Jackson W H, Moscoso H, Nechtman J F, Galileo D S, Garver F A, Lanclos K D
Department of Biology and Geology, University of South Carolina, Aiken, South Carolina, 29801, USA.
Biochem Biophys Res Commun. 1998 Apr 7;245(1):81-4. doi: 10.1006/bbrc.1998.8387.
Tat is a virally expressed regulatory protein involved in the replication of HIV-1, the etiological agent of AIDS. To investigate the effect of tat inhibition on HIV replication, we constructed a retroviral vector to express an anti-tat hammerhead ribozyme as part of the 3' untranslated region of beta-galactosidase transcripts. Initial testing of this vector in tat-expressing COS-7 cells reduced tat activity by 85-95% as measured by tat-dependent CAT assays. Amphotropic and HIV-pseudotyped retroviral particles generated with this vector were used in HIV challenge experiments to determine the ability of this reagent to control HIV replication. CD4(+) peripheral blood lymphocytes (PBLs) stably transduced with this vector were subsequently challenged with HIV. These cells were able to resist HIV infection for up to 20 days as measured by cell death and reverse transcriptase activity. These data yield proof of principle that a pseudotyped retroviral vector can target and deliver a protective ribozyme to CD4(+) cells.
Tat是一种病毒表达的调节蛋白,参与艾滋病病原体HIV-1的复制。为了研究tat抑制对HIV复制的影响,我们构建了一种逆转录病毒载体,以表达一种抗tat锤头状核酶,作为β-半乳糖苷酶转录本3'非翻译区的一部分。通过tat依赖性CAT分析测定,该载体在表达tat的COS-7细胞中的初步测试使tat活性降低了85%-95%。用该载体产生的嗜异性和HIV假型逆转录病毒颗粒用于HIV攻击实验,以确定该试剂控制HIV复制的能力。随后用HIV攻击稳定转导了该载体的CD4(+)外周血淋巴细胞(PBL)。通过细胞死亡和逆转录酶活性测定,这些细胞能够抵抗HIV感染长达20天。这些数据提供了原理证明,即假型逆转录病毒载体可以靶向并向CD4(+)细胞递送保护性核酶。