IOVS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

(Investigative Ophthalmology and Visual Science. 2003;44:590-593.)
© 2003 by The Association for Research in Vision and Ophthalmology, Inc.
DOI:  10.1167/iovs.02-0685
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ambati, B. K.
Right arrow Articles by Ambati, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ambati, B. K.
Right arrow Articles by Ambati, J.

Sustained Inhibition of Corneal Neovascularization by Genetic Ablation of CCR5

Balamurali K. Ambati,1,2 Akshay Anand,3 Antonia M. Joussen,2,4 William A. Kuziel,5 Anthony P. Adamis,2,6 and Jayakrishna Ambati2,3

1From the Department of Ophthalmology, Medical College of Georgia, Augusta, Georgia; the 3Department of Ophthalmology, University of Kentucky, Lexington, Kentucky; the 4Department of Vitreoretinal Surgery, Center of Ophthalmology, University of Cologne, Cologne, Germany; the 5Section of Molecular Genetics and Microbiology and Institute for Cellular and Molecular Biology, University of Texas, Austin, Texas; the 2Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, Massachusetts; and 6Eyetech Pharmaceuticals, Woburn, Massachusetts.


   Abstract
Top
 Abstract
Methods
 Results
 Discussion
 References
 
PURPOSE. To determine whether genetic ablation of the CC chemokine receptor CCR5 (involved in leukocyte and endothelial chemotaxis) inhibits the development of corneal neovascularization.

METHODS. Wild-type C57BL/6J mice and species-specific counterparts with targeted homozygous disruption of the CCR5 gene underwent chemical and mechanical denudation of corneal and limbal epithelium. Corneas were harvested 2 and 4 weeks after injury. Neovascularization was quantified by CD31 immunostaining. Expression of VEGF protein was quantified by ELISA.

RESULTS. The mean percentages of neovascularized corneal area in control mice and CCR5-deficient mice 2 weeks after denudation were 58.3% and 38.5% (P = 0.05), respectively. At 4 weeks after denudation, the corresponding percentages were 67.6% and 44.0% (P = 0.028). In CCR5-deficient mice, VEGF protein levels were reduced 51.1% at 2 weeks (P = 0.05) after injury and 37.3% at 4 weeks (P = 0.03).

CONCLUSIONS. CCR5-deficient mice showed a persistent 34% to 35% inhibition of corneal neovascularization for up to 4 weeks. This inhibition correlates with reduced expression of VEGF. These data implicate CCR5 as one essential component in the development of corneal neovascularization.

Corneal neovascularization (CNV) is a central feature in the pathogenesis of many blinding corneal disorders and a major sight-threatening complication in corneal infections and chemical injury and after keratoplasty, in which neovascularization adversely impacts corneal graft survival.1

Although the molecular mechanisms underlying CNV have not been fully deciphered, vascular endothelial growth factor (VEGF) seems to play an indispensable role. It induces CNV when applied exogenously2 and is the principal endogenous angiogenic force in the neovascularization that follows limbal injury.3 Transmigrating and invading corneal leukocytes appear to provide much of the requisite VEGF that drives CNV.3

The recruitment of leukocytes to inflammatory sites is mediated by chemokines. Chemokines bind to specific receptors that, despite some redundancy, show specificity for individual chemokines. Evidence is emerging that individual chemokines attract specific leukocyte populations through processes determined by ligand specificity and the expression patterns of the corresponding receptors.4 CCR5 receptor ligands include the macrophage inflammatory proteins (MIPs) 1{alpha} and 1ß, which recruit both macrophages and neutrophils.5 6

Endothelial cell migration and proliferation are also essential to angiogenesis, and these processes are known to be influenced by vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF).7 8 Further, endothelial cell chemotaxis and/or proliferation can be stimulated by chemokines, including interleukin (IL)-8, monocyte chemotactic protein (MCP)-1, regulated on activation normal T-cell expressed and secreted (RANTES), and MIP-1{alpha} and -1ß.9 10

