The DOI matches its Crossref record.
Growth factors in the anterior segment: role in tissue maintenance, wound healing and ocular pathology.
Abstract
A number of growth factors and their associated receptors, including epidermal growth factor, transforming growth factor-beta, keratinocyte growth factor, hepatocyte growth factor, fibroblast growth factor and platelet-derived growth factor have been detected in the anterior segment of the eye. On binding to cellular receptors, these factors activate signalling cascades, which regulate functions including mitosis, differentiation, motility and apoptosis. Production of growth factors by corneal cells and their presence in the tear fluid and aqueous humour is essential for maintenance and renewal of normal tissue in the anterior eye and the prevention of undesirable immune or angiogenic reactions. Growth factors also play a vital role in corneal wound healing, mediating the proliferation of epithelial and stromal tissue and affecting the remodelling of the extracellular matrix (ECM). These functions depend on a complex interplay between growth factors of different types, the ECM, and regulatory mechanisms of the affected cells. Imbalances may lead to deficient wound healing and various ocular pathologies, including edema, neovascularization and glaucoma. Growth factors may be targeted in therapeutic ophthalmic applications, through exogenous application or selective inhibition, and may be used to elicit specific cellular responses to ophthalmic materials. A thorough understanding of the mechanism and function of growth factors and their actions in the complex environment of the…
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Improved tissue maintenance is typically accompanied by healthy remodeling.
“Finally, improved tissue maintenance is typically accompanied by a healthy remodeling [77, 84, 85]”
From Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin (2020) · cites this paper as [77]
Modulation of multiple key cell-fate regulatory pathways, including attenuation of pSmad2,3 signaling by follistatin, is important for productive cell proliferation and regeneration in skeletal muscle, heart, and generally throughout the body.
“Modulation of multiple key cell-fate regulatory pathways, including attenuation of pSmad2,3 signaling by follistatin, is important for productive cell proliferation and regeneration in skeletal muscle, heart and generally, throughout the body [77–79].”
From Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin (2020) · cites this paper as [77]
Citations
Cites
No references could be resolved yet.
Research works printed but not linked: 91
- Baldwin, 2002, Growth factors in corneal wound healing following refractive surgery: a review, Acta Ophthalmol. Scand., 80, 238, 10.1034/j.1600-0420.2002.800303.x · DOI
- Blake, 1997, Matrix stimulates the proliferation of human corneal endothelial cells in culture, Invest. Ophthalmol. Vis. Sci., 38, 1119
- Boilly, 2000, FGF signals for cell proliferation and migration through different pathways, Cytokine Growth Factor Rev., 11, 295, 10.1016/S1359-6101(00)00014-9 · DOI
- Brown, 1999, Characterization of proteoglycans synthesized by cultured corneal fibroblasts in response to transforming growth factor β and fetal calf serum, J. Biol. Chem., 274, 7111, 10.1074/jbc.274.11.7111 · DOI
- Carpenter, 1979, Epidermal growth factor, Annu. Rev. Biochem., 48, 193, 10.1146/annurev.bi.48.070179.001205 · DOI
- Chirila T.V., 2001. An overview of the development of artificial corneas with porous skirts and the use of PHEMA for such an application. Biomaterials 22, 3311–3317. · DOI
- Chung, 1989, Treatment of rabbit corneal alkali wounds with human epidermal growth factor, Cornea, 8, 122, 10.1097/00003226-198906000-00008 · DOI
