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转铁蛋白在铁生物学中的已知和潜在作用。

Known and potential roles of transferrin in iron biology.

机构信息

Department of Pathology, Children’s Hospital, Enders 1110, 300 Longwood Avenue, Boston, MA 02115, USA.

出版信息

Biometals. 2012 Aug;25(4):677-86. doi: 10.1007/s10534-012-9520-3.

Abstract

Transferrin is an abundant serum metal-binding protein best known for its role in iron delivery. The human disease congenital atransferrinemia and animal models of this disease highlight the essential role of transferrin in erythropoiesis and iron metabolism. Patients and mice deficient in transferrin exhibit anemia and a paradoxical iron overload attributed to deficiency in hepcidin, a peptide hormone synthesized largely by the liver that inhibits dietary iron absorption and macrophage iron efflux. Studies of inherited human disease and model organisms indicate that transferrin is an essential regulator of hepcidin expression. In this paper, we review current literature on transferrin deficiency and present our recent findings, including potential overlaps between transferrin, iron and manganese in the regulation of hepcidin expression.

摘要

转铁蛋白是一种丰富的血清金属结合蛋白,以其在铁传递中的作用而闻名。人类疾病先天性运铁蛋白血症和这种疾病的动物模型突出了转铁蛋白在红细胞生成和铁代谢中的重要作用。转铁蛋白缺乏的患者和小鼠表现出贫血和铁超载的矛盾现象,这归因于铁调素的缺乏,铁调素是一种主要由肝脏合成的肽激素,它抑制膳食铁的吸收和巨噬细胞铁的流出。对遗传性人类疾病和模式生物的研究表明,转铁蛋白是铁调素表达的必需调节剂。在本文中,我们回顾了转铁蛋白缺乏的现有文献,并介绍了我们的最新发现,包括转铁蛋白、铁和锰在铁调素表达调节中的潜在重叠。

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本文引用的文献

1
The iron transporter ferroportin can also function as a manganese exporter.铁转运蛋白也可作为锰的输出蛋白发挥作用。
Biochim Biophys Acta. 2012 Mar;1818(3):651-7. doi: 10.1016/j.bbamem.2011.12.002. Epub 2011 Dec 8.
5
Role of manganese in neurodegenerative diseases.锰在神经退行性疾病中的作用。
J Trace Elem Med Biol. 2011 Dec;25(4):191-203. doi: 10.1016/j.jtemb.2011.08.144. Epub 2011 Oct 1.
6
The binding and transport of alternative metals by transferrin.转铁蛋白对其他金属的结合与转运
Biochim Biophys Acta. 2012 Mar;1820(3):362-78. doi: 10.1016/j.bbagen.2011.07.003. Epub 2011 Jul 18.
7
Manganese toxicity in a child with iron deficiency and polycythemia.一名缺铁性贫血和红细胞增多症患儿的锰中毒
J Child Neurol. 2011 Jul;26(7):891-4. doi: 10.1177/0883073810393962. Epub 2011 May 18.
9
Congenital disorders of glycosylation.先天性糖基化障碍。
Ann N Y Acad Sci. 2010 Dec;1214:190-8. doi: 10.1111/j.1749-6632.2010.05840.x.

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