Previous work has confirmed that corneal angiogenesis is driven in large part by inflammatory mediators.11 12 MIP-1{alpha} has been associated with CNV in helminth keratitis,13 shown to be required for the development of CNV in HSV keratitis14 15 and demonstrated to be angiogenic in Kaposi’s sarcoma–associated herpes virus infection.16 It has also been associated with angiogenesis in corneal allograft rejection.17 18 Its receptor, CCR5, also found on endothelial cells, is a receptor for CC chemokines that are involved in angiogenesis, including RANTES and MIP-1{alpha} and -1ß.10 19

We therefore examined the role of CCR5 in a clinically relevant ocular model of corneal injury by studying the neovascular response of animals genetically deficient in these molecules.


   Methods
Top
 Abstract
 Methods
Results
 Discussion
 References
 
All animal experiments were approved by the Massachusetts Eye and Ear Infirmary Animal Care Committee and the University of Kentucky Animal Care Committee and conformed to the ARVO Statement for the Use of Animals in Ophthalmic and Vision Research. Mice were anesthetized by intramuscular injection of 50 mg/kg ketamine hydrochloride (Abbott Laboratories, N. Chicago, IL) and 10 mg/kg xylazine (Bayer, Shawnee Mission, KS). Animals were killed by a lethal dose of pentobarbital (150 mg/kg).

Animals
Wild-type C57BL/6J mice (Jackson Laboratories, Bar Harbor, ME) were used as controls. To create the CCR-knockout strain, the entire CCR5 coding region was replaced by insertion of a neomycin-resistant expression cassette, as described previously.20 21 Although the original knockout strains were generated on a mixed C57BL/6 x 129/Ola genetic background, the mice used in the experiments described herein represent the progeny of the eighth generation backcross of the knockout mutations to inbred C57BL/6 animals. Because the CCR2 and CCR5 genes are very closely linked, a wild-type control strain for both knockout strains was developed by backcrossing the wild-type CCR5 locus from 129/Ola to the C57BL/6 background for eight generations. This control strain minimizes the genetic differences flanking the targeted allele. Wild-type C57BL/6 and 129/Ola CCR5 genes were distinguished by the presence of a BglII restriction fragment length polymorphism.20

Genotype Analysis
The genotype of all experimental animals was determined on tail DNA samples. CCR5 knockout alleles were identified by PCR analysis with a set of four primers. Wild-type CCR5 alleles were identified by synthesis of a 450-bp PCR product with primers complementary to sequences on each side of the crossover site (primer 1, 5'-AAGCAGGAGGATCGTGAGCTTGAC-3', and primer 2, 5'-GAAACAAGTTGTTGTGCACCTCAG-3'). Disrupted CCR5 alleles were identified by synthesis of a 350-bp PCR product with a primer that is complementary to a sequence in the neomycin resistance coding region (primer 3, 5'-TTCCATTGCTCAGCGGTGCT-3') combined with a primer complementary to a CCR5 sequence downstream of the crossover site (primer 4, 5'-TGTTTCCTCCTCTAGCCTTCACTATG-3').

Experimental Design
Both groups of mice (control, CCR5 knockout) underwent corneal injury. Corneas were harvested 2 and 4 weeks after injury. An image analyzer was used by a masked investigator to quantify neovascularization in immunostained corneas.

Model of Corneal Neovascularization
Topical proparacaine and 2 µL of 0.15 M NaOH were applied to the right cornea of each mouse. The corneal and limbal epithelia were removed with a Tooke corneal knife (Katena Products, Denville, NJ) in a rotary motion parallel to the limbus. Erythromycin ophthalmic ointment was instilled immediately after epithelial denudation.

