Korean J Parasitol.  2014 Aug;52(4):355-365. 10.3347/kjp.2014.52.4.355.

Amoebic PI3K and PKC Is Required for Jurkat T Cell Death Induced by Entamoeba histolytica

• Lee YA
• Kim KA
• Min A
• Shin MH

• KMID: 1792196
• DOI: http://doi.org/10.3347/kjp.2014.52.4.355

Abstract

The enteric protozoan parasite Entamoeba histolytica is the causative agent of human amebiasis. During infection, adherence of E. histolytica through Gal/GalNAc lectin on the surface of the amoeba can induce caspase-3-dependent or -independent host cell death. Phosphorylinositol 3-kinase (PI3K) and protein kinase C (PKC) in E. histolytica play an important function in the adhesion, killing, or phagocytosis of target cells. In this study, we examined the role of amoebic PI3K and PKC in amoeba-induced apoptotic cell death in Jurkat T cells. When Jurkat T cells were incubated with E. histolytica trophozoites, phosphatidylserine (PS) externalization and DNA fragmentation in Jurkat cells were markedly increased compared to those of cells incubated with medium alone. However, when amoebae were pretreated with a PI3K inhibitor, wortmannin before being incubated with E. histolytica, E. histolytica-induced PS externalization and DNA fragmentation in Jurkat cells were significantly reduced compared to results for amoebae pretreated with DMSO. In addition, pretreatment of amoebae with a PKC inhibitor, staurosporine strongly inhibited Jurkat T cell death. However, E. histolytica-induced cleavage of caspase-3, -6, and -7 were not inhibited by pretreatment of amoebae with wortmannin or staurosporin. In addition, we found that amoebic PI3K and PKC have an important role on amoeba adhesion to host compartment. These results suggest that amebic PI3K and PKC activation may play an important role in caspase-independent cell death in Entamoeba-induced apoptosis.

Keyword

Entamoeba histolytica; phosphorylinositol 3-kinase (PI3K); protein kinase C (PKC); host cell death; adhesion; caspase

MeSH Terms

*Apoptosis
Caspases/metabolism
Entamoeba histolytica/*enzymology/*growth & development
Humans
Hydrolysis
Jurkat Cells
Phosphatidylinositol 3-Kinases/*metabolism
Protein Kinase C/*metabolism
T-Lymphocytes/*parasitology/*physiology
Caspases
Phosphatidylinositol 3-Kinases
Protein Kinase C