Suppr超能文献

造血系统中体内命运图谱的干细胞动力学和谱系拓扑结构。

Stem-cell dynamics and lineage topology from in vivo fate mapping in the hematopoietic system.

作者信息

Höfer Thomas, Barile Melania, Flossdorf Michael

机构信息

Division of Theoretical Systems Biology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany; Bioquant Center, University of Heidelberg, Im Neuenheimer Feld 267, 69120 Heidelberg, Germany.

Division of Theoretical Systems Biology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany; Bioquant Center, University of Heidelberg, Im Neuenheimer Feld 267, 69120 Heidelberg, Germany.

出版信息

Curr Opin Biotechnol. 2016 Jun;39:150-156. doi: 10.1016/j.copbio.2016.04.001. Epub 2016 Apr 20.

Abstract

In recent years, sophisticated fate-mapping tools have been developed to study the behavior of stem cells in the intact organism. These experimental approaches are beginning to yield a quantitative picture of how cell numbers are regulated during steady state and in response to challenges. Focusing on hematopoiesis and immune responses, we discuss how novel mathematical approaches driven by these fate-mapping data have provided insights into the dynamics and topology of cellular differentiation pathways in vivo. The combination of experiment and theory has allowed to quantify the degree of self-renewal in stem and progenitor cells, shown how native hematopoiesis differs fundamentally from post-transplantation hematopoiesis, and uncovered that the diversification of T lymphocytes during immune responses resembles tissue renewal driven by stem cells.

摘要

近年来,已经开发出复杂的命运图谱工具来研究完整生物体中干细胞的行为。这些实验方法开始产生关于细胞数量在稳态期间以及应对挑战时如何调节的定量图景。聚焦于造血作用和免疫反应,我们讨论了由这些命运图谱数据驱动的新型数学方法如何为体内细胞分化途径的动力学和拓扑结构提供了见解。实验与理论的结合使得能够量化干细胞和祖细胞的自我更新程度,表明天然造血作用与移植后造血作用在根本上存在差异,并且揭示了免疫反应期间T淋巴细胞的多样化类似于由干细胞驱动的组织更新。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验