Labeling of Corneal Neovascularization
Immunohistochemical staining for vascular endothelial cells was performed on corneal flatmounts. Fresh corneas were dissected, rinsed in PBS for 30 minutes, and fixed in 100% acetone (Sigma, St. Louis, MO) for 20 minutes. After the corneas were washed in PBS, nonspecific binding was blocked with 0.1 M PBS, 2% albumin (Sigma) for 1 hour at room temperature. Incubation with FITC-coupled monoclonal anti-mouse CD31 antibody (Pharmingen) at a concentration of 1:500 in 0.1 M PBS, 2% albumin at 4°C overnight was followed by subsequent washes in PBS at room temperature. Corneas were mounted with an antifading agent (Gelmount; Biomeda, Inc, San Francisco, CA) and visualized with a fluorescence microscope (Leica, Wetzlar, Germany).

Quantification of Corneal Neovascularization
Digital quantification of corneal neovascularization has been described.22 23 Images of the corneal vasculature were captured with a CD-330 charge-coupled device (CCD) camera (Dage-MIT, Inc., Michigan City, IN) attached to a fluorescence microscope (MZ FLIII; Leica Microsystems Inc., Deerfield, IL). The images were analyzed on computer (Openlab; Improvision Inc., Lexington, MA), resolved at 624 x 480 pixels, and converted to tagged information file format (TIFF) files. The neovascularization was quantified by setting a threshold level of fluorescence above which only vessels were captured. The entire mounted cornea was analyzed to minimize sampling bias. The quantification of the neovascularization was performed in masked fashion. The total corneal area was outlined, with the innermost vessel of the limbal arcade used as the border. The total area of neovascularization was then normalized to the total corneal area, and the percentage of the cornea covered by vessels was calculated.

Corneal Harvest for ELISA
At 1, 3, 14, and 21 days, scraped corneas were dissected and placed in 60 µL lysis buffer (20 mM imidazole hydrochloride, 10 mM potassium chloride, 1 mM magnesium chloride, 10 mM EGTA, 1% Triton, 10 mM sodium fluoride, 1 mM sodium molybdate, and 1 mM EDTA [pH 6.8]), supplemented with protease inhibitor (Sigma) followed by homogenization. The lysate was cleared of debris by centrifugation at 14,000 rpm for 15 minutes (4°C), and the supernatant was collected. Total protein was determined with a Bradford protein assay (Bio-Rad, Hercules, CA).

VEGF ELISA
VEGF was determined by a commercially available ELISA kit (R&D Systems, Minneapolis, MN) which recognizes the 164-amino-acid splice variant of mouse VEGF. The assay was performed according to the manufacturer’s instructions. Briefly, standards or tissue samples (50 µL) were pipetted into an antibody-coated 96-well plate containing 50 µL of assay diluent and incubated for 2 hours at RT on a shaker. The wells were then washed five times with wash buffer, 100 µL of VEGF conjugate was added, and the samples were again incubated for 2 hours at RT. Samples were washed five times, 100 µL substrate buffer was added, the samples were incubated for 30 minutes at RT, the reaction was stopped, and the absorption was measured with an ELISA reader (Emax; Molecular Devices, Sunnyvale, CA) at 450 nm with lambda correction at 570 nm. All measurements were performed in duplicate. The lower limit of ELISA was 3.0 pg/mL. The tissue sample concentration was calculated from the standard curve and corrected for total protein.

Statistics
Data were analyzed by the Kruskal-Wallis test with the Dunn test for multiple comparisons (SPSS, Inc., Chicago, IL). Type I error not exceeding 0.05 was deemed significant.


   Results
Top
 Abstract
 Methods
 Results
Discussion
 References
 
Data on (mean ± SEM) percentages of neovascularized cornea area in mice 2 and 4 weeks after corneal scraping and implantation are presented in Figure 1 .



View larger version (17K):
[in this window]
[in a new window]
  		FIGURE 1. Mean ± SEM fraction of corneal neovascularization, 2 and 4 weeks after denudation in control ({blacksquare}) and CCR5-deficient () mice.

 
Percentage Area of Corneal Neovascularization
At 2 weeks after denudation, CCR5-/- mice (n = 8) had 34.0% less (P = 0.05) neovascularized corneal area than control mice (n = 13). At 4 weeks after denudation, CCR5-/- mice (n = 6) had 34.9% less neovascularized corneal area than control mice (P = 0.028). Representative images are shown in Figure 2 .



