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成人血液干细胞的定位反映了报告的骨髓龛细胞类型及其组合的丰度。

Adult blood stem cell localization reflects the abundance of reported bone marrow niche cell types and their combinations.

机构信息

Department of Biosystems Science and Engineering, Eidgenössische Technische Hochschule (ETH) Zurich, Basel, Switzerland.

Center for Regenerative Medicine, Massachusetts General Hospital, Boston, MA.

出版信息

Blood. 2020 Nov 12;136(20):2296-2307. doi: 10.1182/blood.2020006574.

Abstract

The exact localization of hematopoietic stem cells (HSCs) in their native bone marrow (BM) microenvironment remains controversial, because multiple cell types have been reported to physically associate with HSCs. In this study, we comprehensively quantified HSC localization with up to 4 simultaneous (9 total) BM components in 152 full-bone sections from different bone types and 3 HSC reporter lines. We found adult femoral α-catulin-GFP+ or Mds1GFP/+Flt3Cre HSCs proximal to sinusoids, Cxcl12 stroma, megakaryocytes, and different combinations of those populations, but not proximal to bone, adipocyte, periarteriolar, or Schwann cells. Despite microanatomical differences in femurs and sterna, their adult α-catulin-GFP+ HSCs had similar distributions. Importantly, their microenvironmental localizations were not different from those of random dots, reflecting the relative abundance of imaged BM populations rather than active enrichment. Despite their functional heterogeneity, dormant label-retaining (LR) and non-LR hematopoietic stem and progenitor cells both had indistinguishable localization from α-catulin-GFP+ HSCs. In contrast, cycling juvenile BM HSCs preferentially located close to Cxcl12 stroma and farther from sinusoids/megakaryocytes. We expect our study to help resolve existing confusion regarding the exact localization of different HSC types, their physical association with described BM populations, and their tissue-wide combinations.

摘要

造血干细胞(HSCs)在其天然骨髓(BM)微环境中的精确定位仍然存在争议,因为已经报道了多种细胞类型与 HSCs 物理相关。在这项研究中,我们通过从不同骨类型的 152 个全骨切片和 3 个 HSC 报告细胞系中同时检测多达 4 个(总共 9 个)BM 成分,全面量化了 HSC 的定位。我们发现成年股骨α-微管结合蛋白-GFP+或 Mds1GFP/+Flt3Cre HSCs 靠近窦状隙、Cxcl12 基质、巨核细胞以及这些细胞群体的不同组合,但不靠近骨、脂肪细胞、血管周隙或施万细胞。尽管股骨和胸骨在微观解剖学上存在差异,但它们的成年α-微管结合蛋白-GFP+ HSCs 具有相似的分布。重要的是,它们的微环境定位与随机点没有区别,反映了成像 BM 群体的相对丰度,而不是主动富集。尽管它们具有功能异质性,但休眠标记保留(LR)和非 LR 造血干/祖细胞与α-微管结合蛋白-GFP+ HSCs 的定位没有区别。相比之下,循环的幼年 BM HSCs 优先靠近 Cxcl12 基质,远离窦状隙/巨核细胞。我们希望我们的研究有助于解决关于不同 HSC 类型的精确定位、它们与描述的 BM 群体的物理关联以及它们在组织范围内的组合方面的现有混淆。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe27/8209553/c8899776736a/bloodBLD2020006574absf1.jpg

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