Zebrafish models of inflammation in hematopoietic development and disease

被引:3
作者
Ketharnathan, Sarada [1 ]
Rajan, Vinothkumar [2 ]
Prykhozhij, Sergey V. [1 ]
Berman, Jason N. [1 ,3 ,4 ]
机构
[1] Childrens Hosp Eastern Ontario Res Inst, Ottawa, ON, Canada
[2] Sunnybrook Res Inst, Biol Sci Platform, Toronto, ON, Canada
[3] Univ Ottawa, Dept Pediat, Ottawa, ON, Canada
[4] Univ Ottawa, Dept Cellular & Mol Med, Ottawa, ON, Canada
来源
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2022年 / 10卷
关键词
inflammation; hematopoietic stem and progenitor cell (HSPC); zebrafish; interferon; JAK-STAT signaling pathway; bone marrow failure disorders; inflammasome; clonal hematopoiesis; T-CELL LEUKEMIA; R-LOOPS; STEM; PROGENITOR; MACROPHAGES; EMERGENCE; CYTOKINES; PROVIDE; TRIGGER;
D O I
10.3389/fcell.2022.955658
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Zebrafish offer an excellent tool for studying the vertebrate hematopoietic system thanks to a highly conserved and rapidly developing hematopoietic program, genetic amenability, optical transparency, and experimental accessibility. Zebrafish studies have contributed to our understanding of hematopoiesis, a complex process regulated by signaling cues, inflammation being crucial among them. Hematopoietic stem cells (HSCs) are multipotent cells producing all the functional blood cells, including immune cells. HSCs respond to inflammation during infection and malignancy by proliferating and producing the blood cells in demand for a specific scenario. We first focus on how inflammation plays a crucial part in steady-state HSC development and describe the critical role of the inflammasome complex in regulating HSC expansion and balanced lineage production. Next, we review zebrafish studies of inflammatory innate immune mechanisms focusing on interferon signaling and the downstream JAK-STAT pathway. We also highlight insights gained from zebrafish models harbouring genetic perturbations in the role of inflammation in hematopoietic disorders such as bone marrow failure, myelodysplastic syndrome, and myeloid leukemia. Indeed, inflammation has been recently identified as a potential driver of clonal hematopoiesis and leukemogenesis, where cells acquire somatic mutations that provide a proliferative advantage in the presence of inflammation. Important insights in this area come from mutant zebrafish studies showing that hematopoietic differentiation can be compromised by epigenetic dysregulation and the aberrant induction of signaling pathways.
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页数:8
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