- Dinbergs, 1996, Cellular response to transforming growth factor-β1 and basic fibroblast growth factor depends on release kinetics and extracellular matrix interactions, J. Biol. Chem., 271, 29822, 10.1074/jbc.271.47.29822 · DOI
- Dupuy, 2001, Chemotactic penetration of keratocytes in ePTFE polymer in vitro, J. Biomed. Mater. Res., 56, 487, 10.1002/1097-4636(20010915)56:4<487::AID-JBM1120>3.0.CO;2-# · DOI
- Finch, 1989, Human KGF is FGF-related with properties of a paracrine effector of epithelial cell growth, Science, 245, 752, 10.1126/science.2475908 · DOI
- Fini, 1999, Keratocyte and fibroblast phenotypes in the repairing cornea, Prog. Retin. Eye Res., 18, 529, 10.1016/S1350-9462(98)00033-0 · DOI
- Fujikawa, 1984, Basement membrane components in healing rabbit corneal epithelial wounds: immunofluorescence and ultrastructural studies, J. Cell Biol., 98, 128, 10.1083/jcb.98.1.128 · DOI
- Funderburgh, 2001, Proteoglycan expression during transforming growth factor β-induced keratocyte-myofibroblast transdifferentiation, J. Biol. Chem., 276, 44173, 10.1074/jbc.M107596200 · DOI
- Grant, 1992, Effects of epidermal growth factor, fibroblast growth factor, and transforming growth factor-beta on corneal cell chemotaxis, Invest. Ophthalmol. Vis. Sci., 33, 3292
- Grierson, 2000, Hepatocyte growth factor/scatter factor in the eye, Prog. Retin. Eye Res., 19, 779, 10.1016/S1350-9462(00)00015-X · DOI
- Gupta, 1996, Transforming growth factor beta-1 and beta-2 in human tear fluid, Curr. Eye Res., 15, 605, 10.3109/02713689609008900 · DOI
- Hongo, 1992, Distribution of epidermal growth factor (EGF) receptors in rabbit corneal epithelial cells, keratocytes and endothelial cells, and the changes induced by transforming growth factor-β1, Exp. Eye Res., 54, 9, 10.1016/0014-4835(92)90063-X · DOI
- Honma, 1997, Effect of transforming growth factor-β1 and -β2 on in vitro rabbit corneal epithelial cell proliferation promoted by epidermal growth factor, keratinocyte growth factor, or hepatocyte growth factor, Exp. Eye Res., 65, 391, 10.1006/exer.1997.0338 · DOI
- Imanishi, 2000, Growth factors: importance in wound healing and maintenance of transparency of the cornea, Prog. Retin. Eye Res., 19, 113, 10.1016/S1350-9462(99)00007-5 · DOI
- Ito, 1998, Tissue engineering by immobilized growth factors, Mater. Sci. Eng. C, 6, 267, 10.1016/S0928-4931(98)00061-7 · DOI
- Jester, 2002, TGF beta induced myofibroblast differentiation of rabbit keratocytes requires synergistic TGF beta, PDGF and integrin signaling, Exp. Eye Res., 75, 645, 10.1006/exer.2002.2066 · DOI
- Jones, 2000, Connecting signaling and cell cycle progression in growth factor-stimulated cells, Oncogene, 19, 5558, 10.1038/sj.onc.1203858 · DOI
- Jorissen, 2003, Epidermal growth factor receptor: mechanisms of activation and signaling, Exp. Cell Res., 284, 31, 10.1016/S0014-4827(02)00098-8 · DOI · Paper page
- Joussen, 2003, VEGF-dependent conjunctivalization of the corneal surface, Invest. Ophthalmol. Vis. Sci., 44, 117, 10.1167/iovs.01-1277 · DOI
- Kitazawa, 1990, The mechanism of accelerated corneal epithelial healing by human epidermal growth factor, Invest. Ophthalmol. Vis. Sci., 31, 1773
- Klenkler, B.J., Griffith, M., Sheardown, H., 2004. EGF grafted surfaces in artificial corneal applications. Biomaterials. Submitted. · DOI
- Kokawa, 1996, High total TGF-β levels in normal human tears, Curr. Eye Res., 15, 341, 10.3109/02713689609007630 · DOI
- Kruse, 1993, Growth factors modulate clonal growth and differentiation of cultured rabbit limbal and corneal epithelium, Invest. Ophthalmol. Vis. Sci., 34, 1963
- Kuhl, 1996, Tethered epidermal growth factor as a paradigm for growth factor-induced stimulation from the solid phase, Nat. Med., 2, 1022, 10.1038/nm0996-1022 · DOI
