نتایج جستجو برای: ferroportin

تعداد نتایج: 765  

Journal: :Molecular medicine reports 2015
Li Sun Lixin Wang Zhe Wang Wei He Shuping Zhang Wenli Guo Yi Qian Hong Ji Haiqin Rong Sijin Liu

Cadmium (Cd) is a heavy metal that has detrimental effects on various organs. The widespread contamination of Cd in the environment, crops and food sources poses a severe threat to human health. Acute toxicities of Cd have been extensively investigated; however, the health impact of chronic low‑dose exposure to Cd, particularly exposure under non‑toxic concentrations, has yet to be elucidated. ...

Journal: :Hepatology 2005
Heinz Zoller Ian McFarlane Igor Theurl Sylvia Stadlmann Elizabeta Nemeth David Oxley Tomas Ganz David J Halsall Timothy M Cox Wolfgang Vogel

Ferroportin disease (hemochromatosis type 4) is a recently recognized disorder of human iron metabolism, characterized by iron deposition in macrophages, including Kupffer cells. Mutations in the gene encoding ferroportin 1, a cellular iron exporter, are responsible for this iron storage disease, inherited as an autosomal dominant trait. We present clinical, histopathological, and radiological ...

2014
Nathalie Scheers Ann-Sofie Sandberg

A few tightly regulated transport proteins mediate iron absorption across the intestinal epithelium. At the basolateral border of intestinal cells there is one identified transporter, ferroportin, for the transfer of intracellular iron to the vascular system. Here, we investigate the effects of ascorbate (vitamin C) on the regulation of ferroportin in human intestinal Caco-2 cells using ELISA a...

Journal: :Blood 2007
Irene E Zohn Ivana De Domenico Andrew Pollock Diane McVey Ward Jessica F Goodman Xiayun Liang Amaru J Sanchez Lee Niswander Jerry Kaplan

Ferroportin disease is caused by mutation of one allele of the iron exporter ferroportin (Fpn/IREG1/Slc40a1/MTP1). All reported human mutations are missense mutations and heterozygous null mutations in mouse Fpn do not recapitulate the human disease. Here we describe the flatiron (ffe) mouse with a missense mutation (H32R) in Fpn that affects its localization and iron export activity. Similar t...

Journal: :Histology and histopathology 2007
P S Oates

The field of iron metabolism is moving rapidly. There have been significant advances in our understanding of how proteins carry out the process of iron absorption. The three main tissues involved in iron exchange are the enterocyte which contributes new iron to the system, the hepatocyte which stores and releases iron and the macrophages which recycles iron from effete red blood cells to the pl...

Journal: :Journal of Pediatric Gastroenterology & Nutrition 2016

Journal: :Clinical Liver Disease 2014

2016
Samira Lakhal-Littleton Magda Wolna Yu Jin Chung Helen C Christian Lisa C Heather Marcella Brescia Vicky Ball Rebeca Diaz Ana Santos Daniel Biggs Kieran Clarke Benjamin Davies Peter A Robbins

Hepcidin is the master regulator of systemic iron homeostasis. Derived primarily from the liver, it inhibits the iron exporter ferroportin in the gut and spleen, the sites of iron absorption and recycling respectively. Recently, we demonstrated that ferroportin is also found in cardiomyocytes, and that its cardiac-specific deletion leads to fatal cardiac iron overload. Hepcidin is also expresse...

Journal: :Cell metabolism 2015
Hal Drakesmith Elizabeta Nemeth Tomas Ganz

Maintaining physiologic iron concentrations in tissues is critical for metabolism and host defense. Iron absorption in the duodenum, recycling of iron from senescent erythrocytes, and iron mobilization from storage in macrophages and hepatocytes constitute the major iron flows into plasma for distribution to tissues, predominantly for erythropoiesis. All iron transfer to plasma occurs through t...

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