Evolution of the Developing Myelin Sheath

发育中的髓鞘的进化

• 批准号: 0402188
• 负责人: Robert Gould
• 金额: --
• 依托单位: University of Illinois at Chicago
• 依托单位国家: 美国
• 项目类别: Continuing Grant
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-07-01 至 2005-07-31
• 项目状态: 已结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=0402188&HistoricalAwards=false
• 关键词: Evolution; Developing; Myelin; Sheath

9986132Gould The long-term goal of this research project is to gain understanding of how oligodendrocytes (and Schwann cells) myelinate axons. Realizing that none of the proteins involved in the early recognition and assembly stages of myelination were unknown, a strategy was developed to identify such proteins through isolation of complementary DNA molecules that represent messenger RNAs located at sites where myelin sheaths assemble. Studies of the developmental expression patterns of some of these mRNAs (over 80 were identified) showed that they fell into two developmental groups. One group was not strongly expressed until myelination was well under way (postnatal day 10 in rat). A second group, nearly equal in number to the first group, was expressed earlier and had higher expression in tissues with smaller myelinated fibers. With techniques used to identify these mRNAs, studies will be conducted to identify a third group of mRNAs, those expressed preferentially at times that oligodendrocyte processes first contact the axons they will myelinate. Once these mRNAs are identified, studies will be conducted to locate the sites where mRNAs and proteins are expressed in the developing nervous system to insure that the proteins are indeed important for early stages of myelination. The myelinated nervous system evolved in a common ancestor of all jawed vertebrates, including cartilaginous and teleost fishes, amphibians, reptiles, birds and mammals. This development required recruitment of proteins that allowed myelination to take place in the common ancestor. Comparative studies between rats and sharks are planned and will be used to help us understand how the myelinated nervous system originated.

9986132这个研究项目的长期目标是了解少突胶质细胞(和雪旺细胞)如何形成髓鞘轴突。意识到在髓鞘形成的早期识别和组装阶段涉及的蛋白质都不是未知的，因此开发了一种策略，通过分离代表位于髓鞘组装部位的信使RNA的互补DNA分子来识别此类蛋白质。对其中一些(超过80个)的mRNAs的发育表达模式的研究表明，它们分为两个发育组。其中一组在髓鞘形成过程中(大鼠出生后第10天)才有强烈表达。第二组在数量上几乎与第一组相同，表达较早，并且在有髓纤维较小的组织中表达较高。利用用于识别这些mRNA的技术，将进行研究以识别第三组mRNAs，这些mRNAs优先在少突胶质细胞突起第一次接触它们将形成髓鞘的轴突时表达。一旦确定了这些mRNAs，将进行研究，以定位mRNAs和蛋白质在发育中的神经系统中表达的位置，以确保这些蛋白质确实对髓鞘形成的早期阶段起着重要作用。有髓神经系统在所有有颌脊椎动物的共同祖先中进化，包括软骨和硬骨鱼、两栖动物、爬行动物、鸟类和哺乳动物。这种发育需要招募蛋白质，使髓鞘形成发生在共同的祖先身上。老鼠和鲨鱼之间的比较研究正在计划中，并将用来帮助我们了解有髓神经系统是如何起源的。