DISTRIBUTION OF IGF-I AND IGF-II, IGF BINDING-PROTEINS (IGFBPS) AND IGFBP MESSENGER-RNA IN OCULAR FLUIDS AND TISSUES - POTENTIAL SITES OF SYNTHESIS OF IGFBPS IN AQUEOUS AND VITREOUS

Levels of insulin-like growth factor-I and II (IGF-I and IGF-II) in bovine aqueous humor are twice those found in the vitreous (aqueal IGF-I = 0·62nM, vitreal IGF-I = 0·30 nM; aqueal IGF-II = 0·028 nM, vitreal IGF-II = 0·017 nM). IGF-I and II binding assays and IGF-II Western ligand blots indicate that aqueous and vitreous humor have equal overall levels of binding (binding assays, mean ±S.E.M. bound/free per 50μl of fluid: vitreal IGF-II = 7·28 ± 1·6, IGF-I = 0·3 ± 0·078; aqueal IGF-II = 7·21 ± 0·072; IGF-I = 0·3 ± 0·078). In addition, the ligand blots reveal that aqueous and vitreous have markedly different complements of specific IGF binding proteins (IGFBPs). Aqueal levels of a 34 kDa IGFBP, immunologically identified as IGFBP-2, exceed those in the vitreous by two-fold. In contrast, the vitreous exhibits a two- to three-fold higher level of smaller (28-24 kDa), yet unidentified, IGFBPs. Aqueal and vitreal IGFBP patterns are also different from those found in serum. IGFBP-2 found in the aqueous and vitreous may be synthesized by ciliary body and/or cornea since these structures contain high levels of IGFBP-2 mRNA. Lens epithelial cells may also contribute IGFBP-2 to the aqueous since they also contain IGFBP-2 mRNA, albeit at substantially lower levels than the cornea and ciliary body. The retina has the lowest level of IGFBP-2 mRNA, IGF-II binding assays of cornea, ciliary body, retina and retinal pigment epithelium (RPE) indicate that the cornea has the highest level of binding (mean ± S.E.M. IGF-II B/F per 50μg protein: cornea = 84·52 ± 28·8; iris/ciliary body complex = 0·61 ± 0·078; retina = 0·47 ± 0·096; RPE =0·069 ± 0·019), IGF-II ligand blots confirm these tissue-specific differences in binding and show that each ocular tissue contains IGFBP-2. In addition, ligand blots indicate that each ocular tissue contains a complex and distinctive population of IGFBPs. For example, the cornea and retina (but not the ciliary body, aqueous or vitreous) contain a 46 kDa IGFBP that may be IGFBP-3. The finding that cornea and retina also contain IGFBP-3 mRNA suggests that these structures may synthesize IGFBP-3 for local use within the eye. © 1993 Academic Press, Inc.