Unveiling comprehensive cellular biophysical properties using quantitative phase digital holographic microscopy

使用定量相位数字全息显微镜揭示全面的细胞生物物理特性

• 批准号: RGPIN-2018-06198
• 负责人: Marquet, Pierre
• 金额: $ 2.48万
• 依托单位: Université Laval
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2020
• 资助国家: 加拿大
• 起止时间: 2020-01-01 至 2021-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=714149
• 关键词: Unveiling; comprehensive; cellular; biophysical; properties

The human brain development displays species-specific features, in particular to generate the structures thought to be at the core of human-specific cognitive abilities, such as the cerebral cortex. However, the specific mechanisms underlying this neurodevelopment and leading to this complexity remain incompletely understood, primarily because of the poor experimental accessibility of the human embryonic brain. Nevertheless, recently, the development of technologies based on pluripotent stem cells (PSCs) have permitted to generate, from e.g. a simple skin biopsy of a healthy volunteer, all cell types that comprise his/her tissue including neuronal cells, which constitute the brain tissue. Considering that such generation process of human neuronal cells from PSCs in many ways recapitulates the development of embryonic neurons, its accurate study is providing unique new opportunities for the analysis of human brain development. Obtaining a better understanding of this modeling human brain development in-vitro using PSCs technology represents the main objective of our research program achieved within the framework of the Canada Excellence Research Chair (CERC) in Neurophotonics. Toward this aim, we have been developing new multimodal optical microscopy techniques having the capacity to visualize accurately and non-invasively cells structure and dynamics during the generation process of human mature and functional neurons from PSCs. Specifically, thanks to this research program, we plan to develop multimodal optical microscopy techniques, based on a holographic principle, having not only the capacity to visualize living cells in 3D but also to simultaneously provide information about cell biophysics and biochemistry. Indeed, recent work from a variety of fields has revealed that physical forces and biomechanical cell properties play as important a role in control of cell and tissue development as chemicals and genes. Practically, using such novel multimodal holographic microscopy techniques will make possible to address specifically questions concerning the measurement of cell biophysical properties in relation with the maturation of embryonic neurons into functional neurons. In addition, this multimodal capacity allowing grasping simultaneously several aspects of the multifaceted biological processes represents a promising approach to obtain a more comprehensive understanding of the basic mechanisms underlying the generation of functional neurons from PSCs. Our research program, at the interface between optics, photonics and neurobiology mainly trains physicists, engineers, mathematicians and biologists, who combine their knowledge and skills to advance our understanding of the basic mechanisms of human brain development using PSCs and to improve our methods for advancing cell imaging.

人类大脑发育显示出物种特异性特征，特别是产生被认为是人类特定认知能力核心的结构，如大脑皮层。然而，这种神经发育和导致这种复杂性的具体机制仍然不完全清楚，主要是因为人类胚胎大脑的实验可及性差。然而，最近，基于多能干细胞（PSC）的技术的发展已经允许从例如健康志愿者的简单皮肤活检产生构成他/她的组织的所有细胞类型，包括构成脑组织的神经元细胞。考虑到这种从PSC产生人类神经元细胞的过程在许多方面重演了胚胎神经元的发育，其准确的研究为人类大脑发育的分析提供了独特的新机会。 使用PSC技术更好地了解这种体外模拟人脑发育是我们在加拿大卓越研究主席（CERC）神经光子学框架内实现的研究计划的主要目标。为了实现这一目标，我们一直在开发新的多模态光学显微镜技术，该技术能够在从PSC生成人类成熟和功能性神经元的过程中准确和非侵入性地可视化细胞结构和动力学。 具体来说，由于这项研究计划，我们计划开发基于全息原理的多模态光学显微镜技术，不仅能够以3D方式可视化活细胞，而且还能够同时提供有关细胞生物物理学和生物化学的信息。事实上，最近来自各个领域的研究表明，物理力和生物力学细胞特性在控制细胞和组织发育方面发挥着与化学物质和基因一样重要的作用。实际上，使用这种新的多模态全息显微镜技术将有可能解决具体的问题，有关测量细胞的生物物理特性与胚胎神经元成熟成功能性神经元。此外，这种多模态能力允许同时掌握多方面的生物过程的几个方面，代表了一种有前途的方法，以获得更全面的理解的基本机制的基础上产生的功能神经元从PSC。 我们的研究计划，在光学，光子学和神经生物学之间的接口，主要培养物理学家，工程师，数学家和生物学家，他们联合收割机结合他们的知识和技能，以促进我们对人类大脑发育的基本机制的理解，使用PSC，并改善我们的方法，推进细胞成像。