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Microfabrication of extracellular matrix structures using multipohoton-excited photochemistry: Application to modeling ovarian tissue in vitro.

机译:使用多光子激发光化学法微细化细胞外基质结构:在体外建立卵巢组织模型中的应用。

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摘要

The extracellular matrix plays a crucial role in tissue development, differentiation and homeostasis by providing the necessary biophysical and biochemical cues for the cells. In tumors, the composition and the structure of the microenvironment is thought to be manipulated by the cancers cells to support proliferative growth and enhanced migration as means of facilitated metastasis. Current in vitro tools to address these mechanistic events in tumor progression are lacking in part due to the difficulty in recapitulating the complexity of the composition and nanoarchitecture of the tumor microenvironment. In this thesis, we explore the feasibility of multiphoton-excited photochemistry as a fabrication tool for generating in vitro scaffolds that are highly repeatable, biologically relevant and relatively affordable in a research setting. The power of this technique lays in the capabilities of crosslinking whole extracellular matrix proteins in three dimensions (3D) to recreate key topographical features of the tissue with sub-micron resolution and high fidelity. The technological developments we present here enable direct translation of matrix topographies by using the high resolution image data of the tissue samples as a fabrication template.;To this effect, we have applied the fabrication technique to generate gradients of crosslinked proteins as means of studying the role of haptotaxis in ovarian and breast cancers. Our findings show that cancer cells modulate their migration velocity and persistence in response to the changes in the composition of the extracellular matrix. In addition, we have examined structural features of the stroma in relation to cancer migration dynamics. We find that by recreating highly aligned nanoarchitectural features prevalent in cancer stroma, we see permissive and enhanced cell migration with cell morphologies similar to in vivo.;We believe multiphoton fabrication to be an enabling tool in the next generation of tissue scaffolding. Having the means to carefully recreate complex topographies can ultimately enhance our knowledge of cancer migration in 3D environments as well as provide valued insights in developing novel therapies aim at treating this disease.
机译:细胞外基质通过为细胞提供必要的生物物理和生化线索,在组织发育,分化和体内稳态中起着至关重要的作用。在肿瘤中,微环境的组成和结构被认为是由癌细胞操纵的,以支持增殖生长和作为促进转移的手段而增强的迁移。当前缺少用于解决这些肿瘤进展中的机制事件的体外工具,其部分原因是难以概括肿瘤微环境的组成和纳米结构的复杂性。在本文中,我们探讨了多光子激发光化学作为制备体外支架的制造工具的可行性,该支架在研究环境中具有高度可重复性,生物学相关性和相对负担能力。该技术的强大之处在于可以在三个维度(3D)上交联整个细胞外基质蛋白,从而以亚微米分辨率和高保真度重建组织的关键形貌特征。我们在此提出的技术发展是通过使用组织样本的高分辨率图像数据作为制备模板来直接转换矩阵形貌的;为此,我们已经应用了制备技术来生成交联蛋白的梯度,作为研究蛋白质的方法。触觉在卵巢癌和乳腺癌中的作用。我们的发现表明,癌细胞可调节其迁移速度和持久性,以响应细胞外基质组成的变化。此外,我们检查了与癌症迁移动力学相关的基质结构特征。我们发现,通过重建在癌症基质中普遍存在的高度对齐的纳米结构特征,我们看到了允许的细胞迁移和增强的细胞迁移,其细胞形态类似于体内。我们相信多光子制造将成为下一代组织支架中的使能工具。拥有精心创建复杂地形的方法,最终可以增强我们对3D环境中癌症迁移的了解,并为开发旨在治疗这种疾病的新疗法提供有价值的见解。

著录项

  • 作者

    Ajeti, Visar.;

  • 作者单位

    The University of Wisconsin - Madison.;

  • 授予单位 The University of Wisconsin - Madison.;
  • 学科 Biomedical engineering.;Biology.;Optics.
  • 学位 Ph.D.
  • 年度 2016
  • 页码 128 p.
  • 总页数 128
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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