View larger version (124K):
[in this window]
[in a new window]
  		FIGURE 2. Representative photographs of corneal flatmounts of control (A, C) and CCR5-deficient (B, D) mouse eyes, 2 (A, B) and 4 (C, D) weeks after corneal injury, stained with FITC-coupled monoclonal murine anti-CD31 antibody to visualize endothelial cells.

 
VEGF Expression
Data are presented in Figure 3 . CCR5-/- mice had 51.1% less corneal VEGF than control mice at 14 days after scraping (P = 0.05) and 37.3% less VEGF at 21 days after scraping (P = 0.03).



View larger version (11K):
[in this window]
[in a new window]
  		FIGURE 3. Mean VEGF ± SEM protein expression, normalized to total corneal protein, 2 and 4 weeks after denudation in control ({blacksquare}) and CCR5-deficient ({square}) mice.

 

   Discussion
Top
 Abstract
 Methods
 Results
 Discussion
References
 
In this study, CCR5-deficient mice experienced a sustained inhibition of corneal neovascularization after chemical and mechanical denudation of corneal epithelium, an effect correlated with reduced VEGF expression. These data implicate CCR5 as one of the components in the development of corneal neovascularization, probably because of the effects of this receptor and ligands on endothelial cells and macrophages. Endothelial cells possess CCR519 24 25 and undergo chemotaxis in response to RANTES, MIP-1{alpha}, and MIP-1ß (ligands for CCR5).10

Macrophage involvement in corneal neovascularization is well known24 and infiltration of these cells, which is closely associated with neovascularization, peaks 2 weeks after corneal injury.25 Use of manumycin, a Ras farnesyltransferase inhibitor, inhibits CNV and infiltration of macrophages (but not that of neutrophils).26 Pharmacologic depletion of macrophages dramatically limits CNV in corneal allograft rejection.27 Increased expression of VEGF after corneal injury has been localized to infiltrating inflammatory cells, especially macrophages, after corneal injury,3 which probably accounts for the reduced expression of VEGF observed in this study.

CCR5 plays a role in chemotaxis of mature macrophages, because MIP-1{alpha} is chemotactic for differentiated macrophages.28 29 MIP-1{alpha} is correlated with corneal infiltration of leukocytes, and antibodies to MIP-1{alpha} reduce corneal opacification in herpetic keratitis.30 Previous reports have found upregulation of MIP-1{alpha} after alkali injury, Pseudomonas infection, and HSV infection.30 31 32 A proximate role of MIP-1{alpha}, and thus CCR5, is likely, because it is produced by the corneal stroma in response to injury.31 33

Because inhibition of CNV in CCR5-deficient mice is only approximately one third, it is clear that other mechanisms are involved. However, we may speculate as to the reasons for the persistent inhibition of corneal neovascularization observed in CCR5-/- mice. First, CCR5 may be involved in migration and proliferation of endothelial cells. Second, the reduced expression of VEGF in this model (and thus diminished angiogenic stimulus) may have been due to decreased macrophage infiltration.

In the present study, neovascularization was persistently inhibited in CCR5-deficient mice, which points the way toward a possible therapeutic target for pharmacologic agents. That this inhibition was demonstrated in a mechanical and chemical corneal trauma increases its clinical relevance. The method of inducing neovascularization affects pharmacologic efficacy—for example, integrin antagonists inhibit bFGF-induced corneal neovascularization but not that caused by chemical injury.34

In summary, this finding could advance the management of blinding disorders such as Stevens-Johnson syndrome, cicatricial pemphigoid, corneal allograft rejection, and corneal injury from infection, trauma, or alkali. Future research should also characterize the effect of and the complex molecular interplay among chemokines, leukocytes, and neovascularization and extend this model to other sites of ocular neovascularization.


