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卵黄囊巨噬细胞祖细胞在特定发育阶段迁移至胚胎。

Yolk sac macrophage progenitors traffic to the embryo during defined stages of development.

作者信息

Stremmel C, Schuchert R, Wagner F, Thaler R, Weinberger T, Pick R, Mass E, Ishikawa-Ankerhold H C, Margraf A, Hutter S, Vagnozzi R, Klapproth S, Frampton J, Yona S, Scheiermann C, Molkentin J D, Jeschke U, Moser M, Sperandio M, Massberg S, Geissmann F, Schulz C

机构信息

Medizinische Klinik und Poliklinik I, Klinikum der Universität, Ludwig-Maximilians-Universität, Marchioninistrasse 15, 81377, Munich, Germany.

Walter-Brendel-Center for Experimental Medicine, Ludwig-Maximilians-Universität, Marchioninistrasse 15, 81377, Munich, Germany.

出版信息

Nat Commun. 2018 Jan 8;9(1):75. doi: 10.1038/s41467-017-02492-2.

Abstract

Tissue macrophages in many adult organs originate from yolk sac (YS) progenitors, which invade the developing embryo and persist by means of local self-renewal. However, the route and characteristics of YS macrophage trafficking during embryogenesis are incompletely understood. Here we show the early migration dynamics of YS-derived macrophage progenitors in vivo using fate mapping and intravital microscopy. From embryonic day 8.5 (E8.5) CXCR1+ pre-macrophages are present in the mouse YS where they rapidly proliferate and gain access to the bloodstream to migrate towards the embryo. Trafficking of pre-macrophages and their progenitors from the YS to tissues peaks around E10.5, dramatically decreases towards E12.5 and is no longer evident from E14.5 onwards. Thus, YS progenitors use the vascular system during a restricted time window of embryogenesis to invade the growing fetus. These findings close an important gap in our understanding of the development of the innate immune system.

摘要

许多成体器官中的组织巨噬细胞起源于卵黄囊(YS)祖细胞,这些祖细胞侵入发育中的胚胎并通过局部自我更新得以留存。然而,胚胎发生过程中YS巨噬细胞迁移的途径和特征尚未完全明确。在此,我们利用命运图谱和活体显微镜技术展示了YS来源的巨噬细胞祖细胞在体内的早期迁移动态。从胚胎第8.5天(E8.5)起,CXCR1+前巨噬细胞存在于小鼠YS中,它们在那里迅速增殖并进入血液循环,向胚胎迁移。前巨噬细胞及其祖细胞从YS到组织的迁移在E10.5左右达到峰值,到E12.5时急剧减少,从E14.5起不再明显。因此,YS祖细胞在胚胎发生的有限时间窗口内利用血管系统侵入生长中的胎儿。这些发现填补了我们在理解先天免疫系统发育方面的一个重要空白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fe6/5758709/7cd8485c2449/41467_2017_2492_Fig1_HTML.jpg

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