Molecular Mechanisms Underlying Xenopus Somitogenesis

爪蟾体细胞发生的分子机制

• 批准号: 7599266
• 负责人: CARMEN R. DOMINGO
• 金额: $ 11.5万
• 依托单位: SAN FRANCISCO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-04-01 至 2012-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7599266
• 关键词: Actins; Adult; Affect; Amphibia; Applications Grants; Binding; CXCR4 Receptors; Cells; Complement; Congenital Abnormality; DNA Sequence Rearrangement; Deformity; Dermis; Development; Developmental Biology; Diagnosis; Disease; Embryonic Development; Environment; Event; Evolution; Family; Fiber; Foundations; Genes; Goals; Guanosine Triphosphate Phosphohydrolases; Imaging Techniques; Injection of therapeutic agent; Laboratories; Lead; Mentorship; Mesoderm; Mesoderm Cell; Messenger RNA; Molecular; Morphogenesis; Muscle; Nature; Paraxial Mesoderm; Play; Process; Productivity; Proteins; Public Health; Research; Role; Rotation; Senior Scientist; Signal Pathway; Signal Transduction; Signaling Molecule; Skeletal Muscle; Skeleton; Somites; Spinal; Spinal Cord; Students; Techniques; Testing; Time; Tissues; Training; Training and Education; Underrepresented Minority; Vertebrates; Work; Xenopus; Xenopus laevis; Zebrafish; base; cell behavior; cytokine; gastrulation; improved; in vivo; innovation; interest; knock-down; migration; prevent; progenitor; receptor; rho; rho GTP-Binding Proteins; scoliosis; somitogenesis; spine bone structure; tissue culture; tool

DESCRIPTION (provided by applicant): Somitogenesis consists of the segmentation and differentiation of the paraxial mesoderm into the skeletal muscle, axial skeleton and dermis of the adult. While many genes involved in regulating the periodic nature of somite formation have been characterized, the cell behaviors underlying this process remain poorly understood. The objective of this proposal is to determine the molecular mechanism underlying somite morphogenesis in the vertebrate Xenopus laevis. Our central hypothesis is that the secreted cytokine, stromal-derived factor-1 (SDF-1), regulates Xenopus somite morphogenesis by activating the specific actin regulatory molecules RhoA, Rac1, or Cdc42. Specific support for this hypothesis is based on recent studies in zebrafish that showed that the cell behaviors associated with somite rotation (Hollway et al., 2007; Stellabote et al., 2007) are similar to those documented by our lab and others in Xenopus (Afonin et al., 2006). Furthermore, the secreted cytokine, stromal-derived factor-1 (SDF-1), was shown to be required for the cell rearrangements associated with zebrafish somite rotation (Hollway et al., 2007), which is significant as it is the first signaling molecule shown to regulate somite rotation. In Xenopus, SDF-1 was shown to play a role in mesoderm migration during gastrulation (Fukui et al., 2006) and is expressed in axial tissues throughout early embryonic development (Braun et al., 2002). Thus, SDF-1 is present at the right time and place to play a role in somite morphogenesis. To test our central hypothesis, we will modulate SDF-1 signaling by using morpholinos to knockdown expression levels and in vivo mRNA injections to up-regulate protein levels of SDF-1 and its receptor, CXCR4, in the cell (aim 1). Previous studies have shown that SDF-1 signaling affects changes in cell behaviors by activating specific Rho GTPases (Tan et al., 2006). These actin regulatory molecules have been shown to play an important role in tissue remodeling and thus are likely downstream targets of the SDF-1 signaling pathway during somitogenesis. To test this hypothesis, we will determine whether SDF-1 signaling modulates the activity of specific Rho GTPases during Xenopus somitogenesis (aim 2). Another goal of this proposal is to introduce new molecular approaches that along with the existing expertise in imaging techniques will provide an excellent environment for training students, many of whom are underrepresented minorities (aim 3). Furthermore, we also developed a mentorship plan with three senior scientists (Drs. Amacher, Symes, and Weisblat) whose research expertise complements the objectives presented in this proposal and will increase the research productivity of our lab. Relevance to Public Health: The proposed research is expected to provide critical information on how vertebrate somites are formed. This information will help in developing tools for diagnosing or preventing vertebral disorders such as scoliosis and other congenital spinal cord deformities.

描述（由申请人提供）：躯体发生包括近轴中胚层分割和分化为成人的骨骼肌、轴骨和真皮。虽然许多基因参与调节体节形成的周期性的特点，这一过程的细胞行为仍然知之甚少。本研究的目的是探讨脊椎动物非洲爪蟾体节形态发生的分子机制。我们的中心假设是，分泌的细胞因子，基质衍生因子-1（SDF-1），调节非洲爪蟾体节形态发生激活特定的肌动蛋白调节分子RhoA，Rac 1，或Cdc 42。对这一假设的具体支持是基于最近在斑马鱼中的研究，该研究表明与体节旋转相关的细胞行为（Hollway et al.，2007; Stellabote等人，2007）类似于我们实验室和其他人在非洲爪蟾中记录的那些（Afonin等人，2006年）。此外，分泌的细胞因子，基质衍生因子-1（SDF-1），被证明是与斑马鱼体节旋转相关的细胞重排所需的（Hollway et al.，2007），这是重要的，因为它是第一个显示调节体节旋转的信号分子。在非洲爪蟾中，SDF-1显示在原肠胚形成期间的中胚层迁移中起作用（福井等人，2006）并在整个早期胚胎发育过程中在轴组织中表达（Braun et al.，2002年）。因此，SDF-1在正确的时间和地点存在，在体节形态发生中发挥作用。 为了检验我们的中心假设，我们将通过使用吗啉代敲低表达水平和体内mRNA注射上调细胞中SDF-1及其受体CXCR 4的蛋白水平来调节SDF-1信号传导（目的1）。先前的研究已经表明，SDF-1信号传导通过激活特异性Rho GTP酶来影响细胞行为的变化（Tan等人，2006年）。这些肌动蛋白调节分子已被证明在组织重塑中起重要作用，因此可能是体节发生过程中SDF-1信号通路的下游靶点。为了验证这一假设，我们将确定SDF-1信号传导是否调节非洲爪蟾体节发生过程中特定Rho GTP酶的活性（目的2）。该提案的另一个目标是引入新的分子方法，沿着现有的成像技术专业知识，为培训学生提供一个极好的环境，其中许多学生是代表性不足的少数民族（目标3）。此外，我们还与三位资深科学家（Amacher，Symes和Weisblat博士）制定了一项导师计划，他们的研究专业知识补充了本提案中提出的目标，并将提高我们实验室的研究生产力。与公共卫生的相关性：拟议的研究有望提供有关脊椎动物体节如何形成的关键信息。这些信息将有助于开发诊断或预防脊椎疾病的工具，如脊柱侧凸和其他先天性脊髓畸形。