Central Sterile Corneal Ulceration

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Background

A corneal ulcer is defined as a disruption of the epithelial layer with involvement of the corneal stroma. This condition is associated with inflammation, either sterile or infectious.

The primary purpose of this article is to highlight the pathogenesis of noninfectious stromal ulceration. The infective causes and mechanisms of autoimmune ulcerative keratitis, particularly peripheral, are not included within this article.

See related CME at Cornea and External Disease.

Pathophysiology

An understanding of the pathophysiology of sterile corneal ulceration requires a review of the processes involved in epithelial and stromal wound healing, as well as an examination of the role of precorneal tear film, corneal nerves, proteolytic enzymes, and cytokines.

Epithelial wound healing

Corneal ulceration always begins with an epithelial defect. A persistent epithelial defect allows the corneal stroma to be exposed to the external environment and permits the process of stromal degradation.

Within minutes after a small corneal epithelial injury, cells at the edge of the abrasion begin to migrate centripetally to cover the defect rapidly at a rate of 60-80 µm/h. A longer delay of 4-5 hours is seen in larger defects. This delay is required for preparatory cellular changes prior to rapid cell movement.

Epithelial cells adjacent to the area of the defect flatten, lose their hemidesmosome attachments, and migrate on transient focal contact zones that are formed between cytoplasmic actin filaments and extracellular matrix proteins. Vinculin, a plasma protein, links fibers to talin, which is a cell membrane protein. It, in turn, is linked to integrin. Contraction of actin fibers pulls the cell body forward. Vinculin, integrin, fibronectin, fibrinogen, and fibrin are formed continuously and cleaved to allow for cell migration. Plasmin is the protease responsible for cleaving fibrinogen and fibrin at these focal contact zones.

The basement membrane is also important for epithelial migration, and abnormalities in basement membrane structure, whether due to trauma (eg, recurrent erosion syndrome) or dystrophy (eg, basement membrane dystrophy), can lead to persistence of corneal epithelial defects and stromal ulceration.

After 24-30 hours, mitosis begins to restore epithelial cell population. Basal and limbal stem cells contribute to mitosis. A sufficient supply of progenitor stem cells to facilitate epithelial cell proliferation is important for the cornea. A deficiency of limbal stem cells, from either disease (eg, aniridia) or trauma (eg, chemical burn), can preclude adequate epithelial wound healing.

Stromal wound healing

Stromal wound healing occurs via stromal keratocyte migration, proliferation, and deposition of extracellular matrix molecules, including collagen (specifically type III), adhesion proteins (eg, fibronectin, laminin), and glycosaminoglycans. These processes are facilitated by a phenotypic change among quiescent keratocytes to become active myofibroblasts, a task mediated by transforming growth factor-beta (of presumptive epithelial origin).

Stromal necrosis and degradation

The corneal wound repair process is intricately linked to a complex inflammatory response that must be precisely regulated to ensure proper healing.

Invasion of monocytes/macrophages is critical in wound healing; however, in the corneal stroma, excessive infiltration of monocytes/macrophages is considered to be unfavorable because they secrete matrix metalloproteinases (MMPs) and other proteins undesirable for tissue healing. Numerous cytokines and growth factors that are up-regulated in corneal cells further contribute to tissue inflammation.

Matrix metalloproteinases (MMPs) are a group of structurally related endopeptidases that require a metal cofactor. To date, more than 25 have been identified and are categorized into 6 groups according to their substrate specificity. The main function of metalloproteinases is to degrade extracellular matrix and basement membrane components. MMP-2 and MMP-9 are known as gelatinases and are involved in cleaving collagen types IV, V, VII, and X, as well as fibronectin, laminin, elastin, and gelatins. MMP-1 (neutrophil collagenase) and MMP-8 (fibroblast or keratocyte collagenase) are involved in cleaving collagen types I, II, and III.

