Characterization and regulation of constitutive transport intermediates involved in trafficking from the trans-Golgi network

被引:6
|
作者
McLauchlan, HJ
James, J
Lucocq, JM
Ponnambalam, S [1 ]
机构
[1] Univ Leeds, Sch Biochem & Mol Biol, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Dundee, Dept Biochem, Dundee DD1 4HN, Scotland
[3] Univ Dundee, Dept Anat & Physiol, Dundee DD1 4HN, Scotland
基金
英国医学研究理事会;
关键词
trans-Golgi network; TGN; transport container; TC; trans-Golgi network protein 38 kDa; TGN38; beta; 1.4-galactosyltransferase; GalT; polymeric Ig receptor; plgR; protein kinase C; PKC;
D O I
10.1006/cbir.2001.0717
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transport vesicles or containers (TCs) mediate constitutive protein transport between the trans-Golgi network (TGN) and the plasma membrane. A key question is the nature and regulation of these transport containers or intermediates. We have used a trans-Golgi network resident. TGN38, to investigate TC formation. TGN38 is a recycling membrane glycoprotein that moves to the cell surface via constitutive membrane traffic and returns via the endosomal pathway. An in vitro assay to measure TC formation was devised using rat liver Golgi membranes, cytosolic factors and ATP. Transport intermediates containing TGN38 were produced and found to be smooth vesicles and tubules of up to 200 nm in length. These membrane-enclosed structures contain different constitutively secreted membrane glycoproteins., including molecules involved in immune functions such as MHC Class I and the polymeric Ig receptor, showing that these intermediates correspond to TCs that have been previously identified in vivo. Importantly, TC formation can be stimulated or inhibited by protein kinase and phosphatase inhibitors, showing regulation by intracellular signalling pathways. (C) 2001 Academic Press.
引用
收藏
页码:705 / 713
页数:9
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