首页> 外文期刊>Acta Biotheoretica >Investigating Metalloproteinases MMP-2 and MMP-9 Mechanosensitivity to Feedback Loops Involved in the Regulation of In Vitro Angiogenesis by Endogenous Mechanical Stresses
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Investigating Metalloproteinases MMP-2 and MMP-9 Mechanosensitivity to Feedback Loops Involved in the Regulation of In Vitro Angiogenesis by Endogenous Mechanical Stresses

机译:研究金属蛋白酶MMP-2和MMP-9对涉及内源性机械应力调节体外血管生成的反馈环的机械敏感性

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Angiogenesis is a complex morphogenetic process regulated by growth factors, but also by the force balance between endothelial cells (EC) traction stresses and extracellular matrix (ECM) viscoelastic resistance. Studies conducted with in vitro angiogenesis assays demonstrated that decreasing ECM stiffness triggers an angiogenic switch that promotes organization of EC into tubular cords or pseudo-capillaries. Thus, mechano-sensitivity of EC with regard to proteases secretion, and notably matrix metalloproteinases (MMPs), should likely play a pivotal role in this switching mechanism. While most studies analysing strain regulation of MMPs used cell cultured on stretched membranes, this work focuses on MMP expression during self-assembly of EC into capillary-like structures within fibrin gels, i.e. on conditions that mimics more closely the in vivo cellular mechanical microenvironment. The activity of MMP-2 and MMP-9, two MMPs that have a pivotal role in capillaries formation, has been monitored in pace with the progressive elongation of EAhy926 cells that takes place during the emergence of cellular cords. We found an increase of the zymogen proMMP-2 that correlates with the initial stages of EC cords formation. However, MMP-2 was not detected. ProMMP-9 secretion decreased, with levels of MMP-9 kept at a rather low value. In order to analyse more precisely the observed differences of EAhy926 response on fibrin and plastic substrates, we proposed a theoretical model of the mechano-regulation of proMMP-2 activation in the presence of type 2 tissue inhibitor of MMPs (TIMP-2). Using association/dissociation rates experimentally reported for this enzymatic network, the model adequately describes the synergism of proMMP-2 and TIMP-2 strain activation during pseudo-capillary morphogenesis. All together, these results provide a first step toward a systems biology approach of angiogenesis mechano-regulation by cell-generated extracellular stresses and strains.
机译:血管生成是一个复杂的形态发生过程,受生长因子调控,还受内皮细胞(EC)牵引力和细胞外基质(ECM)粘弹性阻力之间的力平衡影响。用体外血管生成测定法进行的研究表明,降低ECM刚度会触发促血管生成的转换,从而促进EC组织成管状索或假毛细血管。因此,EC对蛋白酶分泌,尤其是基质金属蛋白酶(MMP)的机械敏感性可能在这种转换机制中起关键作用。虽然大多数分析MMP的应变调控的研究都使用在拉伸膜上培养的细胞,但这项工作着重于EC自组装为纤维蛋白凝胶内的毛细管状结构(即更紧密地模拟体内细胞机械微环境的条件)中的MMP表达。 MMP-2和MMP-9(在毛细血管形成中起关键作用的两个MMP)的活性已随着EAhy926细胞在细胞索出现期间逐渐伸长而得到及时监测。我们发现与EC脐带形成的初始阶段相关的酶原proMMP-2的增加。但是,未检测到MMP-2。 ProMMP-9分泌减少,MMP-9水平保持在较低水平。为了更精确地分析在纤维蛋白和塑料底物上观察到的EAhy926反应差异,我们提出了在MMPs 2型组织抑制剂(TIMP-2)存在下proMMP-2激活的机械调节的理论模型。使用针对该酶网络实验报告的缔合/解离速率,该模型充分描述了拟毛细管形态发生过程中proMMP-2和TIMP-2菌株激活的协同作用。总之,这些结果提供了朝着通过细胞产生的细胞外应力和菌株进行血管生成机械调节的系统生物学方法的第一步。

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