The DOI matches its Crossref record.
Analysis of Cholesterol Trafficking with Fluorescent Probes
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Increased cholesterol in APOE4 astrocytes is due to slower exchange to HDL.
“When astrocytes were incubated with the cholesterol efflux acceptor HDL, the percent dehydroergosterol (DHE), a natural fluorescent sterol that mimics cellular/membrane cholesterol (Maxfield and Wustner, 2012), remained significantly increased in APOE4 astrocytes after 24h (Figure S6P), indicating that increased cholesterol is due to slower exchange to HDL.”
From Cholesterol and matrisome pathways dysregulated in astrocytes and microglia (2022) · cites this paper as Maxfield and Wustner, 2012
When astrocytes were incubated with the cholesterol efflux acceptor HDL, the percent dehydroergosterol (DHE) remained significantly increased in APOE4 astrocytes after 24h.
“When astrocytes were incubated with the cholesterol efflux acceptor HDL, the percent dehydroergosterol (DHE), a natural fluorescent sterol that mimics cellular/membrane cholesterol (Maxfield and Wustner, 2012), remained significantly increased in APOE4 astrocytes after 24h (Figure S6P), indicating that increased cholesterol is due to slower exchange to HDL.”
From Cholesterol and matrisome pathways dysregulated in astrocytes and microglia (2022) · cites this paper as Maxfield and Wustner, 2012
Dehydroergosterol (DHE) is a naturally occurring sterol that closely mimics the behavior of cholesterol in cells and membranes.
“Dehydroergosterol (DHE) is a naturally-occurring sterol that closely mimics the behavior of cholesterol in cells and membranes (Hao et al., 2002; Maxfield and Wustner, 2012).”
From Cholesterol and matrisome pathways dysregulated in astrocytes and microglia (2022) · cites this paper as Maxfield and Wustner, 2012
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
No references could be resolved yet.
Research works printed but not linked: 119
- Ahmed, 1997, On the origin of sphingolipid/cholesterol-rich detergent-insoluble cell membranes: physiological concentrations of cholesterol and sphingolipid induce formation of a detergent-insoluble, liquid-ordered lipid phase in model membranes, Biochemistry, 36, 10944, 10.1021/bi971167g · DOI
- Aittoniemi, 2006, Tilt: major factor in sterols’ ordering capability in membranes, J. Phys. Chem. B, 110, 25562, 10.1021/jp064931u · DOI
- Anderton, 2011, Correlated AFM and NanoSIMS imaging to probe cholesterol-induced changes in phase behavior and non-ideal mixing in ternary lipid membranes, Biochim. Biophys. Acta, 1808, 307, 10.1016/j.bbamem.2010.09.016 · DOI
- Altelaar, 2006, Gold-enhanced biomolecular surface imaging of cells and tissue by SIMS and MALDI mass spectrometry, Anal. Chem., 78, 734, 10.1021/ac0513111 · DOI
- Ariola, 2009, Membrane fluidity and lipid order in ternary giant unilamellar vesicles using a new bodipy-cholesterol derivative, Biophys. J., 96, 2696, 10.1016/j.bpj.2008.12.3922 · DOI
- Arthur, J.R., Heinecke, K.A., and Seyfried, T.N. Filipin recognizes both GM1 and cholesterol in GM1 gangliosidosis mouse brain. J. Lipid Res.52, 1345-1351. · DOI
- Baumgart, 2007, Fluorescence probe partitioning between Lo/Ld phases in lipid membranes, Biochim. Biophys. Acta, 1768, 2182, 10.1016/j.bbamem.2007.05.012 · DOI
- Benson, 1985, Digital imaging fluorescence microscopy: spatial heterogeneity of photobleaching rate constants in individual cells, J. Cell Biol., 100, 1309, 10.1083/jcb.100.4.1309 · DOI
