The role of lipids in Plasmodium falciparum invasion of erythrocytes: a coordinated biochemical and microscopic analysis
- PMID: 3045809
- PMCID: PMC281884
- DOI: 10.1073/pnas.85.16.5956
The role of lipids in Plasmodium falciparum invasion of erythrocytes: a coordinated biochemical and microscopic analysis
Erratum in
- Proc Natl Acad Sci U S A 1989 May;86(9):3214
Abstract
The role of lipids in Plasmodium falciparum invasion of erythrocytes was investigated by biochemical and fluorescent microscopic analysis. Metabolic incorporation of radioactive oleate or palmitate and fractionation of radiolabeled phospholipids by thin-layer chromatography revealed no difference in the major phospholipid classes of schizonts and early ring forms after merozoite invasion. Fluorescent anthroyloxy derivatives of oleate and palmitate were also metabolically incorporated into parasite phospholipids. By microscopic analysis, the fluorescent phospholipids were seen localized in the plasma membrane and, within the merozoite, concentrated near the apical end. During invasion fluorescent phospholipid appeared to be injected from the apical end of the merozoite into the host membrane, both within and outside the parasite-host membrane junctions. After invasion fluorescent lipid was only found in the parasite plasma membrane and/or parasitophorous vacuole membrane. Parallel experiments with a fluorescent cholesterol derivative, incorporated into parasite membranes by exchange, revealed neither heterogeneous distribution of label within the parasite nor evidence for cholesterol transfer from merozoite to host cell membrane. Results suggest that during invasion no major covalent alteration of parasite lipids, such as lysophospholipid formation, occurs. However, invasion and formation of the parasitophorous vacuolar membrane apparently involves insertion of parasite phospholipids into the host membrane.
Similar articles
-
Origins of the parasitophorous vacuole membrane of the malaria parasite, Plasmodium falciparum, in human red blood cells.J Cell Sci. 1992 Jul;102 ( Pt 3):527-32. doi: 10.1242/jcs.102.3.527. J Cell Sci. 1992. PMID: 1506432
-
A 60-kDa Plasmodium falciparum protein at the moving junction formed between merozoite and erythrocyte during invasion.Mol Biochem Parasitol. 1989 Sep;36(2):177-85. doi: 10.1016/0166-6851(89)90190-4. Mol Biochem Parasitol. 1989. PMID: 2671726
-
The origin of parasitophorous vacuole membrane lipids in malaria-infected erythrocytes.J Cell Sci. 1993 Sep;106 ( Pt 1):237-48. doi: 10.1242/jcs.106.1.237. J Cell Sci. 1993. PMID: 8270628
-
Cytoskeletal and membrane remodelling during malaria parasite invasion of the human erythrocyte.Br J Haematol. 2011 Sep;154(6):680-9. doi: 10.1111/j.1365-2141.2011.08766.x. Epub 2011 Jul 1. Br J Haematol. 2011. PMID: 21718279 Review.
-
Lipid transport in Plasmodium.Infect Agents Dis. 1992 Oct;1(5):254-62. Infect Agents Dis. 1992. PMID: 1344664 Review.
Cited by
-
Imidazolopiperazine (IPZ)-Induced Differential Transcriptomic Responses on Plasmodium falciparum Wild-Type and IPZ-Resistant Mutant Parasites.Genes (Basel). 2023 Nov 24;14(12):2124. doi: 10.3390/genes14122124. Genes (Basel). 2023. PMID: 38136946 Free PMC article.
-
Endothelial cell-associated platelet-activating factor: a novel mechanism for signaling intercellular adhesion.J Cell Biol. 1990 Feb;110(2):529-40. doi: 10.1083/jcb.110.2.529. J Cell Biol. 1990. PMID: 2153685 Free PMC article.
-
Repurposing Insecticides for Mosquito Control: Evaluating Spiromesifen, a Lipid Synthesis Inhibitor against Aedes aegypti (L.).Trop Med Infect Dis. 2024 Aug 18;9(8):184. doi: 10.3390/tropicalmed9080184. Trop Med Infect Dis. 2024. PMID: 39195622 Free PMC article.
-
Protein sorting in Plasmodium falciparum-infected red blood cells permeabilized with the pore-forming protein streptolysin O.Biochem J. 1996 Apr 1;315 ( Pt 1)(Pt 1):307-14. doi: 10.1042/bj3150307. Biochem J. 1996. PMID: 8670123 Free PMC article.
-
Integrative omics analysis. A study based on Plasmodium falciparum mRNA and protein data.BMC Syst Biol. 2014;8 Suppl 2(Suppl 2):S4. doi: 10.1186/1752-0509-8-S2-S4. Epub 2014 Mar 13. BMC Syst Biol. 2014. PMID: 25033389 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources