从时间和空间维度捕捉胚胎造血过程。

IF 2.5 4区 医学 Q2 HEMATOLOGY Experimental hematology Pub Date : 2024-08-01 DOI:10.1016/j.exphem.2024.104257
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引用次数: 0

摘要

造血干细胞(HSCs)具有在生物体的整个生命周期中持续制造所有血细胞类型的能力。造血干细胞主要分布在成人的骨髓中,但也起源于胚胎发育过程。对造血干细胞的诞生、其发育轨迹以及与其连续龛位之间的特定相互作用进行可视化,极大地促进了我们对造血干细胞形成和扩增的生物学和机理的理解。应用于活胚胎或非固定样本的显像技术为我们深入了解造血干细胞的细胞和解剖起源提供了宝贵的资料。这些成像技术还揭示了造血干细胞与周围微环境或生态位中邻近细胞类型(如内皮细胞或巨噬细胞)之间的动态相互作用。本综述将深入探讨在了解造血干细胞的起源、生成和细胞相互作用方面取得的进展,尤其是在小鼠和斑马鱼胚胎发育过程中,重点关注采用(活体)成像分析的研究。
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Capturing embryonic hematopoiesis in temporal and spatial dimensions

Hematopoietic stem cells (HSCs) possess the ability to sustain the continuous production of all blood cell types throughout an organism's lifespan. Although primarily located in the bone marrow of adults, HSCs originate during embryonic development. Visualization of the birth of HSCs, their developmental trajectory, and the specific interactions with their successive niches have significantly contributed to our understanding of the biology and mechanics governing HSC formation and expansion. Intravital techniques applied to live embryos or non-fixed samples have remarkably provided invaluable insights into the cellular and anatomical origins of HSCs. These imaging technologies have also shed light on the dynamic interactions between HSCs and neighboring cell types within the surrounding microenvironment or niche, such as endothelial cells or macrophages. This review delves into the advancements made in understanding the origin, production, and cellular interactions of HSCs, particularly during the embryonic development of mice and zebrafish, focusing on studies employing (live) imaging analysis.

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来源期刊
Experimental hematology
Experimental hematology 医学-血液学
CiteScore
5.30
自引率
0.00%
发文量
84
审稿时长
58 days
期刊介绍: Experimental Hematology publishes new findings, methodologies, reviews and perspectives in all areas of hematology and immune cell formation on a monthly basis that may include Special Issues on particular topics of current interest. The overall goal is to report new insights into how normal blood cells are produced, how their production is normally regulated, mechanisms that contribute to hematological diseases and new approaches to their treatment. Specific topics may include relevant developmental and aging processes, stem cell biology, analyses of intrinsic and extrinsic regulatory mechanisms, in vitro behavior of primary cells, clonal tracking, molecular and omics analyses, metabolism, epigenetics, bioengineering approaches, studies in model organisms, novel clinical observations, transplantation biology and new therapeutic avenues.
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