   Footnotes
 
Supported by the Heed Ophthalmic Foundation (BKA), American Ophthalmological Society-Knapp Testimonial Fund (JA), a Foundation Fighting Blindness Career Development Award (JA), University of Kentucky Physician-Scientist Award (JA), Grant Jo 324/2-1 from the German Research Foundation (AMJ), the National Eye Institute (APA), Massachusetts Lions Eye Research Fund (APA), and the Roberta Siegel Research Fund (APA).

Submitted for publication July 9, 2002; revised August 19, 2002; accepted September 29, 2002.

Disclosure: B.K. Ambati, None; A. Anand, None; A.M. Joussen, None; W.A. Kuziel, None; A.P. Adamis, Eyetech Pharmaceuticals (E); J. Ambati, None

The publication costs of this article were defrayed in part by page charge payment. This article must therefore be marked "advertisement" in accordance with 18 U.S.C. §1734 solely to indicate this fact.

Corresponding author: Jayakrishna Ambati, Department of Ophthalmology, University of Kentucky, 801 Rose Street, Lexington, KY 40536-0284; jamba2{at}uky.edu.


   References
Top
 Abstract
 Methods
 Results
 Discussion
 References
 

  1. Epstein, RJ, Stulting, RD, Hendricks, RL, Harris, DM. (1987) Corneal neovascularization: pathogenesis and inhibition Cornea 6,250-257[Medline][Order article via Infotrieve]
  2. Kenyon, BM, Voest, EE, Chen, CC, Flynn, E, Folkman, J, D’Amato, RJ. (1996) A model of angiogenesis in the mouse cornea Invest Ophthalmol Vis Sci 37,1625-1632[Abstract/Free Full Text]
  3. Amano, S, Rohan, R, Kuroki, M, Tolentino, M, Adamis, AP. (1998) Requirement for vascular endothelial growth factor in wound- and inflammation-related corneal neovascularization Invest Ophthalmol Vis Sci 39,18-22[Abstract/Free Full Text]
  4. Kim, CH, Broxmeyer, HE. (1999) Chemokines: signal lamps for trafficking of T and B cells for development and effector function J Leukoc Biol 65,6-15[Abstract]
  5. Raport, CJ, Gosling, J, Schweickart, VL, Gray, PW, Charo, IF. (1996) Molecular cloning and functional characterization of a novel human CC chemokine receptor (CCR5) for RANTES, MIP-1beta, and MIP-1alpha J Biol Chem 271,17161-17166[Abstract/Free Full Text]
  6. Samson, M, LaRosa, G, Libert, F, et al (1997) The second extracellular loop of CCR5 is the major determinant of ligand specificity J Biol Chem 272,24934-24941[Abstract/Free Full Text]
  7. Risau, W. (1997) Mechanisms of angiogenesis Nature 386,671-674[CrossRef][Medline][Order article via Infotrieve]
  8. Lindner, V, Majack, RA, Reidy, MA. (1990) Basic fibroblast growth factor stimulates endothelial regrowth and proliferation in denuded arteries J Clin Invest 85,2004-2008
  9. Koch, AE, Polverini, PJ, Kunkel, SL, et al (1992) Interleukin-8 as a macrophage-derived mediator of angiogenesis Science 258,1798-1801[Abstract/Free Full Text]
  10. Berger, O, Gan, X, Gujuluva, C, et al (1999) CXC and CC chemokine receptors on coronary and brain endothelia Mol Med 5,795-805[Medline][Order article via Infotrieve]
  11. Moromizato, Y, Stechschulte, S, Miyamoto, K, et al (2000) CD18 and ICAM-1-dependent corneal neovascularization and inflammation after limbal injury Am J Pathol 157,1277-1281[Abstract/Free Full Text]
  12. Philipp, W, Speicher, L, Humpel, C. (2000) Expression of vascular endothelial growth factor and its receptors in inflamed and vascularized human corneas Invest Ophthalmol Vis Sci 41,2514-2522[Abstract/Free Full Text]
  13. Pearlman, E, Hall, LR, Higgins, AW, et al (1998) The role of eosinophils and neutrophils in helminth-induced keratitis Invest Ophthalmol Vis Sci 39,1176-1182[Abstract/Free Full Text]
  14. Chang, E, Galle, L, Maggs, D, Estes, DM, Mitchell, WJ. (2000) Pathogenesis of herpes simplex virus type 1-induced corneal inflammation in perforin-deficient mice J Virol 74,11832-11840[Abstract/Free Full Text]
  15. Tumpey, TM, Cheng, H, Cook, DN, Smithies, O, Oakes, JE, Lausch, RN. (1998) Absence of macrophage inflammatory protein-1{alpha} prevents the development of blinding herpes stromal keratitis J Virol 72,3705-3710[Abstract/Free Full Text]
