Due to a production error, two sub-section titles lacked the capitalization of “P” for Plasmodium in “Plasmodium-Infected Erythrocytes: a Fight Between Life and Death" and “Plasmodium Induces Eryptosis of Bystander Erythrocytes.” Secondly, in Table 4 (see below), “uRBC” and “iRBC” column titles should be below “Eryptosis,” as subcolumns. All the “ns” should be below “uRBC,” the green arrows below “iRBC,” and the first column of percentages below “Parasitemia decrease.” Lastly, the latest figures in the final publication were not used.
Table 4.
Effect of eryptosis inducers on P. berghei in vivo development.
| P. berghei in vivo assay | |||||||
|---|---|---|---|---|---|---|---|
| Compound | Eryptosis | Parasi-temia decrease | Mice survival | Anemia effect | References | ||
| uRBC | iRBC | ||||||
| Eryptosis inducers | Amiodarone
|
ns | ![]() |
64% | 70% | N/A | Bobbala et al., 2010b |
Anandamide
|
ns | ![]() |
67% | 70% | N/A | Bobbala et al., 2010a | |
Aurothiomalate
|
ns | ![]() |
44% | 55% | ![]() |
Alesutan et al., 2010 | |
Dimethylfumarate
|
ns | ![]() |
83% | 60% | ns | Ghashghaeinia et al., 2010 | |
Amphotericin B
|
ns | ![]() |
ns | 50% | N/A | Siraskar et al., 2010 | |
Eryptosis compounds were administered to P. berghei-infected mice 8 days post-parasite infection. Eryptosis features of infected red blood cells (iRBC) and bystander uninfected red blood cells (uRBC), as well as parasitemia levels, mice survival outcome, and anemia levels effects were measured every day. For clarity purposes, the eryptosis phenotype observed is based only on reported PS exposure measurements. “Parasitemia decrease” indicates the decreased percentage in parasitemia of treated mice when compared to the untreated control (value calculated based on data provided in the original publication) when the difference reached significance. “Mice survival” indicates the percentage of viable treated mice when untreated controls reached 100% lethality rate. Compounds previously described as eryptotic inducers (see Table 1) that did not induce a significant increase in eryptosis of uRBC in these studies are indicated by
. ns, not significant;
, significant increase of PS exposure compared to untreated control; N/A, parameter not discussed in the publication.
The publisher apologizes for this mistake. The original version of this article has been updated.
References
- Alesutan I., Bobbala D., Qadri S. M., Estremera A., Föller M., Lang F. (2010). Beneficial effect of aurothiomalate on murine malaria. Malar. J. 9:118. 10.1186/1475-2875-9-118 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bobbala D., Alesutan I., Föller M., Huber S. M., Lang F. (2010a). Effect of anandamide in Plasmodium berghei-infected mice. Cell. Physiol. Biochem. 26, 355–362. 10.1159/000320559 [DOI] [PubMed] [Google Scholar]
- Bobbala D., Alesutan I., Föller M., Tschan S., Huber S. M., Lang F. (2010b). Protective effect of amiodarone in malaria. Acta Trop. 116, 39–44. 10.1016/j.actatropica.2010.05.005 [DOI] [PubMed] [Google Scholar]
- Ghashghaeinia M., Bobbala D., Wieder T., Koka S., Brück J., Fehrenbacher B., et al. (2010). Targeting glutathione by dimethylfumarate protects against experimental malaria by enhancing erythrocyte cell membrane scrambling. Am. J. Physiol. Cell Physiol. 299, C791–C804. 10.1152/ajpcell.00014.2010 [DOI] [PubMed] [Google Scholar]
- Siraskar B., Ballal A., Bobbala D., Föller M., Lang F. (2010). Effect of amphotericin B on parasitemia and survival of plasmodium berghei-infected mice. Cell. Physiol. Biochem. 26, 347–354. 10.1159/000320558 [DOI] [PubMed] [Google Scholar]
