3D organoid modeling of extramedullary hematopoiesis

被引:1
|
作者
Lara-Gonzalez, Eloisa [1 ]
Wittig, Olga [1 ]
Diaz-Solano, Dylana [1 ]
Cardier, Jose E. [1 ]
机构
[1] Inst Venezolano Invest Cient IVIC, Ctr Med Regenerat, Unidad Terapia Celular, Lab Patol Celular & Mol, Caracas, Venezuela
来源
关键词
Hematopoietic niche model; collagen; fibrin clot; hematopoietic cells; endothelial cells; CELL-CULTURE SYSTEMS; BONE-MARROW NICHE; STEM-CELLS; PROGENITOR CELLS; LIVER; SCAFFOLDS; MAINTENANCE;
D O I
10.1177/03913988221136144
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Background: Under certain clinical and experimental conditions hematopoiesis occurs in other site than bone marrow (BM), such as the liver. Here, we develop a 3D organoid that mimics several components of the hematopoietic niche present during liver extramedullary hematopoiesis. Aim: To evaluate the capacity of a 3D hematopoietic organoid (3D-HO) to function as a hematopoietic like-niche allowing for blood cell production outside of the BM Methods: The 3D-HO is constituted by liver sinusoidal endothelial cells (LSEC) as the stromal component, BM isolated from 5-FU treated mice (FU-BMCs), collagen microspheres and plasma clot as scaffolds. The ability of the 3D-HO to support the survival and functionality of FU-BMCs was investigated by using confocal microscopy, histology analysis, flow cytometry, and clonogenic assays. Results: After 15 and 30 days, post-ectopic implantation, histological studies of the 3D-HO showed the presence of cells with myeloid and lymphoid lineage morphology. Flow cytometry analysis of these cells showed the presence of cells expressing hematopoietic stem progenitor cells (HSPC) (Sca-1(+)/c-Kit(+)), myeloid (Gr-1(+)) and lymphoid (B220(+) and CD19(+)) markers. Clonogenic assays showed that cells from the 3D-HO formed hematopoietic colonies. Expression of the Sry gene by cells from the 3D-HO, implanted for 30 days in female mice, indicated that male donor cells persist in this model of extramedullary hematopoiesis. Conclusions: The 3D-HO constitutes an extramedullary hematopoietic-like niche which supports the survival and functionality of FU-BMCs. It may constitute an efficient model for investigating, in vitro and in vivo, those factors that control hematopoiesis outside BM.
引用
收藏
页码:29 / 39
页数:11
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