Molecular Dissection of Phagocytosis by Proteomic Analysis in Entamoeba histolytica

Genes (Basel). 2023 Jan 31;14(2):379. doi: 10.3390/genes14020379.

Abstract

Entamoeba histolytica is the enteric protozoan parasite responsible for amebiasis. Trophozoites of E. histolytica ingest human cells in the intestine and other organs, which is the hallmark of its pathogenesis. Phagocytosis and trogocytosis are pivotal biological functions for its virulence and also contribute to the proliferation of nutrient uptake from the environment. We previously elucidated the role of a variety of proteins associated with phagocytosis and trogocytosis, including Rab small GTPases, Rab effectors, including retromer, phosphoinositide-binding proteins, lysosomal hydrolase receptors, protein kinases, and cytoskeletal proteins. However, a number of proteins involved in phagocytosis and trogocytosis remain to be identified, and mechanistic details of their involvement must be elucidated at the molecular level. To date, a number of studies in which a repertoire of proteins associated with phagosomes and potentially involved in phagocytosis have been conducted. In this review, we revisited all phagosome proteome studies we previously conducted in order to reiterate information on the proteome of phagosomes. We demonstrated the core set of constitutive phagosomal proteins and also the set of phagosomal proteins recruited only transiently or in condition-dependent fashions. The catalogs of phagosome proteomes resulting from such analyses can be a useful source of information for future mechanistic studies as well as for confirming or excluding a possibility of whether a protein of interest in various investigations is likely or is potentially involved in phagocytosis and phagosome biogenesis.

Keywords: E. histolytica; phagocytosis; proteomics.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Entamoeba histolytica* / metabolism
  • Humans
  • Phagocytosis / physiology
  • Phagosomes / chemistry
  • Phagosomes / metabolism
  • Proteome / metabolism
  • Proteomics
  • rab GTP-Binding Proteins / metabolism

Substances

  • Proteome
  • rab GTP-Binding Proteins

Grants and funding

This research was funded by Grant-in-Aid for a Research Activity start-up (JP20K22758 to N.W.), Sasagawa Scientific Research Grant from The Japan Science Society (2020-4044 to N.W.). Grants-in-Aid for Scientific Research (B) (JP21H02723 to T.N.), Grant for research on emerging, re-emerging infectious diseases from Japan Agency for Medical Research and Development (AMED, JP20fk0108138 to T.N.), Scientific Research on Innovative Areas (JP19H03463 and JP20H05353 to KN-T), Promotion of Joint International Research (Fostering Joint International Research (B)) (21KK0139 to KN-T), and Grant for research on emerging and re-emerging infectious diseases from Japan Agency for Medical Research and Development (AMED, JP20fk0108139 to KN-T).