Barely detected in an unwounded cornea, MMPs are strongly induced during wound healing. Metalloproteinases are secreted as proenzymes by neutrophils infiltrating the wound, injured epithelial cells, and keratocytes. They are activated by proteolytic cleavage of the N-terminal region in the extracellular compartment. In vivo, tissue inhibitors of metalloproteinases (TIMPs) inhibit collagenase activity. TIMPs represent a multigene family that includes at least 4 members. They exert their action by blocking the activation of MMPs and inhibiting proteinase activity.

A relatively higher degree of collagenolysis relative to synthesis is thought to result in degradation, progressive corneal thinning, and, hence, ulceration of the corneal stroma. MMPs are induced at the transcriptional level by various cytokines and growth factors, such as interleukin 1 (IL-1), interleukin 6 (IL-6), tumor necrosis factor-alpha (TNF-alpha), epidermal growth factor (EGF), platelet derived growth factor (PDGF), fibroblast growth factor (FGF), and transforming growth factor-beta (TGF-beta).

Synthetic inhibitors of mammalian metalloproteinase (SIMP) have been studied to determine their effect on the cornea after an alkali burn. It has been shown that SIMP effectively inhibits corneal ulceration when started earlier in treatment as well as in established ulcers.[1]

Studies have shown a role for the extracellular matrix metalloproteinase inducer (EMMPRIN), a cell membrane glycoprotein enriched on epithelial cells during corneal wound healing. It has been shown that it is up-regulated on epithelial cells by EGF and TGF-beta. This, in turn, induces fibroblasts, by direct interaction, to increase their own level of EMMPRIN, leading to induction of MMP. Inhibition of EMMPRIN may represent a promising future therapeutic strategy in situations of excess extracellular matrix degradation associated with chronic wound healing.[2]

Since all metalloproteinase enzymes require metal cofactors Ca2+ and Zn2+, such chelating agents as ethylenediaminetetraacetic acid (EDTA), acetylcysteine, and penicillamine inhibit collagenase activity; however, these agents have been found to have limited efficacy in vivo. Tetracyclines also possess anticollagenolytic activity.

As a result of collagen breakdown, tripeptide products of collagen are released. These are chemotactic for neutrophils, which migrate into the injured tissue where they release additional MMPs as well as superoxide radicals. These agents potentiate further collagenolytic action and corneal degradation. Superoxide dismutase (SOD) enzymatically reduces the superoxide radical to hydrogen peroxide, thus effectively eliminating highly reactive oxygen metabolites before any further damage. Isozymes of SOD are widely found in the corneas of mammals. Therefore, the use of topical SOD is helpful in preventing corneal damage. Studies have shown a beneficial effect of lecithinated SOD, which is retained on the ocular surface longer than native SOD when applied as an eye drop solution.[3]

In cells along the leading edge of the wound, there is a specific activation of the Ser/Thr kinase, Cdk5. Cdk5 activity limits the accumulation of active Src. Active Src promotes epithelial cell migration. However, excessive Src activity can also cause degradation of E-cadherin and a complete loss of cell-cell adhesion, so its activity and localization must be stringently controlled. Inhibiting Cdk5 activity in organ culture after debridement wounding significantly increases the rate of migration but also causes some separation of cells along the leading edge.

The topical application of a Cdk5 inhibitor, olomoucine, increases the rate of debridement wound closure without causing appreciable dissociation or detachment of epithelial cells.[4]

The role of corneal nerves

The cornea is densely innervated by fibers of the ophthalmic division of the trigeminal nerve and sympathetic nerve fibers from the superior cervical ganglion. Corneal nerves provide important protective and trophic functions, and interruption of corneal innervation may result in altered epithelial morphology and function, poor tear film, and delayed wound healing. Decreased corneal sensation from denervation can result in stromal ulceration and perforation. These ulcers result from decreased metabolic and mitotic rates in the corneal epithelium and reduced acetylcholine, choline acetyltransferase, and substance P concentrations.

