Mercher Thomas, Cornejo Melanie G, Sears Christopher, Kindler Thomas, Moore Sandra A, Maillard Ivan, Pear Warren S, Aster Jon C, Gilliland D Gary
Department of Medicine, Division of Hematology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 20115, USA.
Cell Stem Cell. 2008 Sep 11;3(3):314-26. doi: 10.1016/j.stem.2008.07.010.
In the hematopoietic system, Notch signaling specifies T cell lineage fate, in part through negative regulation of B cell and myeloid lineage development. However, we unexpectedly observed the development of megakaryocytes when using heterotypic cocultures of hematopoietic stem cells with OP9 cells expressing Delta-like1, but not with parental OP9 cells. This effect was abrogated by inhibition of Notch signaling either with gamma-secretase inhibitors or by expression of the dominant-negative Mastermind-like1. The importance of Notch signaling for megakaryopoietic development in vivo was confirmed by using mutant alleles that either activate or inhibit Notch signaling. These findings indicate that Notch is a positive regulator of megakaryopoiesis and plays a more complex role in cell-fate decisions among myeloid progenitors than previously appreciated.
在造血系统中,Notch信号通路部分通过对B细胞和髓系谱系发育的负调控来决定T细胞谱系命运。然而,我们意外地观察到,当造血干细胞与表达Delta-like1的OP9细胞进行异型共培养时,会出现巨核细胞的发育,而与亲本OP9细胞共培养则不会。用γ-分泌酶抑制剂或通过表达显性负性的Mastermind样蛋白1抑制Notch信号通路,可消除这种效应。通过使用激活或抑制Notch信号通路的突变等位基因,证实了Notch信号通路在体内巨核细胞生成发育中的重要性。这些发现表明,Notch是巨核细胞生成的正调节因子,并且在髓系祖细胞的细胞命运决定中发挥着比之前认识到的更为复杂的作用。