Monocyte/Macrophage - like cell differentiation induced by TPA in HL60 cells leads to loss of Histone H4 Lysine 16 Acetylation

R. K. Vempati
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Abstract

12-O-Tetradecanoylphorbol-13-acetate (TPA) is a phorbol ester and induces monocyte/macrophage like cell differentiation in HL60 cells. The levels and patterns of gene expression differ greatly between differentiated and undifferentiated HL60 cells. Epigenetic histone modifications play a crucial role in transcriptional activation and alterations in the modification levels greatly affect the gene expression pattern. Acetylation of Histone H4 Lysine 16 (H4K16ac) is one such modification and has a significant role in transcriptional activation. Changes in its acetylation level either due to a physiological or pathological effect will have a dramatic effect on cellular gene expression. Here, a study was done to see the effect of TPA induced differentiation on H4K16ac levels in HL60 cells. Results obtained from flow cytometric analysis showed expression of macrophage cell surface marker CD11b on TPA differentiated HL60 cells and the western blots revealed a drastic downregulation of H4K16ac in differentiated cells. Immunoblotting and co-immunoprecipitation assay revealed DNA damage dependent enhancement of H4K16 acetylation and its co-localization with γH2AX in undifferentiated cells. Whereas, TPA differentiated cells (CD11B+ve) didn’t show any such enhancement in H4K16acetylation levels in the presence of DNA damage. The present study shows that TPA induced differentiation of HL60 cells into macrophages leads to the downregulation of H4K16 acetylation.
TPA诱导HL60细胞单核/巨噬细胞样细胞分化导致组蛋白H4赖氨酸16乙酰化缺失
12- o - tetradecanoylpholl -13-acetate (TPA)是一种pholbol酯,可诱导HL60细胞的单核/巨噬细胞样细胞分化。分化和未分化的HL60细胞的基因表达水平和模式差异很大。表观遗传组蛋白修饰在转录激活中起着至关重要的作用,修饰水平的改变极大地影响了基因的表达模式。Histone H4 Lysine 16 (H4K16ac)的乙酰化就是这样一种修饰,在转录激活中起着重要作用。由于生理或病理作用,其乙酰化水平的变化将对细胞基因表达产生巨大影响。本研究旨在观察TPA诱导分化对HL60细胞H4K16ac水平的影响。流式细胞术分析结果显示巨噬细胞表面标记物CD11b在TPA分化的HL60细胞中表达,western blot结果显示分化细胞中H4K16ac的表达急剧下调。免疫印迹和共免疫沉淀实验显示,DNA损伤依赖性增强了未分化细胞中H4K16乙酰化及其与γ - h2ax的共定位。然而,TPA分化的细胞(CD11B+ve)在DNA损伤的情况下,h4k16乙酰化水平没有任何增强。本研究表明,TPA诱导HL60细胞向巨噬细胞分化,导致H4K16乙酰化下调。
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