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Macrophage Depletion Diminishes Lesion Size and Severity in Experimental Choroidal Neovascularization
Abstract
PURPOSE: Macrophage recruitment to the choroid has been proposed to contribute to the pathogenesis of choroidal neovascularization (CNV) in AMD. The study was conducted to determine whether treatment with clodronate liposomes (CL(2)MDP-lip), which cause depletion of blood monocytes and lymph node macrophages, diminishes the severity of neovascularization in a mouse model of laser-induced CNV. METHODS: Laser-induced CNV was performed in female 16-month-old C57BL/6 mice. Macrophages were depleted by use of CL(2)MDP-lip intraperitoneally and subcutaneously 72 and 24 hours before and every 2 to 3 days after laser injury. Control mice received injections of either PBS alone or PBS liposomes. Blood monocyte and choroidal macrophage depletion were documented by flow cytometry and choroidal flatmount preparation analysis, respectively. Two weeks after laser injury, mice were injected intravenously with fluoresceinated dextran. The right eyes were removed and prepared for flatmount analysis of CNV surface area (in relative disc areas or DA), vascularity (relative fluorescence), and cellularity (propidium iodide stain). The mice were then perfused with 10% formaldehyde, and the left eyes were removed for histopathology. The means of the various parameters for four CNV lesions per eye were calculated. Fluorescein angiography was also performed. RESULTS: Flow cytometry of circulating monocytes and immunohistochemical analysis of choroidal macrophage density confirmed the effective depletion of blood monocytes and choroidal macrophages respectively in CL(2)MDP-lip-treated mice. Compared with the control, flatmount analysis of macrophage depleted mice demonstrated a significant reduction in size of the CNV area (2.8 +/- 0.5 DA vs. 1.4 +/- 0.1 DA; P < 0.043). The treated group also revealed less vascularity (1.6 +/- 0.1 units vs. 1.1 +/- 0.0 units; P < 0.0092) and cellularity of CNV lesions (3.3 +/- 0.6 DA vs. 1.7 +/- 0.1 DA, P < 0.04). Histopathology revealed that, in the macrophage-depleted group, CNV was smaller in diameter (1270 +/- 73 pixels vs. 770 +/- 82 pixels, P < 0.0006) and thickness (120 +/- 7 pixels vs. 96 +/- 7 pixels, P < 0.019). CONCLUSIONS: Macrophage depletion using CL(2)MDP-lip reduces size, cellularity, and vascularity of CNV. This observation supports the hypothesis that macrophages contribute to the severity of CNV lesions.
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Citations
Cites
Rooijen, N. V., & Sanders, A. (1994) · Journal of Immunological Methods · doi:10.1016/0022-1759(94)90012-4 · Cited by 1,779
Dijkstra, C. D., Döpp, E. A., Joling, P., & Kraal, G. (1985) · Microenvironments in the Lymphoid System · doi:10.1007/978-1-4613-2463-8_50 · Cited by 1,598
Macrophage-induced angiogenesis is mediated by tumour necrosis factor-α
Leibovich, S. J., Polverini, P. J., Shepard, H. M., Wiseman, D. M., Shively, V., & Nuseir, N. (1987) · Nature · doi:10.1038/329630a0 · Cited by 1,210
Sunderkötter, C., Steinbrink, K., Goebeler, M., Bhardwaj, R., & Sorg, C. (1994) · Journal of Leukocyte Biology · doi:10.1002/jlb.55.3.410 · Cited by 1,120
A role for local inflammation in the formation of drusen in the aging eye
Anderson, D. H., Mullins, R. F., Hageman, G. S., & Johnson, L. V. (2002) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(02)01624-0 · Cited by 1,087
Intravitreal triamcinolone acetonide for exudative age related macular degeneration
Jonas, J. B. (2003) · British Journal of Ophthalmology · doi:10.1136/bjo.87.4.462 · Cited by 492
Immunological and Aetiological Aspects of Macular Degeneration
Penfold, P. L., Madigan, M. C., Gillies, M. C., & Provis, J. M. (2001) · Progress in Retinal and Eye Research · doi:10.1016/s1350-9462(00)00025-2 · Cited by 460
Grossniklaus, H. E., Ling, J. X., Wallace, T. M., Dithmar, S., Lawson, D., Cohen, C., Elner, V. M., Elner, S. G., & Sternberg, P. (2002) · PubMed · Cited by 434
The mononuclear phagocyte system revisited
Hume, D. A., Ross, I. L., Himes, S. R., Sasmono, R. T., Wells, C. A., & Ravasi, T. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.72.4.621 · Cited by 423
The potential angiogenic role of macrophages in the formation of choroidal neovascular membranes.
