Müller cell response to laser-induced increase in intraocular pressure in rats

The goal of this study was to investigate the reaction of the Müller cells to elevated intraocular pressure (IOP). Elevated IOP is one of the risk factors in glaucomatous retinal ganglion cell (RGC) degeneration. Müller cells play an important role in retinal homeostasis. The reaction of Müller cell...

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Veröffentlicht in:Glia 2004-08, Vol.47 (2), p.109-119
Hauptverfasser: Woldemussie, Elizabeth, Wijono, Mercy, Ruiz, Guadalupe
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description The goal of this study was to investigate the reaction of the Müller cells to elevated intraocular pressure (IOP). Elevated IOP is one of the risk factors in glaucomatous retinal ganglion cell (RGC) degeneration. Müller cells play an important role in retinal homeostasis. The reaction of Müller cells was examined by evaluating temporal changes in glutamate aspartate transporter (GLAST), glutamine synthase (GS), glial fibrillary acidic protein (GFAP), and the B‐cell lymphoma (Bcl‐2) using immunoblotting and immunohistochemical techniques. After IOP was elevated for 4–60 days, there was a time‐related decrease in RGC ranging from 6% to 44%. There was also a time‐related increase in GLAST protein reaching maximum after 3 weeks of elevated IOP. On the other hand, there was very little change in the expression of GS during the first 2 weeks followed by some increase between 21 and 60 days. An increase in Bcl‐2 was biphasic with maximum increase after 4 days followed by decline after 15 and 21 days. GFAP, which is usually not expressed in normal Müller cells, was present at all time points. In all cases, the increase was most intense in the vicinity of the ganglion cells where the astrocytes and endfeet of the Müller cells are located. These results indicate that Müller cells react to the insult of elevated IOP by expressing GFAP and Bcl‐2, proteins that are expressed in reactive gliosis and other pathological conditions. The increase in GLAST along with minimum change in GS indicates a disturbance in glutamate homeostasis. © 2004 Wiley‐Liss, Inc.
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Psychology ; ganglion cells ; Glaucoma - metabolism ; Glaucoma - pathology ; Glaucoma - physiopathology ; Glial Fibrillary Acidic Protein - metabolism ; Glutamate-Ammonia Ligase - metabolism ; Glutamic Acid - metabolism ; Homeostasis - physiology ; Homeostasis - radiation effects ; immunoreactivity ; Intraocular Pressure - physiology ; Intraocular Pressure - radiation effects ; Isolated neuron and nerve. 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Elevated IOP is one of the risk factors in glaucomatous retinal ganglion cell (RGC) degeneration. Müller cells play an important role in retinal homeostasis. The reaction of Müller cells was examined by evaluating temporal changes in glutamate aspartate transporter (GLAST), glutamine synthase (GS), glial fibrillary acidic protein (GFAP), and the B‐cell lymphoma (Bcl‐2) using immunoblotting and immunohistochemical techniques. After IOP was elevated for 4–60 days, there was a time‐related decrease in RGC ranging from 6% to 44%. There was also a time‐related increase in GLAST protein reaching maximum after 3 weeks of elevated IOP. On the other hand, there was very little change in the expression of GS during the first 2 weeks followed by some increase between 21 and 60 days. An increase in Bcl‐2 was biphasic with maximum increase after 4 days followed by decline after 15 and 21 days. GFAP, which is usually not expressed in normal Müller cells, was present at all time points. In all cases, the increase was most intense in the vicinity of the ganglion cells where the astrocytes and endfeet of the Müller cells are located. These results indicate that Müller cells react to the insult of elevated IOP by expressing GFAP and Bcl‐2, proteins that are expressed in reactive gliosis and other pathological conditions. The increase in GLAST along with minimum change in GS indicates a disturbance in glutamate homeostasis. © 2004 Wiley‐Liss, Inc.