Defective hematopoiesis and hepatic steatosis in mice with combined deficiencies of the genes encoding Fancc and Cu/Zn superoxide dismutase
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Mouse genetics of hematopoiesis in Fanconi anemia models.
The study examines gene deficiencies and disease phenotypes in mice.
Mouse genetics of Fanconi anemia and superoxide dismutase; biomedical disease model.
Résumé
Several lines of evidence point to an abnormality in the response of Fanconi anemia cells to reactive oxygen species. To investigate the potential pathologic consequences of an in vivo alteration of redox state in mice lacking one of the Fanconi anemia genes, animals were generated having combined deficiencies of the cytosolic Cu/Zn superoxide dismutase (Sod1) and Fanconi anemia complementation group C (Fancc) genes. Interestingly, hepatocytes of Fancc(-/-)Sod1(-/-) mice exhibited a zonal pattern of microvesicular steatosis, possibly as a result of oxidative stress-induced injury to hepatocyte membranes. Consistent with this idea, freshly explanted Fancc(-/-)Sod1(-/-) hepatocytes demonstrated increased spontaneous production of superoxide in vitro. The second phenotypic feature of Fancc(-/-) Sod1(-/-) mice was that of bone marrow hypocellularity accompanied by significant decreases in peripheral blood erythrocyte and leukocyte numbers as compared with wild-type controls. Although flow cytometry analysis with monoclonal antibodies against cell surface antigens revealed normal numbers of primitive hematopoietic progenitor populations in Fancc(-/-)Sod1(-/-) marrow, lineage-positive progenitor numbers were significantly reduced in these mice. Furthermore, the in vitro clonogenic growth of Fancc(-/-)Sod1(-/-) erythroid, myeloid, and early B-lymphoid colonies in semisolid media was profoundly compromised. These results suggested that the altered redox state likely present in Fancc(-/-) Sod1(-/-) hematopoietic progenitors was responsible for an impairment of cell proliferation or survival. (Blood. 2001;98:1003-1011)
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La notice
- Revue
- Blood
- Thématique
- Hemoglobinopathies and Related Disorders
- Domaine
- Medicine
- Établissements canadiens
- BC Children's HospitalHospital for Sick Children
- Organismes subventionnaires
- National Cancer InstituteCancer Research Society
- Mots-clés
- SOD1BiologySuperoxide dismutaseFanconi anemiaHaematopoiesisProgenitor cellBone marrowSOD2Molecular biologyMyeloidImmunologyCancer researchOxidative stressStem cellCell biologyEndocrinologyDNA repairGeneticsGene
- Résumé présent dans OpenAlex
- oui