The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Red blood cells release microparticles containing human argonaute 2 and miRNAs to target genes of Plasmodium falciparum: MPs and hAgo2-miRNAs targeting P. falciparum
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Red blood cell-derived miRNAs show high expression levels, and some of them are delivered to recipient cells through vesicles and function”
From Red Blood Cells as Potential Repositories of MicroRNAs in the Circulatory System (2020) · cites this paper as Wang et al., 2017
In the citing paper
“(1) mature RBCs may absorb exogenous miRNAs or release internal ones through the circulatory system (Mantel et al., 2016; Wang et al., 2017), and (2) different physiological or pathological conditions may affect the expression of miRNAs in erythroid differentiated cells, thereby affecting the residual amount of miRNAs in mature RBCs (Zhang L. et al., 2012; Shaham et al., 2015; Abraham et al., 2017”
From Red Blood Cells as Potential Repositories of MicroRNAs in the Circulatory System (2020) · cites this paper as Wang et al., 2017
In the citing paper
“Recent research has shown that EVs released from RBCs in large quantities during the blood phase of malarial infection are able to transfer human-derived Ago2–miRNAs (hAgo2–miR-451 and miR-140) complexes into the parasites within infected RBCs, which target the mRNAs of a critical parasite antigen P. falciparum erythrocyte membrane protein-1 (pfEMP1) and downregulated its expression (Wang et al.,”
From Red Blood Cells as Potential Repositories of MicroRNAs in the Circulatory System (2020) · cites this paper as Wang et al., 2017
In the citing paper
“Recent research has shown that EVs released from RBCs in large quantities during the blood phase of malarial infection are able to transfer human-derived Ago2–miRNAs (hAgo2–miR-451 and miR-140) complexes into the parasites within infected RBCs, which target the mRNAs of a critical parasite antigen P. falciparum erythrocyte membrane protein-1 (pfEMP1) and downregulated its expression (Wang et al.,”
From Red Blood Cells as Potential Repositories of MicroRNAs in the Circulatory System (2020) · cites this paper as Wang et al., 2017
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The role of site accessibility in microRNA target recognition
Kertesz, M., Iovino, N., Unnerstall, U., Gaul, U., & Segal, E. (2007) · Nature Genetics · doi:10.1038/ng2135 · Cited by 2,460
Regulation of immune responses by extracellular vesicles
Robbins, P. D., & Morelli, A. E. (2014) · Nature Reviews Immunology · doi:10.1038/nri3622 · Cited by 2,260
Global distribution of the sickle cell gene and geographical confirmation of the malaria hypothesis
Piel, F. B., Patil, A. P., Howes, R. E., Nyangiri, O. A., Gething, P. W., Williams, T. N., Weatherall, D. J., & Hay, S. I. (2010) · Nature Communications · doi:10.1038/ncomms1104 · Cited by 629
(2015) · Advances in Parasitology · doi:10.1016/bs.apar.2015.02.004 · Cited by 162
Flagged first, then by citations
Research works printed but not linked: 50
- Lanier LL.NK cell recognition. Annu Rev Immunol 2005;23: 225–274. · DOI
- Kwiatkowski DP.How malaria has affected the human genome and what human genetics can teach us about malaria. Am J Hum Genet 2005;77: 171–192. · DOI
- Beet EA.Sickle cell disease in the Balovale District of Northern Rhodesia. East Afr Med J 1946;23: 75–86.