- Bergström, 2002, Dimers of Dipyrrometheneboron difluoride (BODIPY) with light spectroscopic applications in chemistry and biology, J. Am. Chem. Soc., 124, 196, 10.1021/ja010983f · DOI
- Boxer, 2009, Advances in imaging secondary ion mass spectrometry for biological samples, Annu. Rev. Biophys., 38, 53, 10.1146/annurev.biophys.050708.133634 · DOI
- Breslow, 1996, Cholesterol recognition and binding by cyclodextrin dimers, J. Am. Chem. Soc., 118, 8495, 10.1021/ja961567b · DOI
- Chen, 1997, Changes in the spectral properties of a plasma membrane lipid analog during the first seconds of endocytosis in living cells, Biophys. J., 72, 37, 10.1016/S0006-3495(97)78645-4 · DOI
- Cheng, 2002, Laser-scanning coherent anti-Stokes Raman scattering microscopy and applications to cell biology, Biophys. J., 83, 502, 10.1016/S0006-3495(02)75186-2 · DOI
- Chiantia, 2008, Role of ceramide in membrane protein organization investigated by combined AFM and FCS, Biochim. Biophys. Acta, 1778, 1356, 10.1016/j.bbamem.2008.02.008 · DOI
- Chien, 2011, Label-free imaging of Drosophila in vivo by coherent anti-Stokes Raman scattering and two-photon excitation autofluorescence microscopy, J. Biomed. Optics, 16, 016012, 10.1117/1.3528642 · DOI
- Chong, 1986, Depolarization of dehydroergosterol in phospholipid bilayers, Biochim. Biophys. Acta, 863, 53, 10.1016/0005-2736(86)90386-X · DOI
- Craig, I.F., Via, D.P., Mantulin, W.W., Pownall, H.J., Gotto, A.M.J., and L.C.S. (1981). Low density lipoproteins reconstituted with steroids containing the nitrobenzoxadiazole fluorophore. J. Lipid Res.22, 687-696. · DOI
- Du, 2011, A role for oxysterol-binding protein-related protein 5 in endosomal cholesterol trafficking, J. Cell Biol., 192, 121, 10.1083/jcb.201004142 · DOI
- Ellinger, 2010, High-pressure freezing combined with in vivo-DAB-cytochemistry: a novel approach for studies of endocytic compartments, J. Struct. Biol., 169, 286, 10.1016/j.jsb.2009.10.011 · DOI
- Fischer, 1984, Delta 5,7,9(11)-Cholestatrien-3 beta-ol: a fluorescent cholesterol analogue, Chem. Phys. Lipids, 36, 1, 10.1016/0009-3084(84)90086-0 · DOI
- Fischer, 1985, Structure and Dynamic Properties of Dehydroergosterol, delta 5,7,9(11),22-ergostatetraen-3 beta-ol, J. Biol. Chem., 13, 13
- Fischer, 1985, Fluorescence of delta 5,7,9(11),22-ergostatetraen-3 beta-ol in micelles, sterol carrier protein complexes, and plasma membranes, Biochemistry, 24, 3322, 10.1021/bi00334a037 · DOI
- Fellmann, 1994, Synthesis and use of spin-labeled lipids for studies of the transmembrane movement of phospholipids, Methods Mol. Biol., 27, 161
- Frolov, 2000, High density lipoprotein-mediated cholesterol uptake and targeting to lipid droplets in intact L-cell fibroblasts, J. Biol. Chem., 275, 12769, 10.1074/jbc.275.17.12769 · DOI
- Garvik, 2008, The fluorescent cholesterol analog dehydroergosterol induces liquid-ordered domains in model membranes, Chem. Phys. Lipids, 159, 114, 10.1016/j.chemphyslip.2009.03.002 · DOI
- Georgiev, 2011, Osh Proteins Regulate Membrane Sterol Organization but Are Not Required for Sterol Movement Between the ER and PM, Traffic, 12, 1341, 10.1111/j.1600-0854.2011.01234.x · DOI
- Gimpl, 2010, Cholesterol-protein interaction: methods and cholesterol reporter molecules, Subcell. Biochem., 51, 1, 10.1007/978-90-481-8622-8_1 · DOI
- Haka, 2009, Diagnosing breast cancer using Raman spectroscopy: prospective analysis, J. Biomed. Optics, 14, 054023, 10.1117/1.3247154 · DOI
