Abstract
We studied the localization of Na+/myo-inositol cotransporter (SMIT) mRNA in normal and hypertonic stress rat eyes by in situ hybridization histochemistry using cRNA probes. SMIT mRNA signals were observed in the iris-ciliary body, the lens epithelial cells, and the ganglion cell layer and the inner nuclear layer of the retina. There was a rapid increase on SMIT mRNA in the retina of hypertonic stress rats compared with control rats. These findings suggest that Na+/myo-inositol cotransporter gene expression is osmotically regulated in vivo to protect retinal neuronal function against hypertonic stress.
MeSH terms
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Animals
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Carrier Proteins / biosynthesis*
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Ciliary Body / metabolism
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Eye / metabolism*
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Gene Expression*
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Heat-Shock Proteins / biosynthesis*
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In Situ Hybridization
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Inositol / metabolism
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Lens, Crystalline / metabolism
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Male
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Membrane Proteins*
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RNA Probes
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RNA, Complementary
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RNA, Messenger / biosynthesis
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Rats
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Rats, Wistar
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Reference Values
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Retina / metabolism
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Retinal Ganglion Cells / metabolism
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Saline Solution, Hypertonic*
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Sodium / metabolism
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Stress, Physiological*
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Symporters*
Substances
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Carrier Proteins
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Heat-Shock Proteins
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Membrane Proteins
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RNA Probes
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RNA, Complementary
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RNA, Messenger
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Saline Solution, Hypertonic
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Symporters
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SLC5A3 protein, human
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Inositol
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Sodium