, activation of either receptor markedly reduced endogenous formation of LXA₄ by the leukocyte-rich stroma. Transcellular biosynthesis is the predominant endogenous route for LXA₄ formation (20, 21, 26, 28). During healthy inflammation, epithelial cells, which highly express 15-LOX, interact with 5-LOX-expressing leukocytes to set in place a temporal amplification loop. This intrinsic feed-forward loop is likely an important factor in the cornea and counterbalances proinflammatory circuits, stimulates noninflammatory activation of macrophages, and drives normal execution of inflammatory-reparative responses. Estradiol attenuates functional expression of this intrinsic corneal circuit at multiple levels by receptor specific regulation in both epithelial cells and leukocytes, which correlates with marked sex-specific differences in the inflammatory and wound-healing response.

In summary, our results provide the first evidence linking sex-specific differences and the action of estradiol to the 15-LOX/LXA₄ circuit. Specifically, ERβ down-regulates epithelial expression and function of key enzymes in the formation of LXA₄, while both ERα and ERβ markedly reduce PMN infiltration and leukocyte-dependent LXA₄ formation. LXA₄, its receptor ALX, and biosynthetic enzymes 15-LOX and 5-LOX have emerged as intrinsic lipid circuits across the visual axis that are critical to the routine execution of healthy inflammatory-reparative responses and the counterregulation of circuits that lead to dysregulated or chronic inflammation (20, 21, 29, 56). Our finding that estrogen negatively regulates the intrinsic LXA₄ circuits, especially ERβ-specific regulation of epithelial 15-LOX, may provide novel insights into the etiology or pathogenesis of sex-specific ocular inflammatory diseases.

Supplementary Material

Acknowledgments

REFERENCES