Franzese Ornella, Adamo Riccardo, Pollicita Michela, Comandini Alessandro, Laudisi Anastasia, Perno Carlo Federico, Aquaro Stefano, Bonmassar Enzo
Department of Neuroscience, Section of Pharmacology and Medical Oncology, University of Rome Tor Vergata, Rome, Italy.
J Med Virol. 2007 May;79(5):639-46. doi: 10.1002/jmv.20855.
Human immunodeficiency virus type 1 (HIV-1) infection is characterized by a progressive decrease of CD4(+) T cells accompanied by other immune dysfunctions. Telomerase is transiently activated in lymphocytes during activation and is able to compensate for the progressive telomeric loss that occurs at each cell division, contributing to ensure the telomere length necessary for multiple proliferative events. The effect of HIV-1 infection on telomerase activity and on the expression of some of the factors involved in its regulation in CD4(+) T cells was investigated. Telomerase was found to be downregulated in both nuclear and cytoplasmic compartments, together with an impairment of human telomerase reverse transcriptase (hTERT) expression and of the cell machinery involved in hTERT phosporylation.
1型人类免疫缺陷病毒(HIV-1)感染的特征是CD4(+) T细胞逐渐减少,并伴有其他免疫功能障碍。端粒酶在淋巴细胞激活过程中被短暂激活,能够补偿每次细胞分裂时发生的端粒渐进性丢失,有助于确保多次增殖事件所需的端粒长度。研究了HIV-1感染对CD4(+) T细胞中端粒酶活性及其调控相关一些因子表达的影响。结果发现,端粒酶在细胞核和细胞质区室中均下调,同时人类端粒酶逆转录酶(hTERT)的表达以及参与hTERT磷酸化的细胞机制也受到损害。