Perfused 3D Tissue Surrogates for Complex Cell-Cell Communication Systems

描述（由申请人提供）：在可用的培养物和动物模型与方法之间存在巨大的差距，这些模型和方法可以提取关于细胞-细胞通信网络的详细信息，该细胞-细胞通信网络控制系统对扰动的反应，例如炎症线索。网络固有地以复杂的、相互关联的方式操作，并且通常在网络中的特定点处表现出来自干预的非直观结果，如在当前可用的临床前试验中有希望的结果之后许多靶向治疗剂在临床环境中操作失败所证明的。细胞-细胞通讯网络包括细胞释放到细胞外环境中的因子（例如，细胞因子、蛋白酶）沿着细胞内信号。虽然大量的努力集中在简单的细胞培养系统中产生的细胞内信号通过直接处理与个别的刺激线索，它是不清楚如何相关的信号所产生的相互作用的多个线索在连续的时间点由不同的细胞类型作为动态级联。阐明细胞外因子在多群体细胞系统中相互作用的重要方面对于理解组织病理生理学是至关重要的，但在体内或传统细胞培养系统中研究是非常困难的。在这个项目中，我们将开发变革性的新方法，将细胞-细胞通信网络的真实的时间分子探针和随后的细胞行为整合到复杂的生理3D培养中，允许从这些培养中获得多路复用的动态信息，以响应系统变量的特定操作，包括涉及的细胞群体和外部扰动，如炎症线索。我们的目标是建立初级人类系统的模型，作为体内复杂性的密切模仿，因此我们专注于开发新的方法，不依赖于细胞群体的遗传操作，以产生有关系统操作的信息。我们的整个项目将通过三个平行但相互交织的努力来推进：开发一种用于连接细胞外和细胞内网络的通信模式的分析形式主义，并提供一个从测量中识别关键细胞外节点的框架（如蛋白质组学分析）;开发新的生物材料微环境，控制和记录细胞周围局部细胞通信信号中的关键节点，以多路复用的方式，具有高的空间和时间分辨率的环境;和这些方法的集成到微尺度灌注培养系统，通过控制因素，包括细胞外基质的性质，培养几何形状，局部氧张力，和机械应力，促进适当的细胞和组织生理学。我们工作中的一个主要创新是以协同方式将这些方法联系起来，以提供可广泛用于各种组织系统的系统，并应用于一系列个体疾病，包括性二型反应突出的疾病。 公共卫生相关性：该项目的目标是通过将系统生物学与组织工程相结合，改变我们探测人类细胞系统中细胞间通讯网络的能力。我们的整个项目将通过三个平行但相互交织的努力来推进：开发一种用于连接细胞外和细胞内网络的通信模式的分析形式主义，并提供一个从测量中识别关键细胞外节点的框架（如蛋白质组学分析）;开发新的生物材料微环境，控制和记录细胞周围局部细胞通信信号中的关键节点，以多路复用的方式，具有高的空间和时间分辨率的环境;和这些方法集成到微尺度灌注培养系统，通过控制因子细胞外基质性质，培养几何形状，局部氧张力和机械应力，促进适当的细胞和组织生理学。

DESCRIPTION (provided by applicant): A tremendous gap exists between available culture and animal models and methods that can extract detailed information on cell-cell communication networks governing system responses to perturbations, such as an inflammatory cue. Networks inherently operate in a complex, interlinked fashion, and often exhibit non-intuitive outcomes from intervention at a particular point in the network, as evidenced by failure of many targeted therapeutics to operate in the clinical setting after promising results in currently- available preclinical trials. Cell-cell communication networks comprise factors the cells release into the extracellular milieu (e.g., cytokines, proteases) along with intracellular signals. While an immense amount of effort has focused on intracellular signals generated in simple cell culture systems by straightforward treatment with individual stimulatory cues, it is not clear how relevant those are to the signals arising from interplay of multiple cues being produced at sequential time-points by diverse cell types as dynamic cascades. Elucidating vital aspects of the interplay of extracellular factors in multi-population cellular systems is crucial for understanding tissue pathophysiology but is exceedingly difficult to study in vivo or in traditional cell culture systems. In this project, we will develop transformative new methods to integrate real time molecular probes of cell-cell communication networks and consequent cell behavior into complex, physiological 3D cultures, allowing multiplexed, dynamic information to be derived from these cultures in response to specific manipulations of the system variables, including cell populations involved and external perturbations such as inflammatory cues. Our goal is to build models of primary human systems to serve as close mimics of in vivo complexity, hence we focus on developing new methods that do not rely on genetic manipulation of the cell populations to generate information about systems operation. Our overall project will advance via three parallel but interwoven efforts: development of an analytical formalism for communication modes that connects extracellular and intracellular networks and provides a framework for identifying key extracellular nodes from measurements (such as proteomic analysis) of extracellular medium; development of new biomaterials microenvironments that both control and record key nodes in local cell communication signals in the pericellular environment in a multiplexed manner, with high spatial and temporal resolution; and integration of these approaches into microscale perfused culture systems that foster appropriate cellular and tissue physiology through control of factors including extracellular matrix properties, culture geometry, local oxygen tension, and mechanical stresses. A major innovation in our work is linking these approaches in a synergistic manner to provide systems that can be used broadly in a wide variety of tissue systems with application to an array of individual diseases, including those where sexually dimorphic responses are prominent. PUBLIC HEALTH RELEVANCE: The goal of this project is transform our ability to probe cell-cell communication networks in human cell systems via linking systems biology with tissue engineering. Our overall project will advance via three parallel but interwoven efforts: development of an analytical formalism for communication modes that connects extracellular and intracellular networks and provides a framework for identifying key extracellular nodes from measurements (such as proteomic analysis) of extracellular medium; development of new biomaterials microenvironments that both control and record key nodes in local cell communication signals in the pericellular environment in a multiplexed manner, with high spatial and temporal resolution; and integration of these approaches into microscale perfused culture systems that foster appropriate cellular and tissue physiology through control of factors extracellular matrix properties, culture geometry, local oxygen tension, and mechanical stresses.