Inhibition of corneal neovascularization by genetic ablation of CCR2

被引:38
作者
Ambati, BK [1 ]
Joussen, AM
Kuziel, WA
Adamis, AP
Ambati, J
机构
[1] Med Coll Georgia, Dept Ophthalmol, Augusta, GA 30907 USA
[2] Harvard Univ, Sch Med, Massachusetts Eye & Ear Infirm, Dept Ophthalmol, Boston, MA 02114 USA
[3] Univ Cologne, Ctr Ophthalmol, Dept Vitreoretinal Surg, D-50931 Cologne, Germany
[4] Univ Texas, Sect Mol Genet & Microbiol, Austin, TX 78712 USA
[5] Univ Texas, Inst Cellular & Mol Biol, Austin, TX 78712 USA
[6] Eyetech Pharmaceut, Woburn, MA 01801 USA
[7] Univ Kentucky, Dept Ophthalmol, Lexington, KY 40536 USA
关键词
angiogenesis; neovascularization; cornea; CCR2; inhibition;
D O I
10.1097/00003226-200307000-00013
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose. To determine if genetic ablation of the chemokine receptor CCR2 (involved in leukocyte and endothelial chemotaxis) inhibits the development of corneal neovascularization. Methods. Wild-type C57BL/6J mice, as well as species-specific counterparts with targeted homozygous disruption of the CCR2. underwent chemical and mechanical denudation of corneal and limbal epithelium. Corneas were harvested 2 weeks after injury. Neovascularization was quantified by CD31 immunostaining. Results. The mean percentages of neovascularized corneal area in control mice and CCR2-deficient mice 2 weeks after denudation were 58.3% and 38.8% (P = 0.047), respectively. Conclusions. Development of corneal neovascularization is inhibited in CCR2-deficient mice.
引用
收藏
页码:465 / 467
页数:3
相关论文
共 33 条
  • [1] Amano S, 1998, INVEST OPHTH VIS SCI, V39, P18
  • [2] Sustained inhibition of corneal neovascularization by genetic ablation of CCR5
    Ambati, BK
    Anand, A
    Joussen, AA
    Kuziel, WA
    Adamis, AP
    Ambati, J
    [J]. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (02) : 590 - 593
  • [3] Monocyte activation in angiogenesis and collateral growth in the rabbit hindlimb
    Arras, M
    Ito, WD
    Scholz, D
    Winkler, B
    Schaper, J
    Schaper, W
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (01) : 40 - 50
  • [4] CXC and CC chemokine receptors on coronary and brain endothelia
    Berger, O
    Gan, XH
    Gujuluva, C
    Burns, AR
    Sulur, G
    Stins, M
    Way, D
    Witte, M
    Weinand, M
    Said, J
    Kim, KS
    Taub, D
    Graves, MC
    Fiala, M
    [J]. MOLECULAR MEDICINE, 1999, 5 (12) : 795 - 805
  • [5] CORNEAL NEOVASCULARIZATION - PATHOGENESIS AND INHIBITION
    EPSTEIN, RJ
    STULTING, RD
    HENDRICKS, RL
    HARRIS, DM
    [J]. CORNEA, 1987, 6 (04) : 250 - 257
  • [6] 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
    Fantuzzi, L
    Borghi, P
    Ciolli, V
    Pavlakis, G
    Belardelli, F
    Gessani, S
    [J]. BLOOD, 1999, 94 (03) : 875 - 883
  • [7] Goede V, 1999, INT J CANCER, V82, P765, DOI 10.1002/(SICI)1097-0215(19990827)82:5<765::AID-IJC23>3.0.CO
  • [8] 2-F
  • [9] Goede V, 1998, LAB INVEST, V78, P1385
  • [10] Human vascular smooth muscle cells express receptors for CC chemokines
    Hayes, IM
    Jordan, NJ
    Towers, S
    Smith, G
    Paterson, JR
    Earnshaw, JJ
    Roach, AG
    Westwick, J
    Williams, RJ
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1998, 18 (03) : 397 - 403