Protection by protein a of apoptotic cell death caused by anti-AIDS drug zidovudine

被引:13
作者
Ghosh, AK
Jana, S
Das, T
Sa, G
Mandal, N
Ray, PK
机构
[1] Bose Inst, Immunotechnol Sect, Calcutta 700054, W Bengal, India
[2] Bose Inst, Anim Physiol Sect, Calcutta, W Bengal, India
关键词
D O I
10.1006/bbrc.1999.1568
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Zidovudine, the anti-AIDS drug, caused inhibition of mitogen-induced proliferation and perturbation of cell-cycle progression of cultured bone marrow cells of mice. There was significant hypoploidy observed in flow cytometric analysis of AZT-treated bone marrow cells. In ape-direct analysis, cells showed apoptosis in G0/G1 phase. In DNA gel analysis, characteristic laddering of apoptosis was observed in AZT-treated bone marrow cells. We demonstrated that, when the animals were pretreated with protein A (PA) of Staphylococcus aureus, the apoptotic changes could be prevented in bone marrow cells of AZT-treated animals. There is a significant (p < 0.05) increase in proliferation of bone marrow cells subjected to mitogen treatment in PA+AZT-treated animals, compared to only AZT-treated animals. However, cell-cycle phase distribution was not hampered and no laddering in DNA gel analysis was also observed in this group. In ape-direct analysis, PA treatment showed significant (p < 0.001) inhibition of AZT-induced apoptosis. These observations indicate that by using a suitable agent such as protein A the toxic side effects of AZT could be minimized. (C) 1999 Academic Press.
引用
收藏
页码:601 / 604
页数:4
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