Feng R, Kabayama A, Uchida K, Hoshino H, Miwa M
Department of Biochemistry and Molecular Oncology, Institute of Basic Medical Sciences and Center for Tsukuba Advanced Research Alliance, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan.
Jpn J Cancer Res. 2001 Apr;92(4):410-6. doi: 10.1111/j.1349-7006.2001.tb01110.x.
Human T-cell leukemia virus type 1 (HTLV-1) is the etiologic agent for adult T-cell leukemia and HTLV-1-associated myelopathy / tropical spastic paraparesis. Recently we infected newborn mice by inoculating HTLV-1-producing human cells, and found that T-cells, B-cells and granulocytes were infected in vivo. To understand the mechanism of viral-cell interaction and the pathogenesis of HTLV-1 using the mouse model, it is important to clarify the cellular tropism using a cell-free HTLV-1 transmission system. We employed a highly transmissible cell-free HTLV-1 produced by a feline kidney cell line, c77, and studied the susceptibility of 9 kinds of mouse cell lines, EL4, RLm1, CTLL-2, J774.1, DA-1, Ba / F3, WEHI-3, NIH3T3 and B1, and two kinds of human cell lines, Molt-4 and Hut78. HTLV-1 proviral sequence was found by PCR in all 9 mouse cell lines as well as in 2 human cell lines and viral entry was blocked with sera from an HTLV-1 carrier and an adult T-cell leukemia patient. Unexpectedly, mouse cell lines EL4 and RLm1 and human cell lines Molt-4 and Hut78 showed similar efficiency for viral entry. These results suggest a wide distribution of HTLV-1 receptor in mouse cells.
人类嗜T淋巴细胞病毒1型(HTLV-1)是成人T细胞白血病和HTLV-1相关脊髓病/热带痉挛性截瘫的病原体。最近,我们通过接种产生HTLV-1的人类细胞感染了新生小鼠,发现T细胞、B细胞和粒细胞在体内均被感染。为了利用小鼠模型了解病毒与细胞相互作用的机制以及HTLV-1的发病机制,使用无细胞HTLV-1传播系统阐明细胞嗜性很重要。我们采用了由猫肾细胞系c77产生的高传染性无细胞HTLV-1,并研究了9种小鼠细胞系EL4、RLm1、CTLL-2、J774.1、DA-1、Ba/F3、WEHI-3、NIH3T3和B1以及两种人类细胞系Molt-4和Hut78的易感性。通过PCR在所有9种小鼠细胞系以及2种人类细胞系中均发现了HTLV-1前病毒序列,并且来自HTLV-1携带者和成人T细胞白血病患者的血清可阻断病毒进入。出乎意料的是,小鼠细胞系EL4和RLm1以及人类细胞系Molt-4和Hut78在病毒进入方面表现出相似的效率。这些结果表明HTLV-1受体在小鼠细胞中广泛分布。