- Haka, 2011, Mechanism of ceroid formation in atherosclerotic plaque: in situ studies using a combination of Raman and fluorescence spectroscopy, J. Biomed. Optics, 16, 011011, 10.1117/1.3524304 · DOI
- Hale, 1982, Asymmetric transbilayer distribution of sterol across plasma membranes determined by fluorescence quenching of dehydroergosterol, Eur. J. Biochem., 122, 649, 10.1111/j.1432-1033.1982.tb06488.x · DOI
- Hao, 2002, Vesicular and non-vesicular sterol transport in living cells. The endocytic recycling compartment is a major sterol storage organelle, J. Biol. Chem., 277, 609, 10.1074/jbc.M108861200 · DOI · Paper page
- Hartwig Petersen, 2008, Kinetic imaging of NPC1L1 and sterol trafficking between plasma membrane and recycling endosomes in hepatoma cells, J. Lipid Res., 49, 2023, 10.1194/jlr.M800145-JLR200 · DOI
- Henriksen, 2004, Vesicle fluctuation analysis of the effects of sterols on membrane bending rigidity, Eur. Biophys. J., 33, 732, 10.1007/s00249-004-0420-5 · DOI
- Henriksen, 2006, Universal behavior of membranes with sterols, Biophys. J., 90, 1639, 10.1529/biophysj.105.067652 · DOI
- Hofsass, 2003, Molecular dynamics simulations of phospholipid bilayers with cholesterol, Biophys. J., 84, 2192, 10.1016/S0006-3495(03)75025-5 · DOI
- Hölttä-Vuori, 2008, BODIPY-cholesterol: a new tool to visualize sterol trafficking in living cells and organisms, Traffic, 9, 1839, 10.1111/j.1600-0854.2008.00801.x · DOI
- Huang, 2010, Use of dansyl-cholestanol as a probe of cholesterol behavior in membranes of living cells, J. Lipid Res., 51, 1157, 10.1194/jlr.M003244 · DOI
- Hyslop, 1990, Organization and interaction of cholesterol and phosphatidylcholine in model bilayer membranes, Biochemistry, 29, 1025, 10.1021/bi00456a027 · DOI
- Jansen, 2011, Role of ORPs in sterol transport from plasma membrane to ER and lipid droplets in mammalian cells, Traffic, 12, 218, 10.1111/j.1600-0854.2010.01142.x · DOI
- Ipsen, 1987, Phase equilibria in the phosphatidylcholine-cholesterol system, Biochim. Biophys. Acta, 905, 162, 10.1016/0005-2736(87)90020-4 · DOI
- Kohut, 2011, The role of ABC proteins Aus1p and Pdr11p in the uptake of external sterols in yeast: Dehydroergosterol fluorescence study, Biochem. Biophys. Res. Commun., 404, 233, 10.1016/j.bbrc.2010.11.099 · DOI
- Krieger, 1986, Reconstitution of the hydrophobic core of low-denstiy lipoprotein, Methods Enzymol., 128, 608, 10.1016/0076-6879(86)28094-5 · DOI
- Lindahl, 2000, Spatial and energetic-entropic decomposition of surface tension in lipid bilayers from molecular dynamics simulations, J. Chem. Phys., 113, 3882, 10.1063/1.1287423 · DOI
- Li, 2005, Quantitative coherent anti-stokes Raman scattering imaging of lipid distribution in coexisting domains, Biophys. J., 89, 3480, 10.1529/biophysj.105.065607 · DOI
- Li, 2006, First synthesis of free cholesterol-BODIPY conjugates, J. Org. Chem., 71, 1718, 10.1021/jo052029x · DOI
- Lim, 2010, Multimodal CARS microscopy determination of the impact of diet on macrophage infiltration and lipid accumulation on plaque formation in ApoE-deficient mice, J. Lipid Res., 51, 1729, 10.1194/jlr.M003616 · DOI
- Loura, 2001, Exclusion of a cholesterol analog from the cholesterol-rich phase in model membranes, Biochim. Biophys. Acta, 1511, 236, 10.1016/S0005-2736(01)00269-3 · DOI
- Luisier, F. (2010). The SURE-LET Approach to Image Denoising. PhD thesis. EPFL, Thesis No. 4566.
