Impact of Cyclic Strain on Elastin Synthesis in a 3D Human Myometrial Culture Model.

IF 2.7 4区 医学 Q3 CELL & TISSUE ENGINEERING Tissue engineering. Part C, Methods Pub Date : 2024-07-01 Epub Date: 2024-07-09 DOI:10.1089/ten.TEC.2024.0038
Carolyn A Nietupski, Andreja Moset Zupan, Stacey C Schutte
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Abstract

The synthesis and assembly of mature, organized elastic fibers remains a limitation to the clinical use of many engineered tissue replacements. There is a critical need for a more in-depth understanding of elastogenesis regulation for the advancement of methods to induce and guide production of elastic matrix structures in engineered tissues that meet the structural and functional requirements of native tissue. The dramatic increase in elastic fibers through normal pregnancy has led us to explore the potential role of mechanical stretch in combination with pregnancy levels of the steroid hormones 17β-estradiol and progesterone on elastic fiber production by human uterine myometrial smooth muscle cells in a three-dimensional (3D) culture model. Opposed to a single strain regimen, we sought to better understand how the amplitude and frequency parameters of cyclic strain influence elastic fiber production in these myometrial tissue constructs (MTC). Mechanical stretch was applied to MTC at a range of strain amplitudes (5%, 10%, and 15% at 0.5 Hz frequency) and frequencies (0.1 Hz, 0.5 Hz, 1 Hz, and constant 0 Hz at 10% amplitude), with and without pregnancy-level hormones, for 6 days. MTC were assessed for cell proliferation, matrix elastin protein content, and expression of the main elastic fiber genes, tropoelastin (ELN) and fibrillin-1 (FBN1). Significant increases in elastin protein and ELN and FBN1 mRNA were produced from samples subjected to a 0.5 Hz, 10% strain regimen, as well as samples stretched at higher amplitude (15%, 0.5 Hz) and higher frequency (1 Hz, 10%); however, no significant effects because of third-trimester mimetic hormone treatment were determined. These results establish that a minimum level of strain is required to stimulate the synthesis of elastic fiber components in our culture model and show this response can be similarly enhanced by increasing either the amplitude or frequency parameter of applied strain. Further, our results demonstrate strain alone is sufficient to stimulate elastic fiber production and suggest hormones may not be a significant factor in regulating elastin synthesis. This 3D culture model will provide a useful tool to further investigate mechanisms underlying pregnancy-induced de novo elastic fiber synthesis and assembly by uterine smooth muscle cells.

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三维人体子宫肌层培养模型中循环应变对弹性蛋白合成的影响
合成和组装成熟、有组织的弹性纤维仍然是许多工程组织替代品临床应用的限制因素。我们亟需更深入地了解弹性生成的调控,以改进方法来诱导和引导工程组织中弹性基质结构的生成,从而满足原生组织的结构和功能要求。正常妊娠过程中弹性纤维的急剧增加促使我们在三维培养模型中探索机械拉伸与妊娠期类固醇激素17β-雌二醇和孕酮水平相结合对人类子宫肌平滑肌细胞产生弹性纤维的潜在作用。与单一应变方案相反,我们试图更好地了解循环应变的振幅和频率参数如何影响这些子宫肌组织构建物(MTC)的弹性纤维生成。在使用或不使用妊娠水平激素的情况下,以不同的应变幅度(5%、10%和 15%,频率为 0.5 Hz)和频率(0.1 Hz、0.5 Hz、1 Hz 和恒定 0 Hz,幅度为 10%)对 MTC 进行机械拉伸,持续 6 天。对 MTC 的细胞增殖、基质弹性蛋白含量以及主要弹性纤维基因弹性蛋白(ELN)和纤连蛋白-1(FBN1)的表达进行评估。在 0.5 Hz、10% 的应变方案下,以及在较高振幅(15%,0.5 Hz)和较高频率(1 Hz,10%)下拉伸的样本中,弹性蛋白、ELN 和 FBN1 mRNA 的表达量均有显著增加;然而,第三孕期模拟激素处理并未产生显著影响。这些结果确定了在我们的培养模型中刺激弹性纤维成分合成所需的最低应变水平,并表明通过增加施加应变的振幅或频率参数,同样可以增强这种反应。此外,我们的研究结果表明,仅应变就足以刺激弹性纤维的生成,并表明激素可能不是调节弹性蛋白合成的重要因素。这种三维培养模型将为进一步研究妊娠诱导子宫平滑肌细胞从头合成和组装弹性纤维的机制提供有用的工具。
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来源期刊
Tissue engineering. Part C, Methods
Tissue engineering. Part C, Methods Medicine-Medicine (miscellaneous)
CiteScore
5.10
自引率
3.30%
发文量
136
期刊介绍: Tissue Engineering is the preeminent, biomedical journal advancing the field with cutting-edge research and applications that repair or regenerate portions or whole tissues. This multidisciplinary journal brings together the principles of engineering and life sciences in the creation of artificial tissues and regenerative medicine. Tissue Engineering is divided into three parts, providing a central forum for groundbreaking scientific research and developments of clinical applications from leading experts in the field that will enable the functional replacement of tissues. Tissue Engineering Methods (Part C) presents innovative tools and assays in scaffold development, stem cells and biologically active molecules to advance the field and to support clinical translation. Part C publishes monthly.
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