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Skipped BSCL2 Transcript in Celia's Encephalopathy (PELD): New Insights on Fatty Acids Involvement, Senescence and Adipogenesis

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dc.contributor.author Sánchez-Iglesias, Sofia
dc.contributor.author Unruh-Pinheiro, Alexander
dc.contributor.author Guillin-Amarelle, Cristina
dc.contributor.author González-Mendez, Blanca
dc.contributor.author Ruiz-Riquelme, Alejandro
dc.contributor.author Leticia-Rodriguez-Canete, Blanca
dc.contributor.author Rodriguez-García, Silvia
dc.contributor.author Araujo-Vilar, David
dc.contributor.author Guillén-Navarro, Encarna
dc.contributor.author Domingo-Jiménez, Rosario
dc.date.accessioned 2026-10-21T06:05:08Z
dc.date.available 2026-10-21T06:05:08Z
dc.date.issued 2016-07-08
dc.identifier.citation Sánchez-Iglesias S, Unruh-Pinheiro A, Guillín-Amarelle C, González-Méndez B, Ruiz-Riquelme A, Rodríguez-Cañete BL, et al. Skipped BSCL2 Transcript in Celia's Encephalopathy (PELD): New Insights on Fatty Acids Involvement, Senescence and Adipogenesis. López M, editor. PLoS ONE. 8 de julio de 2016;11(7):e0158874. doi:10.1371/journal.pone.0158874
dc.identifier.issn 1932-6203
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/28672
dc.description.abstract OBJECTIVE: PELD (Progressive Encephalopathy with or without Lipodystrophy or Celia's Encephalopathy) is a fatal and rare neurodegenerative syndrome associated with the BSCL2 mutation c.985C>T, that results in an aberrant transcript without the exon 7 (Celia seipin). The aim of this study was to evaluate both the process of cellular senescence and the effect of unsaturated fatty acids on preadipocytes from a homozygous c.985C>T patient. Also, the role of aberrant seipin isoform on adipogenesis was studied in adipose-derived human mesenchymal stem cells. MATERIAL AND METHODS: Cellular senescence was evaluated using ?-galactosidase staining of preadipocytes obtained from a homozygous c.985C>T patient. Moreover, these cells were cultured during 24 hours with Intralipid, a soybean oil-based commercial lipid emulsion. The expression of the different BSCL2 transcripts was measured by qPCR. Adipose-derived human mesenchymal stem cells were differentiated to a fat lineage using StemPRO adipogenesis kit, and the expression of BSCL2 transcripts and several adipogenesis-related genes was measured by qPCR. RESULTS: the treatment of preadipocytes with unsaturated fatty acids significantly reduced the expression of the BSCL2 transcript without exon 7 by 34 to 63%. On the other hand, at least in preadipocytes, this mutation does not disturb cellular senescence rate. Finally, during adipocyte differentiation of adipose-derived human mesenchymal stem cells, the expression of adipogenic genes (PPARG, LPIN1, and LPL) increased significantly over 14 days, and noteworthy is that the BSCL2 transcript without exon 7 was differentially expressed by 332 to 723% when compared to day 0, suggesting an underlying role in adipogenesis. CONCLUSIONS: our results suggest that Celia seipin is probably playing an underestimated role in adipocyte maturation, but not in senescence, and its expression can be modified by exogenous factors as fatty acids.
dc.language.iso eng
dc.rights Atribución/Reconocimiento 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by/4.0/deed.es *
dc.subject.mesh Adipocytes/metabolism/pathology
dc.subject.mesh Cellular Senescence/drug effects/genetics
dc.subject.mesh Fatty Acids, Unsaturated/pharmacology
dc.subject.mesh Female
dc.subject.mesh GTP-Binding Protein gamma Subunits/biosynthesis/genetics
dc.subject.mesh Heredodegenerative Disorders, Nervous System/drug therapy/genetics/metabolism/pathology
dc.subject.mesh Humans
dc.subject.mesh Lipodystrophy/drug therapy/genetics/metabolism/pathology
dc.subject.mesh Male
dc.subject.mesh Mesenchymal Stem Cells/metabolism/pathology
dc.subject.mesh Point Mutation
dc.title Skipped BSCL2 Transcript in Celia's Encephalopathy (PELD): New Insights on Fatty Acids Involvement, Senescence and Adipogenesis
dc.type info:eu-repo/semantics/article 
dc.identifier.pmid 27391332
dc.relation.publisherversion https://dx.plos.org/10.1371/journal.pone.0158874
dc.identifier.doi 10.1371/journal.pone.0158874
dc.journal.title Plos One


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