- Lambiase, 1998, Topical treatment with nerve growth factor for corneal neurotrophic ulcers, N. Engl. J. Med., 338, 1174, 10.1056/NEJM199804233381702 · DOI
- Lambiase, 1998, Expression of nerve growth factor receptors on the ocular surface in healthy subjects and during manifestation of inflammatory diseases, Invest. Ophthalmol. Vis. Sci., 39, 1272
- Lambiase, 2000, Nerve growth factor promotes corneal healing: structural, biochemical, and molecular analyses of rat and human corneas, Invest. Ophthalmol. Vis. Sci., 41, 1063
- Lambiase, 2002, Intraocular production and release of nerve growth factor after iridectomy, Invest. Ophthalmol. Vis. Sci., 43, 2334
- Li, 1995, Three patterns of cytokine expression potentially involved in epithelial-fibroblast interactions of human ocular surface, J. Cell. Physiol., 163, 61, 10.1002/jcp.1041630108 · DOI
- Li, 1997, Differential regulation of keratinocyte growth factor and hepatocyte growth factor/scatter factor by different cytokines in human corneal and limbal fibroblasts, J. Cell. Physiol., 172, 361, 10.1002/(SICI)1097-4652(199709)172:3<361::AID-JCP10>3.0.CO;2-9 · DOI
- Lim, 2003, Growth factor, cytokine and protease interactions during corneal wound healing, Ocular Surface, 1, 53, 10.1016/S1542-0124(12)70128-3 · DOI
- Lu, 2001, Corneal epithelial wound healing, Exp. Biol. Med., 226, 653, 10.1177/153537020222600711 · DOI
- Majima, 1998, Cell biological analysis with respect to cause of fibrous opacification of the anterior capsule after cataract extraction, Opthalmologica, 212, 364, 10.1159/000027369 · DOI
- Maldonado, 1995, Epidermal growth factor stimulates integrin-mediated cell migration of cultured human corneal epithelial cells on fibronectin and arginine-glycine-aspartic acid peptide, Invest. Ophthalmol. Vis. Sci., 36, 2120
- Maltseva, 2001, Fibroblast growth factor reversal of the corneal myofibroblast phenotype, Invest. Ophthalmol. Vis. Sci., 42, 2490
- McBain, 2003, HGF, MAPK, and a small physiological electric field interact during corneal epithelial cell migration, Invest. Ophthalmol. Vis. Sci., 44, 540, 10.1167/iovs.02-0570 · DOI
- Nakamura, 2003, Potentiation by cyclic AMP of the stimulatory effect of epidermal growth factor on corneal epithelial migration, Cornea, 22, 355, 10.1097/00003226-200305000-00014 · DOI
- Nakamura, 2001, The epidermal growth factor receptor (EGFR): role in corneal wound healing and homeostasis, Exp. Eye Res., 72, 511, 10.1006/exer.2000.0979 · DOI
- Namiki, 1992, Presence of human epidermal growth factor (hEGF), basic fibroblast growth factor (bFGF) in human aqueous, Nippon Ganka Gakkai Zasshi, 96, 652
- Nathan, 1991, Cytokines in context, J. Cell Biol., 113, 981, 10.1083/jcb.113.5.981 · DOI
- Nezu, 1992, Recombinant human epidermal growth factor and corneal neovascularization, Jpn J. Ophthalmol., 36, 401
- Nishida, 1984, Fibronectin synthesis by the rabbit cornea: effects of mouse epidermal growth factor and cyclic AMP analogs, Jpn J. Ophthalmol., 28, 196
- Nishida, 1990, Differential modes of action of fibronectin and epidermal growth factor on rabbit corneal epithelial migration, J. Cell. Physiol., 145, 549, 10.1002/jcp.1041450323 · DOI
- Ohashi, 1989, Presence of epidermal growth factor in human tears, Invest. Ophthalmol. Vis. Sci., 30, 1879
- Ohji, 1993, Transforming growth factor-beta stimulates collagen and fibronectin synthesis by human corneal stromal fibroblasts in vitro, Curr. Eye Res., 12, 703, 10.3109/02713689308995765 · DOI
- Ohji, 1993, Corneal epithelial cell attachment with endogenous laminin and fibronectin, Invest. Ophthalmol. Vis. Sci., 34, 2487
- Parelman, 1990, Epidermal growth factor in human aqueous humor, Am. J. Ophthalmol., 109, 603, 10.1016/S0002-9394(14)70698-1 · DOI