  16. Boshoff, C, Endo, Y, Collins, PD, et al (1997) Angiogenic and HIV-inhibitory functions of KSHV-encoded chemokines Science 278,290-294[Abstract/Free Full Text]
  17. Torres, PF, De Vos, AF, van der Gaag, R, Martins, B, Kijlstra, A. (1996) Cytokine mRNA expression during experimental corneal allograft rejection Exp Eye Res 63,453-461[CrossRef][Medline][Order article via Infotrieve]
  18. King, WJ, Comer, RM, Hudde, T, Larkin, DF, George, AJ. (2000) Cytokine and chemokine expression kinetics after corneal transplantation Transplantation 70,1225-1233[Medline][Order article via Infotrieve]
  19. Schecter, AD, Calderon, TM, Berman, AB, et al (2000) Human vascular smooth muscle cells possess functional CCR5 J Biol Chem 275,5466-5471[Abstract/Free Full Text]
  20. Kuziel, WA, Maeda, N. (1998) CCR2 and CCR5 Mak, TW eds. The Gene Knockout Facts Book ,118-121 Academic Press London.
  21. Huffnagle, GB, McNeil, LK, McDonald, RA, et al (1999) Cutting edge: role of C-C chemokine receptor 5 in organ-specific and innate immunity to Cryptococcus neoformans J Immunol 163,4642-4646[Abstract/Free Full Text]
  22. Proia, AD, Chandler, DB, Haynes, WL, et al (1988) Quantitation of corneal neovascularization using computerized image analysis Lab Invest 58,473-479[Medline][Order article via Infotrieve]
  23. Goede, V, Schmidt, T, Kimmina, S, Kozian, D, Augustin, HG. (1998) Analysis of blood vessel maturation processes during cyclic ovarian angiogenesis Lab Invest 78,1385-1394[Medline][Order article via Infotrieve]
  24. Polverini, PJ, Cotran, PS, Gimbrone, MA, Jr, Unanue, ER. (1977) Activated macrophages induce vascular proliferation Nature 269,804-806[CrossRef][Medline][Order article via Infotrieve]
  25. Ding, Z, He, Y, Wei, H. (1995) A morphological study of experimental corneal neovascularization [in Chinese] Chung Hua Yen Ko Tsa Chih 31,49-51[Medline][Order article via Infotrieve]
  26. Sonoda, K, Sakamoto, T, Yoshikawa, H, et al (1998) Inhibition of corneal inflammation by the topical use of Ras farnesyltransferase inhibitors: selective inhibition of macrophage localization Invest Ophthalmol Vis Sci 39,2245-2251[Abstract/Free Full Text]
  27. Van der Veen, G, Broersma, L, Dijkstra, CD, Van Rooijen, N, Van Rij, G, Van der Gaag, R. (1994) Prevention of corneal allograft rejection in rats treated with subconjunctival injections of liposomes containing dichloromethylene diphosphonate Invest Ophthalmol Vis Sci 35,3505-3515[Abstract/Free Full Text]
  28. Kaufmann, A, Salentin, R, Gemsa, D, Sprenger, H. (2001) Increase of CCR1 and CCR5 expression and enhanced functional response to MIP-1{alpha} during differentiation of human monocytes to macrophages J Leukoc Biol 69,248-252[Abstract/Free Full Text]
  29. Fantuzzi, L, Borghi, P, Ciolli, V, Pavlakis, G, Belardelli, F, Gessani, S. (1999) Loss of CCR2 expression and functional response to monocyte chemotactic protein (MCP-1) during the differentiation of human monocytes: role of secreted MCP-1 in the regulation of the chemotactic response Blood 94,875-883[Abstract/Free Full Text]
  30. Tumpey, TM, Cheng, H, Yan, XT, et al (1998) Chemokine synthesis in the HSV-1-infected cornea J Leukoc Biol 63,486-492[Abstract]
  31. Sosne, G, Szliter, EA, Barrett, R, et al (2002) Thymosin beta 4 promotes corneal wound healing and decreases inflammation in vivo following alkali injury Exp Eye Res 74,293-299[CrossRef][Medline][Order article via Infotrieve]
  32. Kernacki, KA, Barrett, RP, McClellan, S, et al (2001) MIP-1alpha regulates CD4+ T cell chemotaxis and indirectly enhances PMN persistence in Pseudomonas aeruginosa corneal infection J Leukoc Biol 70,911-919[Abstract/Free Full Text]
  33. Hall, LR, Diaconu, E, Patel, R, et al (2001) CXC chemokine receptor 2 but not C-C chemokine receptor 1 expression is essential for neutrophil recruitment to the cornea in helminth-mediated keratitis (river blindness) J Immunol 166,4035-4041[Abstract/Free Full Text]
  34. Klotz, O, Park, JK, Pleyer, U, et al (2000) Inhibition of corneal neovascularization by alpha(v)-integrin antagonists in the rat Graefes Arch Clin Exp Ophthalmol 238,88-93[CrossRef][Medline][Order article via Infotrieve]



