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正常及再生大鼠肝脏质膜结构域中的纤连蛋白异构体

Fibronectin isoforms in plasma membrane domains of normal and regenerating rat liver.

作者信息

Enrich C, Evans W H, Gahmberg C G

机构信息

National Institute for Medical Research, London, England.

出版信息

FEBS Lett. 1988 Feb 8;228(1):135-8. doi: 10.1016/0014-5793(88)80602-1.

DOI:10.1016/0014-5793(88)80602-1
PMID:3342872
Abstract

Plasma membrane fractions were obtained from the three surface domains of normal and regenerating adult rat livers. It was shown by immunoblotting that sinusoidal plasma membranes contained the characteristic 220 and 210 kDa fibronectin doublet, whereas bile canalicular plasma membranes contained a 220 kDa component. In lateral plasma membranes, 180, 190 and 220 kDa fibronectin isoforms were present. Fibronectin in the sinusoidal and canalicular plasma membranes was shown, by detergent/aqueous phase partitioning, to be more hydrophilic than isoforms in lateral plasma membranes. Changes in the distribution of fibronectin between plasma membrane domains occurred during liver regeneration and their significance, especially in relation to cell division, is discussed.

摘要

从正常成年大鼠肝脏和再生成年大鼠肝脏的三个表面区域获得了质膜部分。免疫印迹显示,窦状质膜含有特征性的220 kDa和210 kDa纤连蛋白双峰,而胆小管质膜含有一个220 kDa的成分。在侧质膜中,存在180 kDa、190 kDa和220 kDa的纤连蛋白异构体。通过去污剂/水相分配显示,窦状和胆小管质膜中的纤连蛋白比侧质膜中的异构体更具亲水性。讨论了肝脏再生过程中质膜区域间纤连蛋白分布的变化及其意义,尤其是与细胞分裂的关系。

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Fibronectin isoforms in plasma membrane domains of normal and regenerating rat liver.正常及再生大鼠肝脏质膜结构域中的纤连蛋白异构体
FEBS Lett. 1988 Feb 8;228(1):135-8. doi: 10.1016/0014-5793(88)80602-1.
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Tissue Eng Part A. 2011 Apr;17(7-8):1055-68. doi: 10.1089/ten.TEA.2010.0398. Epub 2011 Feb 2.
2
HRS/SRp40-mediated inclusion of the fibronectin EIIIB exon, a possible cause of increased EIIIB expression in proliferating liver.HRS/SRp40介导的纤连蛋白EIIIB外显子包含,这可能是增殖性肝脏中EIIIB表达增加的一个原因。
Mol Cell Biol. 1997 Jul;17(7):4096-104. doi: 10.1128/MCB.17.7.4096.
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Identification of a novel glycoprotein (AGp110) involved in interactions of rat liver parenchymal cells with fibronectin.
一种参与大鼠肝实质细胞与纤连蛋白相互作用的新型糖蛋白(AGp110)的鉴定。
J Cell Biol. 1990 Nov;111(5 Pt 1):2117-27. doi: 10.1083/jcb.111.5.2117.
4
Priority targeting of glycosyl-phosphatidylinositol-anchored proteins to the bile-canalicular (apical) plasma membrane of hepatocytes. Involvement of 'late' endosomes.糖基磷脂酰肌醇锚定蛋白优先靶向至肝细胞胆小管(顶端)质膜。“晚期”内体的参与。
Biochem J. 1990 Oct 1;271(1):193-9. doi: 10.1042/bj2710193.
5
Temporal changes in the expression and distribution of adhesion molecules during liver development and regeneration.肝脏发育和再生过程中黏附分子表达及分布的时间变化。
J Cell Biol. 1992 Mar;116(6):1507-15. doi: 10.1083/jcb.116.6.1507.