In 1954, the classic experiment by Sigelman et al demonstrated that ocular surface changes associated with neurotropic keratitis in denervated animals persist despite tarsorrhaphy, suggesting a trophic effect of the corneal nerves.[5] Evidence suggests that sensory neuron loss leads to a severe depletion of acetylcholine in an otherwise acetylcholine rich tissue, resulting in a relative decrease in epithelial cell growth.

Other studies attributed the depletion of substance P associated with sensory denervation as the cause of the changes associated with neurotrophic keratitis. It has been reported that substance P administered with insulinlike growth factor 1 (IGF-1) or EGF synergistically facilitates corneal epithelial migration and adhesion. Nakamura and coworkers (1999) determined that only the four-amino-acid sequence (FGLM) from the C terminal of substance P is necessary.[6] This finding has implications for the clinical use of topically applied neuropeptides, since full-length peptides are more readily degraded and inactivated by peptidases in the tear film and corneal epithelium.

Clinical trials of nerve growth factor (NGF) by Bonini et al (2000) demonstrated a beneficial effect in promoting corneal epithelial wound healing and, possibly, in improving sensitivity in patients with neurotrophic keratitis.[7] The mechanism of action of NGF on the ocular surface is not well defined. It may involve a direct mechanism of sensory innervation and the proliferation and differentiation of epithelial cells. An indirect mechanism, such as increasing the neuropeptides that promote epithelial healing or invoking immune cells through the release of cytokines, could also be involved.

The role of the precorneal tear film in ulceration

The exposure of the bare corneal stroma to its environment secondary to deficient or impaired epithelial wound healing is thought to contribute to stromal degradation through environmental factors, cytokines, lytic enzymes, and neutrophils in the tear film. Direct neutrophil adhesion to the corneal stroma theoretically allows hydrolytic and collagenolytic enzymes, including MMP-8 (neutrophil collagenase), to contribute to the degradation of the corneal stromal extracellular matrix.

Dohlman et al (1969) and subsequently Kenyon et al (1979) demonstrated that a glued on methylacrylate lens applied to a rabbit alkali burn model of corneal ulceration protected the stroma from collagenolysis by neutrophils and injured epithelial cells.[8, 9] Keratocyte fibroblasts also may contribute to this milieu. The prevention of neutrophil infiltration and the promotion of epithelialization are thought to be at least some of the mechanisms responsible for the beneficial effect of amniotic membrane graft use in preventing stromal ulceration.[10]

In addition, cytokines, such as hepatocyte growth factor (HGF), keratocyte growth factor (KGF), and EGF, are produced by the lacrimal gland and, thus, are present in tears. HGF is up-regulated in response to corneal injury in parallel with increased aqueous tear production. In the wounded cornea, these cytokines may play an important role in regulating epithelial healing. Inflammatory cytokines, including IL-1alpha, are detectable in normal human tears and may be important in causing further degradation of the corneal stroma, either directly by inducing keratocyte apoptosis or by recruiting inflammatory cells via their chemotactic properties. In addition, an irregular tear film and a decreased tear film breakup time over the area of the bare stroma can cause a delle effect that may contribute to an unfavorable cellular environment for the viability and proliferation of stromal keratocytes.

The role of cytokines

The complex autocrine and paracrine functions of the cytokines involved in the interactions between the corneal epithelium and stromal keratocytes are important in achieving the appropriate responses to corneal wound healing. While their precise triggers and interactions are still being elucidated, cytokines can induce and mediate many of the fundamental steps involved in wound healing.

Epithelial cell migration, proliferation, and differentiation are influenced by the stromal keratocyte cytokines, KGF and HGF. The cornea is not unique with respect to the stromal-epithelial interactions of these 2 cytokines, which are mediators of similar interactions in the breast, skin, and lung. Although the expression profiles of these cytokines lend themselves toward a linear interpretation of their stromal-epithelial interactions, these cytokines clearly are modulated further in vivo by the effects of other cytokines and truncated receptors of these molecules.

