Sterol, protein and lipid trafficking in Chinese hamster ovary cells with Niemann-Pick type C1 defect.

scientific article published on 7 December 2006

Sterol, protein and lipid trafficking in Chinese hamster ovary cells with Niemann-Pick type C1 defect. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1111/J.1600-0854.2006.00513.X
P698PubMed publication ID17156101
P5875ResearchGate publication ID6643654

P50authorFrederick R. MaxfieldQ44830049
P2093author name stringMingming Hao
Sushmita Mukherjee
Nina H Pipalia
P2860cites workElevated endosomal cholesterol levels in Niemann-Pick cells inhibit rab4 and perturb membrane recyclingQ37537956
Segregation of transferrin to a mildly acidic (pH 6.5) para-Golgi compartment in the recycling pathwayQ39341143
Direct observation of rapid internalization and intracellular transport of sterol by macrophage foam cellsQ40438270
Different transport routes for high density lipoprotein and its associated free sterol in polarized hepatic cellsQ40606710
Rapid nonvesicular transport of sterol between the plasma membrane domains of polarized hepatic cellsQ40727372
Characterization of rapid membrane internalization and recyclingQ40880101
Niemann-Pick C1 is a late endosome-resident protein that transiently associates with lysosomes and the trans-Golgi networkQ40930186
Niemann-pick type C1 (NPC1) overexpression alters cellular cholesterol homeostasisQ42492641
Vesicular and non-vesicular sterol transport in living cells. The endocytic recycling compartment is a major sterol storage organelleQ43781456
Cholesterol accumulates in cell bodies, but is decreased in distal axons, of Niemann-Pick C1-deficient neuronsQ44220275
Acidification of endocytic compartments and the intracellular pathways of ligands and receptorsQ44950371
Maternal Pumilio acts together with Nanos in germline development in Drosophila embryosQ47070377
Cholesterol modulates membrane traffic along the endocytic pathway in sphingolipid-storage diseasesQ47622411
Role of Niemann-Pick type C1 protein in intracellular trafficking of low density lipoprotein-derived cholesterolQ47887125
Lipids, lipid domains and lipid–protein interactions in endocytic membrane trafficQ57356167
Niemann-Pick C1 protein: obligatory roles for N-terminal domains and lysosomal targeting in cholesterol mobilizationQ22008745
Localization of Niemann-Pick C1 protein in astrocytes: implications for neuronal degeneration in Niemann- Pick type C diseaseQ24672011
Niemann-Pick disease type CQ28268777
Sterol resistance in CHO cells traced to point mutation in SREBP cleavage-activating proteinQ28295187
Mobilization of late-endosomal cholesterol is inhibited by Rab guanine nucleotide dissociation inhibitorQ28369794
Accumulation of glycosphingolipids in Niemann-Pick C disease disrupts endosomal transportQ28506553
Endocytic recyclingQ29547737
The NPC1 protein: structure implies function.Q30343740
Lipid changes in Niemann-Pick disease type C brain: personal experience and review of the literatureQ33607709
The Niemann-Pick C1 protein resides in a vesicular compartment linked to retrograde transport of multiple lysosomal cargoQ33856244
Sterol and lipid trafficking in mammalian cellsQ33995960
Niemann-Pick type C mutations cause lipid traffic jam.Q34156605
Cholesterol distribution in living cells: fluorescence imaging using dehydroergosterol as a fluorescent cholesterol analogQ34169116
Glycosphingolipid lysosomal storage diseases: therapy and pathogenesisQ34941895
Endocytosis and sorting of glycosphingolipids in sphingolipid storage diseaseQ35032078
Endocytic trafficking of glycosphingolipids in sphingolipid storage diseasesQ35153223
Lipid and cholesterol trafficking in NPC.Q35909553
Consequences of NPC1 and NPC2 loss of function in mammalian neuronsQ35909562
Functional expression of the human transferrin receptor cDNA in Chinese hamster ovary cells deficient in endogenous transferrin receptorQ36217992
Intracellular fusion of sequentially formed endocytic compartmentsQ36218414
Fusion accessibility of endocytic compartments along the recycling and lysosomal endocytic pathways in intact cellsQ36221883
Iterative fractionation of recycling receptors from lysosomally destined ligands in an early sorting endosomeQ36222118
Isolation and characterization of Chinese hamster ovary cell mutants defective in intracellular low density lipoprotein-cholesterol traffickingQ36222559
The End2 mutation in CHO cells slows the exit of transferrin receptors from the recycling compartment but bulk membrane recycling is unaffectedQ36233462
Endocytic sorting of lipid analogues differing solely in the chemistry of their hydrophobic tails.Q36293356
Sterol trafficking between the endoplasmic reticulum and plasma membrane in yeastQ36482044
Clinical features of Niemann-Pick disease type C. An example of the delayed onset, slowly progressive phenotype and an overview of recent literature.Q36723139
How cholesterol homeostasis is regulated by plasma membrane cholesterol in excess of phospholipidsQ37415722
P433issue2
P304page(s)130-141
P577publication date2006-12-07
P1433published inTrafficQ1572846
P1476titleSterol, protein and lipid trafficking in Chinese hamster ovary cells with Niemann-Pick type C1 defect.
P478volume8

