Red cell vesiculation--a common membrane physiologic event
- PMID: 3760672
Red cell vesiculation--a common membrane physiologic event
Abstract
Loss of red blood cell membrane material in the form of microvesicles has been noted in sickle cells, in Ca++-loaded and adenosine triphosphate (ATP)-depleted normal red blood cells; and during storage of normal red blood cells. To further understand the vesiculation process, we have studied vesicles generated by a variety of perturbations of the red blood cell membrane. Vesicles were isolated by centrifugation at 30,000 X g from plasma of heparinized pathologic blood samples (sickle cell anemia, hemoglobin H disease, hereditary spherocytosis, hereditary elliptocytosis, and protein 4.1 deficiency) incubated overnight at 4 degrees C. Vesicle formation also was induced in normal erythrocytes by ATP depletion, by heating to 49 degrees C, by incubation at pH 5.4, and by incubation in 5 mmol/L diamide. Membrane protein composition was characterized on denaturing polyacrylamide gels and by immunoblot. The vesicles all contained band 3, glycophorin A, and band 4.1. Spectrin was depleted in all vesicles. Thiol disulfide exchange chromatography revealed evidence of oxidative cross-linking of spectrin in pathologic and normal red blood cells that had undergone vesiculation. This suggests that the mechanism of vesiculation may be related to cross-linking of membrane proteins. Membrane phospholipid composition of sickle cell and acid-induced vesicles was similar to that of normal red cells as determined by thin-layer chromatography. Possible pathophysiologic effects of vesiculation were assessed by using a modified Russell's viper venom assay. All vesicles examined shortened Russell's viper venom clotting time by 55% to 70% of control values. In addition, ektacytometer studies reveal that cells remaining after acid-induced vesiculation are rigid. These observations indicate that the vesicles may play a role in the hypercoagulation seen in some hemolytic disorders and that the process of vesiculation itself may contribute to increased rigidity of red cells and their subsequent removal from the circulation.
Similar articles
-
Effects of cross-linking of membrane proteins on vesiculation induced by dimyristoylphosphatidylcholine in human erythrocytes.J Biochem. 1994 Apr;115(4):659-63. doi: 10.1093/oxfordjournals.jbchem.a124392. J Biochem. 1994. PMID: 8089080
-
Vesiculation induced by hydrostatic pressure in human erythrocytes.J Biochem. 1991 Sep;110(3):355-9. doi: 10.1093/oxfordjournals.jbchem.a123585. J Biochem. 1991. PMID: 1769962
-
The effect of spicules obtained from sickle red cells on clotting activity.Br J Haematol. 1984 Apr;56(4):557-62. doi: 10.1111/j.1365-2141.1984.tb02180.x. Br J Haematol. 1984. PMID: 6424699
-
Red cell membrane skeleton: structure-function relationships.Prog Clin Biol Res. 1980;43:21-44. Prog Clin Biol Res. 1980. PMID: 6999502 Review.
-
Red blood cell vesiculation in hereditary hemolytic anemia.Front Physiol. 2013 Dec 13;4:365. doi: 10.3389/fphys.2013.00365. Front Physiol. 2013. PMID: 24379786 Free PMC article. Review.
Cited by
-
Different behavior of ghost-linked acidic and neutral sialidases during human erythrocyte ageing.Glycoconj J. 2001 May;18(5):407-18. doi: 10.1023/a:1014816232197. Glycoconj J. 2001. PMID: 11925508
-
New antimalarial indolone-N-oxides, generating radical species, destabilize the host cell membrane at early stages of Plasmodium falciparum growth: role of band 3 tyrosine phosphorylation.Free Radic Biol Med. 2012 Jan 15;52(2):527-36. doi: 10.1016/j.freeradbiomed.2011.11.008. Epub 2011 Nov 15. Free Radic Biol Med. 2012. PMID: 22142474 Free PMC article.
-
Epidermal-growth-factor-stimulated phosphorylation of calpactin II in membrane vesicles shed from cultured A-431 cells.Biochem J. 1989 Apr 15;259(2):577-83. doi: 10.1042/bj2590577. Biochem J. 1989. PMID: 2524190 Free PMC article.
-
Cyclic Mechanical Stresses Alter Erythrocyte Membrane Composition and Microstructure and Trigger Macrophage Phagocytosis.Adv Sci (Weinh). 2022 Jul;9(20):e2201481. doi: 10.1002/advs.202201481. Epub 2022 May 4. Adv Sci (Weinh). 2022. PMID: 35508805 Free PMC article.
-
Irreversible AE1 tyrosine phosphorylation leads to membrane vesiculation in G6PD deficient red cells.PLoS One. 2011 Jan 5;6(1):e15847. doi: 10.1371/journal.pone.0015847. PLoS One. 2011. PMID: 21246053 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Other Literature Sources