Savickiene J, Gineitis A, Stigbrand T
Laboratory of Developmental Biology, Institute of Biochemistry, 2600 Vilnius, Lithuania.
Cell Death Differ. 1999 Jul;6(7):698-709. doi: 10.1038/sj.cdd.4400541.
The relationship between RA- or dbcaMP-mediated differentiation and subsequent apoptosis in HL-60 cells was assessed by modulating the levels of differentiation suppressing the activity of PKC and PKA with calphostin C or GF 109203X and H89, respectively. Results demonstrated that (1) RA and dbcAMP caused a dose-dependent increase in apoptosis concomitant with progressive differentiation; (2) the suppression of PKC activity resulted in an increase of apoptosis unrelated to the modulated levels of differentiation; (3) the inhibition of PKA decreased granulocytic differentiation, but did not significantly affect apoptosis; (4) the pretreatment of cells with dbcAMP strongly potentiated RA-mediated differentiation without apparent changes in apoptosis; (5) cell differentiation and apoptosis were associated with cell cycle arrest in G1 phase and G2/M phases, respectively. Our findings indicate that the functional maturity of differentiating cells is not directly related to the apoptotic programme, and suggest that induction of cell differentiation and apoptosis are regulated by separate mechanisms in which PKC and PKA are involved.
通过分别用钙泊三醇C或GF 109203X和H89调节抑制蛋白激酶C(PKC)和蛋白激酶A(PKA)活性的分化水平,评估了维甲酸(RA)或二丁酰环磷腺苷(dbcAMP)介导的HL-60细胞分化与随后凋亡之间的关系。结果表明:(1)RA和dbcAMP导致凋亡呈剂量依赖性增加,同时伴有渐进性分化;(2)PKC活性的抑制导致凋亡增加,这与分化水平的调节无关;(3)PKA的抑制降低了粒细胞分化,但对凋亡没有显著影响;(4)用dbcAMP预处理细胞可强烈增强RA介导的分化,而凋亡无明显变化;(5)细胞分化和凋亡分别与G1期和G2/M期的细胞周期停滞有关。我们的研究结果表明,分化细胞的功能成熟与凋亡程序没有直接关系,并提示细胞分化和凋亡的诱导是由涉及PKC和PKA的不同机制调节的。