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Article: Chemotactic effect of ciliary neurotrophic factor on macrophages in retinal ganglion cell survival and axonal regeneration
Title | Chemotactic effect of ciliary neurotrophic factor on macrophages in retinal ganglion cell survival and axonal regeneration |
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Authors | |
Issue Date | 2007 |
Publisher | Association for Research in Vision and Ophthalmology. The Journal's web site is located at http://www.iovs.org |
Citation | Investigative Ophthalmology And Visual Science, 2007, v. 48 n. 9, p. 4257-4266 How to Cite? |
Abstract | PURPOSE. To examine whether ciliary neurotrophic factor (CNTF) has a chemotactic effect on macrophages and whether macrophages are involved in CNTF-induced retinal ganglion cell (RGC) survival and axonal regeneration after optic nerve (ON) injury. METHODS. Adult Fischer 344 rats received an autologous peripheral nerve graft onto transected ON for injured axons to grow. CNTF was applied intravitreally. When needed, clodronate liposomes were applied intravitreally or intravenously to deplete macrophages in the eye. A chemotaxis microchamber system was used to examine whether CNTF has a chemotactic effect on macrophages in vitro, whereas immunohistochemistry was used to identify the location of macrophages/microglia in the retina. The effects of CNTF on RGC neurite outgrowth and macrophage/microglia proliferation were tested in retinal explants. RESULTS. Intravitreal CNTF significantly enhanced RGC survival and axonal regeneration as well as the number of macrophages in the eye. Removal of macrophages significantly reduced CNTF-induced RGC survival and axon regeneration. A chemotaxis assay showed a clear chemotactic effect of CNTF on blood-derived but not peritoneal macrophages. Immunohistochemistry revealed that local microglia was located in a region from the nerve fiber layer (NFL) to the inner nuclear layer, whereas blood-derived macrophages were in the NFL. In vitro experiments revealed that CNTF did not enhance neurite outgrowth or macrophage/microglia proliferation in retinal explants. CONCLUSIONS. CNTF is a chemoattractant but not a proliferation enhancer for blood-derived macrophages, and blood-borne macrophages recruited into the eye by CNTF participate in RGC protection. This finding thus adds an important category to the existing understanding of the biological actions of CNTF. Copyright © Association for Research in Vision and Ophthalmology. |
Persistent Identifier | http://hdl.handle.net/10722/149675 |
ISSN | 2023 Impact Factor: 5.0 2023 SCImago Journal Rankings: 1.422 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Cen, LP | en_US |
dc.contributor.author | Luo, JM | en_US |
dc.contributor.author | Zhang, CW | en_US |
dc.contributor.author | Fan, YM | en_US |
dc.contributor.author | Song, Y | en_US |
dc.contributor.author | So, KF | en_US |
dc.contributor.author | Van Rooijen, N | en_US |
dc.contributor.author | Pang, CP | en_US |
dc.contributor.author | Lam, DSC | en_US |
dc.contributor.author | Cui, Q | en_US |
dc.date.accessioned | 2012-06-26T05:56:56Z | - |
dc.date.available | 2012-06-26T05:56:56Z | - |
dc.date.issued | 2007 | en_US |
dc.identifier.citation | Investigative Ophthalmology And Visual Science, 2007, v. 48 n. 9, p. 4257-4266 | en_US |
dc.identifier.issn | 0146-0404 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/149675 | - |
dc.description.abstract | PURPOSE. To examine whether ciliary neurotrophic factor (CNTF) has a chemotactic effect on macrophages and whether macrophages are involved in CNTF-induced retinal ganglion cell (RGC) survival and axonal regeneration after optic nerve (ON) injury. METHODS. Adult Fischer 344 rats received an autologous peripheral nerve graft onto transected ON for injured axons to grow. CNTF was applied intravitreally. When needed, clodronate liposomes were applied intravitreally or intravenously to deplete macrophages in the eye. A chemotaxis microchamber system was used to examine whether CNTF has a chemotactic effect on macrophages in vitro, whereas immunohistochemistry was used to identify the location of macrophages/microglia in the retina. The effects of CNTF on RGC neurite outgrowth and macrophage/microglia proliferation were tested in retinal explants. RESULTS. Intravitreal CNTF significantly enhanced RGC survival and axonal regeneration as well as the number of macrophages in the eye. Removal of macrophages significantly reduced CNTF-induced RGC survival and axon regeneration. A chemotaxis assay showed a clear chemotactic effect of CNTF on blood-derived but not peritoneal macrophages. Immunohistochemistry revealed that local microglia was located in a region from the nerve fiber layer (NFL) to the inner nuclear layer, whereas blood-derived macrophages were in the NFL. In vitro experiments revealed that CNTF did not enhance neurite outgrowth or macrophage/microglia proliferation in retinal explants. CONCLUSIONS. CNTF is a chemoattractant but not a proliferation enhancer for blood-derived macrophages, and blood-borne macrophages recruited into the eye by CNTF participate in RGC protection. This finding thus adds an important category to the existing understanding of the biological actions of CNTF. Copyright © Association for Research in Vision and Ophthalmology. | en_US |
dc.language | eng | en_US |
dc.publisher | Association for Research in Vision and Ophthalmology. The Journal's web site is located at http://www.iovs.org | en_US |
dc.relation.ispartof | Investigative Ophthalmology and Visual Science | en_US |
dc.title | Chemotactic effect of ciliary neurotrophic factor on macrophages in retinal ganglion cell survival and axonal regeneration | en_US |
dc.type | Article | en_US |
dc.identifier.email | So, KF:hrmaskf@hkucc.hku.hk | en_US |
dc.identifier.authority | So, KF=rp00329 | en_US |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.doi | 10.1167/iovs.06-0791 | en_US |
dc.identifier.pmid | 17724215 | - |
dc.identifier.scopus | eid_2-s2.0-34548016256 | en_US |
dc.identifier.hkuros | 150998 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-34548016256&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 48 | en_US |
dc.identifier.issue | 9 | en_US |
dc.identifier.spage | 4257 | en_US |
dc.identifier.epage | 4266 | en_US |
dc.identifier.isi | WOS:000249061900050 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Cen, LP=36856212100 | en_US |
dc.identifier.scopusauthorid | Luo, JM=51562038700 | en_US |
dc.identifier.scopusauthorid | Zhang, CW=51562967800 | en_US |
dc.identifier.scopusauthorid | Fan, YM=19337163200 | en_US |
dc.identifier.scopusauthorid | Song, Y=51562462900 | en_US |
dc.identifier.scopusauthorid | So, KF=34668391300 | en_US |
dc.identifier.scopusauthorid | Van Rooijen, N=35428581800 | en_US |
dc.identifier.scopusauthorid | Pang, CP=7201425127 | en_US |
dc.identifier.scopusauthorid | Lam, DSC=35500200200 | en_US |
dc.identifier.scopusauthorid | Cui, Q=7103080164 | en_US |
dc.identifier.issnl | 0146-0404 | - |