Literature DB >> 21470123

Following intracellular cholesterol transport by linear and non-linear optical microscopy of intrinsically fluorescent sterols.

Daniel Wüstner1.   

Abstract

Elucidation of intracellular cholesterol transport is important for understanding the molecular basis of several metabolic and neuronal diseases, like atheroclerosis or lysosomal storage disorders. Progress in this field depends crucially on the development of new technical approaches to follow the cellular movement of this essential lipid molecule. In this article, a survey of the various methods being used for analysis of sterol trafficking is given. Various classical biochemical methods are presented and their suitability for analysis of sterol trafficking is assessed. Special emphasis is on recent developments in imaging technology to follow the intracellular fate of intrinsically fluorescent sterols as faithful cholesterol markers. In particular, UV-sensitive wide field and multiphoton microscopy of the sterol dehydroergosterol, DHE, is explained and new methods of quantitative image analysis like pixel-wise bleach rate fitting and multiphoton image correlation spectroscopy are introduced. Several applications of the new technology including observation of vectorial sterol trafficking in polarized human hepatoma cells for investigation of reverse cholesterol transport are presented.

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Year:  2012        PMID: 21470123     DOI: 10.2174/138920112799095301

Source DB:  PubMed          Journal:  Curr Pharm Biotechnol        ISSN: 1389-2010            Impact factor:   2.837


  4 in total

1.  Analysis of cholesterol trafficking with fluorescent probes.

Authors:  Frederick R Maxfield; Daniel Wüstner
Journal:  Methods Cell Biol       Date:  2012       Impact factor: 1.441

2.  Two-photon time-lapse microscopy of BODIPY-cholesterol reveals anomalous sterol diffusion in chinese hamster ovary cells.

Authors:  Frederik W Lund; Michael A Lomholt; Lukasz M Solanko; Robert Bittman; Daniel Wüstner
Journal:  BMC Biophys       Date:  2012-10-18       Impact factor: 4.778

3.  Essentially all excess fibroblast cholesterol moves from plasma membranes to intracellular compartments.

Authors:  Yvonne Lange; Jin Ye; Theodore L Steck
Journal:  PLoS One       Date:  2014-07-11       Impact factor: 3.240

4.  Computational Modeling Explains the Multi Sterol Ligand Specificity of the N-Terminal Domain of Niemann-Pick C1-Like 1 Protein.

Authors:  Vasanthanathan Poongavanam; Jacob Kongsted; Daniel Wüstner
Journal:  ACS Omega       Date:  2019-12-03
  4 in total

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