Does Sirt2 Regulate Cholesterol Biosynthesis During Oligodendroglial Differentiation In Vitro and In Vivo?

• Published in: Cellular and molecular neurobiology 2018, Vol.38 (1), p.329-340
• Main Authors: Thangaraj, Merlin P., Furber, Kendra L., Sobchishin, LaRhonda, Ji, Shaoping, Doucette, J. Ronald, Nazarali, Adil J.
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Biomedical and Life Sciences; Biomedicine; Biosynthesis; Cell Biology; Cell Differentiation - physiology; Cells, Cultured; Central nervous system; Cholesterol; Cholesterol - biosynthesis; Cholesterol - genetics; Gene expression; Kinases; Mice; Mice, 129 Strain; Mice, Inbred C57BL; Mice, Knockout; Myelination; Neurobiology; Neurogenesis - physiology; Neurosciences; Nuclear transport; Oligodendroglia - metabolism; Original Research; RNA-mediated interference; Rodents; Sirtuin 2 - physiology; Sterol regulatory element-binding protein; Substantia alba
• ISSN: 0272-4340; 1573-6830; 1573-6830
• DOI: 10.1007/s10571-017-0537-6

Sirtuin2 (SIRT2) is a deacetylase enzyme predominantly expressed in myelinating glia of the central nervous system (CNS). We have previously demonstrated that Sirt2 expression enhances oligodendrocyte (OL) differentiation and arborization in vitro, but the molecular targets of SIRT2 in OLs remain speculative. SIRT2 has been implicated in cholesterol biosynthesis by promoting the nuclear translocation of sterol regulatory element binding protein (SREBP)-2. We investigated this further in CNS myelination by examining the role of Sirt2 in cholesterol biosynthesis in vivo and in vitro employing Sirt2 − / − mice, primary OL cells and CG4-OL cells. Our results demonstrate that expression of cholesterol biosynthetic genes in the CNS white matter or cholesterol content in purified myelin fractions did not differ between Sirt2 − / − and age-matched wild-type mice. Cholesterol biosynthetic gene expression profiles and total cholesterol content were not altered in primary OLs from Sirt2 − / − mice and in CG4-OLs when Sirt2 was either down-regulated with RNAi or overexpressed. In addition, Sirt2 knockdown or overexpression in CG4-OLs had no effect on SREBP-2 nuclear translocation. Our results indicate that Sirt2 does not impact the expression of genes encoding enzymes involved in cholesterol biosynthesis, total cholesterol content, or nuclear translocation of SREBP-2 during OL differentiation and myelination.