Abstract
Retinopathy is the most common microvascular diabetes complication and represents
a major threat to the eyesight. The aim of this study was to address the role of pro-
and anti-angiogenic molecules in diabetic retinopathy in the aqueous humor of the
eye. Aqueous humor was collected at cataract surgery from 19 diabetic patients and
from 13 age- and sex-matched normoglycemic controls. Levels of pro-angiogenic vascular
endothelial growth factor (VEGF) and angiogenic inhibitor pigment epithelium-derived
factor (PEDF) were determined. Angiogenic activity of the aqueous humor was quantified
by measuring its effect on the migration of capillary endothelial cells.
In the aqueous fluid, VEGF levels were increased in diabetics (mean values: 501 vs. 367 pg/ml; p = 0.05), compared to controls. PEDF was found to be decreased in diabetics
(mean values: 2080 vs. 5780 ng/ml; p = 0.04) compared to controls. In seven diabetic patients with proliferative
retinopathy, the most profound finding was a significant decrease of the PEDF level
(mean value: 237 ng/ml), whereas VEGF levels were comparable to diabetic patients
without proliferation (mean value: 3153; p = 0.003). Angiogenic activity in samples
of patients from the control group was generally inhibitory due to PEDF, and inhibition
was blocked by neutralizing antibodies to PEDF. Likewise, in diabetics without proliferation,
angiogenic activity was also blocked by antibodies to PEDF.
We will demonstrate here that the level of the natural ocular anti-angiogenic agent
PEDF is inversely associated with proliferative retinopathy. PEDF is an important
negative regulator of angiogenic activity of aqueous humor. Our data may have implications
for the development of novel regimens for diabetic retinopathy.
Key words
Angiogenesis - Angiogenic Inhibitors - Aqueous Humor - Diabetic Retinopathy - Pigment
Epithelium-Derived Factor (PEDF) - Vascular Endothelial Growth Factor (VEGF)
References
1 Klein R.
The epidemiology of eye disease. In: Pickup JC, Williams G (eds) Textbook of Diabetes, 2nd edition. Oxford; Blackwell
Sciences 1997: 44.1-44.9
2
The Diabetes Control and Complications Trial Research Group .
The effects of intensive treatment of diabetes on the development and progression
of long-term complications in insulin-dependent diabetes mellitus.
N Engl J Med.
1993;
329
977-986
3
The Diabetes Control and Complications Trial Research Group .
Retinopathy and nephropathy in patients with type 1 diabetes four years after a trial
of intensive therapy. The Diabetes Control and Complications Trial/Epidemiology of
Diabetes Interventions and Complications Research Group.
N Engl J Med.
2000;
342
381-389
4
UK Prospective Diabetes Study (UKPDS) Group .
Intensive blood-glucose control with sulphonylureas or insulin compared with conventional
treatment and risk of complications in patients with type 2 diabetes (UKPDS 33).
Lancet.
1998;
352
837-853
5
Klein R, Klein B EK, Moss S E, Cruickshanks K J.
The Wisconsin Epidemiologic study of diabetic retinopathy. XIV. Ten-year incidence
and progression of diabetic retinopathy.
Arch Ophthalmol.
1994;
112
1217-1228
6
Bouck N, Stellmach V, Hsu S.
How tumors become angiogenic.
Adv Cancer Res.
1996;
69
135-174
7
Hanahan D, Folkman J.
Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis.
Cell.
1996;
86
353-364
8
Bouck N.
PEDF: anti-angiogenic guardian of ocular function.
Trends Mol Med.
2002;
8
330-334
9
Feldmann B, Jehle P M, Mohan S, Lang G E, Lang G K, Brueckel J, Boehm B O.
Diabetic retinopathy is associated with decreased serum levels of free IGF-I and changes
of IGF-binding proteins.
Growth Horm and IGF Res.
2000;
10
53-60
10
Poulaki V, Qin W, Joussen A M, Hurlbut P, Wiegand S J, Rudge J, Yancopoulos G D, Adamis A P.
Acute intensive insulin therapy exacerbates diabetic blood-retinal barrier breakdown
via hypoxia-inducible factor-1α and VEGF.
J Clin Invest.
2002;
109
805-815
11
Adamis A P, Miller J W, Bdernal M-T, D'Amico D J, Folkman J, Yeo T-K, Yeo K-T.
Increased vascular endothelial growth factor levels in the vitreous of eyes with proliferative
diabetic retinopathy.
Am J Ophthalmol.
1994;
118
445-450
12
Aiello L P, Avery R L, Arrigg P G. et al .
Vascular endothelial growth factor in ocular fluid of patients with diabetic retinopathy
and other retinal disorders.
N Engl J Med.
1994;
331
1480-1487
13
Aiello L P, Pierce E A, Foley E D, Takagi H, Chen H, Riddle L, Ferrara N, King G L,
Smith L E.
Suppression of retinal neovascularization in vivo by inhibition of vascular endothelial
growth factor (VEGF) using soluble VEGF-receptor chimeric proteins.
Proc Natl Acad Sci USA.
1995;
92
10 457-10 461
14
Dawson D W, Volpert O V, Gillis P, Crawford S E, Xu H, Benedict W, Bouck N P.
