نتایج جستجو برای: atp7b cu

تعداد نتایج: 61925  

Journal: :The Journal of biological chemistry 2009
Karoline Leonhardt Rolf Gebhardt Joachim Mössner Svetlana Lutsenko Dominik Huster

Cisplatin is a widely used chemotherapeutic agent for treatment of ovarian, testicular, lung, and stomach cancers. The initial response to the drug is robust; however, tumor cells commonly develop resistance to cisplatin, which complicates treatment. Recently, overexpression of the Cu-ATPase ATP7B in ovary cells was linked to the increased cellular resistance to cisplatin; and the role for Cu-A...

Journal: :Biochemistry 2008
Lucia Banci Ivano Bertini Francesca Cantini Amy C Rosenzweig Liliya A Yatsunyk

The Wilson disease protein or ATP7B is a P 1B-type ATPase involved in human copper homeostasis. The extended N-terminus of ATP7B protrudes into the cytosol and contains six Cu(I) binding domains. This report presents the NMR structure of the polypeptide consisting of soluble Cu(I) binding domains 3 and 4. The two domains exhibit ferredoxin-like folds, are linked by a flexible loop, and act inde...

Journal: :American journal of physiology. Regulatory, integrative and comparative physiology 2006
Shannon L Kelleher Bo Lönnerdal

Milk copper (Cu) concentration declines and directly reflects the stage of lactation. Three Cu-specific transporters (Ctr1, Atp7A, Atp7B) have been identified in the mammary gland; however, the integrated role they play in milk Cu secretion is not understood. Whereas the regulation of milk composition by the lactogenic hormone prolactin (PRL) has been documented, the specific contribution of PR...

Journal: :iranian journal of pathology 2012
hamid galehdari raheleh tangestani

wilson disease is a metabolic disorder with an autosomal recessive genetic pattern and occurs in 1-4 of every 100000 individuals. inactivation of the atp7b gene leads to accumulation of the toxic copper to liver and brain causing hepatic and neurological complication. therefore, most patients suffer from chronic hepatic inflammation and central nervous system disorder. nowadays, up to 500 mutat...

2017
Caroline Demily François Parant David Cheillan Emmanuel Broussolle Alice Pavec Olivier Guillaud Lioara Restier Philippe Bernard Fabienne Bourdoncle Patrick Briant Alain Fouilhoux Sandrine Foullu Marie-Hélène Girard-Madoux Caroline Jeanpierre Bernard Joli Marianne Lemarié Sophie Lonjaret Jacques Marescaux Philippe Paulino Lionel Reinheimer Jean-Maurice Tarissan Alain Lachaux Muriel Bost

BACKGROUND Wilson's disease (WD) is a rare autosomal-recessive, inherited disorder caused by a mutation in the copper-transporting gene ATP7B affecting the liver and nervous system. About 30% of patients with WD may initially present with psychiatric symptoms, and diagnosis can be difficult to establish. The objectives of the present preliminary study were [1] to evaluate the relevance of serum...

Journal: :The American journal of clinical nutrition 2008
Bo Lönnerdal

Stable-isotope studies in human infants and adults have shown that copper homeostasis occurs, but the contribution of the small intestine to this regulation is still not well understood. Copper first needs to be reduced to the cuprous form, most likely by Steap proteins on the apical membrane. Copper is subsequently absorbed by Ctr1 and then transferred in the enterocyte by the chaperone Atox1 ...

Journal: :Physiological reviews 2007
Svetlana Lutsenko Natalie L Barnes Mee Y Bartee Oleg Y Dmitriev

Copper-transporting ATPases (Cu-ATPases) ATP7A and ATP7B are evolutionarily conserved polytopic membrane proteins with essential roles in human physiology. The Cu-ATPases are expressed in most tissues, and their transport activity is crucial for central nervous system development, liver function, connective tissue formation, and many other physiological processes. The loss of ATP7A or ATP7B fun...

Journal: :American journal of physiology. Gastrointestinal and liver physiology 2005
Kathryn A Bauerly Shannon L Kelleher Bo Lönnerdal

Infants are exposed to variable copper (Cu) intake; Cu in breast milk is low, whereas infant formulas vary in Cu content as well as the water used for their preparation. Little is known about the regulation of Cu absorption during infancy. The objectives of this study were to determine effects of Cu supplementation on Cu absorption and tissue distribution and the expression of Cu transporters i...

Journal: :Toxicological sciences : an official journal of the Society of Toxicology 2014
Xue Fu Yanshu Zhang Wendy Jiang Andrew Donald Monnot Christopher Alexander Bates Wei Zheng

Regulation of cellular copper (Cu) homeostasis involves Cu-transporting ATPases (Cu-ATPases), i.e., ATP7A and ATP7B. The question as to how these Cu-ATPases in brain barrier systems transport Cu, i.e., toward brain parenchyma, cerebrospinal fluid (CSF), or blood, remained unanswered. This study was designed to characterize roles of Cu-ATPases in regulating Cu transport at the blood-brain barrie...

Journal: :American journal of physiology. Gastrointestinal and liver physiology 2009
Lelita Braiterman Lydia Nyasae Yan Guo Rodrigo Bustos Svetlana Lutsenko Ann Hubbard

ATP7B is a copper-transporting P-type ATPase present predominantly in liver. In basal copper, hepatic ATP7B is in a post-trans-Golgi network (TGN) compartment where it loads cytoplasmic Cu(I) onto newly synthesized ceruloplasmin. When copper levels rise, the protein redistributes via unique vesicles to the apical periphery where it exports intracellular Cu(I) into bile. We want to understand th...

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