- Marks, 2008, Use of Bodipy-labeled sphingolipid and cholesterol analogs to examine membrane microdomains in cells, Histochem. Cell Biol., 130, 819, 10.1007/s00418-008-0509-5 · DOI
- Markham, 2001, Artefacts in restored images due to intensity loss in three-dimensional fluorescence microscopy, J. Microsc., 204, 93, 10.1046/j.1365-2818.2001.00961.x · DOI
- Marsan, 1999, Cholesterol orientation and dynamics in dimyristoylphosphatidylcholine bilayers: a solid state deuterium NMR analysis, Biophys. J., 76, 351, 10.1016/S0006-3495(99)77202-4 · DOI
- Matyash, 2001, Distribution and transport of cholesterol in Caenorhabditis elegans, Mol. Biol. Cell, 12, 1725, 10.1091/mbc.12.6.1725 · DOI
- McIntosh, 2003, Fluorescence and multiphoton imaging resolve unique structural forms of sterol in membranes of living cells, J. Biol. Chem., 278, 6384, 10.1074/jbc.M205472200 · DOI
- McIntosh, 2008, Fluorescence techniques using dehydroergosterol to study cholesterol trafficking, Lipids, 43, 1185, 10.1007/s11745-008-3194-1 · DOI
- Mesmin, 2009, Intracellular sterol dynamics, Biochim. Biophys. Acta, 1791, 636, 10.1016/j.bbalip.2009.03.002 · DOI
- Mondal, 2009, Sterols are mainly in the cytoplasmic leaflet of the plasma membrane and the endocytic recycling compartment in CHO cells, Mol. Biol. Cell, 20, 581, 10.1091/mbc.E08-07-0785 · DOI
- Mörck, 2009, Statins inhibit protein lipidation and induce the unfolded protein response in the non-sterol producing nematode Caenorhabditis elegans, Proc. Natl. Acad. Sci. U.S.A., 106, 18285, 10.1073/pnas.0907117106 · DOI
- Mukherjee, 1998, Cholesterol distribution in living cells: fluorescence imaging using dehydroergosterol as a fluorescent cholesterol analog, Biophys. J., 75, 1915, 10.1016/S0006-3495(98)77632-5 · DOI · Paper page
- Mukherjee, 2004, Membrane domains, Annu. Rev. Cell Dev. Biol., 20, 839, 10.1146/annurev.cellbio.20.010403.095451 · DOI
- Munro, 2003, Lipid rafts: elusive or illusive?, Cell, 115, 377, 10.1016/S0092-8674(03)00882-1 · DOI
- Nagle, 2000, Structure of lipid bilayers, Biochim. Biophys. Acta, 1469, 159, 10.1016/S0304-4157(00)00016-2 · DOI
- Nan, 2003, Vibrational imaging of lipid droplets in live fibroblast cells with coherent anti-Stokes Raman scattering microscopy, J. Lipid Res., 44, 2202, 10.1194/jlr.D300022-JLR200 · DOI
- Nygren, 2004, Silver deposition on freeze-dried cells allows subcellular localization of cholesterol with imaging TOF-SIMS, J. Microsc., 215, 156, 10.1111/j.0022-2720.2004.01374.x · DOI
- Ohvo-Rekila, 2002, Cholesterol interactions with phospholipids in membranes, Prog. Lipid Res., 41, 66, 10.1016/S0163-7827(01)00020-0 · DOI · Paper page
- Orci, 1981, Heterogeneous distribution of filipin--cholesterol complexes across the cisternae of the Golgi apparatus, Proc. Natl. Acad. Sci. U.S.A., 78, 293, 10.1073/pnas.78.1.293 · DOI
- Ostrowski, 2007, Secondary ion MS imaging to relatively quantify cholesterol in the membranes of individual cells from differentially treated populations, Anal. Chem., 79, 3554, 10.1021/ac061825f · DOI
- Pagano, 1991, A novel fluorescent ceramide analogue for studying membrane traffic in animal cells: accumulation at the Golgi apparatus results in altered spectral properties of the sphingolipid precursor, J. Cell Biol., 113, 1267, 10.1083/jcb.113.6.1267 · DOI
- Peake, 2010, Defective cholesterol trafficking in Niemann-Pick C-deficient cells, FEBS Lett., 584, 2731, 10.1016/j.febslet.2010.04.047 · DOI
- Piehowski, 2008, MS/MS methodology to improve subcellular mapping of cholesterol using TOF-SIMS, Anal. Chem., 80, 8662, 10.1021/ac801591r · DOI
