Single-cell analysis of cultured bone marrow stromal cells reveals high similarity to fibroblasts in situ

被引:5
|
作者
Stalmann, Ursula S. A. [1 ,2 ]
Banjanin, Bella [1 ,2 ]
Snoeren, Inge A. M. [1 ,2 ]
Nagai, James S. [3 ]
Leimkuehler, Nils B. [4 ]
Li, Ronghui [3 ]
Benabid, Adam [5 ]
Pritchard, Jessica E. [1 ,2 ,5 ]
Malyaran, Hanna [6 ,7 ]
Neuss, Sabine [6 ,7 ]
Bindels, Eric M. [8 ]
Costa, Ivan G. [3 ]
Schneider, Rebekka K. [1 ,2 ,5 ]
机构
[1] Erasmus MC, Dept Dev Biol, Rotterdam, Netherlands
[2] Erasmus MC, Oncode Inst, Inst Canc, Rotterdam, Netherlands
[3] Rhein Westfal TH Aachen, RWTH, Inst Computat Genom, Aachen, Germany
[4] Univ Duisburg Essen, Univ Hosp Essen, Dept Hematol & Stem Cell Transplantat, Essen, Germany
[5] Rhein Westfal TH Aachen, Inst Biomed Engn, Fac Med, Dept Cell Biol,RWTH, Aachen, Germany
[6] Rhein Westfal TH Aachen, RWTH, Inst Pathol, Fac Med Rhein, Aachen, Germany
[7] Rhein Westfal TH Aachen, RWTH, Helmholtz Inst Biomed Engn, Biointerface Grp, Aachen, Germany
[8] Erasmus MC, Dept Hematol, Inst Canc, Rotterdam, Netherlands
关键词
D O I
10.1016/j.exphem.2022.03.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Within the heterogenous pool of bone marrow stromal cells, mesenchymal stromal cells (MSCs) are of particular interest because of their hematopoiesis-supporting capacities, contribution to disease progression, therapy resistance, and leukemic initiation. Cultured bone marrow-derived stromal cells (cBMSCs) are used for in vitro modeling of hematopoiesis-stroma interactions, validation of disease mechanisms, and screening for therapeutic targets. Here, we place cBMSCs (mouse and human) in a bone marrow tissue context by systematically comparing the transcriptome of plastic-adherent cells on a single-cell level with in vivo counterparts. Cultured BMSCs encompass a rather homogenous cell population, independent of the isolation method used and, although still possessing hematopoiesis-supporting capacity, are distinct from freshly isolated MSCs and more akin to in vivo fibroblast populations. Informed by combined cell trajectories and pathway analyses, we illustrate that TGFb inhibition in vitro can preserve a more "MSC"-like phenotype (c) 2022 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
引用
收藏
页码:28 / 33
页数:6
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