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dc.date.accessioned 2019-10-25T13:15:54Z
dc.date.available 2019-10-25T13:15:54Z
dc.date.issued 2011-07-04
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/84041
dc.description.abstract Purpose. Simple sphingolipids control crucial cellular processes in several cell types. Previous work demonstrated that sphingolipids, such as ceramide, sphingosine, and sphingosine-1-phosphate, are key mediators in the regulation of survival, differentiation, and proliferation of retina photoreceptors. Ceramide-1-phosphate (C1P) regulates growth and survival in several cell types; however, little is known concerning its functions in the retina. Whether C1P also participates in controlling photoreceptor development was also explored. Methods. Rat retina neuronal cultures were supplemented with 1 to 10 μM C1P. Proliferation was determined by evaluating 5-bromo-2-deoxyuridine (BrdU) uptake and the number of mitotic figures and differentiation by evaluating opsin and peripherin expression by immunocytochemistry and Western blot. Apoptosis was inhibited with the pan caspase inhibitor ZVADFMK and evaluated by TUNEL assay, propidium iodide/annexin V, and DAPI labeling. Preservation of mitochondrial membrane potential was evaluated. Results. C1P enhanced BrdU uptake and increased mitosis in retinal progenitors. C1P addition advanced photoreceptor differentiation, enhancing opsin and peripherin expression and stimulating development of the apical processes in which these proteins were concentrated. In the absence of these trophic factors, photoreceptors degenerated after 4 days in vitro, and at day 6, almost 50% of photoreceptors were apoptotic. C1P decreased photoreceptor apoptosis, reducing this percentage by half. Inhibiting caspase activity reduced photoreceptor apoptosis in the controls, but did not increase opsin expression, implying that C1P has separate effects on differentiation and survival. Conclusions. These results suggest for the first time that C1P is a novel mediator that has multiple functions in photoreceptors, initially regulating their proliferation and then promoting their survival and differentiation. en
dc.format.extent 6580-6588 es
dc.language en es
dc.subject Sphingolipids es
dc.subject Ceramide-1-phosphate es
dc.subject Retina es
dc.subject Biología Celular es
dc.title Ceramide-1-phosphate, a new mediator of development and survival in retina photoreceptors en
dc.type Articulo es
sedici.identifier.other http://dx.doi.org/10.1167/iovs.10-7065 es
sedici.identifier.issn 0146-0404 es
sedici.creator.person Miranda, Gisela E. es
sedici.creator.person Abrahan, Carolina E. es
sedici.creator.person Agnolazza, Daniela L. es
sedici.creator.person Politi, Luis E. es
sedici.creator.person Rotstein, Nora P. es
sedici.subject.materias Biología es
sedici.description.fulltext true es
mods.originInfo.place Instituto Multidisciplinario de Biología Celular es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Investigative Ophthalmology and Visual Science es
sedici.relation.journalVolumeAndIssue vol. 52, no. 9 es
sedici.rights.sherpa * Color: verde* Pre-print del autor: si* Post-print del autor: no* Versión de editor/PDF:si* Condiciones:>>Author's pre-print on preprint server>>Author's pre-print deposit must be updated with published version upon publication>>On any website or open access repository>>La versión de editor/PDF debe utilizarse>>Creative Commons Attribution Non-Commercial No Derivatives License or Creative Commons Attribution License available>>NIH, HHMI and Wellcome Trust authors will have their articles automatically deposited in PubMed Central on their behalf>>Debe ir enlazado a la versión de editor>>All titles are open access journals>>Publisher last reviewed on 24/03/2016* Link a Sherpa: http://sherpa.ac.uk/romeo/issn/0146-0404/es/


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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)