Inserm UMRS-940, Université Denis Diderot Paris-7, Hôpital Saint-Louis, Paris, France.
Leuk Res. 2012 Mar;36(3):358-62. doi: 10.1016/j.leukres.2011.09.022. Epub 2011 Oct 11.
Survival of acute myeloid leukemia (AML) cells is regulated by their adherence to bone marrow stromal environment. Several adhesion molecules mediate interactions between AML cells and stroma, but their specific role in AML cell survival is still poorly understood. Here, we show that CD44 activation with the Hermes-3 monoclonal antibody enhances primary AML5 blast survival and increases apoptosis resistance of THP-1 monoblastic leukemia cells. Moreover, we show that CD44 activation upregulates the anti-apoptotic Mcl-1 protein and that Mcl-1 is essential for apoptosis resistance of THP-1 cells. These results suggest that Mcl-1 inhibitors might be required to block pro-survival activity of CD44 in AML5.
急性髓细胞白血病(AML)细胞的存活受到其与骨髓基质环境黏附的调节。几种黏附分子介导 AML 细胞与基质之间的相互作用,但它们在 AML 细胞存活中的具体作用仍知之甚少。在这里,我们表明,使用 Hermes-3 单克隆抗体激活 CD44 可增强原发性 AML5 原始细胞的存活并增加 THP-1 单核白血病细胞的抗凋亡能力。此外,我们表明 CD44 的激活上调了抗凋亡的 Mcl-1 蛋白,并且 Mcl-1 对于 THP-1 细胞的抗凋亡至关重要。这些结果表明,可能需要 Mcl-1 抑制剂来阻断 AML5 中 CD44 的促生存活性。