- Pipalia, 2006, Automated microscopy screening for compounds that partially revert cholesterol accumulation in Niemann-Pick C cells, J. Lipid Res., 47, 284, 10.1194/jlr.M500388-JLR200 · DOI
- Pipalia, 2011, Histone deacetylase inhibitor treatment dramatically reduces cholesterol accumulation in Niemann-Pick type C1 mutant human fibroblasts, Proc. Natl. Acad. Sci. U.S.A., 108, 5620, 10.1073/pnas.1014890108 · DOI · Paper page
- Puri, 1999, Cholesterol modulates membrane traffic along the endocytic pathway in sphingolipid-storage diseases, Nat. Cell Biol., 1, 386, 10.1038/14084 · DOI
- Puri, 2001, Clathrin-dependent and -independent internalization of plasma membrane sphingolipids initiates two Golgi targeting pathways, J. Cell Biol., 154, 535, 10.1083/jcb.200102084 · DOI
- Qin, 2005, Photophysical properties of borondipyrromethene analogues in solution, J. Phys. Chem. A, 109, 7371, 10.1021/jp052626n · DOI
- Qin, 2006, Elevated plasma membrane cholesterol content alters macrophage signaling and function, Arterioscler. Thromb. Vasc. Biol., 26, 372, 10.1161/01.ATV.0000197848.67999.e1 · DOI
- Reiner, 2005, Saccharomyces cerevisiae, a model to study sterol uptake and transport in eukaryotes, Biochem. Soc. Trans., 33, 1186, 10.1042/BST20051186 · DOI
- Rinia, 2008, Quantitative label-free imaging of lipid composition and packing of individual cellular lipid droplets using multiplex CARS microscopy, Biophys. J., 95, 4908, 10.1529/biophysj.108.137737 · DOI
- Rogers, 1979, The organisation of cholesterol and ergosterol in lipid bilayers based on studies using non-perturbing fluorescent sterol probes, Biochim. Biophys. Acta, 552, 23, 10.1016/0005-2736(79)90243-8 · DOI
- Röhrl, C., Meisslitzer-Ruppitsch, C., Bittman, R., Li, Z., Pabst, G., Prassl, R., Strobl, W., Neumüller, J., Ellinger, A., Pavelka, M., and Stangl, H. (2011). Combined light and electron microscopy using diaminobenzidine photooxidation to monitor trafficking of lipids derived from lipoprotein particles. Curr. Pharm. Biotechnol. In press. PMID: 21470121.
- Rosenbaum, 2011, Niemann-Pick type C disease: molecular mechanisms and potential therapeutic approaches, J. Neurochem., 116, 789, 10.1111/j.1471-4159.2010.06976.x · DOI
- Rosenbaum, 2009, Chemical screen to reduce sterol accumulation in Niemann-Pick C disease cells identifies novel lysosomal acid lipase inhibitors, Biochim. Biophys. Acta, 1791, 1155, 10.1016/j.bbalip.2009.08.005 · DOI
- Rujoi, 2010, Cholesterol pathways affected by small molecules that decrease sterol levels in Niemann-Pick type C mutant cells, PLoS One, 5, e12788, 10.1371/journal.pone.0012788 · DOI
- Scheidt, 2003, The potential of fluorescent and spin-labeled steroid analogs to mimic natural cholesterol, J. Biol. Chem., 278, 45563, 10.1074/jbc.M303567200 · DOI
- Schrader, 1997, Three-photon-excitation microscopy: theory, experiment and applications, Optik, 104, 116
- Schroeder, 1987, A fluorescence study of dehydroergosterol in phosphatidylcholine bilayer vesicles, Biochemistry, 26, 2441, 10.1021/bi00383a007 · DOI
- Schroeder, 1988, Fluorescence properties of cholestatrienol in phosphatidylcholine bilayer vesicles, Biophys. Chem., 32, 57, 10.1016/0301-4622(88)85034-8 · DOI
- Sharma, 2003, Glycosphingolipids internalized via caveolar-related endocytosis rapidly merge with the clathrin pathway in early endosomes and form microdomains for recycling, J. Biol. Chem., 278, 7564, 10.1074/jbc.M210457200 · DOI