Oh, H., Takagi, H., Takagi, C., Suzuma, K., Otani, A., Ishida, K., Matsumura, M., Ogura, Y., & Honda, Y. (1999) · PubMed · Cited by 393
Risk Factors for Age-related Macular Degeneration
Evans, J. R. (2001) · Progress in Retinal and Eye Research · doi:10.1016/s1350-9462(00)00023-9 · Cited by 339
Exudative macular degeneration and intravitreal triamcinolone: 18 month follow up
Challa, J. K., Gillies, M. C., Penfold, P. L., Gyory, J. F., Hunyor, A. B., & Billson, F. A. (1998) · Australian and New Zealand Journal of Ophthalmology · doi:10.1111/j.1442-9071.1998.tb01330.x · Cited by 324
Senile macular degeneration: The involvement of immunocompetent cells
Penfold, P. L., Killingsworth, M. C., & Sarks, S. H. (1985) · Graefe's Archive for Clinical and Experimental Ophthalmology · doi:10.1007/bf02150948 · Cited by 293
Epidemiology of Age-Related Macular Degeneration
Klein, R. (2005) · Macular Degeneration · doi:10.1007/3-540-26977-0_5 · Cited by 283
Ishibashi, T., Miki, K., Sorgente, N., Patterson, R., & Ryan, S. J. (1985) · Archives of Ophthalmology · doi:10.1001/archopht.1985.01050050100026 · Cited by 192
Ciulla, T. A. (2001) · Archives of Ophthalmology · doi:10.1001/archopht.119.3.399 · Cited by 181
Penfold, P. L., Wen, L., Madigan, M. C., Gillies, M. C., King, N. J. C., & Provis, J. M. (2001) · Clinical and Experimental Immunology · doi:10.1046/j.1365-2249.2000.01316.x · Cited by 167
Softening of drusen and subretinal neovascularization.
Sarks, S. H., Van Driel, D., Maxwell, L., & Killingsworth, M. C. (1980) · PubMed · Cited by 144
Naito, M., Nagai, H., Kawano, S., et al. (1996) · Journal of Leukocyte Biology · doi:10.1002/jlb.60.3.337 · Cited by 137
The distribution of immune cells in the uveal tract of the normal eye
McMenamin, P. G. (1997) · Eye · doi:10.1038/eye.1997.49 · Cited by 117
MPhil, P. P., BSppSc, M. K., & Sarks, S. H. (1984) · Australian Journal of Opthalmology · doi:10.1111/j.1442-9071.1984.tb01120.x · Cited by 115
Ageing changes in Bruch's membrane and their functional implications.
Cf, G., & Marshall, J.-C. (1978) · PubMed · Cited by 111
Age-Related Macular Degeneration: Epidemiology and Optimal Treatment
la Cour, M., Kiilgaard, J. F., & Nissen, M. H. (2002) · Drugs & Aging · doi:10.2165/00002512-200219020-00003 · Cited by 111
Biewenga, J., van der Ende, M. B., Krist, L. F. G., Borst, A., Ghufron, M., & van Rooijen, N. (1995) · Cell and Tissue Research · doi:10.1007/bf00304524 · Cited by 111
Forrester, J. V., Huitinga, I., Lumsden, L., & Dijkstra, C. D. (1998) · Current Eye Research · doi:10.1080/02713689808951224 · Cited by 105
Penfold, P. L., Killingsworth, M. C., & Sarks, S. H. (1986) · PubMed · Cited by 100
Penfold, P. L., Wong, J. G., Gyory, J., & Billson, F. A. (2001) · Clinical & Experimental Ophthalmology · doi:10.1046/j.1442-9071.2001.00407.x · Cited by 97
Genetic susceptibility to age related macular degeneration
Yates, J. R. W., & Moore, A. T. (2000) · Journal of Medical Genetics · doi:10.1136/jmg.37.2.83 · Cited by 89
Choroidal neovascularization in younger patients
Spaide, R. F. (1999) · Current Opinion in Ophthalmology · doi:10.1097/00055735-199906000-00005 · Cited by 89
Dendritic cells and macrophages in the uveal tract of the normal mouse eye
McMenamin, P. G. (1999) · British Journal of Ophthalmology · doi:10.1136/bjo.83.5.598 · Cited by 88
Age as an independent risk factor for severity of experimental choroidal neovascularization.
