Huelsz-Prince Guizela, Belkin Alexey M, VanBavel Ed, Bakker Erik N T P
Department of Biomedical Engineering and Physics, Academic Medical Center, Amsterdam, The Netherlands.
J Vasc Res. 2013;50(5):383-95. doi: 10.1159/000354222. Epub 2013 Aug 24.
Inward remodeling of small arteries occurs after prolonged vasoconstriction, low blood flow, and in several models of hypertension. The cross-linking enzyme, transglutaminases 2 (TG2), is able to induce inward remodeling and stiffening of arteries. The activity of TG2 is dependent on its conformation, which can be open or closed, and on its redox state. Several factors have been shown to be involved in modulating TG2 activity, including Ca(2+) and GTP/GDP concentrations, as well as the redox state of the environment. This review introduces the hypothesis that mechanical force could be involved in regulating the activity of TG2 during inward remodeling by promoting its open and reduced active state. Several aspects of TG2, such as its structure and localization, are assessed in order to provide arguments that support the hypothesis. We conclude that a direct activation of TG2 by mechanical force exerted by smooth muscle cells may explain the link between smooth muscle activation and inward remodeling, as observed in several physiological and pathological conditions.
在长期血管收缩、低血流量以及多种高血压模型中,小动脉会发生内向性重塑。交联酶转谷氨酰胺酶2(TG2)能够诱导动脉的内向性重塑和僵硬。TG2的活性取决于其构象(可以是开放或关闭状态)以及氧化还原状态。已表明有多种因素参与调节TG2的活性,包括钙离子(Ca²⁺)和鸟苷三磷酸/鸟苷二磷酸(GTP/GDP)浓度,以及环境的氧化还原状态。本综述提出一种假说,即在内向性重塑过程中,机械力可能通过促进TG2处于开放和还原的活性状态来参与调节其活性。为了提供支持该假说的论据,对TG2的几个方面,如结构和定位进行了评估。我们得出结论,平滑肌细胞施加的机械力直接激活TG2,可能解释了在多种生理和病理状况下观察到的平滑肌激活与内向性重塑之间的联系。