- Allison AC.Protection afforded by sickle-cell trait against subtertian malareal infection. Br Med J 1954;1: 290–294. · DOI
- Bunn HF.The triumph of good over evil: protection by the sickle gene against malaria. Blood 2013;121: 20–25. · DOI
- Howes RE, Battle KE, Satyagraha AWet al.G6PD deficiency: global distribution, genetic variants and primaquine therapy. Adv Parasitol 2013;81: 133–201. · DOI
- Ruwende C, Hill A.Glucose-6-phosphate dehydrogenase deficiency and malaria. J Mol Med 1998;76: 581–588. · DOI
- Buzas EI, Gyorgy B, Nagy Get al.Emerging role of extracellular vesicles in inflammatory diseases. Nat Rev Rheumatol 2014;10: 356–364. · DOI
- Couper KN, Barnes T, Hafalla JCet al.Parasite-derived plasma microparticles contribute significantly to malaria infection-induced inflammation through potent macrophage stimulation. PLoS Pathog 2010;6: e1000744. · DOI
- Campos FM, Franklin BS, Teixeira-Carvalho Aet al.Augmented plasma microparticles during acute Plasmodium vivax infection. Malar J 2010;9: 327. · DOI
- Nantakomol D, Dondorp AM, Krudsood Set al.Circulating red cell-derived microparticles in human malaria. J Infect Dis 2011;203: 700–706. · DOI
- Mantel PY, Hoang AN, Goldowitz Iet al.Malaria-infected erythrocyte-derived microvesicles mediate cellular communication within the parasite population and with the host immune system. Cell Host Microbe 2013;13: 521–534. · DOI
- Martin-Jaular L, Nakayasu ES, Ferrer Met al.Exosomes from Plasmodium yoelii-infected reticulocytes protect mice from lethal infections. PLoS One 2011;6: e26588. · DOI
- LaMonte G, Philip N, Reardon Jet al.Translocation of sickle cell erythrocyte microRNAs into Plasmodium falciparum inhibits parasite translation and contributes to malaria resistance. Cell Host Microbe 2012;12: 187–199. · DOI · Paper page
- Trager W, Jensen JB.Human malaria parasites in continuous culture. Science 1976;193: 673–675. · DOI
- Lambros C, Vanderberg JP.Synchronization of Plasmodium falciparum erythrocytic stages in culture. J Parasitol 1979;65: 418–420. · DOI
- Smythe WA, Joiner KA, Hoppe HC.Actin is required for endocytic trafficking in the malaria parasite Plasmodium falciparum. Cell Microbiol 2008;10: 452–464.
- Chen C, Ridzon DA, Broomer AJet al.Real-time quantification of microRNAs by stem-loop RT-PCR. Nucleic Acids Res 2005;33: e179. · DOI
- Kramer MF.Stem-loop RT-qPCR for miRNAs. Curr Protoc Mol Biol 2011;Chapter 15: Unit 15 10.
- Millholland MG, Mishra S, Dupont CDet al.A host GPCR signaling network required for the cytolysis of infected cells facilitates release of apicomplexan parasites. Cell Host Microbe 2013;13: 15–28. · DOI
- Maniataki E, De Planell Saguer MD, Mourelatos Z.Immunoprecipitation of microRNPs and directional cloning of microRNAs. Methods Mol Biol 2005;309: 283–294.
- Kaestli M, Cockburn IA, Cortes Aet al.Virulence of malaria is associated with differential expression of Plasmodium falciparum var gene subgroups in a case-control study. J Infect Dis 2006;193: 1567–1574. · DOI
- Muhle RA, Adjalley S, Falkard Bet al.A var gene promoter implicated in severe malaria nucleates silencing and is regulated by 3' untranslated region and intronic cis-elements. Int J Parasitol 2009;39: 1425–1439. · DOI
- Enright AJ, John B, Gaul Uet al.MicroRNA targets in Drosophila. Genome Biol 2003;5: R1. · DOI · Paper page
- Kaess BM, Harris WS, Lacey Set al.The relation of red blood cell fatty acids with vascular stiffness, cardiac structure and left ventricular function: The Framingham Heart Study. Vasc Med 2015;20: 5–13. · DOI
- Newbold CI, Craig AG, Kyes Set al.PfEMP1, polymorphism and pathogenesis. Ann Trop Med Parasitol 1997;91: 551–557. · DOI
- Flick K, Chen Q.var genes, PfEMP1 and the human host. Mol Biochem Parasitol 2004;134: 3–9. · DOI
- Mantel PY, Hjelmqvist D, Walch Met al.Infected erythrocyte-derived extracellular vesicles alter vascular function via regulatory Ago2-miRNA complexes in malaria. Nat Commun 2016;7: 12727. · DOI · Paper page
- Yoon SK, Hur W, Lee YKet al.MiR-451 inhibits fatty acid-induced increases in NF-kappa B transactivation through ampk in non-alcoholic steatohepatitis (nash). J Hepatol 2013;58: S528–S528. · DOI
- Jamal MS, Hafeez BB, Verma AK.Chronic ultraviolet radiation exposure of mouse skin activates GATA and PAX families of transcription factors, which regulate expression of cell survival genes. Cancer Res 2011;71: 4204. · DOI
- Zhou M, Bai X, Wei M.Effect of microRNA in progressing of breast cancer and drug resistance. Chin J Cancer Prev Treat 2011;18: 1732–1735.
