• 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

相似文献

1
The molecular and cellular hematopoietic stem cell specification niche.造血干细胞分子和细胞特化龛。
Exp Hematol. 2024 Aug;136:104280. doi: 10.1016/j.exphem.2024.104280. Epub 2024 Jul 14.
2
Exploring Epigenetic Complexity in Regulation of Hematopoietic Stem Cells Niche: A Mechanistic Journey from Normal to Malignant Hematopoiesis.探索造血干细胞微环境调控中的表观遗传复杂性:从正常造血到恶性造血的机制之旅。
Adv Exp Med Biol. 2025;1483:49-67. doi: 10.1007/5584_2024_846.
3
Widespread presence of bone marrow-like hematopoietic stem cell niche in invertebrate skeletons.无脊椎动物骨骼中广泛存在类似骨髓的造血干细胞生态位。
Sci Adv. 2025 Jun 27;11(26):eadw0958. doi: 10.1126/sciadv.adw0958. Epub 2025 Jun 25.
4
Bone Marrow Niche in Cardiometabolic Disease: Mechanisms and Therapeutic Potential.心血管代谢疾病中的骨髓微环境:机制与治疗潜力
Circ Res. 2025 Jan 31;136(3):325-353. doi: 10.1161/CIRCRESAHA.124.323778. Epub 2025 Jan 30.
5
A capsular myofibroblastic niche maintains hematopoietic stem cells in the spleen.被膜肌成纤维细胞微环境维持脾脏中的造血干细胞。
EMBO J. 2025 Jun 5. doi: 10.1038/s44318-025-00477-2.
6
An unbiased genomewide screen uncovers 7 genes that drive hematopoietic stem cell fate from mouse embryonic stem cells.一项无偏差的全基因组筛选发现了7个驱动小鼠胚胎干细胞向造血干细胞命运转变的基因。
Blood. 2025 Jul 17;146(3):328-340. doi: 10.1182/blood.2024027742.
7
DNMT3A regulates murine megakaryocyte-biased hematopoietic stem cell fate decisions.DNMT3A调控小鼠巨核细胞偏向性造血干细胞的命运决定。
Blood Adv. 2025 May 13;9(9):2285-2299. doi: 10.1182/bloodadvances.2024015061.
8
The Aryl Hydrocarbon Receptor Modulates Murine Hematopoietic Stem Cell Homeostasis and Influences Lineage-Biased Stem and Progenitor Cells.芳香烃受体调节小鼠造血干细胞的稳态并影响谱系偏向的干细胞和祖细胞。
Stem Cells Dev. 2021 Oct 1;30(19):970-980. doi: 10.1089/scd.2021.0096. Epub 2021 Sep 20.
9
Stem cell insights into human trophoblast lineage differentiation.干细胞对人类滋养层谱系分化的研究。
Hum Reprod Update. 2016 Dec;23(1):77-103. doi: 10.1093/humupd/dmw026. Epub 2016 Sep 2.
10
KLF4 enhances transplantation-induced hematopoiesis by inhibiting TLRs and noncanonical NFκB signaling at a steady state.KLF4通过在稳态下抑制Toll样受体(TLRs)和非经典核因子κB(NFκB)信号通路来增强移植诱导的造血作用。
Exp Hematol. 2025 Apr;144:104730. doi: 10.1016/j.exphem.2025.104730. Epub 2025 Feb 1.

引用本文的文献

1
Restraint of TGFβ family signaling by SMAD7 is necessary for hematopoietic stem cell maturation in the embryo.SMAD7对转化生长因子β(TGFβ)家族信号的抑制作用是胚胎中造血干细胞成熟所必需的。
bioRxiv. 2025 Aug 28:2025.08.23.671940. doi: 10.1101/2025.08.23.671940.
2
The evolving hematopoietic niche during development.发育过程中不断演变的造血微环境。
Front Mol Biosci. 2024 Oct 2;11:1488199. doi: 10.3389/fmolb.2024.1488199. eCollection 2024.