- Sharma, 2004, Selective stimulation of caveolar endocytosis by glycosphingolipids and cholesterol, Mol. Biol. Cell, 15, 3114, 10.1091/mbc.E04-03-0189 · DOI
- Shaw, 2006, Correlated fluorescence-atomic force microscopy of membrane domains: structure of fluorescence probes determines lipid localization, Biophys. J., 90, 2170, 10.1529/biophysj.105.073510 · DOI
- Shrivastava, 2009, Orientation and dynamics of a novel fluorescent cholesterol analogue in membranes of varying phase, J. Phys. Chem. B, 113, 4475, 10.1021/jp808309u · DOI
- Sibarita, 2005, Deconvolution microscopy, Adv. Biochem. Eng. Biotechnol., 95, 201
- Smutzer, 1986, Physical properties of the fluorescent sterol probe dehydroergosterol, Biochim. Biophys. Acta, 862, 361, 10.1016/0005-2736(86)90239-7 · DOI
- Sokolov, 2010, Accessibility of cholesterol in endoplasmic reticulum membranes and activation of SREBP-2 switch abruptly at a common cholesterol threshold, J. Biol. Chem., 285, 29480, 10.1074/jbc.M110.148254 · DOI · Paper page
- Sostarecz, 2004, Phosphatidylethanolamine-induced cholesterol domains chemically identified with mass spectrometric imaging, J. Am. Chem. Soc., 126, 13882, 10.1021/ja0472127 · DOI
- Steer, 1984, Detection of membrane cholesterol by filipin in isolated rat liver coated vesicles is dependent upon removal of the clathrin coat, J. Cell Biol., 99, 315, 10.1083/jcb.99.1.315 · DOI
- Swedlow, 2007, Quantitative fluorescence microscopy and image deconvolution, Methods Cell Biol., 81, 447, 10.1016/S0091-679X(06)81021-6 · DOI
- van Manen, 2009, Cholesterol esters are detected by Raman microspectroscopy in HeLa cells, J. Raman Spectrosc., 40, 117, 10.1002/jrs.2168 · DOI
- Vist, 1990, Phase equilibria of cholesterol/dipalmitoylphosphatidylcholine mixtures: 2H nuclear magnetic resonance and differential scanning calorimetry, Biochemistry, 29, 451, 10.1021/bi00454a021 · DOI
- Wang, 2009, Imaging and quantitative analysis of atherosclerotic lesions by CARS-based multimodal nonlinear optical microscopy, Arterioscler. Thromb. Vasc. Biol., 29, 1342, 10.1161/ATVBAHA.109.189316 · DOI
- Wiegand, V., Chang, T.Y., Strauss, J.F. r., Fahrenholz, F., and Gimpl, G. (2003). Transport of plasma membrane-derived cholesterol and the function of Niemann-Pick C1 Protein. FASEB J. 17, 782–784. · DOI
- Wüstner, D. (2010). Following intracellular cholesterol transport by linear and non-linear optical microscopy of intrinsically fluorescent sterols. Curr. Pharm. Biotechnol. In press. PMID: 21470123.
- Wüstner, 2011, Potential of ultraviolet widefield imaging and multiphoton microscopy for analysis of dehydroergosterol in cellular membranes, Microsc. Res. Tech., 74, 92, 10.1002/jemt.20878 · DOI
- Wüstner, 2008, Spatiotemporal analysis of endocytosis and membrane distribution of fluorescent sterols in living cells, Histochem. Cell Biol., 130, 891, 10.1007/s00418-008-0488-6 · DOI
- Wüstner, 2008, Chromatic aberration correction and deconvolution for UV sensitive imaging of fluorescent sterols in cytoplasmic lipid droplets, Cytometry A, 73, 727, 10.1002/cyto.a.20593 · DOI
- Wüstner, 2002, Rapid nonvesicular transport of sterol between the plasma membrane domains of polarized hepatic cells, J. Biol. Chem., 277, 30325, 10.1074/jbc.M202626200 · DOI
- Wüstner, 2010, Selective visualization of fluorescent sterols in Caenorhabditis elegans by bleach-rate based image segmentation, Traffic, 11, 440, 10.1111/j.1600-0854.2010.01040.x · DOI
- Wüstner, 2005, Direct observation of rapid internalization and intracellular transport of sterol by macrophage foam cells, Traffic, 6, 396, 10.1111/j.1600-0854.2005.00285.x · DOI
