The Tunicate Ciona: A New Model for the Effects of Aging on Tissue Regeneration

被囊动物 Ciona：衰老对组织再生影响的新模型

• 批准号: 8132928
• 负责人: WILLIAM R JEFFERY
• 金额: $ 9.07万
• 依托单位: UNIV OF MARYLAND, COLLEGE PARK
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-01 至 2012-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8132928
• 关键词: Ablation; Adolescent; Adult; Age; Aging; Aging-Related Process; Animals; Apoptosis; Appearance; Area; Biological Models; Biology; Brain; Candidate Disease Gene; Cell Aging; Cell Death; Cell Proliferation; Cell physiology; Cerebrum; Chordata; Ciona intestinalis; Collection; Complementary DNA; Complex; Defect; Development; Embryo; Event; Expressed Sequence Tags; Face; Ganglia; Gene Expression; Gene Silencing; Genes; Genome; Growth; Guanosine Triphosphate; Heart Atrium; Human; In Situ Hybridization; Invertebrates; Life; Life Cycle Stages; Lobe; Maintenance; Methods; Microarray Analysis; Microsurgery; Modeling; Molecular; Muscle Fibers; Natural regeneration; Nerve; Nervous system structure; Oral; Oranges; Organ; Pattern; Photoreceptors; Phylogenetic Analysis; Pigments; Positioning Attribute; Process; RNA Interference; Receptor Cell; Relative (related person); Research; Role; Screening procedure; Sensory; Signal Transduction; Sister; Site; Speed; Staining method; Stains; Stem cells; Study models; System; Taxon; Techniques; Tissues; Transgenic Animals; Transgenic Organisms; Urochordata; Vertebrates; Wound Healing; age effect; age related; cell motility; design; gene function; genome sequencing; inhibitor/antagonist; injured; life history; member; middle age; migration; notch protein; novel strategies; organ regeneration; polarized cell; precursor cell; progenitor; public health relevance; regenerative; small molecule; stem; tissue regeneration; wound

DESCRIPTION (provided by applicant): Many vertebrates have robust capacities for tissue regeneration as embryos and juveniles but this power fades during development and aging. The mechanisms of age-related decline in regenerative capacity are unknown and an area in which new approaches and model systems are necessary. This proposal develops the tunicate Ciona intestinalis as a chordate model for studying the effects of aging on tissue regeneration. Although not previously used as an aging model, Ciona has many favorable attributes for this purpose: it has powerful capacities for regeneration, which decline during aging, a sequenced genome, a collection of cDNA and ESTs covering 80% of the total genes, stable transgenic lines with tagged gene expression in specific tissues, and a short life history in which age is directly related to size. As a member of a chordate invertebrate group that is inferred to be the sister taxon of vertebrates, information obtained about the relationship between aging and regeneration in tunicates may be relevant to humans. The five specific aims of this proposal are designed to obtain a molecular and cellular understanding of defective oral siphon regeneration during aging. We will focus on the sensory pigment organs of the oral siphon, possible photoreceptors that regenerate with high fidelity in young and middle age animals, but show specific defects in old animals. The first three aims will focus on the cellular events involved in producing age-related defects in pigment organ regeneration. The first aim will investigate the effects of aging on maintenance of the stem/progenitor cell niche for pigment organ precursors and precursor cell migration to the wound site during regeneration. The second aim will focus on age-related changes in cell death and proliferation in the siphon wound site, the stem/precursor niche, and the reforming pigment organs during regeneration. The third aim explores the role of siphon nerves and the CNS in regenerative aging using ablation techniques and a transgenic line with GFP staining throughout the nervous system. The fourth and fifth aims investigate the molecular mechanisms responsible for age-related defects in pigment organ regeneration. The fourth aim will identify and determine the expression patterns of genes involved in regeneration, including components of the Notch signaling system, which preliminary studies have implicated in the regenerative process. The fifth aim will use RNAi gene silencing to establish how functional changes in regeneration genes are involved in the cellular aging processes revealed in the first three aims. This research is expected to fill a major gap in understanding how regenerative capacity declines with aging in a model chordate representing the closest living relative of vertebrates. PUBLIC HEALTH RELEVANCE: The ability to replace injured tissues fades with aging in most vertebrates, including humans. This study will develop the tunicate Ciona intestinalis, a vertebrate relative with powerful regeneration abilities that also recede with age, as a model to study the relationship between aging and tissue regeneration.

描述（由申请人提供）：许多脊椎动物在胚胎和幼年时具有强大的组织再生能力，但这种能力在发育和衰老过程中逐渐消失。与年龄相关的再生能力下降的机制是未知的，在这一领域，新的方法和模型系统是必要的。本研究将被囊玻璃海鞘作为研究衰老对组织再生影响的脊索动物模型。虽然以前没有被用作衰老模型，但玻璃海鞘具有许多有利的属性：它具有强大的再生能力，在衰老过程中会下降，测序的基因组，覆盖80%总基因的cDNA和EST集合，在特定组织中具有标记基因表达的稳定转基因系，以及年龄与大小直接相关的短生活史。作为脊索动物无脊椎动物群的一员，被推断为脊椎动物的姐妹分类群，有关被囊动物衰老和再生之间的关系的信息可能与人类有关。本提案的五个具体目标旨在获得衰老过程中有缺陷的口腔虹吸管再生的分子和细胞理解。我们将集中在口腔虹吸管的感觉色素器官，可能的光感受器，在年轻和中年动物中以高保真度再生，但在老年动物中表现出特定的缺陷。前三个目标将集中在色素器官再生中产生年龄相关缺陷的细胞事件。第一个目的是研究衰老对维持色素器官前体干/祖细胞生态位和再生过程中前体细胞迁移到伤口部位的影响。第二个目标将集中在虹吸伤口部位，干/前体生态位和再生过程中的重组色素器官中细胞死亡和增殖的年龄相关变化。第三个目标探讨虹吸神经和中枢神经系统再生老化的作用，使用消融技术和转基因线与GFP染色整个神经系统。第四和第五个目标是研究色素器官再生中与年龄相关的缺陷的分子机制。第四个目标将识别和确定参与再生的基因的表达模式，包括Notch信号系统的组成部分，初步研究表明这些基因与再生过程有关。第五个目标将使用RNAi基因沉默来确定再生基因的功能变化如何参与前三个目标中揭示的细胞衰老过程。这项研究有望填补一个主要的空白，了解再生能力如何随着模型脊索动物的衰老而下降，脊索动物代表了脊椎动物的最接近的生活亲属。 公共卫生相关性：在大多数脊椎动物中，包括人类，替换受损组织的能力随着年龄的增长而减弱。本研究将开发被囊玻璃海鞘，一种具有强大再生能力的脊椎动物亲戚，也随着年龄的增长而衰退，作为研究衰老和组织再生之间关系的模型。