Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Science 10 November 1978:
Vol. 202. no. 4368, pp. 650 - 652
DOI: 10.1126/science.360396

Articles

Science, Vol 202, Issue 4368, 650-652
Copyright © 1978 by American Association for the Advancement of Science


articles

Sickling rates of human AS red cells infected in vitro with Plasmodium falciparum malaria

EF Roth Jr, M Friedman, Y Ueda, I Tellez, W Trager, and RL Nagel

The kinetics of sickling of malaria-infected red cells from humans with sickle cell trait were studied in vitro in an attempt to obtain direct experimental evidence for a selective advantage of the hemoglobin S heterozygote in a malarious region. The sickling rates of cells infected with Plasmodium falciparum and of non-infected cells were studied both in the total absence of oxygen (by dithionite addition) and at several different concentrations of oxyhemoglobin which might obtain in vivo. In all cases, red cells containing small plasmodium parasite forms (ring forms) sickled approximately eight times as readily as uninfected cells. Cells containing large parasitic forms (trophozoites and schizonts) appeared to sickle less readily than uninfected cells, by light microscopy criteria, but electron micrographs demonstrated the presence of polymerized deoxyhemoglobin S with a high frequency. It is concluded that enhanced sickling of plasmodium-infected AS cells may be one mechanism whereby the hemoglobin S polymorphism is balanced in favor of the heterozygote.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Aspartic Acid Homozygosity at Codon 57 of HLA-DQ {beta} Is Associated with Susceptibility to Pulmonary Tuberculosis in Cambodia.
J. C. Delgado, A. Baena, S. Thim, and A. E. Goldfeld (2006)
J. Immunol. 176, 1090-1097
   Abstract »    Full Text »    PDF »
Association Between a Functional Variant of the KLOTHO Gene and High-Density Lipoprotein Cholesterol, Blood Pressure, Stroke, and Longevity.
D. E. Arking, G. Atzmon, A. Arking, N. Barzilai, and H. C. Dietz (2005)
Circ. Res. 96, 412-418
   Abstract »    Full Text »    PDF »
Enhanced phagocytosis of ring-parasitized mutant erythrocytes: a common mechanism that may explain protection against falciparum malaria in sickle trait and beta-thalassemia trait.
K. Ayi, F. Turrini, A. Piga, and P. Arese (2004)
Blood 104, 3364-3371
   Abstract »    Full Text »    PDF »
Transgenic Mice Expressing Human Fetal Globin Are Protected From Malaria by a Novel Mechanism.
H. L. Shear, L. Grinberg, J. Gilman, M. E. Fabry, G. Stamatoyannopoulos, D. E. Goldberg, and R. L. Nagel (1998)
Blood 92, 2520-2526
   Abstract »    Full Text »    PDF »
Association of human aging with a functional variant of klotho.
D. E. Arking, A. Krebsova, M. Macek Sr., M. Macek Jr., A. Arking, I. S. Mian, L. Fried, A. Hamosh, S. Dey, I. McIntosh, et al. (2002)
PNAS 99, 856-861
   Abstract »    Full Text »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)