本文引用的文献

1
Lineage-tracing hematopoietic stem cell origins in vivo to efficiently make human HLF+ HOXA+ hematopoietic progenitors from pluripotent stem cells.在体追踪造血干细胞起源,高效地从多能干细胞产生人 HLF+HOXA+ 造血祖细胞。
Dev Cell. 2024 May 6;59(9):1110-1131.e22. doi: 10.1016/j.devcel.2024.03.003. Epub 2024 Apr 2.
2
Fetal liver macrophages contribute to the hematopoietic stem cell niche by controlling granulopoiesis.胎肝巨噬细胞通过控制粒细胞生成来促进造血干细胞龛的形成。
Elife. 2024 Mar 25;13:e86493. doi: 10.7554/eLife.86493.
3
A multistep computational approach reveals a neuro-mesenchymal cell population in the embryonic hematopoietic stem cell niche.一种多步骤计算方法揭示了胚胎造血干细胞龛中的神经-间质细胞群体。
Development. 2024 Apr 1;151(7). doi: 10.1242/dev.202614. Epub 2024 Apr 4.
4
Runx1+ vascular smooth muscle cells are essential for hematopoietic stem and progenitor cell development in vivo.Runx1+ 血管平滑肌细胞对于体内造血干细胞和祖细胞的发育是必不可少的。
Nat Commun. 2024 Feb 23;15(1):1653. doi: 10.1038/s41467-024-44913-z.
5
Cis inhibition of NOTCH1 through JAGGED1 sustains embryonic hematopoietic stem cell fate.通过 JAGGED1 抑制 NOTCH1 维持胚胎造血干/祖细胞命运。
Nat Commun. 2024 Feb 21;15(1):1604. doi: 10.1038/s41467-024-45716-y.
6
An interactive resource of molecular signalling in the developing human haematopoietic stem cell niche.一个发育中人造血干细胞龛中分子信号传导的交互式资源。
Development. 2023 Dec 1;150(23). doi: 10.1242/dev.201972. Epub 2023 Dec 6.
7
Dermomyotome-derived endothelial cells migrate to the dorsal aorta to support hematopoietic stem cell emergence.皮肌节衍生的内皮细胞迁移到背主动脉以支持造血干细胞的出现。
Elife. 2023 Sep 11;12:e58300. doi: 10.7554/eLife.58300.
8
Haematopoietic stem and progenitor cell heterogeneity is inherited from the embryonic endothelium.造血干细胞和祖细胞的异质性是从胚胎内皮细胞遗传而来的。
Nat Cell Biol. 2023 Aug;25(8):1135-1145. doi: 10.1038/s41556-023-01187-9. Epub 2023 Jul 17.
9
Activation of lineage competence in hemogenic endothelium precedes the formation of hematopoietic stem cell heterogeneity.在造血干细胞异质性形成之前,造血内皮细胞中的谱系潜能被激活。
Cell Res. 2023 Jun;33(6):448-463. doi: 10.1038/s41422-023-00797-0. Epub 2023 Apr 4.
10
Alcam-a and Pdgfr-α are essential for the development of sclerotome-derived stromal cells that support hematopoiesis.Alcam-a 和 PDGFR-α 对于支持造血的由生骨节衍生而来的基质细胞的发育是必不可少的。
Nat Commun. 2023 Mar 1;14(1):1171. doi: 10.1038/s41467-023-36612-y.

造血干细胞分子和细胞特化龛。

The molecular and cellular hematopoietic stem cell specification niche.

机构信息

Department of Hematology, St. Jude Children's Research Hospital, Memphis, TN.

Department of Hematology, St. Jude Children's Research Hospital, Memphis, TN.

出版信息

Exp Hematol. 2024 Aug;136:104280. doi: 10.1016/j.exphem.2024.104280. Epub 2024 Jul 14.

DOI:10.1016/j.exphem.2024.104280
PMID:39009276
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11338702/
Abstract

Hematopoietic stem cells (HSCs) are a population of tissue-specific stem cells that reside in the bone marrow of adult mammals, where they self-renew and continuously regenerate the adult hematopoietic lineages over the life of the individual. Prominence as a stem cell model and clinical usefulness have driven interest in understanding the physiologic processes that lead to the specification of HSCs during embryonic development. High-efficiency directed differentiation of HSCs by the instruction of defined progenitor cells using sequentially defined instructive molecules and conditions remains impossible, indicating that comprehensive knowledge of the complete set of precursor intermediate identities and required inductive inputs remains incompletely understood. Recently, interest in the molecular and cellular microenvironment where HSCs are specified from endothelial precursors-the "specification niche"-has increased. Here we review recent progress in understanding these niche spaces across vertebrate phyla, as well as how a better characterization of the origin and molecular phenotypes of the niche cell populations has helped inform and complicate previous understanding of signaling required for HSC emergence and maturation.

摘要

造血干细胞(HSCs)是一种组织特异性干细胞,存在于成年哺乳动物的骨髓中,在个体的一生中,它们自我更新并不断再生成体造血谱系。HSCs 作为干细胞模型的重要性及其在临床应用上的价值,推动了人们对理解胚胎发育过程中导致 HSCs 特化的生理过程的兴趣。使用顺序定义的有指导作用的分子和条件,通过定义明确的祖细胞指令,高效地定向分化 HSCs 仍然是不可能的,这表明对完整的前体细胞中间身份和所需诱导输入的综合认识仍不完全清楚。最近,人们对造血干细胞从内皮前体细胞(“特化龛位”)特化的分子和细胞微环境的兴趣增加了。在这里,我们综述了在理解这些龛位空间方面在脊椎动物门之间的最新进展,以及更好地表征龛位细胞群体的起源和分子表型如何帮助阐明和复杂化以前对 HSC 出现和成熟所需信号的理解。