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Sox17 和其他 SoxF 家族蛋白在小鼠胚胎造血中发挥关键作用。

Sox17 and Other SoxF-Family Proteins Play Key Roles in the Hematopoiesis of Mouse Embryos.

机构信息

Department of Stem Cell Regulation, Medical Research Institute, Tokyo Medical and Dental University (TMDU), 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan.

Department of Nutritional Sciences, Faculty of Nutritional Sciences, Nakamura Gakuen University, 5-7-1 Befu, Jonan-ku, Fukuoka 814-0198, Japan.

出版信息

Cells. 2024 Nov 7;13(22):1840. doi: 10.3390/cells13221840.

DOI:10.3390/cells13221840
PMID:39594589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11593047/
Abstract

During mouse development, hematopoietic cells first form in the extraembryonic tissue yolk sac. Hematopoietic stem cells (HSCs), which retain their ability to differentiate into hematopoietic cells for a long time, form intra-aortic hematopoietic cell clusters (IAHCs) in the dorsal aorta at midgestation. These IAHCs emerge from the hemogenic endothelium, which is the common progenitor of hematopoietic cells and endothelial cells. HSCs expand in the fetal liver, and finally migrate to the bone marrow (BM) during the peripartum period. IAHCs are absent in the dorsal aorta in mice deficient in transcription factors such as Runx-1, GATA2, and c-Myb that are essential for definitive hematopoiesis. In this review, we focus on the transcription factor Sry-related high mobility group (HMG)-box (Sox) F family of proteins that is known to regulate hematopoiesis in the hemogenic endothelium and IAHCs. The SoxF family is composed of Sox7, Sox17, and Sox18, and they all have the HMG box, which has a DNA-binding ability, and a transcriptional activation domain. Here, we describe the functional and phenotypic properties of SoxF family members, with a particular emphasis on Sox17, which is the most involved in hematopoiesis in the fetal stages considering that enhanced expression of Sox17 in hemogenic endothelial cells and IAHCs leads to the production and maintenance of HSCs. We also discuss SoxF-inducing signaling pathways.

摘要

在小鼠发育过程中,造血细胞最初在胚外组织卵黄囊中形成。造血干细胞(HSCs)能够长期保持分化为造血细胞的能力,在中孕期形成主动脉内造血细胞簇(IAHCs)位于背主动脉。这些 IAHCs 起源于造血细胞和内皮细胞的共同祖细胞——造血内皮细胞。HSCs 在胎儿肝脏中扩增,最终在围产期迁移到骨髓(BM)。在缺乏对确定造血至关重要的转录因子(如 Runx-1、GATA2 和 c-Myb)的小鼠中,背主动脉中不存在 IAHCs。在这篇综述中,我们重点介绍了已知在造血内皮细胞和 IAHCs 中调节造血的 Sry 相关高迁移率族(HMG)-盒(Sox)F 家族蛋白的转录因子。SoxF 家族由 Sox7、Sox17 和 Sox18 组成,它们都具有 HMG 盒,具有 DNA 结合能力和转录激活结构域。在这里,我们描述了 SoxF 家族成员的功能和表型特性,特别强调 Sox17,因为考虑到 Sox17 在造血内皮细胞和 IAHCs 中的高表达会导致 HSCs 的产生和维持,Sox17 在胎儿期的造血中最为重要。我们还讨论了 SoxF 诱导的信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de98/11593047/74b7d71c66d3/cells-13-01840-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de98/11593047/a467d7b8a825/cells-13-01840-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de98/11593047/7a788e2dc43d/cells-13-01840-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de98/11593047/74b7d71c66d3/cells-13-01840-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de98/11593047/a467d7b8a825/cells-13-01840-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de98/11593047/7a788e2dc43d/cells-13-01840-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de98/11593047/74b7d71c66d3/cells-13-01840-g003.jpg

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本文引用的文献

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Long-term engrafting multilineage hematopoietic cells differentiated from human induced pluripotent stem cells.长期植入由人类诱导多能干细胞分化而来的多谱系造血细胞。
Nat Biotechnol. 2024 Sep 2. doi: 10.1038/s41587-024-02360-7.
2
Efficient hemogenic endothelial cell specification by RUNX1 is dependent on baseline chromatin accessibility of RUNX1-regulated TGFβ target genes.RUNX1 通过调控 TGFβ 靶基因的基础染色质可及性来实现高效的造血内皮细胞特化。
Genes Dev. 2021 Nov 1;35(21-22):1475-1489. doi: 10.1101/gad.348738.121. Epub 2021 Oct 21.
3
SOX18 enhances the proliferation and migration of airway smooth muscle cells induced by tumor necrosis factor-α via the regulation of Notch1 signaling.
SOX18 通过调节 Notch1 信号增强肿瘤坏死因子-α诱导的气道平滑肌细胞增殖和迁移。
Int Immunopharmacol. 2021 Jul;96:107746. doi: 10.1016/j.intimp.2021.107746. Epub 2021 May 15.
4
SOX17 integrates HOXA and arterial programs in hemogenic endothelium to drive definitive lympho-myeloid hematopoiesis.SOX17 将 HOXA 和动脉程序整合到造血内皮中,以驱动确定性淋巴-髓系造血。
Cell Rep. 2021 Feb 16;34(7):108758. doi: 10.1016/j.celrep.2021.108758.
5
Protocol for the Generation of Definitive Hematopoietic Progenitors from Human Pluripotent Stem Cells.从人类多能干细胞生成确定性造血祖细胞的方案。
STAR Protoc. 2020 Oct 16;1(3):100130. doi: 10.1016/j.xpro.2020.100130. eCollection 2020 Dec 18.
6
Sox17-mediated expression of adherent molecules is required for the maintenance of undifferentiated hematopoietic cluster formation in midgestation mouse embryos.Sox17 介导的黏附分子表达对于维持中孕期小鼠胚胎未分化造血集落的形成是必需的。
Differentiation. 2020 Sep-Oct;115:53-61. doi: 10.1016/j.diff.2020.08.001. Epub 2020 Aug 16.
7
SOX18 exerts tumor-suppressive functions in papillary thyroid carcinoma through inhibition of Wnt/β-catenin signaling.SOX18 通过抑制 Wnt/β-catenin 信号通路在甲状腺乳头状癌中发挥肿瘤抑制作用。
Exp Cell Res. 2020 Nov 1;396(1):112249. doi: 10.1016/j.yexcr.2020.112249. Epub 2020 Aug 25.
8
Notch ligand Dll4 impairs cell recruitment to aortic clusters and limits blood stem cell generation.Notch 配体 Dll4 会损害细胞向主动脉丛的募集,从而限制血液干细胞的生成。
EMBO J. 2020 Apr 15;39(8):e104270. doi: 10.15252/embj.2019104270. Epub 2020 Mar 9.
9
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Stem Cells. 2020 Jun;38(6):756-768. doi: 10.1002/stem.3169. Epub 2020 Mar 16.
10
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F1000Res. 2019 Dec 20;8. doi: 10.12688/f1000research.21129.1. eCollection 2019.