Shear stress mediates tyrosylprotein sulfotransferase isoform shift in human endothelial cells.

Abstract:

:In this study, we examined expression of tyrosylprotein sulfotransferase (TPST) isoforms TPST1 and TPST2 in primary cultures of human umbilical vein endothelial cells. For the first time coexpression of both isoforms is shown in primary human cells. Application of physiological levels of shear stress regulates expression of TPST isoforms in a time- and dose-dependent manner. Sustained application of arterial laminar shear stress causes downregulation of TPST1 mRNA and protein expression, while TPST2 is upregulated. This TPST isoform shift is mediated by different signaling pathways. Shear stress-dependent downregulation of TPST1 involves tyrosine kinase, while upregulation of TPST2 is mediated by a protein kinase C-dependent pathway [corrected].

authors

Goettsch S,Goettsch W,Morawietz H,Bayer P

doi

10.1016/S0006-291X(02)00511-9

subject

Has Abstract

pub_date

2002-06-14 00:00:00

pages

541-6

issue

3

eissn

0006-291X

issn

1090-2104

pii

S0006-291X(02)00511-9

journal_volume

294

pub_type

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