- Pasquale, 1993, Immunolocalization of TGF-beta 1, TGF-beta 2, and TGF-beta 3 in the anterior segment of the human eye, Invest. Ophthalmol. Vis. Sci., 34, 23
- Rieck, 2001, Intracellular signaling pathway of FGF-2-modulated corneal endothelial cell migration during wound healing in vitro, Exp. Eye Res., 73, 639, 10.1006/exer.2001.1067 · DOI
- Roberts, 2002, The ever-increasing complexity of TGF-β signaling, Cytokine Growth Factor Rev., 13, 3, 10.1016/S1359-6101(01)00027-2 · DOI
- Rolando, 2001, The ocular surface and tear film and their dysfunction in dry eye disease, Surv. Ophthalmol., 45, S203, 10.1016/S0039-6257(00)00203-4 · DOI
- Rubin, 1989, Purification and characterization of a newly identified growth factor specific for epithelial cells, Proc. Natl Acad. Sci. USA, 86, 802, 10.1073/pnas.86.3.802 · DOI
- Saghizadeh, 2001, Altered expression of growth factors and cytokines in keratoconus, bullous keratopathy and diabetic human corneas, Exp. Eye Res., 73, 179, 10.1006/exer.2001.1028 · DOI
- Sakamoto, 2000, Blockade of TGF-β by in vivo gene transfer of a soluble TGF-β type II receptor in the muscle inhibits corneal opacification, edema and angiogenesis, Gene Ther., 7, 1915, 10.1038/sj.gt.3301320 · DOI
- Sheardown, 1996, Mechanisms of corneal epithelial wound healing, Chem. Eng. Sci., 51, 4517, 10.1016/0009-2509(96)00299-0 · DOI
- Shimmura, S., Doillon, C.J., Griffith, M., Nakamura, M., Gagnon, E., Usui, A., Tsubota, K., 2003. Collagen‐poly (N‐isopropylacrylamide) based membranes for corneal stroma scaffolds. Cornea 22, S81–S88. · DOI
- Smith, 1998, Clearing the cornea with nerve growth factor, N. Engl J. Med., 338, 1222, 10.1056/NEJM199804233381710 · DOI
- Song, 2001, Injury and EGF mediate the expression of α6β4 integrin subunits in corneal epithelium, J. Cell. Biochem., 80, 397, 10.1002/1097-4644(20010301)80:3<397::AID-JCB140>3.0.CO;2-W · DOI
- Song, 2002, TGF-β1 regulates TGF-β1 and FGF-2 mRNA expression during fibroblast wound healing, Mol. Pathol., 55, 164, 10.1136/mp.55.3.164 · DOI
- Song, 2003, Role of epidermal growth factor and epidermal growth factor receptor on hemidesmosome complex formation and integrin subunit β4, Cell Tissue Res., 312, 203, 10.1007/s00441-002-0693-x · DOI
- Sorkin, 2002, Signal transduction and endocytosis: close encounters of many kinds, Nat. Rev. Mol. Cell. Biol., 3, 600, 10.1038/nrm883 · DOI
- Sotozono, 1994, Paracrine role of keratinocyte growth factor in rabbit corneal epithelial cell growth, Exp. Eye Res., 59, 385, 10.1006/exer.1994.1122 · DOI
- Streilein, 2000, Does innate immune privilege exist?, J. Leukoc. Biol., 67, 479, 10.1002/jlb.67.4.479 · DOI
- Streilein, 2002, The eye's view of antigen presentation, Hum. Immunol., 63, 435, 10.1016/S0198-8859(02)00393-2 · DOI
- Suuronen, E.J., Nakamura, M., Watsky, M.A., Stys, P.K., Muller, L.J., Munger, R., Shinozaki, N., Griffith, M., 2004. Innervated human corneal equivalents as in vitro models for nerve‐target cell interactions. FASEB J. 18, 170–172. · DOI
- Suzuki, 2003, Cell-matrix and cell–cell interactions during corneal epithelial wound healing, Prog. Retin. Eye Res., 22, 113, 10.1016/S1350-9462(02)00042-3 · DOI
- Taniguchi, 1991, The effect of recombinant epidermal growth factor in corneal angiogenesis, Nippon Ganka Gakkai Zasshi, 95, 52
- Tervo, 1997, Tear hepatocyte growth factor (HGF) availability increases markedly after excimer laser surface ablation, Exp. Eye Res., 64, 501, 10.1006/exer.1996.0226 · DOI
- Trinkaus-Randall, 1998, Biological response to a synthetic cornea, J. Control. Release, 53, 205, 10.1016/S0168-3659(97)00254-X · DOI
- Tripathi, 1991, Analysis of human aqueous humor for epidermal growth factor, Exp. Eye. Res., 53, 407, 10.1016/0014-4835(91)90247-C · DOI