In what is likely to be merely the tip of the iceberg with respect to the understanding of cytokine-cytokine interactions, both KGF and HGF mRNA production are altered by the fibroblast cytokines, EGF, TGF-alpha, PDGF, and IL-1. In addition, EGF, PDGF, IL-1alpha, IL-6, and TNF at low concentrations appear to enhance fibronectin (FN)-induced epithelial cell migration.

Not to be eclipsed by stromal influences, epithelial cells modulate important keratocyte responses to epithelial cell injury. Keratocyte wound healing processes, including MMP production and regulation, HGF and KGF production, and keratocyte apoptosis, are mediated via various cytokines, including stimulators like IL-1 and soluble Fas ligand and major inhibitor TGF-beta2. Anterior stromal keratocyte cell death is an important feature of corneal wounding and stromal degradation.

Beyond keratocyte cell death caused by mechanical injury or necrosis associated with neutrophil infiltration, IL-1– and Fas ligand–mediated apoptosis is an important stromal response to epithelial injury. Since both of these cytokines can be produced by keratocytes, autocrine modulation of these responses may occur. IL-1 and PDGF also regulate MMP expression in stromal keratocytes. The exact keratocyte response to IL-1 is likely to be determined by the cytokine milieu in which the targeted keratocyte resides. Other cytokine systems that have demonstrated fibroblast apoptosis include TNF and bone morphogenic protein (BMP).

Studies have shown that autologous serum and umbilical cord serum harbor many growth factors and neuropeptides like EGF, TGF-beta, vitamin A, fibronectin, substance P, IGF-1, NGF, and other cytokines that are essential for the proliferation, differentiation, and maturation of the ocular surface epithelium. Treatment with autologous serum and umbilical cord serum eye drops seem promising for the restoration of the ocular surface epithelial integrity in patients with neurotrophic keratitis and severe dry eye syndrome.[11]

Platelets are known for their ability to heal epithelial and internal wounds. They have storage pools of growth factors, including platelet-derived growth factors, TGF-beta, epithelial growth factors, fibroblast growth factors, insulinlike growth factor I, and vascular endothelial growth factors. Autologous platelet-rich plasma has a large quantity of growth factors that have been found to promote the healing of dormant corneal ulcers and to reduce pain and inflammation.[12]

Platelet-activating factor (PAF) is a potent bioactive lipid that is generated in the cornea after injury. Corneal cells synthesize PAF as early as 30 minutes after injury and increased accumulation is observed at later times, which is, in part, due to the presence of inflammatory cells that arrive at the cornea and actively produce PAF. PAF is a strong inflammatory mediator and inducer of the expression of specific genes, such as some metalloproteinases, urokinase plasminogen activators, and TIMPs. It delays corneal epithelial wound healing by inhibiting adhesion of epithelial cells to the basement membrane and by increasing apoptosis of stromal cells. All these activities exerted by PAF are receptor mediated. Corneal epithelial cells, keratocytes, and endothelial cells express the PAF receptor, and, in corneal epithelial cells, injury up-regulates PAF receptor gene expression. The role of PAF receptor antagonists in preventing corneal injury is under investigation.

Plasminogen is synthesized in the cornea and can be activated to plasmin by a plasminogen activator. This synthesis is stimulated by IL-1alpha and IL-1beta. In turn, plasmin is able to activate latent collagenase. This system could lead to the collagen degradation of corneal ulceration. Studies have demonstrated that uPA (urokinase plasminogen activator), but not tPA (tissue plasminogen activator), is induced in the migrating epithelial cells during corneal epithelial wound healing. Amiloride, a specific uPA inhibitor, effectively decreases uPA activity in the cornea as well as in the tear fluid and favorably affects corneal healing.

