کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2077762 | 1079742 | 2012 | 12 صفحه PDF | دانلود رایگان |
SummaryIntact cholesterol homeostasis helps to maintain hematopoietic stem and multipotential progenitor cell (HSPC) quiescence. Mice with defects in cholesterol efflux pathways due to deficiencies of the ATP binding cassette transporters ABCA1 and ABCG1 displayed a dramatic increase in HSPC mobilization and extramedullary hematopoiesis. Increased extramedullary hematopoiesis was associated with elevated serum levels of G-CSF due to generation of IL-23 by splenic macrophages and dendritic cells. This favored hematopoietic lineage decisions toward granulocytes rather than macrophages in the bone marrow leading to impaired support for osteoblasts and decreased Cxcl12/SDF-1 production by mesenchymal progenitors. Greater HSPC mobilization and extramedullary hematopoiesis were reversed by raising HDL levels in Abca1−/−Abcg1−/− and Apoe−/− mice or in a mouse model of myeloproliferative neoplasm mediated by Flt3-ITD mutation. Our data identify a role of cholesterol efflux pathways in the control of HSPC mobilization. This may translate into therapeutic strategies for atherosclerosis and hematologic malignancies.
Graphical AbstractFigure optionsDownload high-quality image (404 K)Download as PowerPoint slideHighlights
► Cholesterol efflux in splenic DCs and macrophages regulate HSPC mobilization
► Cholesterol efflux causes reduced G-CSF production and alters the osteoblastic niche
► Cholesterol efflux prevents HSPC mobilization and extramedullary hematopoiesis
Journal: - Volume 11, Issue 2, 3 August 2012, Pages 195–206