In vivo mouse models for inducible hematopoietic- and hematopoietic stem cell-spe

诱导型造血细胞和造血干细胞特异性小鼠体内模型

• 批准号: 8719927
• 负责人: CAMILLA FORSBERG
• 金额: $ 18.11万
• 依托单位: UNIVERSITY OF CALIFORNIA SANTA CRUZ
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-09-01 至 2016-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8719927
• 关键词: Ablation; Animals; Antibodies; Blood; Cell physiology; Cells; Cessation of life; Clinical; Complex; Diphtheria Toxin; Engraftment; Ensure; Environment; Equilibrium; Excision; Future; Goals; Gold; Hematological Disease; Hematopoiesis; Hematopoietic; Hematopoietic Stem Cell Transplantation; Hematopoietic stem cells; Homeostasis; Immune; Immune system; Immunosuppression; In Situ; Laboratories; Lead; Life; Mediating; Methods; Modeling; Mus; Outcome; Pathway interactions; Physiological; Process; Protocols documentation; Radiation; Regimen; Relative (related person); Research; Role; Safety; Stem cell transplant; Stem cells; Testing; Toxin; Transplantation; Vascular blood supply; cancer therapy; cell type; chemotherapy; clinically relevant; conditioning; congenic; diphtheria toxin receptor; hematopoietic stem cell fate; immune clearance; improved; in vivo; insight; interest; irradiation; mouse model; novel; progenitor; public health relevance; receptor; reconstitution; research study; self-renewal; stem cell differentiation; stem cell fate; stem cell niche; tool

DESCRIPTION (provided by applicant): Our long-term research goals are to understand the mechanisms that regulate stem cell fate decisions. To ensure a life-long supply of blood and immune cells, the hematopoietic stem cell (HSC) must balance self-renewal with differentiation by responding properly to complex and dynamic inputs from the environment. The goal of this proposal is to develop two new mouse models that will serve as important tools for dissecting the intrinsic and extrinsic mechanisms that govern HSC function. These new models will enable us to pursue the mechanisms regulating hematopoietic homeostasis, the role of niches in HSC fate decisions and engraftment, how radiation-induced effects influence these processes, and a range of other questions that cannot be answered by existing methods. The outcomes will facilitate ex vivo HSC expansion and guide strategies for improving the safety and efficiency of HSC transplantation therapies. .

描述（由申请人提供）：我们的长期研究目标是了解调节干细胞命运决定的机制。为了确保血液和免疫细胞的终身供应，造血干细胞（HSC）必须通过适当地响应来自环境的复杂和动态输入来平衡自我更新与分化。本提案的目标是开发两种新的小鼠模型，这两种模型将作为解剖支配HSC功能的内在和外在机制的重要工具。这些新的模型将使我们能够追求造血稳态的调节机制，在HSC的命运决定和移植的作用，小生境，辐射诱导的影响如何影响这些过程，以及一系列其他问题，不能回答现有的方法。这些结果将促进体外HSC扩增，并指导提高HSC移植治疗安全性和有效性的策略。.

项目成果

ROBO4-mediated vascular integrity regulates the directionality of hematopoietic stem cell trafficking.

• DOI: 10.1016/j.stemcr.2014.12.013
• 发表时间: 2015-02-10
• 期刊: STEM CELL REPORTS
• 影响因子: 5.9
• 作者: Smith-Berdan, Stephanie;Nguyen, Andrew;Hong, Matthew A.;Forsberg, E. Camilla
• 通讯作者: Forsberg, E. Camilla