A majority of inflammatory cytokines use the nuclear factor (NF)-κB pathway for signaling. Saika et al 2005 studied a mouse corneal alkali burn model to evaluate the therapeutic potential of topical administration of SN50, a cell-permeable peptide inhibitor of NF-κB.[13] They showed that topical administration of SN50 prevents epithelial defects and corneal ulceration after a central alkali burn.[13]

Thymosin beta-4 is a water-soluble polypeptide that promotes corneal wound healing and decreases inflammation.[14] Thymosin beta-4 interferes with NF-κB signaling pathways and suppresses NF-κB phosphorylation, activity, and nuclear translocation in cultured human corneal epithelial cells. Thymosin beta-4 can potentially be used as a potent anti-inflammatory therapy in inflammatory corneal conditions.[14]

Saika et al (2007) concluded that overexpression of peroxisome proliferator-activated receptor-gamma (PPARgamma) may represent an effective new strategy for the treatment of ocular surface burns.[15] Adenoviral gene introduction of PPARgamma inhibited activation of ocular fibroblasts and macrophages in vitro and also induced anti-inflammatory and antifibrogenic responses in an alkali-burned mouse cornea.

Cytokines and trophic factors from the corneal nerves, tear film, conjunctiva, conjunctival vessels, endothelium, and anterior chamber may have important modulating effects on corneal epithelial and stromal healing responses and, thus, corneal ulceration.

Epidemiology

Frequency

United States

The incidence rate depends on the etiology of the corneal ulcer.

Mortality/Morbidity

Corneal scarring, decreased vision, neovascularization, perforation, and blindness are associated with this condition.

Sex

Because of an increased incidence of injuries, this condition may be seen more frequently in males than females.

History

Physical

Causes

A thorough history and physical examination should allow a clinician to narrow down the differential diagnosis.

Laboratory Studies

Procedures

Medical Care

Individual treatment should be tailored toward the coconspirators that are identified by the history and physical examination. Again, the importance of first excluding infectious etiologies is paramount. Once identified, each contributing factor needs to be treated appropriately. All toxic drops should be eliminated if medicamentosa is suspected. Lagophthalmos should be treated with copious lubrication, with taping for variable amounts of time, beginning with sleeping hours. Tarsorrhaphy is indicated if previous method fails. Patients with sicca need copious lubrication and punctal plugs. Evaluate these patients for systemic rheumatologic disease if suspected by clinical history or examination. If immune disease is suspected, systemic immunomodulatory therapy may be necessary.

Treatment modalities are outlined below.

Surgical Care

See Medical Care for possible surgical treatments.

Consultations

Medication Summary

As discussed in Medical Care, a number of medications for sterile corneal ulcers refractory to conventional treatment are currently being investigated with respect to their clinical efficacy (eg, fibronectin, vitamin A, ascorbic acid, serum-derived tears, metalloproteinase inhibitors, neurotrophic growth factor). Therefore, standard dosing, indications, treatment regimens, and contraindications with respect to these medications are not available. The authors recommend that interested physicians directly contact clinical investigators for specific treatment regimens currently used in treatment trials.

Antibiotics often are used prophylactically in treating patients with sterile corneal ulcerations. Specific dosing and medication information on topical antibiotics are not included in this article.

Immunomodulatory treatment regimens are complex, and elaborating on medication dosing and treatment regimens for specific rheumatologic diseases is beyond the scope of this article.

Prednisolone ophthalmic (AK-Pred, Pred Forte, Pred Mild, Inflamase Forte) Suspension 0.12%

Clinical Context:  Decreases inflammation and corneal neovascularization. Suppresses migration of polymorphonuclear leukocytes and reverses increased capillary permeability.

Class Summary

Minimize the activity of inflammatory cells and formation of granulomas. Used in symptomatic patients and commonly provides symptomatic improvement.

Further Outpatient Care

Deterrence/Prevention

Complications

Prognosis

Author

Saadia Zohra Farooqui, MBBS, Aga Khan University Medical College, Pakistan

Disclosure: Nothing to disclose.

