نتایج جستجو برای: pick type c1 npc1

تعداد نتایج: 1363808  

Journal: :International journal of sciences 2023

Male patients with NPC1 heterozygous mutation (Npc1+/-) are prone to obesity and diabetes, yet the mechanism remains unclear. In this study, male Npc1+/- mice (C57BL/6C-Npc1) were used evaluate effects of combined 60% high-fat diet (HFD) on glucolipid metabolism, cholesterol accumulation, islet dysfunction β-cell dedifferentiation. Compared HFD-Npc1+/+ or fed low-fat (LFD), body weight HFD-Npc1...

2016
A. V. Degtyareva S. V. Mikhailova E. Y. Zakharova E. L. Tumanova A. A. Puchkova

BACKGROUND Niemann-Pick disease type C is a rare metabolic disease characterized by progressive neurological deterioration with childhood onset, and often results in premature mortality. Niemann-Pick disease type C has an extremely heterogeneous clinical presentation with a wide range of visceral and neurological signs and symptoms that are not specific to the disease, and which progress over v...

2015
Franziska Dahlmann Nadine Biedenkopf Anne Babler Willi Jahnen-Dechent Christina B. Karsten Kerstin Gnirß Heike Schneider Florian Wrensch Christopher A. O'Callaghan Stephanie Bertram Georg Herrler Stephan Becker Stefan Pöhlmann Heike Hofmann-Winkler

Ebolaviruses constitute a public health threat, particularly in Central and Western Africa. Host cell factors required for spread of ebolaviruses may serve as targets for antiviral intervention. Lectins, TAM receptor tyrosine kinases (Tyro3, Axl, Mer), T cell immunoglobulin and mucin domain (TIM) proteins, integrins, and Niemann-Pick C1 (NPC1) have been reported to promote entry of ebolaviruses...

Journal: :Developmental Cell 2021

Niemann-Pick type C is a neurological disorder caused by mutations in the lysosome cholesterol exporter NPC1. In this issue of Developmental Cell, Davis et al. dissect how NPC1 loss elevates mTORC1 signaling, and demonstrate that suppression signaling can rescue disease pathology NPC1-deficient cell models. Lysosomes are key degradation organelles. As centers catabolic metabolism, they receive ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Jinwoo Lee David A Nyenhuis Elizabeth A Nelson David S Cafiso Judith M White Lukas K Tamm

Ebolavirus (EBOV), an enveloped filamentous RNA virus causing severe hemorrhagic fever, enters cells by macropinocytosis and membrane fusion in a late endosomal compartment. Fusion is mediated by the EBOV envelope glycoprotein GP, which consists of subunits GP1 and GP2. GP1 binds to cellular receptors, including Niemann-Pick C1 (NPC1) protein, and GP2 is responsible for low pH-induced membrane ...

Journal: :Circulation research 2010
Tomas Blom Nils Bäck Aino-Liisa Mutka Robert Bittman Zaiguo Li Angel de Lera Petri T Kovanen Ulf Diczfalusy Elina Ikonen

RATIONALE The synthetic sphingosine analog FTY720 is undergoing clinical trials as an immunomodulatory compound, acting primarily via sphingosine 1-phosphate receptor activation. Sphingolipid and cholesterol homeostasis are closely connected but whether FTY720 affects atherogenesis in humans is not known. OBJECTIVE We examined the effects of FTY720 on the processing of scavenged lipoprotein c...

2009
Cristin D. Davidson Nafeeza F. Ali Matthew C. Micsenyi Gloria Stephney Sophie Renault Kostantin Dobrenis Daniel S. Ory Marie T. Vanier Steven U. Walkley

BACKGROUND Niemann-Pick type C (NPC) disease is a fatal neurodegenerative disorder caused most commonly by a defect in the NPC1 protein and characterized by widespread intracellular accumulation of unesterified cholesterol and glycosphingolipids (GSLs). While current treatment therapies are limited, a few drugs tested in Npc1(-/-) mice have shown partial benefit. During a combination treatment ...

2007
Marc C. Patterson Marie T. Vanier Kinuko Suzuki Jill A. Morris Eugene Carstea Edward B. Neufeld Joan E. Blanchette-Mackie Peter G. Pentchev

1. Niemann-Pick disease type C (NP-C) is an autosomal recessive lipidosis with protean clinical manifestations, distinguished biochemically by a unique error in cellular trafficking of exogenous cholesterol that is associated with lysosomal accumulation of unesterified cholesterol. A majority of patients with this phenotype are linked genetically to chromosome 18, the locus of Niemann-Pick dise...

2017
Xiaoyang Xu Aolin Zhang Matthew S. Halquist Xinxu Yuan Scott C. Henderson William L. Dewey Pin‐Lan Li Ningjun Li Fan Zhang

Statins, 3-hydroxyl-3-methylglutaryl coenzyme A reductase inhibitors, are the first-line medications prescribed for the prevention and treatment of coronary artery diseases. The efficacy of statins has been attributed not only to their systemic cholesterol-lowering actions but also to their pleiotropic effects that are unrelated to cholesterol reduction. These pleiotropic effects have been incr...

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