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dc.date.accessioned 2020-10-28T14:26:10Z
dc.date.available 2020-10-28T14:26:10Z
dc.date.issued 2019
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/107850
dc.description.abstract Gaucher and Fabry diseases are the most prevalent sphingolipidoses. Chronic inflammation is activated in those disorders, which could play a role in pathogenesis. Significant degrees of amelioration occur in patients upon introduction of specific therapies; however, restoration to complete health status is not always achieved. The idea of an adjunctive therapy that targets inflammation may be a suitable option for patients. PPS is a mixture of semisynthetic sulfated polyanions that have been shown to have anti-inflammatory effects in mucopolysaccharidosis type I and II patients and animal models of type I, IIIA and VI. We hypothesized PPS could be a useful adjunctive therapy to inflammation for Gaucher and Fabry diseases. The objective of this work is to analyze the in vitro effect of PPS on inflammatory cytokines in cellular models of Gaucher and Fabry diseases, and to study its effect in Gaucher disease associated in vitro bone alterations. Cultures of peripheral blood mononuclear cells from Fabry and Gaucher patients were exposed to PPS. The secretion of proinflammatory cytokines was significantly reduced. Peripheral blood cells exposed to PPS from Gaucher patients revealed a reduced tendency to differentiate to osteoclasts. Osteoblasts and osteocytes cell lines were incubated with an inhibitor of glucocerebrosidase, and conditioned media was harvested in order to analyze if those cells secrete factors that induce osteoclastogenesis. Conditioned media from this cell cultures exposed to PPS produced lower numbers of osteoclasts. We could demonstrate PPS is an effective molecule to reduce the production of proinflammatory cytokines in in vitro models of Fabry and Gaucher diseases. Moreover, it was effective at ameliorating bone alterations of in vitro models of Gaucher disease. These results serve as preclinical supportive data to start clinical trials in human patients to analyze the effect of PPS as a potential adjunctive therapy for Fabry and Gaucher diseases. en
dc.language en es
dc.subject Gaucher's disease es
dc.subject cytokines es
dc.subject inflammatory diseases es
dc.subject osteoclasts es
dc.subject cytokine therapy es
dc.subject lysosomes es
dc.subject osteoblasts es
dc.subject Fabry disease es
dc.title Efficacy of pentosan polysulfate in in vitro models of lysosomal storage disorders: Fabry and Gaucher Disease en
dc.type Articulo es
sedici.identifier.uri http://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC6544267&blobtype=pdf es
sedici.identifier.uri https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0217780 es
sedici.identifier.other pmid:31150494 es
sedici.identifier.other pmcid:PMC6544267 es
sedici.identifier.other https://doi.org/10.1371/journal.pone.0217780 es
sedici.identifier.issn 1932-6203 es
sedici.creator.person Crivaro, Andrea Natalia es
sedici.creator.person Mucci, Juan Marcos es
sedici.creator.person Bondar, Constanza María es
sedici.creator.person Ormazabal, Maximiliano Emanuel es
sedici.creator.person Ceci, Romina es
sedici.creator.person Simonaro, Calogera es
sedici.creator.person Rozenfeld, Paula Adriana es
sedici.subject.materias Ciencias Exactas es
sedici.description.fulltext true es
mods.originInfo.place Facultad de Ciencias Exactas es
mods.originInfo.place Instituto de Estudios Inmunológicos y Fisiopatológicos es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution 4.0 International (CC BY 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle PLoS ONE es
sedici.relation.journalVolumeAndIssue vol. 14, no. 5 es


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