- Wang XC, Tian LL, Jiang XYet al.The expression and function of miRNA-451 in non-small cell lung cancer. Cancer Lett 2011;311: 203–209. · DOI
- Bancells C, Deitsch KW.A molecular switch in the efficiency of translation reinitiation controls expression of var2csa, a gene implicated in pregnancy-associated malaria. Mol Microbiol 2013;90: 472–488. · DOI
- Zhang Q, Siegel TN, Martins RMet al.Exonuclease-mediated degradation of nascent RNA silences genes linked to severe malaria. Nature 2014;513: 431–435. · DOI
- Duraisingh MT, Voss TS, Marty AJet al.Heterochromatin silencing and locus repositioning linked to regulation of virulence genes in Plasmodium falciparum. Cell 2005;121: 13–24. · DOI
- Freitas-Junior LH, Hernandez-Rivas R, Ralph SAet al.Telomeric heterochromatin propagation and histone acetylation control mutually exclusive expression of antigenic variation genes in malaria parasites. Cell 2005;121: 25–36. · DOI
- Kyes S, Christodoulou Z, Pinches Ret al.Plasmodium falciparum var gene expression is developmentally controlled at the level of RNA polymerase II-mediated transcription initiation. Mol Microbiol 2007;63: 1237–1247. · DOI
- Deitsch KW, Calderwood MS, Wellems TE.Malaria. cooperative silencing elements in var genes. Nature 2001;412: 875–876. · DOI
- Voss TS, Healer J, Marty AJet al.A var gene promoter controls allelic exclusion of virulence genes in Plasmodium falciparum malaria. Nature 2006;439: 1004–1008. · DOI
- Regev-Rudzki N, Wilson DW, Carvalho TGet al.Cell-cell communication between malaria-infected red blood cells via exosome-like vesicles. Cell 2013;153: 1120–1133. · DOI · Paper page
- Faille D, Combes V, Mitchell AJet al.Platelet microparticles: a new player in malaria parasite cytoadherence to human brain endothelium. FASEB J 2009;23: 3449–3458. · DOI
- Combes V, Coltel N, Alibert Met al.ABCA1 gene deletion protects against cerebral malaria: potential pathogenic role of microparticles in neuropathology. Am J Pathol 2005;166: 295–302. · DOI
- Trecul A, Morceau F, Gaigneaux Aet al.Valproic acid regulates erythro-megakaryocytic differentiation through the modulation of transcription factors and microRNA regulatory micro-networks. Biochem Pharmacol 2014;92: 299–311. · DOI
- Svasti S, Masaki S, Penglong Tet al.Expression of microRNA-451 in normal and thalassemic erythropoiesis. Ann Hematol 2010;89: 953–958. · DOI
- Lai K, Jia S, Yu S, Luo J, He Y.Genome-wide analysis of aberrantly expressed lncRNAs and miRNAs with associated co-expression and ceRNA networks in beta-thalassemia and hereditary persistence of fetal hemoglobin. Oncotarget 2017;8: 49931–49943. · DOI
- Chen SY, Wang Y, Telen MJ, Chi JT.The genomic analysis of erythrocyte microRNA expression in sickle cell diseases. PLoS One 2008;3: e2360. · DOI · Paper page
- Choong ML, Yang HH, McNiece I.MicroRNA expression profiling during human cord blood-derived CD34 cell erythropoiesis. Exp Hematol 2007;35: 551–564. · DOI · Paper page
- Masaki S, Ohtsuka R, Abe Yet al.Expression patterns of microRNAs 155 and 451 during normal human erythropoiesis. Biochem Bioph Res Co 2007;364: 509–514. · DOI · Paper page
- Prugnolle F, Durand P, Ollomo Bet al.A fresh look at the origin of Plasmodium falciparum, the most malignant malaria agent. PLoS Pathog 2011;7: e1001283. · DOI
- Prugnolle F, Ollomo B, Durand Pet al.African monkeys are infected by Plasmodium falciparum nonhuman primate-specific strains. Proc Natl Acad Sci USA 2011;108: 11948–11953. · DOI
Cited by
Sorted by citations
Red Blood Cells as Potential Repositories of MicroRNAs in the Circulatory System
Sun, L., Yu, Y., Niu, B., & Wang, D. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.00442 · Cited by 83
Yan, X., Zeng, D., Zhu, H., Zhang, Y., Shi, Y., Wu, Y., Tang, H., & Li, D. (2020) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s251152 · Cited by 29
Metadata
- Authors
- Wang, Z., Xi, J., Hao, X., Deng, W., Liu, J., Wei, C., Gao, Y., Zhang, L., & Wang, H.
- Affiliations
- Department of Microbiology and Parasitology, Institute of Basic Medical Sciences/Chinese Academy of Medical Sciences, School of Basic Medicine/Peking Union Medical College, Beijing 100005, China
- Venue
- Emerging Microbes & Infections
- Publisher
- Informa UK Limited
- Published
- 2017-01
- Volume
- 6
- Issue
- 1
- Pages
- 1-11
- ISSN
- 2222-1751
- PMC
- PMC5583671
- Cited by
- 57
- References
- 4
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review