Espinosa‐Heidmann, D. G., Suñer, I. J., Hernandez, E. P., Frazier, W. D., Csaky, K. G., & Cousins, S. W. (2002) · PubMed · Cited by 81
Self-citationGrossniklaus, H. E. (2000) · Archives of Ophthalmology · doi:10.1001/archopht.118.5.625 · Cited by 76
Roles of Macrophages in Measles Virus Infection of Genetically Modified Mice
Roscic, B., Schwendener, R. A., Odermatt, B. F., Zúñiga, A., Pavlovic, J., Billeter, M. A., & Cattaneo, R. (2001) · Journal of Virology · doi:10.1128/jvi.75.7.3343-3351.2001 · Cited by 76
Pouvreau, I., Zech, J., Thillaye-Goldenberg, B., Naud, M., van Rooijen, N., & de Kozak, Y. (1998) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(98)00042-3 · Cited by 72
Optimal methods for preparation and immunostaining of iris, ciliary body, and choroidal wholemounts.
McMenamin, P. G. (2000) · PubMed · Cited by 68
Mechanism of age related macular degeneration
Husain, D., Ambati, B. K., ADAMIS, A., & Miller, J. W. (2002) · Ophthalmology Clinics of North America · doi:10.1016/s0896-1549(01)00009-8 · Cited by 55
Ultrastructure of Bruch's Membrane After Krypton Laser Photocoagulation
Pollack, A. (1986) · Archives of Ophthalmology · doi:10.1001/archopht.1986.01050210131040 · Cited by 43
Bauer, D., Mrzyk, S., van Rooijen, N., Steuhl, K., & Heiligenhaus, A. (2001) · Experimental Eye Research · doi:10.1006/exer.2000.0947 · Cited by 26
Flow cytometric detection of lymphocyte proliferation in eyes with immunogenic inflammation.
Cousins, S. W., & Streilein, J. W. (1990) · PubMed · Cited by 18
Self-citationNieuwenhuijzen, G. A. P. (1997) · Archives of Surgery · doi:10.1001/archsurg.1997.01430290079016 · Cited by 14
Immunohistochemical proof of origin of macrophages in laser photocoagulation lesion in the retina.
Yi, X., Takahashi, K., Ogata, N., & Uyama, M. (1996) · PubMed · Cited by 12
Immunology of Age-Related Macular Degeneration
Cousins, S. W., & Csaky, K. G. (2002) · doi:10.3109/9780203909157-7 · Cited by 9
Self-citation
Cited by
Hageman, G. S., Anderson, D. H., Johnson, L. V., Hancox, L. S., Taiber, A. J., Hardisty, L. I., Hageman, J. L., Stockman, H. A., Borchardt, J. D., Gehrs, K. M., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501536102 · Cited by 1,961
Fantin, A., Vieira, J. M., Gestri, G., Denti, L., Schwarz, Q., Prykhozhij, S., Peri, F., Wilson, S. W., & Ruhrberg, C. (2010) · Blood · doi:10.1182/blood-2009-12-257832 · Cited by 1,153
Molecular pathology of age-related macular degeneration
Ding, X., Patel, M., & Chan, C.-C. (2009) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2008.10.001 · Cited by 582
“Espinosa-Heidmann et al. (2003) and Sakurai et al. (2003) and their colleagues showed that when administered to mice, these liposomes markedly impaired macrophage recruitment to areas of laser retinal injury.”
BackgroundThe impact of microglial activation on blood-brain barrier in brain diseases
da Fonseca, A. C. C., Matias, D., Garcia, C., Amaral, R., Geraldo, L. H., Freitas, C., & Lima, F. R. S. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00362 · Cited by 572
Mettu, P. S., Allingham, M. J., & Cousins, S. W. (2021) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2020.100906 · Cited by 370
Self-citation
Metadata
- Authors
- Espinosa-Heidmann, D. G., Suner, I. J., Hernandez, E. P., Monroy, D., Csaky, K. G., & Cousins, S. W.
- Venue
- Investigative Opthalmology & Visual Science
- Published
- 2003-08-01
- Volume
- 44
- Issue
- 8
- Pages
- 3586
- ISSN
- 0146-0404 (ISSN-L)
- 1552-5783
- OpenAlex
- W2068403296
- Cited by
- 401
- References
- 42
- FWCI
- 14.36
- Type
- journal article
- Language
- en
- Open access
- closed
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