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Genetic manipulation of cell line derived reticulocytes enables dissection of host malaria invasion requirements
Investigating the role that host erythrocyte proteins play in malaria infection is hampered by the genetic intractability of this anucleate cell. Here we report that reticulocytes derived through in vitro differentiation of an enucleation-competent immortalized erythroblast cell line (BEL-A) support...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707200/ https://www.ncbi.nlm.nih.gov/pubmed/31444345 http://dx.doi.org/10.1038/s41467-019-11790-w |
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author | Satchwell, Timothy J. Wright, Katherine E. Haydn-Smith, Katy L. Sánchez-Román Terán, Fernando Moura, Pedro L. Hawksworth, Joseph Frayne, Jan Toye, Ashley M. Baum, Jake |
author_facet | Satchwell, Timothy J. Wright, Katherine E. Haydn-Smith, Katy L. Sánchez-Román Terán, Fernando Moura, Pedro L. Hawksworth, Joseph Frayne, Jan Toye, Ashley M. Baum, Jake |
author_sort | Satchwell, Timothy J. |
collection | PubMed |
description | Investigating the role that host erythrocyte proteins play in malaria infection is hampered by the genetic intractability of this anucleate cell. Here we report that reticulocytes derived through in vitro differentiation of an enucleation-competent immortalized erythroblast cell line (BEL-A) support both successful invasion and intracellular development of the malaria parasite Plasmodium falciparum. Using CRISPR-mediated gene knockout and subsequent complementation, we validate an essential role for the erythrocyte receptor basigin in P. falciparum invasion and demonstrate rescue of invasive susceptibility by receptor re-expression. Successful invasion of reticulocytes complemented with a truncated mutant excludes a functional role for the basigin cytoplasmic domain during invasion. Contrastingly, knockout of cyclophilin B, reported to participate in invasion and interact with basigin, did not impact invasive susceptibility of reticulocytes. These data establish the use of reticulocytes derived from immortalized erythroblasts as a powerful model system to explore hypotheses regarding host receptor requirements for P. falciparum invasion. |
format | Online Article Text |
id | pubmed-6707200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67072002019-08-26 Genetic manipulation of cell line derived reticulocytes enables dissection of host malaria invasion requirements Satchwell, Timothy J. Wright, Katherine E. Haydn-Smith, Katy L. Sánchez-Román Terán, Fernando Moura, Pedro L. Hawksworth, Joseph Frayne, Jan Toye, Ashley M. Baum, Jake Nat Commun Article Investigating the role that host erythrocyte proteins play in malaria infection is hampered by the genetic intractability of this anucleate cell. Here we report that reticulocytes derived through in vitro differentiation of an enucleation-competent immortalized erythroblast cell line (BEL-A) support both successful invasion and intracellular development of the malaria parasite Plasmodium falciparum. Using CRISPR-mediated gene knockout and subsequent complementation, we validate an essential role for the erythrocyte receptor basigin in P. falciparum invasion and demonstrate rescue of invasive susceptibility by receptor re-expression. Successful invasion of reticulocytes complemented with a truncated mutant excludes a functional role for the basigin cytoplasmic domain during invasion. Contrastingly, knockout of cyclophilin B, reported to participate in invasion and interact with basigin, did not impact invasive susceptibility of reticulocytes. These data establish the use of reticulocytes derived from immortalized erythroblasts as a powerful model system to explore hypotheses regarding host receptor requirements for P. falciparum invasion. Nature Publishing Group UK 2019-08-23 /pmc/articles/PMC6707200/ /pubmed/31444345 http://dx.doi.org/10.1038/s41467-019-11790-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Satchwell, Timothy J. Wright, Katherine E. Haydn-Smith, Katy L. Sánchez-Román Terán, Fernando Moura, Pedro L. Hawksworth, Joseph Frayne, Jan Toye, Ashley M. Baum, Jake Genetic manipulation of cell line derived reticulocytes enables dissection of host malaria invasion requirements |
title | Genetic manipulation of cell line derived reticulocytes enables dissection of host malaria invasion requirements |
title_full | Genetic manipulation of cell line derived reticulocytes enables dissection of host malaria invasion requirements |
title_fullStr | Genetic manipulation of cell line derived reticulocytes enables dissection of host malaria invasion requirements |
title_full_unstemmed | Genetic manipulation of cell line derived reticulocytes enables dissection of host malaria invasion requirements |
title_short | Genetic manipulation of cell line derived reticulocytes enables dissection of host malaria invasion requirements |
title_sort | genetic manipulation of cell line derived reticulocytes enables dissection of host malaria invasion requirements |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707200/ https://www.ncbi.nlm.nih.gov/pubmed/31444345 http://dx.doi.org/10.1038/s41467-019-11790-w |
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