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Neuronal and glial cell expression of angiotensin II type 1 (AT1) and type 2 (AT2) receptors in the rat retina
Authors:LE Downie  K Vessey  A Miller  MM Ward  MJ Pianta  AJ Vingrys  JL Wilkinson-Berka  EL Fletcher
Institution:1. Department of Anatomy and Cell Biology, The University of Melbourne, Grattan Street, Parkville 3010, Victoria, Australia 3010;2. Department of Optometry and Vision Sciences, The University of Melbourne, Cnr Keppel and Cardigan Sts, Carlton, Victoria, Australia, 3053;3. Department of Immunology, Monash University, Commercial Road, Prahran, Victoria, Australia 3004
Abstract:The bio-active peptide, angiotensin II (Ang II), has been suggested to exert a neuromodulatory effect on inner retinal neurons. In this study, we examined the distribution of angiotensin receptors (ATRs) in the developing and mature rat retina and optic nerve using immunofluorescence immunocytochemistry. Double-labeling experiments were performed with established markers to identify different retinal cell populations. In adult retinae, ATRs were observed on neurons involved in “ON” pathways of neurotransmission. Angiotensin II type 1 receptors (AT1Rs) were expressed by a sub-population of “ON” cone bipolar cells that also labeled for Gα0 and islet-1. Extra-neuronal expression of AT1Rs was evident on retinal astrocytes, Müller cells and blood vessels. Immunoreactivity for the angiotensin II type 2 receptor (AT2R) was observed on conventional and displaced GABAergic amacrine cells. Co-localization studies showed that AT2R-expressing amacrine cells constituted at least two separate sub-populations. Cell counts revealed that all wide-field amacrine cells expressing protein kinase C-alpha were also AT2R-positive; a further subset of amacrine cells expressing AT2Rs and stratifying in sublamina “b” of the inner plexiform layer (IPL) was identified. Developmental expression of AT1Rs was dynamic, involving multiple inner neuronal classes. At postnatal day 8 (P8), AT1R immunoreactivity was observed on putative ganglion cells. The characteristic bipolar cell labeling observed in adults was not evident until P13. In contrast, AT2Rs were detected as early as P2 and localized specifically to amacrine cells from this age onward. These data provide further evidence for the potential role of angiotensin II in the modulation of retinal neurons and glia. The differential pattern of expression of these receptors across these cell types is similar to that observed in the brain and suggests that a similar functional role for Ang II may also exist within the retina.
Keywords:astrocyte  bipolar cell  amacrine cell  renin-angiotensin system  neuromodulation
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