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整合跨物种转录组分析显示,与小鼠相比,在循环前的灵长类动物中更早地发生了髓系细胞生成。

Integrative cross-species transcriptome analysis reveals earlier occurrence of myelopoiesis in pre-circulation primates compared to mice.

机构信息

Chinese PLA Medical School, Chinese PLA General Hospital, Beijing 100853, China.

State Key Laboratory of Experimental Hematology, Haihe Laboratory of Cell Ecosystem, Senior Department of Hematology, Fifth Medical Center of Chinese PLA General Hospital, Beijing 100071, China.

出版信息

Zool Res. 2024 Nov 18;45(6):1276-1286. doi: 10.24272/j.issn.2095-8137.2024.173.

DOI:10.24272/j.issn.2095-8137.2024.173
PMID:39397246
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11668956/
Abstract

Hematopoiesis originates in the yolk sac, which forms prior to the establishment of blood circulation and exhibits distinct developmental processes between primates and mice. Despite increasing appreciation of yolk sac hematopoiesis for its lifelong contribution to the adult hematopoietic system and its regulatory roles in organogenesis, cross-species differences, particularly before the onset of blood circulation, remain incompletely understood. In this study, we constructed an integrative cross-species transcriptome atlas of pre-circulation hematopoiesis in humans, monkeys ( ), and mice. This analysis identified conserved populations between primates and mice, while also revealing more differentiated myeloid, erythroid, and megakaryocytic lineages in pre-circulation primates compared to mice. Specifically, -expressing macrophages were detected in primates before the onset of blood circulation but were absent in mice. Cell-cell communication analysis identified extraembryonic mesoderm cells as a potential supportive niche for macrophage generation, with ligand-receptor interactions between macrophages and other cell populations in the human yolk sac. Interestingly, pre-circulation macrophages exhibited hallmark signatures reminiscent of a macrophage subset that positively regulates hematopoietic stem cell generation. Our findings provide a valuable cross-species resource, advancing our understanding of human pre-circulation yolk sac hematopoiesis and offering a theoretical basis for the regeneration of functional blood cells.

摘要

造血发生于卵黄囊,其形成于血液循环建立之前,并在灵长类动物和小鼠之间表现出明显的发育过程。尽管人们越来越认识到卵黄囊造血对于成年造血系统的终身贡献及其在器官发生中的调节作用,但种间差异,尤其是在血液循环开始之前,仍不完全清楚。在这项研究中,我们构建了人类、猴子( )和小鼠的血液循环前造血的综合跨物种转录组图谱。这项分析鉴定了灵长类动物和小鼠之间的保守群体,同时还揭示了与小鼠相比,血液循环前的灵长类动物中更分化的髓样、红系和巨核细胞谱系。具体而言,在血液循环开始之前,在灵长类动物中检测到表达 的巨噬细胞,但在小鼠中不存在。细胞间通讯分析将 胚外中胚层细胞鉴定为巨噬细胞生成的潜在支持龛,人类卵黄囊中巨噬细胞与其他细胞群体之间存在配体-受体相互作用。有趣的是,血液循环前的 巨噬细胞表现出类似于正向调节造血干细胞生成的巨噬细胞亚群的特征标志。我们的研究结果提供了一个有价值的跨物种资源,推进了我们对人类血液循环前卵黄囊造血的理解,并为功能性血细胞的再生提供了理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd5/11668956/f4caed589f40/zr-45-6-1276-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd5/11668956/a44ba9167066/zr-45-6-1276-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd5/11668956/ef33ab600633/zr-45-6-1276-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd5/11668956/d0a5d712fb09/zr-45-6-1276-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd5/11668956/f4caed589f40/zr-45-6-1276-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd5/11668956/a44ba9167066/zr-45-6-1276-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd5/11668956/ef33ab600633/zr-45-6-1276-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd5/11668956/d0a5d712fb09/zr-45-6-1276-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd5/11668956/f4caed589f40/zr-45-6-1276-4.jpg

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本文引用的文献

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Yolk sac cell atlas reveals multiorgan functions during human early development.卵黄囊细胞图谱揭示了人类早期发育过程中的多器官功能。
Science. 2023 Aug 18;381(6659):eadd7564. doi: 10.1126/science.add7564.
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The genesis of human hematopoietic stem cells.人类造血干细胞的起源。
Blood. 2023 Aug 10;142(6):519-532. doi: 10.1182/blood.2022017934.
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Gas6/Axl Axis Activation Dampens the Inflammatory Response in Osteoarthritic Fibroblast-like Synoviocytes and Synovial Explants.Gas6/Axl轴激活可减轻骨关节炎成纤维细胞样滑膜细胞和滑膜外植体中的炎症反应。
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Geniposide ameliorates atherosclerosis by regulating macrophage polarization via perivascular adipocyte-derived CXCL14.栀子苷通过血管周脂肪细胞衍生的趋化因子 14 调节巨噬细胞极化来改善动脉粥样硬化。
J Ethnopharmacol. 2023 Oct 5;314:116532. doi: 10.1016/j.jep.2023.116532. Epub 2023 May 5.
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Platelet-instructed SPP1 macrophages drive myofibroblast activation in fibrosis in a CXCL4-dependent manner.血小板指导的 SPP1 巨噬细胞以 CXCL4 依赖的方式驱动纤维化中的肌成纤维细胞激活。
Cell Rep. 2023 Feb 28;42(2):112131. doi: 10.1016/j.celrep.2023.112131. Epub 2023 Feb 18.
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Primate gastrulation and early organogenesis at single-cell resolution.灵长类动物原肠胚形成和早期器官发生的单细胞分辨率研究
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Towards a primate single-cell atlas.迈向灵长类单细胞图谱。
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Exosomal CXCL14 Contributes to M2 Macrophage Polarization through NF-B Signaling in Prostate Cancer.外泌体 CXCL14 通过 NF-B 信号通路促进前列腺癌中 M2 型巨噬细胞的极化。
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