Title
TERT inhibition leads to reduction of IL-6 expression induced by palmitic acid and interferes with the protective effects of tibolone in an astrocytic cell model
Date Issued
01 January 2019
Access level
metadata only access
Resource Type
journal article
Author(s)
Pontificia Universidad Javeriana
Publisher(s)
Blackwell Publishing Ltd
Abstract
Although it has been shown that telomerase has neuroprotective effects, mainly as a result of its non-canonical functions in neuronal cells, its role with respect to glial cells remains unknown. There is growing evidence indicating that telomerase plays an important role with respect to inflammation, especially in the regulation of pro-inflammatory cytokine gene expression. The present study aimed to evaluate the role of telomerase in an astrocyte cell model treated with palmitic acid (PA) and tibolone. Cell death, reactive oxygen species production and interleukin-6 expression were evaluated under telomerase inhibition with the BIBR1532 compound in T98G cells treated with tibolone and PA, using fluorometry, flow cytometry, enzyme-linked immunosorbent assays and the quantitative polymerase chain reaction. The results obtained showed that telomerase protein was increased by PA after 36 hours, alone or in combination with tibolone, and that its activity was affected by PA. Telomerase inhibition reduced interleukin-6 expression and it interfered with the protective effects of tibolone on cell death. Moreover, tibolone increased Tyr707 phosphorylation in PA-treated cells. In the present study, we provide novel findings about the regulation of telomerase by PA and tibolone. Telomerase was involved in inflammation by PA and in protective effects of tibolone. Therefore, we conclude that telomerase could play a dual role in these cells.
Volume
31
Issue
8
Language
English
OCDE Knowledge area
Bioquímica, Biología molecular
Neurociencias
Subjects
Scopus EID
2-s2.0-85069928303
PubMed ID
Source
Journal of Neuroendocrinology
ISSN of the container
09538194
Sponsor(s)
YG-G is supported by a PhD fellowship from the Centro de Estudios Interdisciplinarios Básicos y Aplicados CEIBA (Rodolfo Llinás Program). The present study was supported by a research grant from Colciencias (Grant No. 824-2017).
YG‐G is supported by a PhD fellowship from the Centro de Estudios Interdisciplinarios Básicos y Aplicados C?IBA (Rodolfo Llinás Program). The present study was supported by a research grant from Colciencias (Grant No. 824‐2017).
Sources of information:
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