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Significance During malaria infections, Plasmodium falciparum parasites invade RBCs. Identification of host factors for parasite invasion guides the development of vaccines and host-targeted therapeutics. Here we describe the development of an in vitro culture system for the functional analysis of RBC determinants using the immortal erythroleukemia cell line JK-1. JK-1 cells can be induced to differentiate synchronously, support parasite invasion, and are amenable to genetic manipulation. Using this system, we validated two host factors, basigin and CD44, as strain-transcendent host factors for parasite invasion, and we demonstrated a functional interaction between these two proteins. The ability to perform gene editing to produce RBC mutants will augment our ability to study malaria infection.
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Kanjee et al. (2017) studied this question.
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