Synthetic development: dissection of morphogenetic programs via reconstructive and perturbative approaches

综合发展：通过重建和微扰方法剖析形态发生程序

• 批准号: 10452672
• 负责人: Leonardo Morsut
• 金额: $ 41.25万
• 依托单位: UNIVERSITY OF SOUTHERN CALIFORNIA
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-09-15 至 2025-06-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10452672
• 关键词: Behavior; Biological Models; Cells; Communication; Complex; Computer Models; Congenital Disorders; Defect; Development; Developmental Biology; Developmental Process; Disease; Dissection; Embryo; Embryonic Development; Environment; Event; Extracellular Matrix; Genes; Genetic; Growth; Lead; Light; Link; Logic; Mesoderm; Microfluidics; Modernization; Molecular; Morphogenesis; Optics; Organ; Pathway interactions; Pattern; Periodicity; Population; Process; Proteins; Resolution; Shapes; Signal Pathway; Signal Transduction; Somites; System; Time; Tissues; base; in vivo; insight; notch protein; optogenetics; programs; reconstruction; reverse genetics; single cell sequencing; spatiotemporal; spine bone structure; tool

Project Summary A fundamental question in developmental biology concerns the origin and control of patterns and shapes, also known as morphogenesis. Multicellular signaling networks, encoded in genetic networks, underlie the normal development of embryos and drive their morphogenesis. Paradigmatic example is the periodic segmentation of mesoderm into somites, the precursors of the vertebrae, during vertebrate development. Changes in genes, effector proteins, and cellular environments can lead to altered embryonic development as seen in congenital disorders. To cure diseases we need to understand how genes control cells at multiple scales and how groups of cells form coherent, functional tissues and organs. The last years have witnessed a boom in discoveries in developmental biology with single-cell sequencing, microfluidics, optics, increased computational power leading to unprecedented spatiotemporal resolution of the multiscale dynamics of morphogenetic systems, from molecules to cells to whole embryos. While these advancements have produced detailed roadmaps of the events orchestrated during develop- ment, we still lack a clear picture of which cellular networks drive collective morphogenetic programs. The classical forward and reverse genetic perturbative screenings, and even modern perturbative tools like optogenetics, still mainly focus at the level of the gene(s) or single signaling pathways. This makes it challenging to infer causal relationship between complex multicellular networks and developmental transitions. New perturbative tools are needed that could construct similar complexity as the ones observed in vivo. As these complex networks in vivo are based on cell-cell and cell-environment communication pathways, we need controllable versions of those pathways that we can (i) link in complex synthetic networks, (ii) use to control endogenous developmental pathways. Such a system would enable the introduction of precise and complex spatiotemporal perturbations at the level of the networks instead of the gene(s), ultimately delivering increased understanding of the relationship between complex networks and resulting developmental transitions. In our lab we develop synthetic cell-cell and cell-ECM pathways, connect them in networks, and use them to investigate developmental processes. Here we propose to (i) use these tools to investigate the mechanistic contribution of Notch signaling to the formation and propagation of signaling waves in the presomitic mesoderm and, (ii) develop new tools for cell-ECM communication, inspired by developmental signaling. We expect to enter a cycle of toolsàtestàanswersànew questionsànew tools. These studies will advance the field of developmental biology by shedding light on the behavior and logic of multicellular systems and how complex networks enable control across scales of space and time. Gaining insight and tools to direct developmental cell populations would have widespread relevance for the treatment of developmental defects and our capacity to control the growth of tissue and organs in a dish.

项目摘要 发育生物学中的一个基本问题涉及图案和形状的起源和控制， 也称为形态发生。多细胞信号网络，编码在遗传网络中，是 胚胎的正常发育并驱动其形态发生。典型的例子是 在脊椎动物发育过程中，中胚层分裂成体节，即椎骨的前体。 基因、效应蛋白和细胞环境的变化可以导致胚胎发育的改变， 常见于先天性疾病为了治愈疾病，我们需要了解基因如何控制细胞在多个 规模和细胞群如何形成连贯的功能性组织和器官。 在过去的几年里，单细胞测序在发育生物学方面的发现激增， 微流体、光学、计算能力的提高带来了前所未有的时空分辨率 形态发生系统的多尺度动力学，从分子到细胞到整个胚胎。 虽然这些进步已经产生了详细的路线图的事件精心策划的发展过程中， 然而，我们仍然缺乏一个清晰的图片，哪些细胞网络驱动集体形态发生程序。的 经典的正向和反向遗传微扰筛选，甚至现代微扰工具， 光遗传学仍然主要集中在基因或单个信号通路的水平。这使得 推断复杂多细胞网络与发育转变之间的因果关系具有挑战性。 需要新的微扰工具，可以构建类似的复杂性，在体内观察。作为 这些复杂的体内网络是基于细胞-细胞和细胞-环境的通讯途径，我们需要 这些途径的可控版本，我们可以（i）在复杂的合成网络中连接，（ii）用来控制 内源性发展途径。这样的系统将能够引入精确和复杂的 在网络而不是基因水平上的时空扰动，最终提供增加的 理解复杂网络和由此产生的发展转型之间的关系。 在我们的实验室中，我们开发了合成的细胞-细胞和细胞-ECM通路，将它们连接在网络中，并使用它们来 研究发展过程。在这里，我们建议（i）使用这些工具来调查机制 Notch信号对分裂前期信号波形成和传播的贡献 中胚层，（ii）开发新的工具，细胞外基质通信，发育信号的启发。我们 期待进入一个工具测试答案新问题新工具的循环。 这些研究将通过阐明发育生物学的行为和逻辑来推进发育生物学领域。 多细胞系统以及复杂的网络如何实现跨时空尺度的控制。获得 指导发育细胞群的见解和工具将对治疗具有广泛的相关性 发育缺陷和我们控制培养皿中组织和器官生长的能力。