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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.
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页码:29 / 39
页数:11
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