Miyagi T, Murakami K, Sawada T, Taguchi H, Miyoshi I
Department of Medicine, Kochi Medical School, Japan.
Leukemia. 1998 Oct;12(10):1645-50. doi: 10.1038/sj.leu.2401154.
The abnormal lymphocytes in adult T cell leukemia (ATL) reveal a peculiar morphology that is characterized by indented or lobulated nuclei. While human T lymphotropic virus type I (HTLV-I) is thought to be integrated in ATL cells, the correlation between the nuclear irregularities and HTLV-I infection is obscure. We have devised a novel single cell polymerase chain reaction (PCR) technique to examine the integration of HTLV-I provirus genome in cells from two patients with ATL. To isolate single cells, peripheral blood smears were prepared on thin polyester slides and stained with May-Grünwald-Giemsa. Morphologically defined single cells were cut out after light microscopy. The HTLV-I DNA sequences were detected not only in ATL cells but also in normal-looking lymphocytes. This novel PCR method may provide a valuable tool for understanding the molecular events associated with HTLV-I infection at the single cell level.
成人T细胞白血病(ATL)中的异常淋巴细胞呈现出一种特殊的形态,其特征为核呈凹陷或分叶状。虽然人们认为I型人类嗜T淋巴细胞病毒(HTLV-I)整合于ATL细胞中,但核不规则与HTLV-I感染之间的相关性尚不清楚。我们设计了一种新型单细胞聚合酶链反应(PCR)技术,以检测两名ATL患者细胞中HTLV-I前病毒基因组的整合情况。为了分离单细胞,在薄聚酯载玻片上制备外周血涂片,并用May-Grünwald-Giemsa染色。在光学显微镜下观察后,切下形态学上确定的单细胞。不仅在ATL细胞中检测到了HTLV-I DNA序列,在看似正常的淋巴细胞中也检测到了该序列。这种新型PCR方法可能为在单细胞水平上理解与HTLV-I感染相关的分子事件提供一个有价值的工具。