Cook Brandoch D, Evans Todd
Department of Surgery, Weill Cornell Medical College, New York, NY.
Blood. 2014 Jul 17;124(3):393-402. doi: 10.1182/blood-2014-02-556993. Epub 2014 Jun 3.
Bone morphogenetic protein (BMP) signaling regulates early hematopoietic development, proceeding from mesoderm patterning through the progressive commitment and differentiation of progenitor cells. The BMP pathway signals largely through receptor-mediated activation of Mothers Against Decapentaplegic homolog (SMAD) proteins, although alternate pathways are modulated through various components of mitogen-activated protein kinase (MAPK) signaling. Using a conditional, short hairpin RNA (shRNA)-based knockdown system in the context of differentiating embryonic stem cells (ESCs), we demonstrated previously that Smad1 promotes hemangioblast specification, but then subsequently restricts primitive progenitor potential. Here we show that co-knockdown of Smad5 restores normal progenitor potential of Smad1-depleted cells, suggesting opposing functions for Smad1 and Smad5. This balance was confirmed by cotargeting Smad1/5 with a specific chemical antagonist, LDN193189 (LDN). However, we discovered that LDN treatment after hemangioblast commitment enhanced primitive myeloid potential. Moreover, inhibition with LDN (but not SMAD depletion) increased expression of Delta-like ligands Dll1 and Dll3 and NOTCH activity; abrogation of NOTCH activity restored LDN-enhanced myeloid potential back to normal, corresponding with expression levels of the myeloid master regulator, C/EBPα. LDN but not SMAD activity was also associated with activation of the p38MAPK pathway, and blocking this pathway was sufficient to enhance myelopoiesis. Therefore, NOTCH and p38MAPK pathways balance primitive myeloid progenitor output downstream of the BMP pathway.
骨形态发生蛋白(BMP)信号传导调节早期造血发育,从中胚层模式开始,经过祖细胞的逐步定向分化过程。BMP信号通路主要通过受体介导的对果蝇抗五体不全同源蛋白(SMAD)的激活来传递信号,尽管其他途径是通过丝裂原活化蛋白激酶(MAPK)信号传导的各种组分来调节的。在分化的胚胎干细胞(ESC)背景下,我们使用基于条件性短发夹RNA(shRNA)的敲低系统,先前已经证明Smad1促进成血管细胞的特化,但随后限制原始祖细胞的潜能。在这里,我们表明Smad5的共敲低恢复了Smad1缺失细胞的正常祖细胞潜能,表明Smad1和Smad5具有相反的功能。用特异性化学拮抗剂LDN193189(LDN)共靶向Smad1/5证实了这种平衡。然而,我们发现成血管细胞定向分化后用LDN处理可增强原始髓系潜能。此外,用LDN抑制(而非SMAD缺失)可增加Delta样配体Dll1和Dll3的表达以及NOTCH活性;NOTCH活性的消除将LDN增强的髓系潜能恢复到正常水平,这与髓系主调节因子C/EBPα的表达水平相对应。LDN而非SMAD活性也与p38MAPK途径的激活相关,阻断该途径足以增强髓系造血。因此,NOTCH和p38MAPK途径在BMP途径下游平衡原始髓系祖细胞的输出。