祖细胞
干细胞
造血
内皮干细胞
细胞生物学
骨髓
髓系白血病
癌症研究
生物
川地34
白血病
祖细胞
髓样
免疫学
体外
生物化学
作者
Patricia Torres-Barrera,Dafné Moreno-Lorenzana,José Antonio Alvarado-Moreno,Elena Garcı́a-Ruiz,Cesar Lagunas,Héctor Mayani,Antonieta Chávez‐González
标识
DOI:10.3390/ijms231810326
摘要
Chronic Myeloid Leukemia (CML) originates in a leukemic stem cell that resides in the bone marrow microenvironment, where they coexist with cellular and non-cellular elements. The vascular microenvironment has been identified as an important element in CML development since an increase in the vascularization has been suggested to be related with poor prognosis; also, using murine models, it has been reported that bone marrow endothelium can regulate the quiescence and proliferation of leukemic stem and progenitor cells. This observation, however, has not been evaluated in primary human cells. In this report, we used a co-culture of primitive (progenitor and stem) CML cells with endothelial colony forming cells (ECFC) as an in vitro model to evaluate the effects of the vascular microenvironment in the leukemic hematopoiesis. Our results show that this interaction allows the in vitro maintenance of primitive CML cells through an inflammatory microenvironment able to regulate the proliferation of progenitor cells and the permanence in a quiescent state of leukemic stem cells.
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