PURPOSE: To study the distribution of milk fat globule epidermal growth factor E8 (MFG-E8) in the rodent eye and to investigate a potential role for this molecule in the phagocytosis of photoreceptor outer segments (POS) by the retinal pigment epithelium (RPE). METHODS: We have used immunohistochemistry, in situ hybridization, Northern and Western blotting to demonstrate the presence and distribution of MFG-E8 in the rat and mouse retina. siRNA technology was used to knock down MFG-E8 mRNA and to study the effect of such knockdown on the phagocytosis of POS by the RPE. RESULTS: We identified a novel long form of this protein (MFG-E8L) in rat tissues, which contains a 56 amino acid insert that is rich in proline and threonine. This is the first demonstration that MFG-E8L is present in a species other than the mouse. Immunohistochemistry and in situ hybridization demonstrate that MFG-E8 is present in the retina and RPE. Northern blotting and PCR show that the short form of MFG-E8 (MFG-E8S) is present in both the retina and RPE, but MFG-E8L is found only in the RPE. Our results do not demonstrate a role for MFG-E8 in POS phagocytosis by cultured RPE cells. CONCLUSIONS: In all tissues in which MFG-E8 has been localized, it has been shown to perform an important role in cell-cell binding, or in promoting phagocytosis. The localization of this glycoprotein in the retina and RPE, and particularly the specific localization of MFG-E8L in the RPE, suggests that this molecule may play an important, but as yet unknown role in retinal function.
PURPOSE: To study the distribution of milk fat globule epidermal growth factor E8 (MFG-E8) in the rodent eye and to investigate a potential role for this molecule in the phagocytosis of photoreceptor outer segments (POS) by the retinal pigment epithelium (RPE). METHODS: We have used immunohistochemistry, in situ hybridization, Northern and Western blotting to demonstrate the presence and distribution of MFG-E8 in the rat and mouse retina. siRNA technology was used to knock down MFG-E8 mRNA and to study the effect of such knockdown on the phagocytosis of POS by the RPE. RESULTS: We identified a novel long form of this protein (MFG-E8L) in rat tissues, which contains a 56 amino acid insert that is rich in proline and threonine. This is the first demonstration that MFG-E8L is present in a species other than the mouse. Immunohistochemistry and in situ hybridization demonstrate that MFG-E8 is present in the retina and RPE. Northern blotting and PCR show that the short form of MFG-E8 (MFG-E8S) is present in both the retina and RPE, but MFG-E8L is found only in the RPE. Our results do not demonstrate a role for MFG-E8 in POS phagocytosis by cultured RPE cells. CONCLUSIONS: In all tissues in which MFG-E8 has been localized, it has been shown to perform an important role in cell-cell binding, or in promoting phagocytosis. The localization of this glycoprotein in the retina and RPE, and particularly the specific localization of MFG-E8L in the RPE, suggests that this molecule may play an important, but as yet unknown role in retinal function.
Authors: Emeline F Nandrot; Monika Anand; Dena Almeida; Kamran Atabai; Dean Sheppard; Silvia C Finnemann Journal: Proc Natl Acad Sci U S A Date: 2007-07-09 Impact factor: 11.205
Authors: Mingyi Wang; Zongming Fu; James Wu; Jing Zhang; Liqun Jiang; Benjamin Khazan; Richard Telljohann; Mingming Zhao; Alexander W Krug; Maria Pikilidou; Robert E Monticone; Robert Wersto; Jennifer Van Eyk; Edward G Lakatta Journal: Aging Cell Date: 2012-04-04 Impact factor: 9.304
Authors: Irene E Whitney; Mary A Raven; Daniel C Ciobanu; Robert W Williams; Benjamin E Reese Journal: Invest Ophthalmol Vis Sci Date: 2009-01-24 Impact factor: 4.799