Computing hepatic intercellular communications in response to toxicant exposures

计算肝脏细胞间通讯以响应有毒物质暴露

• 批准号: 8718528
• 负责人: Allison N Tegge
• 金额: $ 5.33万
• 依托单位: VIRGINIA POLYTECHNIC INST AND ST UNIV
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-08-15 至 2017-08-14
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8718528
• 关键词: Affect; Algorithms; Animal Model; Automobile Driving; Behavior; Benchmarking; Bile fluid; Biological Assay; Biomedical Engineering; Cell physiology; Chemicals; Cholesterol Homeostasis; Coagulation Process; Communication; Computing Methodologies; Coupling; Data; Databases; Endothelial Cells; Environment; Environmental Exposure; Exposure to; Future; Genes; Genomics; Goals; Graph; Health; Heart Diseases; Hepatic; Hepatocyte; Human; In Vitro; Intervention; Kupffer Cells; Ligands; Light; Literature; Liver; Lung diseases; Malignant Neoplasms; Methodology; Methods; Modeling; Network-based; Organ; Parkinson Disease; Pathway Analysis; Pathway interactions; Pattern; Phenotype; Physiological; Primary carcinoma of the liver cells; Process; Production; Proteins; Proteomics; Publishing; Rattus; Research; Research Proposals; Role; Signal Pathway; Signal Transduction; Stimulus; Stream; System; Techniques; Testing; Tissues; Toxic Environmental Substances; Toxicant exposure; Tweens; base; career; cell type; data integration; environmental chemical; experience; genetic regulatory protein; human disease; improved; in vivo; insight; intercellular communication; liver function; liver-specific protein; nervous system disorder; novel; population based; public health relevance; receptor; receptor binding; research study; response; skills; toxicant; transcriptomics

DESCRIPTION (provided by applicant): On a daily basis, the population is exposed to environmental chemicals. This exposure has been associated with many human diseases ranging from heart disease to Parkinson's disease, and even several cancers. The liver is an essential organ to study for understanding how environmental toxicants affect the body due to its capability of detoxifying these foreign chemicals, among other key responsibilities. The liver contains multiple cell types, each having distinct functionality, and investigating how these cell types communicate is imperative to understanding physiological functions of the liver. However, in vivo studies of inter-cellular communications in the liver are difficult for both humans and model organisms. Emerging as an attractive alternative, in vitro bioengineered liver models have been developed that represent the most important cell types (hepatocytes, liver sinusoidal endothelial cells (LSECs), and Kupffer cells) and maintain cell-type-specific phenotypes and behaviors as a surrogate for costly experiments. Using these liver models, in combination with genomic and computational methods, promises to improve our understanding of the cellular signaling that occurs within the liver models under both normal conditions and after an exposure to environmental toxicants, thereby resulting in more impactful and biologically meaningful insights. Developing novel computational methods seek to quantitatively identify the normal inter-cellular communication patterns between the liver cell types and utilize transcriptomic and proteomic data for predicting how environmental chemicals perturb the normal hepatic inter-cellular communication patterns. This research proposal will develop novel network based computational methods related to inter-cellular signaling and communication in the liver. Computational methods will be tested, benchmarked and validated using experimental data from both toxicant response assays and bioengineered liver models. These approaches will make predictions and prioritizations that are biologically informative and relevant, thus driving future experiments. To this end, a database of rat-related liver-specific protein-protein and regulatory interactions and signaling pathways derived from published literature as a starting framework for computing liver-specific signaling networks will be created. This network will be used to predict dysregulated signaling patterns from high-throughput response assays. The liver-specific background network will be extended to include inter-cellular interactions and integrate transcriptomic and proteomic data from 3D bioengineered liver models. This data integration will result in the identification of inter-cellular communication patterns specific for bioengineered liver systems. Additionally, toxicant-specific signaling network as a result of the liver models' exposure to various environmental chemicals will be computed. From these toxicant-specific networks, differential network analysis will be performed to identify chemical specific signaling patterns, which subsequently will prioritize future experiments. Taken together, this proposal will characterize and propose mechanisms in which toxicants alter the natural inter-cellular communication patterns.

描述（由申请人提供）：在日常生活中，人口暴露于环境化学品。这种暴露与许多人类疾病有关，从心脏病到帕金森病，甚至是几种癌症。肝脏是研究环境毒物如何影响身体的重要器官，因为它具有解毒这些外来化学物质的能力，以及其他关键责任。肝脏含有多种细胞类型，每种细胞类型都具有不同的功能，研究这些细胞类型如何交流对于了解肝脏的生理功能至关重要。然而，在肝脏中的细胞间通信的体内研究是困难的人类和模式生物。作为一种有吸引力的替代方案，已经开发了体外生物工程肝脏模型，其代表了最重要的细胞类型（肝细胞，肝窦内皮细胞（LSEC）和枯否细胞），并保持细胞类型特异性表型和行为作为昂贵实验的替代品。使用这些肝脏模型，结合基因组和计算方法，有望提高我们对正常条件下和暴露于环境毒物后肝脏模型内发生的细胞信号传导的理解，从而产生更具影响力和生物学意义的见解。开发新的计算方法寻求定量识别肝细胞类型之间的正常细胞间通信模式，并利用转录组学和蛋白质组学数据来预测环境化学物质如何干扰正常的肝细胞间通信模式。这项研究计划将开发新的基于网络的计算方法，与肝脏中的细胞间信号传导和通信相关。计算方法将使用来自毒物反应测定和生物工程肝脏模型的实验数据进行测试、基准测试和验证。这些方法将做出生物信息和相关的预测和优先级排序，从而推动未来的实验。为此，将创建一个大鼠相关肝脏特异性蛋白质-蛋白质和调控相互作用以及来自已发表文献的信号通路的数据库，作为计算肝脏特异性信号网络的起始框架。该网络将用于预测来自高通量反应测定的失调信号模式。肝脏特异性背景网络将扩展到包括细胞间相互作用，并整合来自3D生物工程肝脏模型的转录组学和蛋白质组学数据。这种数据整合将导致识别特定于 生物工程肝脏系统此外，还将计算肝脏模型暴露于各种环境化学物质导致的毒物特异性信号网络。从这些毒物特异性网络中，将进行差异网络分析以识别化学特异性信号模式，随后将优先考虑未来的实验。两者合计，这一建议将表征和提出机制，其中毒物改变自然细胞间的通信模式。