- Tripathi, 1994, Trabecular cells express the TGF-β2 gene and secrete the cytokine, Exp. Eye Res., 58, 523, 10.1006/exer.1994.1046 · DOI
- Tripathi, 1994, Aqueous humor in glaucomatous eyes contains an increased level of TGF-β2, Exp. Eye Res., 59, 723, 10.1006/exer.1994.1158 · DOI
- Van Setten, 1997, Vascular endothelial growth factor (VEGF) in normal human corneal epithelium: detection and physiological importance, Acta Ophthalmol. Scand., 75, 649, 10.1111/j.1600-0420.1997.tb00623.x · DOI
- Van Setten, 1996, Growth factors and their receptors in the anterior chamber. Absence of epidermal growth factor and transforming growth factor alpha in human aqueous humor, Ophthalmic Res., 28, 361
- Welge-Lüβen, 2001, Role of tissue growth factors in aqueous humor homeostasis, Curr. Opin. Ophthalmol., 12, 94, 10.1097/00055735-200104000-00003 · DOI
- Wilson, 1999, Stimulus-specific and cell type-specific cascades: emerging principles relating to control of apoptosis in the eye, Exp. Eye Res., 69, 255, 10.1006/exer.1999.0698 · DOI
- Wilson, 1994, Epidermal growth factor, transforming growth factor alpha, transforming growth factor beta, acidic fibroblast growth factor, basic fibroblast growth factor, and interleukin-1 proteins in the cornea, Exp. Eye Res., 59, 63, 10.1006/exer.1994.1081 · DOI
- Wilson, 1994, Effect of epidermal growth factor, hepatocyte growth factor, and keratinocyte growth factor, on proliferation, motility and differentiation of human corneal epithelial cells, Exp. Eye Res., 59, 665, 10.1006/exer.1994.1152 · DOI
- Wilson, 1999, Expression of HGF, KGF, EGF and receptor messenger RNAs following corneal epithelial wounding, Exp. Eye Res., 68, 377, 10.1006/exer.1998.0603 · DOI
- Wilson, 1999, Stromal–epithelial interactions in the cornea, Prog. Retin. Eye Res., 18, 293, 10.1016/S1350-9462(98)00017-2 · DOI
- Wilson, 1999, Lacrimal gland HGF, KGF, and EGF mRNA levels increase after corneal epithelial wounding, Invest. Ophthalmol. Vis. Sci., 40, 2185
- Wilson, 2001, The corneal wound healing response: cytokine-mediated interaction of the epithelium, stroma, and inflammatory cells, Prog. Retin. Eye Res., 20, 625, 10.1016/S1350-9462(01)00008-8 · DOI
- Wu, 1998, In vivo comparison of three different porous materials intended for use in a keratoprosthesis, Br. J. Ophthalmol., 82, 569, 10.1136/bjo.82.5.569 · DOI
- Yanai, 2002, Mitogenic and antiapoptotic effects of various growth factors on human corneal fibroblasts, Invest. Ophthalmol. Vis. Sci., 43, 2122
- You, 2000, Neurotrophic factors in the human cornea, Invest. Ophthalmol. Vis. Sci., 41, 692
- Zhao, 2001, Role of tears in keratocyte loss after epithelial removal in mouse cornea, Invest. Ophthalmol. Vis. Sci., 42, 1743
Cited by
Sorted by citations
Rejuvenation of three germ layers tissues by exchanging old blood plasma with saline-albumin
Mehdipour, M., Skinner, C., Wong, N., Lieb, M., Liu, C., Etienne, J., Kato, C., Kiprov, D., Conboy, M. J., & Conboy, I. M. (2020) · Aging · doi:10.18632/aging.103418 · Cited by 115
Keeping an Eye on Decellularized Corneas: A Review of Methods, Characterization and Applications
Wilson, S., Sidney, L., Dunphy, S., Rose, J., & Hopkinson, A. (2013) · Journal of Functional Biomaterials · doi:10.3390/jfb4030114 · Cited by 100
Lee, J. H., Ryu, I. H., Kim, E. K., Lee, J. E., Hong, S., & Lee, H. K. (2006) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.05-0596 · Cited by 17
Metadata
- Authors
- Klenkler, B., & Sheardown, H.
- Venue
- Experimental Eye Research
- Publisher
- Elsevier BV
- Published
- 2004-11
- Volume
- 79
- Issue
- 5
- Pages
- 677-688
- ISSN
- 0014-4835
- Cited by
- 146
- References
- 0
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review