- Wüstner, 2007, Fluorescent sterols as tools in membrane biophysics and cell biology, Chem. Phys. Lipids, 146, 1, 10.1016/j.chemphyslip.2006.12.004 · DOI
- Wüstner, 2007, Plasma membrane sterol distribution resembles the surface topography of living cells, Mol. Biol. Cell, 18, 211, 10.1091/mbc.E06-05-0445 · DOI
- Wüstner, 2011, Quantitative assessment of sterol traffic in living cells by dual labeling with dehydroergosterol and BODIPY-cholesterol, Chem. Phys. Lipids, 164, 221, 10.1016/j.chemphyslip.2011.01.004 · DOI
- Wüstner, 2010, Multicolor bleach-rate imaging enlightens in vivo sterol transport, Commun. Integr. Biol., 3, 1, 10.4161/cib.3.4.11972 · DOI
- Yeagle, 1990, Cholesterol dynamics in membranes, Biophys. J., 57, 413, 10.1016/S0006-3495(90)82558-3 · DOI
- Yeagle, 1982, Molecular packing of cholesterol in phospholipid vesicles as probed by dehydroergosterol, Biochim. Biophys. Acta, 692, 139, 10.1016/0005-2736(82)90511-9 · DOI
- Yen, 2010, A comparative study of fat storage quantitation in nematode Caenorhabditis elegans using label and label-free methods, PLoS One, 5, e12810, 10.1371/journal.pone.0012810 · DOI
- Young, 1989, Image fidelity: characterizing the imaging transfer function, Methods Cell Biol., 30, 2
- Zhang, 2005, Structural analysis of sterol distributions in the plasma membrane of living cells, Biochemistry, 44, 2864, 10.1021/bi048172m · DOI
- Zheng, 2007, Sphingomyelin/phosphatidylcholine and cholesterol interactions studied by imaging mass spectrometry, J. Am. Chem. Soc., 129, 15730, 10.1021/ja0741675 · DOI
- Zidovetzki, 2007, Use of cyclodextrins to manipulate plasma membrane cholesterol content: evidence, misconceptions and control strategies, Biochim. Biophys. Acta, 1768
- Zipfel, 2003, Nonlinear magic: multiphoton microscopy in the biosciences, Nat. Biotechnol., 21, 1369, 10.1038/nbt899 · DOI
Cited by
Sorted by citations
Cholesterol and matrisome pathways dysregulated in astrocytes and microglia
TCW, J., Qian, L., Pipalia, N. H., Chao, M. J., Liang, S. A., Shi, Y., Jain, B. R., Bertelsen, S. E., Kapoor, M., Marcora, E., et al. (2022) · Cell · doi:10.1016/j.cell.2022.05.017 · Cited by 411
Self-citationAPOE4 disrupts intracellular lipid homeostasis in human iPSC-derived glia
Sienski, G., Narayan, P., Bonner, J. M., Kory, N., Boland, S., Arczewska, A. A., Ralvenius, W. T., Akay, L., Lockshin, E., He, L., et al. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.aaz4564 · Cited by 336
A Carbon Nanotube Optical Reporter Maps Endolysosomal Lipid Flux
Jena, P. V., Roxbury, D., Galassi, T. V., Akkari, L., Horoszko, C. P., Iaea, D. B., Budhathoki-Uprety, J., Pipalia, N., Haka, A. S., Harvey, J. D., et al. (2017) · ACS Nano · doi:10.1021/acsnano.7b04743 · Cited by 125
Self-citationDefects in a liver-bone axis contribute to hepatic osteodystrophy disease progression
Lu, K., Shi, T.-S., Shen, S.-Y., Shi, Y., Gao, H.-L., Wu, J., Lu, X., Gao, X., Ju, H.-X., Wang, W., et al. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.02.006 · Cited by 126
Santos-Pereira, C., Andrés, M. T., Chaves, S. R., Fierro, J. F., Gerós, H., Manon, S., Rodrigues, L. R., & Côrte-Real, M. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.12.224 · Cited by 21
Metadata
- Authors
- Maxfield, F. R., & Wüstner, D.
- Venue
- Methods in Cell Biology
- Publisher
- Elsevier
- Published
- 2012
- Pages
- 367-393
- ISSN
- 0091-679X
- PMC
- PMC3626500
- Cited by
- 240
- References
- 0
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review