Pigment epithelium-derived factor: a potent inhibitor of angiogenesis.
Science.
1999;
285
245-248
15
Brausewetter F, Jehle P M, Jung M F, Boehm B O, Brueckel J, Hombach V, Osterhues H H.
Microvascular permeability is increased in both types of diabetes and correlates differentially
with serum levels of insulin-like growth factor I (IGF-I) and vascular endothelial
growth factor (VEGF).
Horm Metab Res.
2001;
33
713-720
16
Miller A D, Robinson G S, Smith L EH, Becerra S P.
Regulation of pigment epithelium-derived factor (PEDF) production by oxygen.
Invest Ophthalmol Vis Sci.
2000;
41 (Suppl)
S869-S874
17
Gao G, Li Y, Zhang D, Gee S, Crosson G, Ma J.
Unbalanced expression of VEGF and PEDF in ischemia-induced retinal neovascularization.
FEBS Lett.
2001;
489
270-276
18
Okamoto T, Oikawa S, Toyota T.
Absence of angiogenesis-inhibitory activity in aqueous humor of diabetic rabbits.
Diabetes.
1990;
39
12-16
19
Tapper D, Langer R, Bellows A R, Folkman J.
Angiogenesis capacity as a diagnostic marker for human eye tumors.
Surgery.
1979;
86
36-40
20
Ortego J, Escribano J, Beccera S P, Coca-Prados M.
Gene expression of the neurotrophic pigment epithelium-derived factor in the human
ciliary epithelium: synthesis and secretion into the aqueous humor.
Invest Ophthalmol Vis Sci.
1996;
37
2759-2767
21
Ogata N, Wada M, Otsuji T, Jo N, Tombran-Tink J, Matsumura M.
Expression of pigment epithelium-derived factor in normal adult rat eye and experimental
choroidal neovascularization.
Invest Ophthalmol Vis Sci.
2002;
43
1168-1175
22
Stellmach V, Crawford S E, Zhou W, Bouck N.
Prevention of ischemia induced retinopathy by the natural ocular anti-angiogenic agent
pigment epithelium-derived factor.
Proc Natl Acad Sci USA.
2001;
98
2593-2597
23
Chader G J.
PEDF: raising both hopes and questions in controlling angiogenesis.
Proc Natl Acad Sci USA.
2001;
98
2122-2124
24
Becerra S P.
Structure-function studies on PEDF a noninhibitory serpin with neurotrophic activity.
Adv Exp Med Biol.
1997;
425
223-237
25
Mori K, Gehlbach P, Ando A, McVey D, Wei L, Campochiaro P A.
Regression of ocular neovascularization in response to increased expression of pigment
epithelium-derived factor.
Invest Ophthalmol Vis Sci.
2002;
43
2428-2434
26
Cayouette M, Smith S B, Becerra S P, Gravel C.
Pigment epithelium-derived factor delays the death of photoreceptors in mouse models
of inherited retinal degenerations.
Neurobiol Dis.
1999;
6
523-532
27
Bilak M M, Corse A M, Bilak S R, Lehar M, Tombran-Tink J, Kuncl R W.
Pigment epithelium-derived factor (PEDF) protects motor neurons from chronic glutamate-mediated
neurodegeneration.
J Neuropathol Exp Neurol.
1999;
58
719-728
28
Cao W, Tombran-Tink J, Elias R, Sezate S, Mrazek D, McGinns J F.
In vivo protection of photoreceptors from light damage by pigment epithelium-derived
factor.
Investigative Ophthalmol Vis Sci.
2001;
42
1646-1652
29
Ohno-Matsui K, Morita I, Tombran-Tink J, Mrazek D, Onodera M, Uetama T, Hayano M,
Murota S-I, Mochizuki M.
Novel mechanisms for age-related macular degeneration: An equilibrium shift between
the angiogenesis factors VEGF and PEDF.
J Cell Physiol.
2001;
189
323-333
30
Holekamp N M, Bouck N, Volpert O.
Pigment epithelium-derived factor is deficient in the vitreous of patients with choroidal
neovascularization due to age-related macular degeneration.
Am J Ophthalmol.
2002;
134
220-227
31
Spranger J, Osterhoff M, Reimann M, Möhlig M, Ristow M, Francis M F, Cristofalo V,
Hames H-P, Smith G, Boulton M, Pfeiffer A FH.
Loss of the antiangiogenic pigment epithelium-derived factor in patients with angiogenic
eye disease.
Diabetes.
2001;
50
2641-2645
32
Boehm B O, Lang G K, Jehle P M, Feldmann B*, Lang G E*.
Octreotide reduces risk for vitreous hemorrhages and loss of visual acuity in patients
with high risk proliferative diabetic retinopathy.
Horm Metab Res.
2001;
33
300-306 (* contributed equally)
Prof. Bernhard O. Boehm, M. D.
Division of Endocrinology and Diabetes, University of Ulm ·
Robert-Koch-Strasse 8, 89081 Ulm, Germany
Telefon: + 49 (731) 500-24304
Fax: + 49 (731) 500-23938 ·
eMail: bernhard.boehm@medizin.uni-ulm.de