微管参与发育中的鸡心肌对机械负荷改变的适应

E. Schroder, K. Tobita, J. P. Tinney, J. Foldes, B. Keller
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引用次数: 40

摘要

摘要-机械负荷调节心室生长、功能和结构,从心脏形态发生的最早阶段到衰老。心脏形态和功能的剧烈变化已被定义为心血管系统的发展,机械负荷条件的变化可产生结构畸形,如左心发育不全。迄今为止,关于机械负荷、形态发生和胚胎心脏材料特性变化之间的相互作用,我们所知相对较少。我们验证了一个假设,即胚胎心脏中的被动材料特性会随着机械负荷的改变而改变,而微管在这种适应性反应中起着重要作用。在21期左房结扎(LAL)后,我们测量了汉堡-汉密尔顿第27期鸡胚胎左室(LV)心肌条的双轴被动应力-应变关系,以减少左室体积负荷并造成左心发育不全。LAL后,给定应变下的心肌应力和周向刚度较对照条增加。LAL胚胎的Western blot分析显示,总微管蛋白和聚合微管蛋白均增加,共聚焦显微镜证实,与对照组相比,LV致密层的微管密度增加。经秋水仙碱处理后,LAL样本的左室应力和刚度归一化,且经秋水仙碱处理后的LAL微管密度与对照组相似。相比之下,紫杉醇处理使对照条的心肌应力和刚度增加到超过LAL标本的水平。因此,发育中的心肌的材料特性受到机械负荷的调节,而微管在心脏形态发生过程中发挥了这种适应性反应的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microtubule Involvement in the Adaptation to Altered Mechanical Load in Developing Chick Myocardium
Abstract— Mechanical load regulates ventricular growth, function, and structure from the earliest stages of cardiac morphogenesis through senescence. Dramatic changes in cardiac form and function have been defined for developing cardiovascular systems, and changes in mechanical loading conditions can produce structural malformations such as left heart hypoplasia. To date, relatively little is known regarding the interactions between changes in mechanical load, morphogenesis, and the material properties of the embryonic heart. We tested the hypothesis that passive material properties in the embryonic heart change in response to altered mechanical load and that microtubules play an important role in this adaptive response. We measured biaxial passive stress-strain relations in left ventricular (LV) myocardial strips in chick embryos at Hamburger-Hamilton stage 27 following left atrial ligation (LAL) at stage 21 to reduce LV volume load and create left heart hypoplasia. Following LAL, myocardial stresses at given strains and circumferential stiffness increased versus control strips. Western blot analysis of LAL embryos showed an increase in both total and polymerized &bgr;-tubulin and confocal microscopy confirmed an increase in microtubule density in the LV compact layer versus control. Following colchicine treatment, LV stresses and stiffness normalized in LAL specimens and microtubule density following colchicine was similar in LAL to control. In contrast, Taxol treatment increased myocardial stresses and stiffness in control strips to levels beyond LAL specimens. Thus, the material properties of the developing myocardium are regulated by mechanical load and microtubules play a role in this adaptive response during cardiac morphogenesis.
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