نتایج جستجو برای: npc1

تعداد نتایج: 544  

2013
Ting Yu Andrew P. Lieberman

Cholesterol availability is rate-limiting for myelination, and prior studies have established the importance of cholesterol synthesis by oligodendrocytes for normal CNS myelination. However, the contribution of cholesterol uptake through the endocytic pathway has not been fully explored. To address this question, we used mice with a conditional null allele of the Npc1 gene, which encodes a tran...

Journal: :American journal of physiology. Gastrointestinal and liver physiology 2005
Robert P Erickson Achyut Bhattacharyya Robert J Hunter Randall A Heidenreich Nathan J Cherrington

Cholestatic hepatitis is frequently found in Niemann-Pick C (NPC) disease. We studied the influence of diet and the low density lipoprotein receptor (LDLR, Ldlr in mice, known to be the source of most of the stored cholesterol) on liver disease in the mouse model of NPC. Npc1-/- mice of both sexes, with or without the Ldlr knockout, were fed a 18% fat, 1% cholesterol ("high-fat") diet and were ...

Journal: :Chemistry & biology 2013
Kenji Ohgane Fumika Karaki Kosuke Dodo Yuichi Hashimoto

Niemann-Pick type C1 (NPC1) is a polytopic endosomal membrane protein required for efflux of LDL-derived cholesterol from endosomes, and mutations of this protein are associated with Niemann-Pick disease type C, a fatal neurodegenerative disease. At least one prevalent mutation (I1061T) has been shown to cause a folding defect, which results in failure of endosomal localization, leading to a lo...

2013
Michael Zech Georg Nübling Florian Castrop Angela Jochim Eva C. Schulte Brit Mollenhauer Peter Lichtner Annette Peters Christian Gieger Thorsten Marquardt Marie T. Vanier Philippe Latour Hans Klünemann Claudia Trenkwalder Janine Diehl-Schmid Robert Perneczky Thomas Meitinger Konrad Oexle Bernhard Haslinger Stefan Lorenzl Juliane Winkelmann

Niemann-Pick type C (NPC) disease is a rare autosomal-recessively inherited lysosomal storage disorder caused by mutations in NPC1 (95%) or NPC2. Given the highly variable phenotype, diagnosis is challenging and particularly late-onset forms with predominantly neuropsychiatric presentations are likely underdiagnosed. Pathophysiologically, genetic alterations compromising the endosomal/lysosomal...

Journal: :Glia 2007
Gang Chen Hai-Min Li Yi-Ren Chen Xiao-Song Gu Shumin Duan

Niemann-Pick disease type C (NPC) is a deadly neurodegenerative disease often caused by mutation in a gene called NPC1, which results in the accumulation of unesterified cholesterol and glycosphingolipids in the endosomal-lysosomal system. Most studies on the mechanisms of neurodegeneration in NPC have focused on neurons. However, the possibility also exists that NPC1 affects neuronal functions...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Nina H Pipalia Casey C Cosner Amy Huang Anamitra Chatterjee Pauline Bourbon Nathan Farley Paul Helquist Olaf Wiest Frederick R Maxfield

Niemann-Pick type C (NPC) disease is predominantly caused by mutations in the NPC1 protein that affect intracellular cholesterol trafficking and cause accumulation of unesterified cholesterol and other lipids in lysosomal storage organelles. We report the use of a series of small molecule histone deacetylase (HDAC) inhibitors in tissue culture models of NPC human fibroblasts. Some HDAC inhibito...

Journal: :Cell 2009
J. Fernando Bazan Frederic J. de Sauvage

The molecular details of how cholesterol exits lysosomes and is integrated into cellular and endoplasmic reticulum membranes remain unclear. Two proteins implicated in this exit process, the 13-transmembrane transporter NPC1 and secreted NPC2, are known to be mutated in Niemann-Pick type C (NPC) disease in humans, characterized by cholesterol accumulation. A recent X-ray crystallographic study ...

2014
Ahmed A. Eltoukhy Gaurav Sahay James M. Cunningham Daniel G. Anderson

Despite intensive research effort, the rational design of improved nanoparticulate drug carriers remains challenging, in part due to a limited understanding of the determinants of nanoparticle entry and transport in target cells. Recent studies have shown that Niemann-Pick C1 (NPC1), the lysosome membrane protein that mediates trafficking of cholesterol in cells, is involved in the endosomal es...

2013
Nicholas L. Cianciola Diane J. Greene Richard E. Morton Cathleen R. Carlin

Niemann-Pick disease type C (NPC) is caused by mutations in NPC1 or NPC2, which coordinate egress of low-density-lipoprotein (LDL)-cholesterol from late endosomes. We previously reported that the adenovirus-encoded protein RIDα rescues the cholesterol storage phenotype in NPC1-mutant fibroblasts. We show here that RIDα reconstitutes deficient endosome-to-endoplasmic reticulum (ER) transport, al...

2013
Mahua Maulik Gopal Thinakaran Satyabrata Kar

Niemann-Pick type C (NPC) disease, a rare autosomal recessive disorder caused mostly by mutation in NPC1 gene, is pathologically characterized by the accumulation of free cholesterol in brain and other tissues. This is accompanied by gliosis and loss of neurons in selected brain regions, including the cerebellum. Recent studies have shown that NPC disease exhibits intriguing parallels with Alzh...

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