| Literature DB >> 35971894 |
James L C Che1,2,3, Daniel Bode1,2,3, Iwo Kucinski1,2, Alyssa H Cull3, Fiona Bain3, Hans J Becker4,5, Maria Jassinskaja3, Melania Barile1,2, Grace Boyd3, Miriam Belmonte1,2, Andy G X Zeng6,7, Kyomi J Igarashi8, Juan Rubio-Lara3, Mairi S Shepherd1,2, Anna Clay1, John E Dick6,7, Adam C Wilkinson9, Hiromitsu Nakauchi4,5,8, Satoshi Yamazaki10,11, Berthold Göttgens1,2, David G Kent1,2,3.
Abstract
Hematopoietic stem cells (HSCs) cultured outside the body are the fundamental component of a wide range of cellular and gene therapies. Recent efforts have achieved > 200-fold expansion of functional HSCs, but their molecular characterization has not been possible since the majority of cells are non-HSCs and single cell-initiated cultures have substantial clone-to-clone variability. Using the Fgd5 reporter mouse in combination with the EPCR surface marker, we report exclusive identification of HSCs from non-HSCs in expansion cultures. By directly linking single-clone functional transplantation data with single-clone gene expression profiling, we show that the molecular profile of expanded HSCs is similar to proliferating fetal HSCs and reveals a gene expression signature, including Esam, Prdm16, Fstl1, and Palld, that can identify functional HSCs from multiple cellular states. This "repopulation signature" (RepopSig) also enriches for HSCs in human datasets. Together, these findings demonstrate the power of integrating functional and molecular datasets to better derive meaningful gene signatures and opens the opportunity for a wide range of functional screening and molecular experiments previously not possible due to limited HSC numbers.Entities:
Keywords: HSC expansion; hematopoiesis; hematopoietic stem cells; self-renewal gene signature; single cell biology
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Year: 2022 PMID: 35971894 PMCID: PMC9535767 DOI: 10.15252/embr.202255502
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 9.071