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Am J Physiol Cell Physiol 289: C748-C756, 2005. First published April 20, 2005; doi:10.1152/ajpcell.00019.2005
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Protein and Vesicle Trafficking, Cytoskeleton

Constitutive secretion of serum albumin requires reversible protein tyrosine phosphorylation events in trans-Golgi

Rachel J. Webb,1 Jacob D. Judah,1 Lee-Chiang Lo,2 and Geraint M. H. Thomas1

1Department of Physiology, University College London, London, United Kingdom; and 2Department of Chemistry, National Taiwan University, Taipei, Taiwan

Submitted 18 January 2005 ; accepted in final form 12 April 2005

Serum albumin secretion from rat hepatocytes proceeds via the constitutive pathway. Although much is known about the role of protein tyrosine phosphorylation in regulated secretion, nothing is known about its function in the constitutive process. Here we show that albumin secretion is inhibited by the tyrosine kinase inhibitor genistein but relatively insensitive to subtype-selective inhibitors or treatments. Secretion is also blocked in a physiologically identical manner by the tyrosine phosphatase inhibitors pervanadate and bisperoxo(1,10-phenanthroline)-oxovanadate. Inhibition of either the kinase(s) or phosphatase(s) leads to the accumulation of albumin between the trans-Golgi and the plasma membrane, whereas the immediate precursor proalbumin builds up in a proximal compartment. The trans-Golgi marker TGN38 is rapidly dispersed under conditions that inhibit tyrosine phosphatase action, whereas the distribution of the cis-Golgi marker GM130 is insensitive to genistein or pervanadate. By using a specifically reactive biotinylation probe, we detected protein tyrosine phosphatases in highly purified rat liver Golgi membranes. These membranes also contain both endogenous tyrosine kinases and their substrates, indicating that enzymes and substrates for reversible tyrosine phosphorylation are normal membrane-resident components of this trafficking compartment. In the absence of perturbation of actin filaments and microtubules, we conclude that reversible protein tyrosine phosphorylation in the trans-Golgi network is essential for albumin secretion and propose that the constitutive secretion of albumin is in fact a regulated process.

vesicular trafficking; liver; genistein; pervanadate



Address for reprint requests and other correspondence: G. M. H. Thomas, Dept. of Physiology, Univ. College London, Rockefeller Bldg., 21 Univ. St., London WC1E 6JJ, UK (e-mail: g.thomas{at}ucl.ac.uk)




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