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Obligate Role of Anti-Apoptotic MCL-1 in the Survival of Hematopoietic Stem Cells

机译:抗凋亡MCL-1在造血干细胞存活中的重要作用。

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Apoptosis is important in controlling hematopoietic stem cell (HSC) numbers. However, the specific BCL-2 family member(s) that regulate HSC homeostasis are not precisely defined. We tested myeloid leukemia-1 (MCL-1) as an attractive candidate that is highly expressed in HSCs and regulated by growth factor signals. Inducible deletion of Mcl-1 in mice resulted in ablation of bone marrow. This resulted in the loss of early bone marrow progenitor populations, including HSCs. Moreover, growth factors including stem cell factor increased transcription of the Mcl-1 gene and required MCL-1 to augment survival of purified bone marrow progenitors. Deletion of Mcl-1 in other tissues, including liver, did not impair survival. Thus, MCL-1 is a critical and specific regulator essential for ensuring the homeostasis of early hematopoietic progenitors.
机译:凋亡在控制造血干细胞(HSC)数量中很重要。但是,尚不清楚调节HSC稳态的特定BCL-2家族成员。我们测试了髓样白血病1(MCL-1)作为在HSC中高表达并受生长因子信号调节的诱人候选物。小鼠中Mcl-1的诱导型缺失导致骨髓消融。这导致了包括HSCs在内的早期骨髓祖细胞的流失。此外,包括干细胞因子在内的生长因子增加了Mcl-1基因的转录,并需要MCL-1来提高纯化的骨髓祖细胞的存活率。在包括肝脏在内的其他组织中删除Mcl-1不会损害存活率。因此,MCL-1是确保早期造血祖细胞体内稳态必不可少的关键和特定调节剂。

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