Palker T J, Fong A M, Scearce R M, Patel D D, Haynes B F
Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA.
Hybridoma. 1998 Dec;17(6):497-507. doi: 10.1089/hyb.1998.17.497.
The lymphocyte specific protein 1 (LSP1) phosphoprotein is an F-actin binding molecule restricted to cells of hematopoietic origin in mice and humans. LSP1 is localized to the internal surface of the plasma membrane, the cytoplasm, and NP-40-insoluble actin filaments and is thought to mediate cytoskeleton-driven responses in activated leukocytes that involve receptor capping, cell-cell interactions and cell motility. Here, we generated two monoclonal antibodies (MAbs), 5E3 and 14G8, that are specific for human LSP1 to define the expression of LSP1 throughout human T-cell development. Both MAbs reacted with a 52-kDa protein in BW5147 cells transfected with human LSP1 cDNA in pcDNA3, but not in cells transfected with cDNA in an antisense orientation, indicating the specificity of 5E3 and 14G8 for human LSP1. In developing T cells, LSP1 was expressed on human fetal liver CD7+ NK and T-cell precursors, the CD7+, CD3-, CD4-, CD8- human stem cell line DU-528, and on CD4-, CD8- double-negative (DN) thymocytes. Immunohistochemistry and three-color flow cytometry analysis of fetal or postnatal thymocytes revealed that LSP1 was increasingly expressed during intrathymic human T-cell maturation. While immature CD4+CD8+ double-positive (DP) thymocytes expressed low to undetectable levels of LSP1, mature CD4+CD8- and CD4-CD8+ single-positive (SP) thymocytes expressed high levels of LSP1. Thus, LSP1 is developmentally regulated during T-cell maturation within the human thymus and may play a functional role in the motility of DN and SP thymocytes.
淋巴细胞特异性蛋白1(LSP1)磷酸蛋白是一种F-肌动蛋白结合分子,在小鼠和人类中仅限于造血起源的细胞。LSP1定位于质膜内表面、细胞质和NP-40不溶性肌动蛋白丝,被认为在活化的白细胞中介导细胞骨架驱动的反应,这些反应涉及受体封帽、细胞间相互作用和细胞运动。在这里,我们生成了两种针对人LSP1的单克隆抗体(MAb)5E3和14G8,以确定LSP1在整个人类T细胞发育过程中的表达。两种单克隆抗体均与用pcDNA3中的人LSP1 cDNA转染的BW5147细胞中的一种52 kDa蛋白发生反应,但与用反义方向的cDNA转染的细胞不发生反应,表明5E3和14G8对人LSP1具有特异性。在发育中的T细胞中,LSP1在人类胎儿肝脏CD7+NK和T细胞前体、CD7+、CD3-、CD4-、CD8-人类干细胞系DU-528以及CD4-、CD8-双阴性(DN)胸腺细胞上表达。对胎儿或产后胸腺细胞的免疫组织化学和三色流式细胞术分析显示,LSP1在胸腺内人类T细胞成熟过程中表达逐渐增加。虽然未成熟的CD4+CD8+双阳性(DP)胸腺细胞表达低至无法检测到的LSP1水平,但成熟的CD4+CD8-和CD4-CD8+单阳性(SP)胸腺细胞表达高水平的LSP1。因此,LSP1在人类胸腺内的T细胞成熟过程中受到发育调控,可能在DN和SP胸腺细胞的运动中发挥功能作用。