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Pneumocystis carinii inhibits cyclin-dependent kinase activity in lung epithelial cells
被引:28
|作者:
Limper, AH
Edens, N
Anders, RA
Leof, EB
机构:
[1] Mayo Clin & Mayo Fdn, Thorac Dis Res Unit, Div Pulm Crit Care & Internal Med, Dept Med, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
来源:
关键词:
Pneumocystis carinii;
epithelium;
cyclin-dependent kinase;
cell cycle;
D O I:
10.1172/JCI659
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Pneumorystis carinii remains an important cause of pneumonia in patients with AIDS, Attachment of the organism to epithelial cells is a central event in establishing infection, impairing the growth potential of lung epithelial cells and thereby slowing repair, In light of investigations documenting a central role for cyclin-dependent kinases in controlling the cell cycle, we addressed the hypothesis that P. carinii inhibits epithelial cell growth by interfering with host epithelial cyclin-dependent kinase (cdk) activity, We observed that P. carinii significantly impaired growth of cultured mink lung epithelial cells, with effects observed after 48-72 h of treatment, However, the kinase activity associated with p34(cdc2) or p33(cdk2) was maximally inhibited as early as 24 h after P. carinii exposure, The inhibitory effect on cyclin-dependent kinase activity was mediated by the trophozoite form of P. carinii, in that highly purified trophozoites exerted marked inhibition of p34(cdc2) activity, Growth impairment was similarly preceded by P. carinii-induced alteration in the state of epithelial cell p34(cdc2) phosphorylation, with no change in p34(cdc2) Or p33(cdk2) protein levels. These data strongly suggest that the antiproliferative activity of P. carinii on respiratory epithelium is mediated in part. through modulation of the host cell cycle machinery.
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页码:1148 / 1155
页数:8
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