Literature DB >> 17378665

Precholesterol sterols accumulate in lipid rafts of patients with Smith-Lemli-Opitz syndrome and X-linked dominant chondrodysplasia punctata.

Dinesh Rakheja1, Richard L Boriack.   

Abstract

Systemic fetal dysmorphogenesis in disorders of postsqualene cholesterol biosynthesis is thought to be caused by disruption of Hedgehog signaling. Because precholesterol sterols such as 7-dehydrocholesterol and lathosterol can replace cholesterol in the activation of Hedgehog proteins, it is currently believed that cholesterol deficiency-related Hedgehog signaling block occurs further downstream, probably at the level of Smoothened. Experimentally, such a block in Hedgehog signaling occurs at sterol levels of <40 mug/mg protein. Recently, we studied autopsy material from 2 infants with fatal cholesterol biosynthetic disorders (Smith-Lemli-Opitz syndrome and X-linked dominant chondrodysplasia punctata) in which the hepatic cholesterol levels were far greater. In this study, we demonstrate abnormal accumulation of sterol precursors of cholesterol in membrane lipid rafts (detergent resistance membranes) prepared from liver tissues of these 2 infants: 8-dehydrocholesterol and 7-dehydrocholesterol in lipid rafts of the infant with Smith-Lemli-Opitz syndrome and cholest-8(9)-ene-3beta-ol in lipid rafts of the infant with X-linked dominant chondrodysplasia punctata. We suggest that such alterations in the lipid raft sterol environment may affect the biology of cells and the development of fetuses with cholesterol biosynthetic disorders.

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Year:  2007        PMID: 17378665     DOI: 10.2350/06-10-0179.1

Source DB:  PubMed          Journal:  Pediatr Dev Pathol        ISSN: 1093-5266


  7 in total

1.  Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay.

Authors:  Miao He; Lisa E Kratz; Joshua J Michel; Abbe N Vallejo; Laura Ferris; Richard I Kelley; Jacqueline J Hoover; Drazen Jukic; K Michael Gibson; Lynne A Wolfe; Dhanya Ramachandran; Michael E Zwick; Jerry Vockley
Journal:  J Clin Invest       Date:  2011-03       Impact factor: 14.808

2.  Alterations in membrane caveolae and BKCa channel activity in skin fibroblasts in Smith-Lemli-Opitz syndrome.

Authors:  Gongyi Ren; Robert F Jacob; Yuri Kaulin; Paul Dimuzio; Yi Xie; R Preston Mason; G Stephen Tint; Robert D Steiner; Jean-Baptiste Roullet; Louise Merkens; Diana Whitaker-Menezes; Philippe G Frank; Michael P Lisanti; Robert H Cox; Thomas N Tulenko
Journal:  Mol Genet Metab       Date:  2011-05-27       Impact factor: 4.797

3.  Corpus callosum measurements correlate with developmental delay in Smith-Lemli-Opitz syndrome.

Authors:  Ryan W Y Lee; Shoko Yoshida; Eun Sol Jung; Susumu Mori; Eva H Baker; Forbes D Porter
Journal:  Pediatr Neurol       Date:  2013-08       Impact factor: 3.372

4.  Brain magnetic resonance imaging findings in Smith-Lemli-Opitz syndrome.

Authors:  Ryan W Y Lee; Sandra K Conley; Andrea Gropman; Forbes D Porter; Eva H Baker
Journal:  Am J Med Genet A       Date:  2013-08-05       Impact factor: 2.802

Review 5.  The role of sterol-C4-methyl oxidase in epidermal biology.

Authors:  Miao He; Laurie D Smith; Richard Chang; Xueli Li; Jerry Vockley
Journal:  Biochim Biophys Acta       Date:  2013-10-18

6.  Hypothesis: the role of sterols in autism spectrum disorder.

Authors:  Ryan W Y Lee; Elaine Tierney
Journal:  Autism Res Treat       Date:  2011-04-27

7.  Quantitative profiling of brain lipid raft proteome in a mouse model of fragile X syndrome.

Authors:  Magdalena Kalinowska; Catherine Castillo; Anna Francesconi
Journal:  PLoS One       Date:  2015-04-07       Impact factor: 3.240

  7 in total

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