Gurbuxani Sandeep, Xu Yanfei, Keerthivasan Ganesan, Wickrema Amittha, Crispino John D
The Ben May Institute for Cancer Research and Department of Pathology, University of Chicago, Chicago, IL 60637, USA.
Proc Natl Acad Sci U S A. 2005 Aug 9;102(32):11480-5. doi: 10.1073/pnas.0500303102. Epub 2005 Jul 29.
Although erythroid cells and megakaryocytes arise from a common progenitor, their terminal maturation follows very different paths; erythroid cells undergo cell-cycle exit and enucleation, whereas megakaryocytes continue to progress through the cell cycle but skip late stages of mitosis to become polyploid cells. In our efforts to identify genes that participate in this process, we discovered that survivin, a member of the inhibitor of apoptosis family that also has an essential role in cytokinesis, is differentially expressed during erythroid versus megakaryocyte development. Erythroid cells express survivin throughout their maturation, whereas megakaryocytes express approximately 4-fold lower levels of survivin mRNA and no detectable protein. To investigate the role of survivin in these lineages, we overexpressed or knocked down survivin from mouse bone marrow cells and then examined erythroid and megakaryocyte development. These studies revealed that overexpression of survivin antagonized megakaryocyte growth, maturation, and polyploidization but had no effect on erythroid development. This block in polyploidization was accompanied by increased expression of p21 and decreased expression of megakaryocyte genes such as von Willebrand factor and beta(1)-tubulin. In contrast, a reduction in survivin expression interfered with the formation of erythroid cells but not megakaryocytes. Last, consistent with the requirement for survivin in the survival of proliferating cells, survivin-deficient hematopoietic progenitors failed to give rise to either erythroid or megakaryocytic colonies. Together, these studies show that whereas survivin expression is essential for megakaryocyte and erythroid progenitors, its down-regulation is required for terminal differentiation of megakaryocytes.
尽管红系细胞和巨核细胞起源于共同的祖细胞,但它们的终末成熟遵循非常不同的路径;红系细胞经历细胞周期退出和去核过程,而巨核细胞则继续通过细胞周期,但跳过有丝分裂后期成为多倍体细胞。在我们致力于鉴定参与这一过程的基因时,我们发现survivin,一种凋亡抑制家族成员,在细胞分裂中也起着重要作用,在红系与巨核细胞发育过程中差异表达。红系细胞在整个成熟过程中都表达survivin,而巨核细胞中survivin mRNA的表达水平大约低4倍,且未检测到蛋白质。为了研究survivin在这些谱系中的作用,我们在小鼠骨髓细胞中过表达或敲低survivin,然后检测红系和巨核细胞的发育。这些研究表明,survivin的过表达拮抗巨核细胞的生长、成熟和多倍体化,但对红系发育没有影响。这种多倍体化的阻滞伴随着p21表达的增加以及巨核细胞基因如血管性血友病因子和β1微管蛋白表达的减少。相反,survivin表达的降低会干扰红系细胞的形成,但不影响巨核细胞。最后,与survivin对增殖细胞存活的需求一致,survivin缺陷的造血祖细胞无法产生红系或巨核细胞集落。总之,这些研究表明,虽然survivin的表达对巨核细胞和红系祖细胞至关重要,但其下调是巨核细胞终末分化所必需的。