Montes-Olivas Sandra, Marucci Lucia, Homer Martin
Department of Engineering Mathematics, University of Bristol, Bristol, United Kingdom.
School of Cellular and Molecular Medicine, University of Bristol, Bristol, United Kingdom.
Front Genet. 2019 Sep 19;10:873. doi: 10.3389/fgene.2019.00873. eCollection 2019.
Organoids are engineered three-dimensional tissue cultures derived from stem cells and capable of self-renewal and self-organization into a variety of progenitors and differentiated cell types. An organoid resembles the cellular structure of an organ and retains some of its functionality, while still being amenable to experimental study. Compared with two-dimensional cultures, the three-dimensional structure of organoids provides a more realistic environment and structural organization of organs. Similarly, organoids are better suited to reproduce signaling pathway dynamics , due to a more realistic physiological environment. As such, organoids are a valuable tool to explore the dynamics of organogenesis and offer routes to personalized preclinical trials of cancer progression, invasion, and drug response. Complementary to experiments, mathematical and computational models are valuable instruments in the description of spatiotemporal dynamics of organoids. Simulations of mathematical models allow the study of multiscale dynamics of organoids, at both the intracellular and intercellular levels. Mathematical models also enable us to understand the underlying mechanisms responsible for phenotypic variation and the response to external stimulation in a cost- and time-effective manner. Many recent studies have developed laboratory protocols to grow organoids resembling different organs such as the intestine, brain, liver, pancreas, and mammary glands. However, the development of mathematical models specific to organoids remains comparatively underdeveloped. Here, we review the mathematical and computational approaches proposed so far to describe and predict organoid dynamics, reporting the simulation frameworks used and the models' strengths and limitations.
类器官是由干细胞衍生而来的工程化三维组织培养物,能够自我更新并自我组织形成多种祖细胞和分化细胞类型。类器官类似于器官的细胞结构,并保留其部分功能,同时仍便于进行实验研究。与二维培养相比,类器官的三维结构为器官提供了更真实的环境和结构组织。同样,由于生理环境更真实,类器官更适合重现信号通路动态。因此,类器官是探索器官发生动态并为癌症进展、侵袭和药物反应的个性化临床前试验提供途径的宝贵工具。作为实验的补充,数学和计算模型是描述类器官时空动态的重要工具。数学模型的模拟允许在细胞内和细胞间水平研究类器官的多尺度动态。数学模型还使我们能够以经济高效的方式理解导致表型变异和对外部刺激反应的潜在机制。最近的许多研究已经开发出实验室方案来培养类似于不同器官(如肠道、大脑、肝脏、胰腺和乳腺)的类器官。然而,针对类器官的数学模型的开发仍然相对滞后。在这里,我们回顾了迄今为止提出的用于描述和预测类器官动态的数学和计算方法,报告了所使用的模拟框架以及模型的优缺点。