Department of Microbiology, University of Virginia, Charlottesville, VA 22908-1340, USA.
Int J Parasitol. 2010 Jun;40(7):833-43. doi: 10.1016/j.ijpara.2009.12.007. Epub 2010 Jan 18.
Entamoeba histolytica contains a large and novel family of transmembrane kinases (TMKs). The expression patterns of the E. histolytica TMKs in individual trophozoites and the roles of the TMKs for sensing and responding to extracellular cues were incompletely characterised. Here we provide evidence that single cells express multiple TMKs and that TMK39 and TMK54 likely serve non-redundant cellular functions. Laser-capture microdissection was used in conjunction with microarray analysis to demonstrate that single trophozoites express more than one TMK gene. Anti-peptide antibodies were raised against unique regions in the extracellular domains of TMK39, TMK54 and PaTMK, and TMK expression was analysed at the protein level. Flow cytometric assays revealed that populations of trophozoites homogeneously expressed TMK39, TMK54 and PaTMK, while confocal microscopy identified different patterns of cell surface expression for TMK39 and TMK54. The functions of TMK39 and TMK54 were probed by the inducible expression of dominant-negative mutants. While TMK39 co-localised with ingested beads and expression of truncated TMK39 interfered with trophozoite phagocytosis of apoptotic lymphocytes, expression of a truncated TMK54 inhibited growth of amoebae and altered the surface expression of the heavy subunit of the E. histolytica Gal/GalNAc lectin. Overall, our data indicates that multiple members of the novel E. histolytica TMK family are utilised for non-redundant functions by the parasite.
溶组织内阿米巴含有一个大型的新型跨膜激酶(TMK)家族。单个滋养体中溶组织内阿米巴 TMK 的表达模式以及 TMK 对细胞外信号的感应和反应的作用尚未完全阐明。在这里,我们提供的证据表明单个细胞表达多种 TMK,并且 TMK39 和 TMK54 可能具有非冗余的细胞功能。激光捕获显微切割与微阵列分析结合使用,证明单个滋养体表达多种 TMK 基因。针对 TMK39、TMK54 和 PaTMK 胞外结构域中的独特区域制备了抗肽抗体,并在蛋白质水平上分析了 TMK 表达。流式细胞术检测显示,滋养体群体均匀表达 TMK39、TMK54 和 PaTMK,而共聚焦显微镜鉴定了 TMK39 和 TMK54 的不同细胞表面表达模式。通过诱导表达显性负突变体来探究 TMK39 和 TMK54 的功能。虽然 TMK39 与摄入的珠子共定位,并且截断的 TMK39 表达干扰了滋养体对凋亡淋巴细胞的吞噬作用,但表达截断的 TMK54 抑制了阿米巴的生长并改变了溶组织内阿米巴 Gal/GalNAc 凝集素的重链的表面表达。总体而言,我们的数据表明新型溶组织内阿米巴 TMK 家族的多个成员被寄生虫用于非冗余的功能。