MSM - Multiscale Studies of Segmentation in Vertebrate *

MSM - 脊椎动物分割的多尺度研究*

• 批准号: 7283086
• 负责人: James Alexander Glazier
• 金额: $ 27.99万
• 依托单位: TRUSTEES OF INDIANA UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-09-01 至 2008-09-25
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7283086
• 关键词: Address; Anterior; Behavior; Biocompatible Materials; Biological Pacemakers; Birth; Cell Adhesion; Cell Adhesion Molecules; Cells; Complex; Development; Developmental Biology; Developmental Process; Disease; Embryonic Development; Extracellular Matrix; Failure; Feedback; Goldenhar Syndrome; Growth Factor; Infant; Knowledge; Kyphosis deformity of spine; Limb structure; Methodology; Modeling; Molecular; Movement; Muscle; Pattern; Peripheral Nervous System; Prevention; Process; Property; Public Health; Purpose; Range; Regulation; Research; Research Personnel; Segmentation Clock Pathway; Simulate; Somites; Spinal Dysraphism; Structure; Syndrome; Techniques; Testing; Tissues; Vertebrates; Work; insight; malformation; millimeter; multi-scale modeling; novel; open source; research study; rib bone structure; scoliosis; simulation; software development; somitogenesis; spine bone structure; theories

DESCRIPTION (provided by applicant): In vertebrates, segmentation during early embryogenesis forms somites, recurring tissue modules, distributed along the anterior-posterior axis. Segmental structures give rise to the ribs, vertebrae, limbs, associated muscles, and central and peripheral nervous system. Failures in segmentation can be lethal or cause serious developmental abnormalities. Somitogenesis relies on a molecular clock, growth factor gradients and the expression of cell-adhesion and extracellular matrix (ECM) molecules. Segmentation requires complex, large-scale (millimeter) coordinated movement of cells and ECM. Despite increasing knowledge of the molecular mechanisms underlying segmentation, the interplay of molecular-, cell- and tissue-level mechanisms during somitogenesis remains obscure. Because of the tight feedback between subcellular and large-scale processes, no single-scale model can simulate somitogenesis. Current models address only the subcellular or macroscopic levels and do so separately. A successful multiscale model will answer one of developmental biology's great open problems: how do the molecular mechanisms of fate determination couple to large-scale tissue deformations? The proposed work will test the hypothesis that during segmentation, physical forces and biomaterial properties must coordinate with a moving biological oscillator, the segmentation clock, for successful somitogenesis. We will both model and conduct experiments on key developmental mechanisms ranging from local regulation of cell adhesion proteins (micrometers) to global tissue deformations (millimeters). We will develop novel theories and modeling approaches to bridge these scales. Our methodology has four major components: 1) Identifying (discovering) mechanisms and relevant models at each scale. 2) Determining the parameters for each level of model. 3) Validating model results. 4) Testing model predictions of normal and abnormal behaviors, e.g. inhibition or overproduction of adhesion molecules. The techniques and insights the research will produce will apply to other developmental processes. The software we develop will form the core of an open-source, multiscale and general purpose Tissue Simulation Toolkit, which other researchers can apply to this and other developmental problems. The proposed research contributes to public health by addressing the causes of a significant subset of the developmental malformations which occur in approximately 150,000 infants born each year in the USA (1 out of 28 births). Disturbing somite formation results in Klippel-Feil syndrome.spondylocostal dysostosis.Jarcho-Levin syndrome, congenital scoliosis and kyphosis, Goldenhar syndrome, and spina bifida, among others disorders. Studying the developmental mechanisms in vertebral patterning will aid in the identification of protective or potentially disruptive factors for normal somitogenesis and could potentially impact treatments for the prevention of vertebral patterning disorders.

描述（由申请人提供）： 在脊椎动物中，早期胚胎发生期间的分节形成体节，体节是沿着前后轴沿着分布的重复组织模块。节段性结构产生肋骨、椎骨、四肢、相关肌肉以及中枢和外周神经系统。分割失败可能是致命的或导致严重的发育异常。躯体发生依赖于分子时钟、生长因子梯度以及细胞粘附和细胞外基质（ECM）分子的表达。分割需要细胞和ECM的复杂的、大规模（毫米）的协调运动。尽管越来越多的知识的分子机制的分割，相互作用 在体节发生的分子，细胞和组织水平的机制仍然是模糊的。由于亚细胞和大尺度过程之间的紧密反馈，没有单一尺度的模型可以模拟体节发生。目前的模型只涉及亚细胞或宏观水平，并单独进行。一个成功的多尺度模型将回答发育生物学的一个巨大的开放问题：命运决定的分子机制如何与大尺度组织变形耦合？拟议的工作将测试的假设，即在分割，物理力和生物材料的属性必须协调与移动的生物振荡器，分割时钟，成功的体节。我们将对关键的发育机制进行建模和实验，从细胞粘附蛋白的局部调节（微米）到全球组织变形（毫米）。我们将开发新的理论和建模方法来弥合这些规模。我们的方法有四个主要组成部分：1）识别（发现）机制和相关模型在每个规模。2)确定模型每个级别的参数。3)验证 模型结果4)测试正常和异常行为的模型预测，例如粘附分子的抑制或过度产生。研究将产生的技术和见解将适用于其他发展过程。我们开发的软件将形成一个开源，多尺度和通用组织模拟工具包的核心，其他研究人员可以应用于这个和其他发展问题。拟议的研究通过解决美国每年出生的约15万名婴儿（28名新生儿中的1名）中发生的发育畸形的重要子集的原因，为公共卫生做出贡献。扰乱体节形成导致Klippel-Feil综合征、脊椎肋骨发育不全、Jarcho-Levin综合征、先天性脊柱侧凸和脊柱后凸、Goldenhar综合征和脊柱裂等疾病。研究发展 脊椎图案形成中的机制将有助于识别正常体节发生的保护性或潜在破坏性因素，并可能影响预防脊椎图案形成障碍的治疗。