Shutt D C, Stapleton J T, Kennedy R C, Soll D R
Department of Biological Sciences, University of Iowa, Iowa City 52242, USA.
Cell Immunol. 1995 Dec;166(2):261-74. doi: 10.1006/cimm.1995.9971.
It was previously demonstrated that HIV-induced syncytia of the immortalized T cell line SupT1 reorganize their cytoskeleton and form a spherical supernuclear complex, thus mimicking the organization, polarity, and morphology of a single SupT1 cell. Then, through extension of a single, giant pseudopod, these syncytia, which grow to more than 100 times the volume of a single SupT1 cell, translocate along a substratum. To verify that syncytium motility is not peculiar to the SupT1 cell line, we have analyzed the cytoskeletal organization and motile capabilities of HIV-induced syncytia formed in peripheral blood cell cultures containing more than 90% CD4-positive cells. The results demonstrate that although peripheral blood T cells differ from SupT1 cells in size and morphology, they are continuously motile and translocate along a substratum in a manner quite similar to that of SupT1 cells, and peripheral blood T cell syncytia induced by HIV-1LAI as well as two additional clinical isolates translocate by the extension of a giant anterior pseudopod in a fashion indistinguishable from that of HIV-induced SupT1 syncytia. Together, these results support the generalization that HIV-induced T cell syncytia are motile.
先前已证明,永生化T细胞系SupT1的HIV诱导的多核巨细胞会重组其细胞骨架并形成球形核上复合体,从而模拟单个SupT1细胞的组织、极性和形态。然后,通过伸出单个巨大的伪足,这些体积增长到单个SupT1细胞体积100倍以上的多核巨细胞会沿着基质移位。为了验证多核巨细胞的运动性并非SupT1细胞系所特有,我们分析了在含有超过90% CD4阳性细胞的外周血细胞培养物中形成的HIV诱导的多核巨细胞的细胞骨架组织和运动能力。结果表明,尽管外周血T细胞在大小和形态上与SupT1细胞不同,但它们持续运动,并以与SupT1细胞非常相似的方式沿着基质移位,并且HIV-1LAI以及另外两种临床分离株诱导的外周血T细胞多核巨细胞通过伸出巨大的前伪足以与HIV诱导的SupT1多核巨细胞无法区分的方式移位。总之,这些结果支持HIV诱导的T细胞多核巨细胞具有运动性这一普遍观点。