Acquisition of a core research microscope for imaging long-term cellular signaling dynamics and optogenetic manipulation

购买核心研究显微镜，用于长期细胞信号动力学和光遗传学操作成像

• 批准号: 10797751
• 负责人: Adam David Hoppe
• 金额: $ 19.98万
• 依托单位: SOUTH DAKOTA STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2022
• 资助国家: 美国
• 起止时间: 2022-03-20 至 2027-01-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10797751
• 关键词: Administrative Supplement; Award; Bioinformatics; Biomedical Research; CRISPR imaging; CRISPR/Cas technology; Cell Death; Cell physiology; Cells; Cellular biology; Centers of Research Excellence; Charge; Consult; Development; Devices; Educational process of instructing; Educational workshop; Faculty; Filtration; Funding; Gene Expression; Genes; Genetic; Genetic Transcription; Goals; Graduate Education; Hour; Image; Immune; Individual; Inflammation; Inflammation Process; Inflammatory; Investigation; Laboratories; Lasers; Letters; Lighting; Lymphatic; Macrophage; Maintenance; Microscope; Microscopy; Molecular; Motor; Movement; Optics; Outcome; Oxidative Stress; PTPN6 gene; Parents; Pathway Analysis; Phosphoric Monoester Hydrolases; Phosphotransferases; Pinocytosis; Plants; Process; Proteins; Regulation; Research; Research Personnel; Research Project Grants; Research Support; Resolution; Resources; Shapes; Signal Transduction; Site; South Dakota; Stimulus; Students; System; Technology; Testing; Time; Tissues; Training; Training and Education; United States National Institutes of Health; Universities; VDAC1 gene; Visualization; Work; base; biological systems; cell motility; cellular imaging; digital; drinking; graduate student; healing; imaging capabilities; imaging study; insight; institutional capacity; instrument; instrumentation; interdisciplinary approach; microscopic imaging; minimally invasive; novel therapeutic intervention; optogenetics; parent project; polarized cell; programs; response; single cell sequencing; student training; tool; transcriptome sequencing; transcriptomics; whole genome

Project Summary This project is an administrative supplement request in response to NOT-GM-22-017. The objective of this project is to expand the capabilities of the CRISPR-IMAGE research support core as part of parent award (COBRE, 5P20GM135008) with a microscope to enable optogenetic manipulating and imaging of signaling dynamics, molecular reorganization, and cellular movements on the time scale of inflammation and resolution (hours to days). This instrumentation’s implementation capitalizes on new expertise brought into the COBRE center with the hire of a new director for our CRIPSR-IMAGE core. This direction will expand our institutional capacity for the analyses of cellular-to-tissue inflammatory process by direct visualization and quantification of cellular dynamics during cellular and tissue-level processes such as differentiation, immune polarization, and responses to oxidative stress. In addition to increasing our capacity for research within the COBRE, this instrument will be used for graduate education via a hands-on course taught by the director (with currently 18 students/year) and it will be available to users from across campus studying diverse cellular processes ranging from bacterial to plant systems.

项目摘要 本项目是响应NOT-GM-22-017的行政补充请求。的目的 该项目旨在扩大CRISPR-IMAGE研究支持核心的能力，作为家长奖的一部分 （COBRE，5 P20 GM 135008）与显微镜进行光遗传学操作和信号传导成像 动力学、分子重组和炎症时间尺度上的细胞运动， 分辨率（小时至天）。该仪器的实施利用了引入的新专业知识， COBRE中心为我们的CRIPSR-IMAGE核心聘请了一位新主任。这一方向将扩大 我们通过直接可视化分析细胞到组织炎症过程的机构能力 以及细胞和组织水平过程（例如分化）期间细胞动力学的量化， 免疫极化和对氧化应激的反应。除了提高我们的研究能力之外， 在COBRE内，该仪器将通过由美国国防部教授的实践课程用于研究生教育。 董事（目前有18名学生/年），它将提供给用户从整个校园学习 从细菌到植物系统的各种细胞过程。