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January 1, 2002Arteriosclerosis Thrombosis and Vascular Biology188 citations

Stromal Cells Are the Main Plasminogen Activator Inhibitor-1-Producing Cells in Human Fat

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DBDelphine BastelicaAix-Marseille Université
Pierre‐Emmanuel Morange
Pierre‐Emmanuel MorangeVascular Medicine
BBB BerthetMedStar Washington Hospital Center

Key Points

  • The research aims to compare how plasminogen activator inhibitor-1 (PAI-1) is distributed in human visceral versus subcutaneous fat.
  • Localized PAI-1 expression in visceral and subcutaneous fat using mRNA analysis and in vitro adipocyte differentiation
  • Used real-time polymerase chain reaction to measure PAI-1 mRNA content in stromal and adipocyte fractions
  • Applied in situ hybridization for PAI-1 mRNA detection in cultured adipocytes
  • PAI-1 mRNA levels were 5-fold higher in the visceral versus subcutaneous stromal area (P=0.004)
  • PAI-1 production is primarily derived from stromal cells, more prevalent in visceral fat
  • PAI-1 secretion during adipocyte differentiation did not correlate with adipocyte maturation

Abstract

Elevated plasma plasminogen activator inhibitor (PAI)-1 observed during insulin resistance has been connected with an excessive PAI-1 adipose tissue secretion mainly by visceral fat. Our aim was to compare the localization of PAI-1 in human visceral and subcutaneous fats. PAI-1 secretion was also investigated in vitro during human adipocyte differentiation. PAI-1 antigen and mRNA were localized in the stromal area of the tissue and were also present in a few CD14-positive monocytes, in direct contact with adipocytes. In addition, in subcutaneous tissue, PAI-1 mRNA contents, determined by using real-time polymerase chain reaction, were higher in the stromal fraction than in the adipocyte fraction. PAI-1 mRNA-positive cells were 5-fold more frequent in the visceral area than in the subcutaneous stromal area (P=0.004). Such a difference was also observed for PAI-1 mRNA content between both whole adipose tissues. In contrast to leptin, during adipocyte differentiation, PAI-1 secretion did not follow adipocyte maturation. In situ hybridization in culture did not reveal PAI-1 mRNA in lipid-filled cells. Our results demonstrate that PAI-1 production is mainly due to stromal cells, which were more numerous in the visceral than in the subcutaneous depot. These results could explain the strong relationship observed between circulating PAI-1 levels and the accumulation of visceral fat.

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Cite This Study

Bastelica et al. (2002) studied this question.

synapsesocial.com/papers/69dd608c7808b00a4799d514https://doi.org/10.1161/hq0102.101552
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