</description><subject>Amino Acid Transport System X-AG - metabolism</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Count</subject><subject>Disease Models, Animal</subject><subject>Down-Regulation - physiology</subject><subject>Down-Regulation - radiation effects</subject><subject>Eye and associated structures. Visual pathways and centers. Vision</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>ganglion cells</subject><subject>Glaucoma - metabolism</subject><subject>Glaucoma - pathology</subject><subject>Glaucoma - physiopathology</subject><subject>Glial Fibrillary Acidic Protein - metabolism</subject><subject>Glutamate-Ammonia Ligase - metabolism</subject><subject>Glutamic Acid - metabolism</subject><subject>Homeostasis - physiology</subject><subject>Homeostasis - radiation effects</subject><subject>immunoreactivity</subject><subject>Intraocular Pressure - physiology</subject><subject>Intraocular Pressure - radiation effects</subject><subject>Isolated neuron and nerve. Neuroglia</subject><subject>laser photocoagulation</subject><subject>Lasers - adverse effects</subject><subject>Male</subject><subject>Müller cells</subject><subject>Neuroglia - metabolism</subject><subject>Neuroglia - pathology</subject><subject>Neuroglia - radiation effects</subject><subject>ocular hypertension</subject><subject>Proto-Oncogene Proteins c-bcl-2 - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reaction Time - physiology</subject><subject>Reaction Time - radiation effects</subject><subject>Retina - metabolism</subject><subject>Retina - pathology</subject><subject>Retina - physiopathology</subject><subject>Retinal Degeneration - etiology</subject><subject>Retinal Degeneration - pathology</subject><subject>Retinal Degeneration - physiopathology</subject><subject>Retinal Ganglion Cells - pathology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0894-1491</issn><issn>1098-1136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKxDAUhoMoOo5ufADpRhdC9STpLUsRHS-jo6AIbkKanko1045Ji_pu7nwxMxcvK0MgJ4fv_w_nJ2SLwj4FYAePplL7DPxZIj0KIgsp5cky6UEmopBGgq6RdeeeAKj_pKtkjcY0i7mAHhldfn4YgzbQaExg0U2a2mHQNoFRDm1Y1UWnsQiqWlv0HV_421rV6M4oG0y8xHV21reqdRtkpVTG4ebi7ZO7k-Pbo9NwOBqcHR0OQ80Fh5AVuowpR57rUqs0UhlGHMqsSFiJAhjmScZ4hnmesiTRuQbIIS40L7TIElS8T3bnvhPbvHToWjmu3HQHVWPTOZnO8gDhwb05qG3jnMVSTmw1VvZdUpDT-OQ0PjnDPby9cO3yMRa_6CIvD-wsAOW0MqVVta7cH05EImHMc3TOvVYG3_8ZKQfDs8Pv4eFcU7kW3340yj7LJOVpLO-vBvKG3z-cxxfXcsi_AM46mCs</recordid><startdate>20040801</startdate><enddate>20040801</enddate><creator>Woldemussie, Elizabeth</creator><creator>Wijono, Mercy</creator><creator>Ruiz, Guadalupe</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20040801</creationdate><title>Müller cell response to laser-induced increase in intraocular pressure in rats</title><author>Woldemussie, Elizabeth ; Wijono, Mercy ; Ruiz, Guadalupe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3930-2dcf513e3bcfca74a8e430f8d62fe902eb68238ebb7266cbc00b05dc3dc986ea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Amino Acid Transport System X-AG - metabolism</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Count</topic><topic>Disease Models, Animal</topic><topic>Down-Regulation - physiology</topic><topic>Down-Regulation - radiation effects</topic><topic>Eye and associated structures. 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In all cases, the increase was most intense in the vicinity of the ganglion cells where the astrocytes and endfeet of the Müller cells are located. These results indicate that Müller cells react to the insult of elevated IOP by expressing GFAP and Bcl‐2, proteins that are expressed in reactive gliosis and other pathological conditions. The increase in GLAST along with minimum change in GS indicates a disturbance in glutamate homeostasis. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15185390</pmid><doi>10.1002/glia.20000</doi><tpages>11</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Amino Acid Transport System X-AG - metabolism
Animals
Biological and medical sciences
Cell Count
Disease Models, Animal
Down-Regulation - physiology
Down-Regulation - radiation effects
Eye and associated structures. Visual pathways and centers. Vision
Fundamental and applied biological sciences. Psychology
ganglion cells
Glaucoma - metabolism
Glaucoma - pathology
Glaucoma - physiopathology
Glial Fibrillary Acidic Protein - metabolism
Glutamate-Ammonia Ligase - metabolism
Glutamic Acid - metabolism
Homeostasis - physiology
Homeostasis - radiation effects
immunoreactivity
Intraocular Pressure - physiology
Intraocular Pressure - radiation effects
Isolated neuron and nerve. Neuroglia
laser photocoagulation
Lasers - adverse effects
Male
Müller cells
Neuroglia - metabolism
Neuroglia - pathology
Neuroglia - radiation effects
ocular hypertension
Proto-Oncogene Proteins c-bcl-2 - metabolism
Rats
Rats, Wistar
Reaction Time - physiology
Reaction Time - radiation effects
Retina - metabolism
Retina - pathology
Retina - physiopathology
Retinal Degeneration - etiology
Retinal Degeneration - pathology
Retinal Degeneration - physiopathology
Retinal Ganglion Cells - pathology
Vertebrates: nervous system and sense organs
title Müller cell response to laser-induced increase in intraocular pressure in rats
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