Mouse Models of Erythropoiesis and Associated Diseases
- 27 October 2017
- book chapter
- Published by Springer Nature
- Vol. 1698, 37-65
Abstract
Animal models of erythropoiesis have been, and will continue to be, important tools for understanding molecular mechanisms underlying the development of this cell lineage and the pathophysiology associated with various human erythropoietic diseases. In this regard, the mouse is probably the most valuable animal model available to investigators. The physiology and short gestational period of mice make them ideal for studying developmental processes and modeling human diseases. These attributes, coupled with cutting-edge genetic tools such as transgenesis, gene knockouts, conditional gene knockouts, and genome editing, provide a significant resource to the research community to test a plethora of hypotheses. This review summarizes the mouse models available for studying a wide variety of erythroid-related questions, as well as the properties inherent in each one.Keywords
This publication has 116 references indexed in Scilit:
- Establishing Rps6 hemizygous mice as a model for studying how ribosomal protein haploinsufficiency impairs erythropoiesisExperimental Hematology, 2012
- Protein Phosphatase 2A Catalytic Subunit α (PP2Acα) Maintains Survival of Committed Erythroid Cells in Fetal Liver Erythropoiesis through the STAT5 PathwayThe American Journal of Pathology, 2011
- Specific erythroid-lineage defect in mice conditionally deficient for Mediator subunit Med1Proceedings of the National Academy of Sciences, 2010
- Loss of autophagy in erythroid cells leads to defective removal of mitochondria and severe anemia in vivoProceedings of the National Academy of Sciences, 2009
- ADAR1 is required for hematopoietic progenitor cell survival via RNA editingProceedings of the National Academy of Sciences, 2009
- LRF Is an Essential Downstream Target of GATA1 in Erythroid Development and Regulates BIM-Dependent ApoptosisDevelopmental Cell, 2009
- Targeted deletion of the γ-adducin gene (Add3) in mice reveals differences in α-adducin interactions in erythroid and nonerythroid cellsAmerican Journal of Hematology, 2009
- Generation of mice with a conditional allele for Trim33Genesis, 2008
- Unrestrained erythroblast development in Nix −/− mice reveals a mechanism for apoptotic modulation of erythropoiesisProceedings of the National Academy of Sciences, 2007
- Tie2-Cre Transgenic Mice: A New Model for Endothelial Cell-Lineage Analysis in VivoDevelopmental Biology, 2001