Regulation of plasminogen activators in human thyroid follicular cells and their relationship to differentiated function
✍ Scribed by Radhika Susarla; John C. Watkinson; Margaret C. Eggo
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 430 KB
- Volume
- 212
- Category
- Article
- ISSN
- 0021-9541
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✦ Synopsis
Abstract
Human thyroid cells in culture take up and organify ^125^I when cultured in TSH (acting through cAMP) and insulin. They also secrete urokinase (uPA) and tissue‐type (tPA) plasminogen activators (5–100 IU/10^6^cells/day). TSH and insulin both decreased secreted PA activity (PAA), uPA and tPA protein and their mRNAs. Autocrine fibroblast growth factor increased secreted PAA and inhibited thyroid cell ^125^I uptake. Epidermal growth factor (EGF) and the protein kinase C (PKC) activator, TPA significantly increased PAA and inhibited thyroid differentiated function, (TPA > EGF). For TPA, effects were rapid, increased PAA secretion and decreased ^125^I uptake being seen at 4 h whereas for EGF, a 24 h incubation was required. qRT‐PCR showed significantly increased mRNA expression of uPA with lesser effects on tPA. Aprotinin, which inhibits PAA, increased ^125^I uptake but did not abrogate the effects of TPA and EGF. The MEKK inhibitor, PD98059 partially reversed the effects of EGF and TPA on PAA, and largely reversed the effects of EGF but not TPA on differentiated function. PKC inhibitors bisindoylmaleimide 1, and the specific PKCβ inhibitor, LY379196 completely reversed the effects of TPA on ^125^I uptake and PAA whereas EGF effects were unaffected. TPA inhibited follicle formation and this effect was blocked by LY379196 but not PD98059. We conclude that in thyroid cells, MAPK activation inversely correlates with ^125^I uptake and directly correlates with PA expression, in contrast to the effects of cAMP. TPA effects on iodide metabolism, dissolution of follicles and uPA synthesis are mediated predominantly through PKCβ whereas EGF exerts its effects through MAPK but not PKCβ. J. Cell. Physiol. 212:643–654, 2007. © 2007 Wiley‐Liss, Inc.