Literature DB >> 23230282

What dictates the accumulation of desmosterol in the developing brain?

Maurice Jansen1, Wei Wang, Dario Greco, Gian Carlo Bellenchi, Umberto di Porzio, Andrew J Brown, Elina Ikonen.   

Abstract

The brain is the most cholesterol-enriched tissue in the body. During brain development, desmosterol, an immediate precursor of cholesterol, transiently accumulates up to 30% of total brain sterols. This massive desmosterol deposition appears to be present in all mammalian species reported so far, including humans, but how it is achieved is not well understood. Here, we propose that desmosterol accumulation in the developing brain may be primarily caused by post-transcriptional repression of 3β-hydroxysterol 24-reductase (DHCR24) by progesterone. Furthermore, distinct properties of desmosterol may serve to increase the membrane active pool of sterols in the brain: desmosterol cannot be hydroxylated to generate 24S-hydroxycholesterol, a brain derived secretory sterol, desmosterol has a reduced propensity to be esterified as compared to cholesterol, and desmosterol may activate LXR to stimulate astrocyte sterol secretion. This regulated accumulation of desmosterol by progesterone-induced suppression of DHCR24 may facilitate the rapid enrichment and distribution of membrane sterols in the developing brain.

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Year:  2012        PMID: 23230282     DOI: 10.1096/fj.12-211235

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  17 in total

1.  Cholesterol metabolism changes under long-term dietary restrictions while the cholesterol homeostasis remains unaffected in the cortex and hippocampus of aging rats.

Authors:  Kosara Smiljanic; Tim Vanmierlo; Aleksandra Mladenovic Djordjevic; Milka Perovic; Sanja Ivkovic; Dieter Lütjohann; Selma Kanazir
Journal:  Age (Dordr)       Date:  2014-04-23

Review 2.  Post-translational control of the long and winding road to cholesterol.

Authors:  Laura J Sharpe; Hudson W Coates; Andrew J Brown
Journal:  J Biol Chem       Date:  2020-12-18       Impact factor: 5.157

3.  The terminal enzymes of cholesterol synthesis, DHCR24 and DHCR7, interact physically and functionally.

Authors:  Winnie Luu; Gene Hart-Smith; Laura J Sharpe; Andrew J Brown
Journal:  J Lipid Res       Date:  2015-01-31       Impact factor: 5.922

4.  Desmosterolosis and desmosterol homeostasis in the developing mouse brain.

Authors:  Luke B Allen; Thiago C Genaro-Mattos; Ned A Porter; Károly Mirnics; Zeljka Korade
Journal:  J Inherit Metab Dis       Date:  2019-04-08       Impact factor: 4.982

Review 5.  Post-translational control of the long and winding road to cholesterol.

Authors:  Laura J Sharpe; Hudson W Coates; Andrew J Brown
Journal:  J Biol Chem       Date:  2020-10-13       Impact factor: 5.157

6.  Desmosterol in brain is elevated because DHCR24 needs REST for Robust Expression but REST is poorly expressed.

Authors:  G S Tint; Luxing Pan; Quan Shang; Laura J Sharpe; Andrew J Brown; Man Li; Hongwei Yu
Journal:  Dev Neurosci       Date:  2014-05-24       Impact factor: 2.984

7.  Analysis of hedgehog signaling in cerebellar granule cell precursors in a conditional Nsdhl allele demonstrates an essential role for cholesterol in postnatal CNS development.

Authors:  David Cunningham; Andrea E DeBarber; Natalie Bir; Laura Binkley; Louise S Merkens; Robert D Steiner; Gail E Herman
Journal:  Hum Mol Genet       Date:  2015-02-04       Impact factor: 6.150

8.  Signaling regulates activity of DHCR24, the final enzyme in cholesterol synthesis.

Authors:  Winnie Luu; Eser J Zerenturk; Ika Kristiana; Martin P Bucknall; Laura J Sharpe; Andrew J Brown
Journal:  J Lipid Res       Date:  2013-12-20       Impact factor: 5.922

9.  Inhibitors of 7-Dehydrocholesterol Reductase: Screening of a Collection of Pharmacologically Active Compounds in Neuro2a Cells.

Authors:  Hye-Young H Kim; Zeljka Korade; Keri A Tallman; Wei Liu; C David Weaver; Karoly Mirnics; Ned A Porter
Journal:  Chem Res Toxicol       Date:  2016-04-28       Impact factor: 3.739

Review 10.  Controlling cholesterol synthesis beyond 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR).

Authors:  Laura J Sharpe; Andrew J Brown
Journal:  J Biol Chem       Date:  2013-05-21       Impact factor: 5.157

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