纤维蛋白溶解系统在脂肪组织发育中的功能作用。

H R Lijnen
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引用次数: 0

摘要

肥胖的发展与脂肪组织的广泛改变有关,包括脂肪生成、血管生成和细胞外基质蛋白水解。纤溶(纤溶酶原/纤溶酶)系统有助于这些过程。纤溶系统的主要生理抑制剂纤溶酶原激活物抑制剂-1 (PAI-1)在小鼠和人类脂肪组织中表达,PAI-1水平高易导致血栓并发症。然而,PAI-1在脂肪组织发育中的潜在作用仍然是一个谜。我们利用野生型和转基因小鼠的营养诱导肥胖模型来研究纤溶系统在肥胖发生中的作用。我们的主要发现是:1)肥胖与血浆PAI-1水平显著升高有关;2) PAI-1对体内脂肪组织发育的影响呈浓度依赖性;3) PAI-1在脂肪形成中无显著作用,但可能影响血管生成;4).组织型纤溶酶原激活物(t-PA), PAI-1的主要靶点,损害脂肪组织发育;5) PAI-1参与肥胖对血栓性缺血性脑卒中预后的有害影响;6)使用人工合成的PAI-1低Mr抑制剂可能具有减少肥胖的潜力。因此,这些研究支持了纤溶活性的作用,并表明其调节可能会影响脂肪组织的发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional role of the fibrinolytic system in development of adipose tissue.

Development of obesity is associated with extensive modifications in adipose tissue involving adipogenesis, angiogenesis and extracellular matrix proteolysis. The fibrinolytic (plasminogen/plasmin) system contributes to these processes. The main physiological inhibitor of the fibrinolytic system, plasminogen activator inhibitor-1 (PAI-1), is expressed in murine and human adipose tissues, and high PAI-1 levels predispose to thrombotic complications. The potential role of PAI-1 in development of adipose tissue remains, however, enigmatic. We have used nutritionally induced obesity models in wild-type and transgenic mice to study the role of the fibrinolytic system in the development of obesity. Our main findings are: 1) Obesity is associated with markedly enhanced plasma levels of PAI-1; 2) The effect of PAI-1 on in vivo adipose tissue development is concentration-dependent; 3) PAI-1 does not play a significant role in adipogenesis but may affect angiogenesis; 4). Tissue-type plasminogen activator (t-PA), the main target of PAI-1, impairs adipose tissue development; 5) PAI-1 contributes to the deleterious effect of obesity on the outcome of thrombotic ischemic stroke; and 6) The use of synthetic low Mr inhibitors of PAI-1 may have the potential to reduce obesity. These studies thus support a role for fibrinolytic activity and suggest that its modulation may allow to affect development of adipose tissue.

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