Abstract | PURPOSE: METHODS: RESULTS: The histopathological findings demonstrated that PDR membranes consisted of a variety of endothelial cells forming a microvascular cavity with red blood cells and non-vascular stromal mononuclear cells. Membranous and cytoplasmic immunoreactivity for EpoR was strongly detected in endothelial cells and stromal cells in all PDR patients. Although microvessels were not observed in IERMs and ILMs, immunoreactivity for EpoR was noted in the cellular component of IERMs, and was weakly detected in ILMs. Epo was not expressed in any membrane. CONCLUSION: EpoR was strongly expressed in microvessels of all PDR membranes. The in vivo evidence in this study suggests that Epo in the vitreous binds to EpoR in PDR membranes, which subsequently leads to the proliferation of new retinal vessels. EpoR immunoreactivity in non-vascular stromal cells in PDR membranes, and IERMs and ILMs might be indirectly correlated with ischaemia.
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Authors | Satoru Kase, Wataru Saito, Kazuhiro Ohgami, Kazuhiko Yoshida, Naoki Furudate, Akari Saito, Masahiko Yokoi, Manabu Kase, Shigeaki Ohno |
Journal | The British journal of ophthalmology
(Br J Ophthalmol)
Vol. 91
Issue 10
Pg. 1376-8
(Oct 2007)
ISSN: 0007-1161 [Print] England |
PMID | 17522145
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Receptors, Erythropoietin
- Erythropoietin
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Topics |
- Aged
- Diabetic Retinopathy
(metabolism, pathology)
- Endothelial Cells
(pathology)
- Epiretinal Membrane
(metabolism, pathology)
- Erythropoietin
(analysis)
- Female
- Humans
- Immunohistochemistry
(methods)
- Male
- Microcirculation
- Middle Aged
- Receptors, Erythropoietin
(analysis)
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