This article has been cited by other articles:


Home page
 J. Immunol.Home page
P. Lu, L. Li, K. Kuno, Y. Wu, T. Baba, Y.-y. Li, X. Zhang, and N. Mukaida
Protective Roles of the Fractalkine/CX3CL1-CX3CR1 Interactions in Alkali-Induced Corneal Neovascularization through Enhanced Antiangiogenic Factor Expression
J. Immunol., March 15, 2008; 180(6): 4283 - 4291.
[Abstract] [Full Text] [PDF]

Home page
 IOVSHome page
T. Usui, S. Yamagami, S. Kishimoto, Y. Seiich, T. Nakayama, and S. Amano
Role of Macrophage Migration Inhibitory Factor in Corneal Neovascularization
Invest. Ophthalmol. Vis. Sci., August 1, 2007; 48(8): 3545 - 3550.
[Abstract] [Full Text] [PDF]

Home page
 IOVSHome page
P. D. Jani, N. Singh, C. Jenkins, S. Raghava, Y. Mo, S. Amin, U. B. Kompella, and B. K. Ambati
Nanoparticles Sustain Expression of Flt Intraceptors in the Cornea and Inhibit Injury-Induced Corneal Angiogenesis
Invest. Ophthalmol. Vis. Sci., May 1, 2007; 48(5): 2030 - 2036.
[Abstract] [Full Text] [PDF]

Home page
 IOVSHome page
S. Dell, S. Peters, P. Muther, N. Kociok, and A. M. Joussen
The Role of PDGF Receptor Inhibitors and PI3-Kinase Signaling in the Pathogenesis of Corneal Neovascularization
Invest. Ophthalmol. Vis. Sci., May 1, 2006; 47(5): 1928 - 1937.
[Abstract] [Full Text] [PDF]

Home page
 IOVSHome page
N. Singh, S. Amin, E. Richter, S. Rashid, V. Scoglietti, P. D. Jani, J. Wang, R. Kaur, J. Ambati, Z. Dong, et al.
Flt-1 Intraceptors Inhibit Hypoxia-Induced VEGF Expression In Vitro and Corneal Neovascularization In Vivo
Invest. Ophthalmol. Vis. Sci., May 1, 2005; 46(5): 1647 - 1652.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ambati, B. K.
Right arrow Articles by Ambati, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ambati, B. K.
Right arrow Articles by Ambati, J.

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS