• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

通过胚状体形成将人类胚胎干细胞分化为造血内皮细胞和血液祖细胞。

differentiation of human embryonic stem cells to hemogenic endothelium and blood progenitors via embryoid body formation.

机构信息

Developmental Haematopoiesis Group, Faculty of Biology, Medicine and Health, the University of Manchester, Manchester M13 9PT, UK.

Stem Cell Process Development, Adaptimmune Ltd., 60 Jubilee Avenue Milton Park, Abingdon, Oxfordshire OX14 4RX, UK.

出版信息

STAR Protoc. 2021 Mar 2;2(1):100367. doi: 10.1016/j.xpro.2021.100367. eCollection 2021 Mar 19.

DOI:10.1016/j.xpro.2021.100367
PMID:33718891
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7933812/
Abstract

Little is known about the emergence of blood progenitors during human embryogenesis due to ethical reasons and restricted embryo access. The use of human embryonic stem cells (hESCs) as a model system offers unique opportunities to dissect human blood cell formation. Here, we describe a protocol allowing the differentiation of hESCs via embryoid bodies toward hemogenic endothelium and its subsequent differentiation to blood progenitors. This protocol relies on the formation of embryoid bodies, which is tricky if not carefully performed. For complete details on the use and execution of this protocol, please refer to Garcia-Alegria et al. (2018).

摘要

由于伦理原因和胚胎获取受限,人类胚胎发生过程中血液祖细胞的出现知之甚少。使用人类胚胎干细胞 (hESC) 作为模型系统为解析人类血细胞形成提供了独特的机会。在这里,我们描述了一种通过胚状体将 hESC 分化为造血内皮细胞并随后分化为血液祖细胞的方案。该方案依赖于胚状体的形成,如果操作不仔细,这将很棘手。有关此方案的使用和执行的完整详细信息,请参阅 Garcia-Alegria 等人。(2018)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/379d39d74820/gr13.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/7e07373040c2/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/8407f41137e2/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/5fbcdea15769/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/60aab3bea1a7/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/8977b924d9fb/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/8d9cabb44919/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/8920b1f2450d/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/c9ff8dcfbb3f/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/44b223fdcf73/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/253147a1736d/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/c13c32a0c5c2/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/2d00050224c2/gr11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/c70681d9c5c6/gr12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/379d39d74820/gr13.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/7e07373040c2/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/8407f41137e2/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/5fbcdea15769/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/60aab3bea1a7/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/8977b924d9fb/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/8d9cabb44919/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/8920b1f2450d/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/c9ff8dcfbb3f/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/44b223fdcf73/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/253147a1736d/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/c13c32a0c5c2/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/2d00050224c2/gr11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/c70681d9c5c6/gr12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97fd/7933812/379d39d74820/gr13.jpg

相似文献

1
differentiation of human embryonic stem cells to hemogenic endothelium and blood progenitors via embryoid body formation.通过胚状体形成将人类胚胎干细胞分化为造血内皮细胞和血液祖细胞。
STAR Protoc. 2021 Mar 2;2(1):100367. doi: 10.1016/j.xpro.2021.100367. eCollection 2021 Mar 19.
2
Early Human Hemogenic Endothelium Generates Primitive and Definitive Hematopoiesis In Vitro.早期人类造血内皮细胞在体外产生原始和定向造血。
Stem Cell Reports. 2018 Nov 13;11(5):1061-1074. doi: 10.1016/j.stemcr.2018.09.013. Epub 2018 Oct 25.
3
Targeted Disruption of TCF12 Reveals HEB as Essential in Human Mesodermal Specification and Hematopoiesis.靶向敲除 TCF12 揭示 HEB 在人类中胚层特化和造血中的必需性。
Stem Cell Reports. 2017 Sep 12;9(3):779-795. doi: 10.1016/j.stemcr.2017.07.011. Epub 2017 Aug 10.
4
Directed differentiation of definitive hemogenic endothelium and hematopoietic progenitors from human pluripotent stem cells.从人多能干细胞定向分化出确定的造血内皮细胞和造血祖细胞。
Methods. 2016 May 15;101:65-72. doi: 10.1016/j.ymeth.2015.10.001. Epub 2015 Oct 9.
5
Application of small molecule CHIR99021 leads to the loss of hemangioblast progenitor and increased hematopoiesis of human pluripotent stem cells.小分子CHIR99021的应用导致血管母细胞祖细胞的丧失,并增加了人类多能干细胞的造血作用。
Exp Hematol. 2018 Sep;65:38-48.e1. doi: 10.1016/j.exphem.2018.05.007. Epub 2018 Jun 5.
6
In vitro human embryonic stem cell hematopoiesis mimics MYB-independent yolk sac hematopoiesis.体外人胚胎干细胞造血模拟不依赖MYB的卵黄囊造血。
Haematologica. 2015 Feb;100(2):157-66. doi: 10.3324/haematol.2014.112144. Epub 2014 Nov 7.
7
Efficient and simultaneous generation of hematopoietic and vascular progenitors from human induced pluripotent stem cells.高效且同时从人诱导多能干细胞中生成造血和血管祖细胞。
Cytometry A. 2013 Jan;83(1):114-26. doi: 10.1002/cyto.a.22090. Epub 2012 Jun 26.
8
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.
9
ID1 and ID3 represent conserved negative regulators of human embryonic and induced pluripotent stem cell hematopoiesis.ID1 和 ID3 是人类胚胎和诱导多能干细胞造血的保守负调控因子。
J Cell Sci. 2011 May 1;124(Pt 9):1445-52. doi: 10.1242/jcs.077511. Epub 2011 Apr 12.
10
Expression of angiotensin-converting enzyme (CD143) identifies and regulates primitive hemangioblasts derived from human pluripotent stem cells.血管紧张素转换酶(CD143)的表达可识别并调节源自人类多能干细胞的原始成血管细胞。
Blood. 2008 Nov 1;112(9):3601-14. doi: 10.1182/blood-2008-03-144766. Epub 2008 Aug 26.

引用本文的文献

1
ETV2 Overexpression Promotes Efficient Differentiation of Pluripotent Stem Cells to Endothelial Cells.ETV2过表达促进多能干细胞高效分化为内皮细胞。
Biotechnol Bioeng. 2025 Jul;122(7):1914-1928. doi: 10.1002/bit.28979. Epub 2025 Mar 25.
2
Combining the induced pluripotent stem cell (iPSC) technology with chimeric antigen receptor (CAR)-based immunotherapy: recent advances, challenges, and future prospects.将诱导多能干细胞(iPSC)技术与基于嵌合抗原受体(CAR)的免疫疗法相结合:最新进展、挑战与未来前景。
Front Cell Dev Biol. 2024 Nov 18;12:1491282. doi: 10.3389/fcell.2024.1491282. eCollection 2024.
3
Blood-generating heart-forming organoids recapitulate co-development of the human haematopoietic system and the embryonic heart.

本文引用的文献

1
Direct Comparison of Four Hematopoietic Differentiation Methods from Human Induced Pluripotent Stem Cells.人诱导多能干细胞四种造血分化方法的直接比较
Stem Cell Reports. 2020 Sep 8;15(3):735-748. doi: 10.1016/j.stemcr.2020.07.009. Epub 2020 Aug 6.
2
Early Human Hemogenic Endothelium Generates Primitive and Definitive Hematopoiesis In Vitro.早期人类造血内皮细胞在体外产生原始和定向造血。
Stem Cell Reports. 2018 Nov 13;11(5):1061-1074. doi: 10.1016/j.stemcr.2018.09.013. Epub 2018 Oct 25.
3
Activation of the Arterial Program Drives Development of Definitive Hemogenic Endothelium with Lymphoid Potential.
造血心形成类器官再现了人类造血系统和胚胎心脏的共同发育。
Nat Cell Biol. 2024 Nov;26(11):1984-1996. doi: 10.1038/s41556-024-01526-4. Epub 2024 Oct 8.
4
CD82 expression marks the endothelium to hematopoietic transition at the onset of blood specification in human.CD82的表达标志着人类血液特化开始时内皮细胞向造血细胞的转变。
iScience. 2023 Aug 9;26(9):107583. doi: 10.1016/j.isci.2023.107583. eCollection 2023 Sep 15.
5
Endothelial and hematopoietic hPSCs differentiation via a hematoendothelial progenitor.通过造血内皮祖细胞分化内皮和造血 hPSCs。
Stem Cell Res Ther. 2022 Jun 17;13(1):254. doi: 10.1186/s13287-022-02925-w.
6
Use of standard U-bottom and V-bottom well plates to generate neuroepithelial embryoid bodies.使用标准 U 底和 V 底培养板生成神经上皮类胚体。
PLoS One. 2022 May 10;17(5):e0262062. doi: 10.1371/journal.pone.0262062. eCollection 2022.
7
Hematopoietic Cells from Pluripotent Stem Cells: Hope and Promise for the Treatment of Inherited Blood Disorders.多能干细胞来源的造血细胞:遗传性血液疾病治疗的希望与承诺。
Cells. 2022 Feb 5;11(3):557. doi: 10.3390/cells11030557.
8
The RUNX1b Isoform Defines Hemogenic Competency in Developing Human Endothelial Cells.RUNX1b 异构体定义了发育中的人类内皮细胞的造血能力。
Front Cell Dev Biol. 2021 Dec 16;9:812639. doi: 10.3389/fcell.2021.812639. eCollection 2021.
动脉程序的激活驱动具有淋巴样潜能的定型血发生内皮的发育。
Cell Rep. 2018 May 22;23(8):2467-2481. doi: 10.1016/j.celrep.2018.04.092.
4
Hemangioblast, hemogenic endothelium, and primitive versus definitive hematopoiesis.成血管细胞、造血内皮细胞以及原始造血与定向造血
Exp Hematol. 2017 May;49:19-24. doi: 10.1016/j.exphem.2016.12.009. Epub 2016 Dec 30.
5
Chromosomal Modification in Human Embryonic Stem Cells Cultured in a Feeder-Free Condition after Single Cell Dissociation using Accutase.使用Accutase进行单细胞解离后,在无饲养层条件下培养的人胚胎干细胞中的染色体修饰
Dev Reprod. 2012 Dec;16(4):353-61. doi: 10.12717/DR.2012.16.4.353.
6
A novel serum-free monolayer culture for orderly hematopoietic differentiation of human pluripotent cells via mesodermal progenitors.一种新型无血清单层培养方法,通过中胚层祖细胞有序地进行人多能干细胞的造血分化。
PLoS One. 2011;6(7):e22261. doi: 10.1371/journal.pone.0022261. Epub 2011 Jul 27.
7
Human ESCs predisposition to karyotypic instability: Is a matter of culture adaptation or differential vulnerability among hESC lines due to inherent properties?人类胚胎干细胞易患核型不稳定性:是培养适应性问题,还是由于内在特性导致的不同人类胚胎干细胞系之间的易感性差异?
Mol Cancer. 2008 Oct 3;7:76. doi: 10.1186/1476-4598-7-76.
8
Induction of T cell development and establishment of T cell competence from embryonic stem cells differentiated in vitro.从体外分化的胚胎干细胞诱导T细胞发育并建立T细胞功能。
Nat Immunol. 2004 Apr;5(4):410-7. doi: 10.1038/ni1055. Epub 2004 Mar 21.