Coauthor(s)

C Stephen Foster, MD, FACS, FACR, FAAO, Clinical Professor of Ophthalmology, Harvard Medical School; Consulting Staff, Department of Ophthalmology, Massachusetts Eye and Ear Infirmary; Founder and President, Ocular Immunology and Uveitis Foundation, Massachusetts Eye Research and Surgery Institution

Disclosure: Nothing to disclose.

Joseph JK Ma, MD, Assistant Professor, Department of Ophthalmology, University of Toronto Faculty of Medicine, Canada

Disclosure: Nothing to disclose.

Specialty Editors

Fernando H Murillo-Lopez, MD, Senior Surgeon, Unidad Privada de Oftalmologia CEMES

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Medscape Salary Employment

Christopher J Rapuano, MD, Professor, Department of Ophthalmology, Jefferson Medical College of Thomas Jefferson University; Director of the Cornea Service, Co-Director of Refractive Surgery Department, Wills Eye Institute

Disclosure: Allergan Honoraria Speaking and teaching; Allergan Consulting fee Consulting; Alcon Honoraria Speaking and teaching; RPS Ownership interest Other; Bausch & Lomb Honoraria Speaking and teaching; Merck Consulting fee Consulting; Bausch & Lomb Consulting; Merck Honoraria Speaking and teaching

Ralph Garzia, OD, Assistant Dean for Clinical and Academic Programs, Associate Professor, College of Optometry, University of Missouri at St Louis

Disclosure: Nothing to disclose.

Chief Editor

Hampton Roy Sr, MD, Associate Clinical Professor, Department of Ophthalmology, University of Arkansas for Medical Sciences

Disclosure: Nothing to disclose.

