Novel spontaneous myelodysplastic syndrome mouse model
Autor: | Grant Morahan, Lingyan Zhang, Weisha Li, Mengyuan Li, Zhiqi Song, Chuan Qin, Lin Cao, Ran Gao, Xingjiu Yang, Xinpei Wang, Wenlong Zhang |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Genetically modified mouse
Medicine (General) Population The Collaborative Cross Mice Biology Pathogenesis Mice R5-920 Bone Marrow hemic and lymphatic diseases medicine Animals education education.field_of_study Strain (biology) Anemia myelodysplastic syndrome (MDS) Original Articles Leukopenia General Medicine medicine.disease Phenotype Disease Models Animal Haematopoiesis Leukemia medicine.anatomical_structure Myelodysplastic Syndromes Cancer research Original Article spontaneous mouse model Bone marrow |
Zdroj: | Animal Models and Experimental Medicine, Vol 4, Iss 2, Pp 169-180 (2021) Animal Models and Experimental Medicine |
ISSN: | 2576-2095 |
Popis: | Background Myelodysplastic syndrome (MDS) is a group of disorders involving hemopoietic dysfunction leading to leukemia. Although recently progress has been made in identifying underlying genetic mutations, many questions still remain. Animal models of MDS have been produced by introduction of specific mutations. However, there is no spontaneous mouse model of MDS, and an animal model to simulate natural MDS pathogenesis is urgently needed. Methods In characterizing the genetically diverse mouse strains of the Collaborative Cross (CC) we observed that one, designated JUN, had abnormal hematological traits. This strain was thus further analyzed for phenotypic and pathological identification, comparing the changes in each cell population in peripheral blood and in bone marrow. Results In a specific‐pathogen free environment, mice of the JUN strain are relatively thin, with healthy appearance. However, in a conventional environment, they become lethargic, develop wrinkled yellow hair, have loose and light stools, and are prone to infections. We found that the mice were cytopenic, which was due to abnormal differentiation of multipotent bone marrow progenitor cells. These are common characteristics of MDS. Conclusions A mouse strain, JUN, was found displaying spontaneous myelodysplastic syndrome. This strain has the advantage over existing models in that it develops MDS spontaneously and is more similar to human MDS than genetically modified mouse models. JUN mice will be an important tool for pathogenesis research of MDS and for evaluation of new drugs and treatments. |
Databáze: | OpenAIRE |
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