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Modeling Hematopoietic Disorders in Zebrafish

Overview
Journal Dis Model Mech
Specialty General Medicine
Date 2019 Sep 15
PMID 31519693
Citations 16
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Abstract

Zebrafish offer a powerful vertebrate model for studies of development and disease. The major advantages of this model include the possibilities of conducting reverse and forward genetic screens and of observing cellular processes by imaging of single cells. Moreover, pathways regulating blood development are highly conserved between zebrafish and mammals, and several discoveries made in fish were later translated to murine and human models. This review and accompanying poster provide an overview of zebrafish hematopoiesis and discuss the existing zebrafish models of blood disorders, such as myeloid and lymphoid malignancies, bone marrow failure syndromes and immunodeficiencies, with a focus on how these models were generated and how they can be applied for translational research.

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References
1.
Kissa K, Herbomel P . Blood stem cells emerge from aortic endothelium by a novel type of cell transition. Nature. 2010; 464(7285):112-5. DOI: 10.1038/nature08761. View

2.
Danilova N, Sakamoto K, Lin S . Ribosomal protein S19 deficiency in zebrafish leads to developmental abnormalities and defective erythropoiesis through activation of p53 protein family. Blood. 2008; 112(13):5228-37. DOI: 10.1182/blood-2008-01-132290. View

3.
Brothers K, Newman Z, Wheeler R . Live imaging of disseminated candidiasis in zebrafish reveals role of phagocyte oxidase in limiting filamentous growth. Eukaryot Cell. 2011; 10(7):932-44. PMC: 3147414. DOI: 10.1128/EC.05005-11. View

4.
Fraenkel P, Traver D, Donovan A, Zahrieh D, Zon L . Ferroportin1 is required for normal iron cycling in zebrafish. J Clin Invest. 2005; 115(6):1532-41. PMC: 1089797. DOI: 10.1172/JCI23780. View

5.
Shafizadeh E, Paw B, Foott H, Liao E, Barut B, Cope J . Characterization of zebrafish merlot/chablis as non-mammalian vertebrate models for severe congenital anemia due to protein 4.1 deficiency. Development. 2002; 129(18):4359-70. DOI: 10.1242/dev.129.18.4359. View