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Diabetes, Vol 48, Issue 4 890-895, Copyright © 1999 by American Diabetes Association
Glucocorticoids and insulin promote plasminogen activator inhibitor 1 production by human adipose tissue
PE Morange, J Aubert, F Peiretti, HR Lijnen, P Vague, M Verdier, R Negrel, I Juhan-Vague and MC Alessi
Laboratoire d'Hematologie, CR INSERM, Faculte de Medecine Timone, Marseille, France.
Plasminogen activator inhibitor 1 (PAI-1) is likely to play a role in
vascular disease, primarily in subjects with android obesity. It has been
demonstrated that PAI-1 is overexpressed in adipose tissue from obese
subjects and that visceral adipose tissue produced more PAI-1 than
subcutaneous fat. In the present study, the effect of insulin and
glucocorticoids, which are key mediators of adipose tissue metabolism, was
examined in relation to PAI-1 synthesis by human adipose tissue explants
(HAT), collagenase isolated human adipocytes (IHA), cultured human stromal
cells (cSC), and differentiated adipocytes from the murine clonal cell line
3T3-F442A. A significant increase in PAI-1 antigen release (1.5-fold) from
HAT was detectable after 16 h of treatment with insulin concentrations of
at least 10(-8) mol/l. This was associated with a PAI-1 mRNA increase.
Concomitant addition of insulin (10(-8) mol/l) to forskolin (5 x 10(-5)
mol/l) reversed the decrease in PAI-1 antigen caused by forskolin alone. No
effect on PAI-1 antigen was observed when insulin was incubated with IHA or
cSC. 3T3 F442A cells were sensitive to insulin with a four- and twofold
increase in PAI-1 antigen and mRNA levels, respectively, after 16 h of
stimulation with 10(-8) mol/l. Dexamethasone (DXM) significantly enhanced
PAI-1 antigen and mRNA expression by HAT (1.5- and 2.5-fold increase,
respectively) at concentrations of at least 10(-8) mol/l. A higher
stimulation was observed with IHA (sevenfold increase) and with the
differentiated 3T3 F442 cell line. Cortisol was found to be less potent
than DXM. No effect was observed when glucocorticoids were incubated with
cSC. Coincubation of HAT with insulin (10(-7) mol/l) and DXM (10(-7) mol/l)
led to an additive effect on PAI-1 synthesis. These results support the
hypothesis that PAI-1 expression in human adipose tissue is controlled by
insulin and glucocorticoids and may help to explain the increase in plasma
PAI-1 levels observed in patients with android obesity.

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Copyright © 1999 by the American Diabetes Association.
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