References

  1. Wentworth JS, Paterson CA, Gray RD. Effect of a metalloproteinase inhibitor on established corneal ulcers after an alkali burn. Invest Ophthalmol Vis Sci. Jun 1992;33(7):2174-9. [View Abstract]
  2. Gabison EE, Mourah S, Steinfels E, et al. Differential expression of extracellular matrix metalloproteinase inducer (CD147) in normal and ulcerated corneas: role in epithelio-stromal interactions and matrix metalloproteinase induction. Am J Pathol. Jan 2005;166(1):209-19. [View Abstract]
  3. Shimmura S, Igarashi R, Yaguchi H, et al. Lecithin-bound superoxide dismutase in the treatment of noninfectious corneal ulcers. Am J Ophthalmol. May 2003;135(5):613-9. [View Abstract]
  4. Tripathi BK, Stepp MA, Gao CY, et al. The Cdk5 inhibitor olomoucine promotes corneal debridement wound closure in vivo. Mol Vis. Mar 17 2008;14:542-9. [View Abstract]
  5. Sigelman S, Friedenwald JS. Mitotic and wound-healing activities of the corneal epithelium; effect of sensory denervation. AMA Arch Ophthalmol. Jul 1954;52(1):46-57. [View Abstract]
  6. Nakamura M, Chikama T, Nishida T. Synergistic effect with Phe-Gly-Leu-Met-NH2 of the C-terminal of substance P and insulin-like growth factor-1 on epithelial wound healing of rabbit cornea. Br J Pharmacol. May 1999;127(2):489-97. [View Abstract]
  7. Bonini S, Lambiase A, Rama P, et al. Topical treatment with nerve growth factor for neurotrophic keratitis. Ophthalmology. Jul 2000;107(7):1347-51; discussion 1351-2. [View Abstract]
  8. Dohlman CH, Slansky HH, Laibson PR, et al. Artificial corneal epithelium in acute alkali burns. Ann Ophthalmol. 1969;112.
  9. Kenyon KR, Berman M, Rose J, et al. Prevention of stromal ulceration in the alkali-burned rabbit cornea by glued-on contact lens. Evidence for the role of polymorphonuclear leukocytes in collagen degradation. Invest Ophthalmol Vis Sci. Jun 1979;18(6):570-87. [View Abstract]
  10. Nubile M, Dua HS, Lanzini M, Ciancaglini M, Calienno R, Said DG, et al. In vivo analysis of stromal integration of multilayer amniotic membrane transplantation in corneal ulcers. Am J Ophthalmol. May 2011;151(5):809-822.e1. [View Abstract]
  11. Yoon KC, You IC, Im SK, et al. Application of umbilical cord serum eyedrops for the treatment of neurotrophic keratitis. Ophthalmology. Sep 2007;114(9):1637-42. [View Abstract]
  12. Alio JL, Abad M, Artola A, et al. Use of autologous platelet-rich plasma in the treatment of dormant corneal ulcers. Ophthalmology. Jul 2007;114(7):1286-1293.e1. [View Abstract]
  13. Saika S, Miyamoto T, Yamanaka O, et al. Therapeutic effect of topical administration of SN50, an inhibitor of nuclear factor-kappaB, in treatment of corneal alkali burns in mice. Am J Pathol. May 2005;166(5):1393-403. [View Abstract]
  14. Sosne G, Qiu P, Christopherson PL, et al. Thymosin beta 4 suppression of corneal NFkappaB: a potential anti-inflammatory pathway. Exp Eye Res. Apr 2007;84(4):663-9. [View Abstract]
  15. Saika S, Yamanaka O, Okada Y, et al. Effect of overexpression of PPARgamma on the healing process of corneal alkali burn in mice. Am J Physiol Cell Physiol. Jul 2007;293(1):C75-86. [View Abstract]
  16. Ioannidis AS, Zagora SL, Wechsler AW. A non-healing corneal ulcer as the presenting feature of type 1 diabetes mellitus: a case report. J Med Case Reports. Nov 4 2011;5(1):539. [View Abstract]
  17. Albert DM, Jakobiec FA, eds. Principles and Practice of Ophthalmology. 2nd ed. Boston: WB Saunders Co; 2000.
  18. Dua HS, Gomes JA, Singh A. Corneal epithelial wound healing. Br J Ophthalmol. May 1994;78(5):401-8. [View Abstract]
  19. Geerling G, Joussen AM, Daniels JT, et al. Matrix metalloproteinases in sterile corneal melts. Ann N Y Acad Sci. Jun 30 1999;878:571-4. [View Abstract]
  20. Gipson IK, Inatomi T. Extracellular matrix and growth factors in corneal wound healing. Curr Opin Ophthalmol. Aug 1995;6(4):3-10. [View Abstract]
  21. He J, Bazan NG, Bazan HE. Alkali-induced corneal stromal melting prevention by a novel platelet-activating factor receptor antagonist. Arch Ophthalmol. Jan 2006;124(1):70-8. [View Abstract]
  22. Imanishi J, Kamiyama K, Iguchi I, et al. Growth factors: importance in wound healing and maintenance of transparency of the cornea. Prog Retin Eye Res. Jan 2000;19(1):113-29. [View Abstract]
  23. Kaufman HE, et al, eds. The Cornea. 2nd ed. Boston: Butterworth-Heinemann; 1998.
  24. Nagano T, Nakamura M, Nakata K, et al. Effects of substance P and IGF-1 in corneal epithelial barrier function and wound healing in a rat model of neurotrophic keratopathy. Invest Ophthalmol Vis Sci. Sep 2003;44(9):3810-5. [View Abstract]
  25. Watanabe M, Yano W, Kondo S, et al. Up-regulation of urokinase-type plasminogen activator in corneal epithelial cells induced by wounding. Invest Ophthalmol Vis Sci. Aug 2003;44(8):3332-8. [View Abstract]
  26. Wilson SE, Liu JJ, Mohan RR. Stromal-epithelial interactions in the cornea. Prog Retin Eye Res. May 1999;18(3):293-309. [View Abstract]