Inhibition of reactive gliosis attenuates excitotoxicity-mediated death of retinal ganglion cells.
Reactive gliosis is a hallmark of many retinal neurodegenerative conditions, including glaucoma. Although a majority of studies to date have concentrated on reactive gliosis in the optic nerve head, very few studies have been initiated to investigate the role of reactive gliosis in the retina. We ha...
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Public Library of Science (PLoS)
2011-03-01
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| Series: | PLoS ONE |
| Online Access: | https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0018305&type=printable |
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| author | Bhagyalaxmi S Ganesh Shravan K Chintala |
| author_facet | Bhagyalaxmi S Ganesh Shravan K Chintala |
| author_sort | Bhagyalaxmi S Ganesh |
| collection | DOAJ |
| description | Reactive gliosis is a hallmark of many retinal neurodegenerative conditions, including glaucoma. Although a majority of studies to date have concentrated on reactive gliosis in the optic nerve head, very few studies have been initiated to investigate the role of reactive gliosis in the retina. We have previously shown that reactive glial cells synthesize elevated levels of proteases, and these proteases, in turn, promote the death of retinal ganglion cells (RGCs). In this investigation, we have used two glial toxins to inhibit reactive gliosis and have evaluated their effect on protease-mediated death of RGCs. Kainic acid was injected into the vitreous humor of C57BL/6 mice to induce reactive gliosis and death of RGCs. C57BL/6 mice were also treated with glial toxins, alpha-aminoadipic acid (AAA) or Neurostatin, along with KA. Reactive gliosis was assessed by immunostaining of retinal cross sections and retinal flat-mounts with glial fibrillary acidic protein (GFAP) and vimentin antibodies. Apoptotic cell death was assessed by TUNEL assays. Loss of RGCs was determined by immunostaining of flat-mounted retinas with Brn3a antibodies. Proteolytic activities of matrix metalloproteinase-9 (MMP-9), tissue plasminogen activator (tPA), and urokinase plasminogen activator (uPA) were assessed by zymography assays. GFAP-immunoreactivity indicated that KA induced reactive gliosis in both retinal astrocytes and in Muller cells. AAA alone or in combination with KA decreased GFAP and vimentin-immunoreactivity in Mϋller cells, but not in astrocytes. In addition AAA failed to decrease KA-mediated protease levels and apoptotic death of RGCs. In contrast, Neurostatin either alone or in combination with KA, decreased reactive gliosis in both astrocytes and Mϋller cells. Furthermore, Neurostatin decreased protease levels and prevented apoptotic death of RGCs. Our findings, for the first time, indicate that inhibition of reactive gliosis decreases protease levels in the retina, prevents apoptotic death of retinal neurons, and provides substantial neuroprotection. |
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| id | doaj-art-b71cc18841cd437c97d720fedf0bfe27 |
| institution | Kabale University |
| issn | 1932-6203 |
| language | English |
| publishDate | 2011-03-01 |
| publisher | Public Library of Science (PLoS) |
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| spelling | doaj-art-b71cc18841cd437c97d720fedf0bfe272025-08-20T03:45:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-03-0163e1830510.1371/journal.pone.0018305Inhibition of reactive gliosis attenuates excitotoxicity-mediated death of retinal ganglion cells.Bhagyalaxmi S GaneshShravan K ChintalaReactive gliosis is a hallmark of many retinal neurodegenerative conditions, including glaucoma. Although a majority of studies to date have concentrated on reactive gliosis in the optic nerve head, very few studies have been initiated to investigate the role of reactive gliosis in the retina. We have previously shown that reactive glial cells synthesize elevated levels of proteases, and these proteases, in turn, promote the death of retinal ganglion cells (RGCs). In this investigation, we have used two glial toxins to inhibit reactive gliosis and have evaluated their effect on protease-mediated death of RGCs. Kainic acid was injected into the vitreous humor of C57BL/6 mice to induce reactive gliosis and death of RGCs. C57BL/6 mice were also treated with glial toxins, alpha-aminoadipic acid (AAA) or Neurostatin, along with KA. Reactive gliosis was assessed by immunostaining of retinal cross sections and retinal flat-mounts with glial fibrillary acidic protein (GFAP) and vimentin antibodies. Apoptotic cell death was assessed by TUNEL assays. Loss of RGCs was determined by immunostaining of flat-mounted retinas with Brn3a antibodies. Proteolytic activities of matrix metalloproteinase-9 (MMP-9), tissue plasminogen activator (tPA), and urokinase plasminogen activator (uPA) were assessed by zymography assays. GFAP-immunoreactivity indicated that KA induced reactive gliosis in both retinal astrocytes and in Muller cells. AAA alone or in combination with KA decreased GFAP and vimentin-immunoreactivity in Mϋller cells, but not in astrocytes. In addition AAA failed to decrease KA-mediated protease levels and apoptotic death of RGCs. In contrast, Neurostatin either alone or in combination with KA, decreased reactive gliosis in both astrocytes and Mϋller cells. Furthermore, Neurostatin decreased protease levels and prevented apoptotic death of RGCs. Our findings, for the first time, indicate that inhibition of reactive gliosis decreases protease levels in the retina, prevents apoptotic death of retinal neurons, and provides substantial neuroprotection.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0018305&type=printable |
| spellingShingle | Bhagyalaxmi S Ganesh Shravan K Chintala Inhibition of reactive gliosis attenuates excitotoxicity-mediated death of retinal ganglion cells. PLoS ONE |
| title | Inhibition of reactive gliosis attenuates excitotoxicity-mediated death of retinal ganglion cells. |
| title_full | Inhibition of reactive gliosis attenuates excitotoxicity-mediated death of retinal ganglion cells. |
| title_fullStr | Inhibition of reactive gliosis attenuates excitotoxicity-mediated death of retinal ganglion cells. |
| title_full_unstemmed | Inhibition of reactive gliosis attenuates excitotoxicity-mediated death of retinal ganglion cells. |
| title_short | Inhibition of reactive gliosis attenuates excitotoxicity-mediated death of retinal ganglion cells. |
| title_sort | inhibition of reactive gliosis attenuates excitotoxicity mediated death of retinal ganglion cells |
| url | https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0018305&type=printable |
| work_keys_str_mv | AT bhagyalaxmisganesh inhibitionofreactivegliosisattenuatesexcitotoxicitymediateddeathofretinalganglioncells AT shravankchintala inhibitionofreactivegliosisattenuatesexcitotoxicitymediateddeathofretinalganglioncells |