Reverse relations

cites work (P2860)
Q36916857(-)-Epigallocatechin gallate causes internalization of the epidermal growth factor receptor in human colon cancer cells
Q958401112-Hydroxypropyl-gamma-cyclodextrin overcomes NPC1 deficiency by enhancing lysosome-ER association and autophagy
Q42013607A comparative study on fluorescent cholesterol analogs as versatile cellular reporters
Q36307272A novel intrinsically fluorescent probe for study of uptake and trafficking of 25-hydroxycholesterol.
Q36278707ARF6-mediated endocytic recycling impacts cell movement, cell division and lipid homeostasis
Q33429998ARF6-mediated endosome recycling reverses lipid accumulation defects in Niemann-Pick Type C disease
Q36950303Abnormal accumulation and recycling of glycoproteins visualized in Niemann-Pick type C cells using the chemical reporter strategy
Q30872586Chemical screen to reduce sterol accumulation in Niemann-Pick C disease cells identifies novel lysosomal acid lipase inhibitors
Q33705255Cholesterol pathways affected by small molecules that decrease sterol levels in Niemann-Pick type C mutant cells
Q37289281Cholesterol regulation of rab-mediated sphingolipid endocytosis
Q30612009Cholesterol-mediated activation of acid sphingomyelinase disrupts autophagy in the retinal pigment epithelium
Q39971390Chromatic aberration correction and deconvolution for UV sensitive imaging of fluorescent sterols in cytoplasmic lipid droplets
Q40066539Endocytic trafficking of sphingomyelin depends on its acyl chain length
Q33777920Endocytosis of beta-cyclodextrins is responsible for cholesterol reduction in Niemann-Pick type C mutant cells
Q37201335Galectin-3 guides intracellular trafficking of some human serotransferrin glycoforms
Q42705344Hepatic metabolic response to restricted copper intake in a Niemann-Pick C murine model
Q38716617Histone deacetylase inhibitors correct the cholesterol storage defect in most Niemann-Pick C1 mutant cells.
Q34399659Improvement in lipid and protein trafficking in Niemann-Pick C1 cells by correction of a secondary enzyme defect
Q34320547Insights into the mechanisms of sterol transport between organelles
Q37228012Intracellular sterol dynamics
Q64275517Lipid⁻Protein Interactions in Niemann⁻Pick Type C Disease: Insights from Molecular Modeling
Q34104368Niemann-Pick C1 affects the gene delivery efficacy of degradable polymeric nanoparticles
Q41899989Niemann-Pick type C cells show cholesterol dependent decrease of APP expression at the cell surface and its increased processing through the beta-secretase pathway
Q37784257Niemann‐Pick type C disease: molecular mechanisms and potential therapeutic approaches
Q41484671One-Step Selective Exoenzymatic Labeling (SEEL) Strategy for the Biotinylation and Identification of Glycoproteins of Living Cells
Q46966340Plasma membrane rafts complete cholesterol synthesis by participating in retrograde movement of precursor sterols
Q37809216Probes for studying cholesterol binding and cell biology
Q24316973Regulation of sterol transport between membranes and NPC2
Q38897940Role of STARD4 and NPC1 in intracellular sterol transport
Q33563385Role of STARD4 in sterol transport between the endocytic recycling compartment and the plasma membrane
Q38954364SpatTrack: an imaging toolbox for analysis of vesicle motility and distribution in living cells
Q42248628Sterol transfer between cyclodextrin and membranes: similar but not identical mechanism to NPC2-mediated cholesterol transfer
Q33676201Tracking the subcellular fate of 20(s)-hydroxycholesterol with click chemistry reveals a transport pathway to the Golgi
Q36954877Transport of LDL-derived cholesterol from the NPC1 compartment to the ER involves the trans-Golgi network and the SNARE protein complex