Modulated red blood cell survival by membrane protein clustering View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1995-03

AUTHORS

Laura Chiarantini, Luigia Rossi, Alessandra Fraternale, Mauro Magnani

ABSTRACT

Human and murine blood cells treated with ZnCl2 and bis(sulfosuccinimidyl)suberate (BS3) (a cross linking agent) undergo band 3 clustering and binding of hemoglobin to red blood cell membrane proteins. These clusters induce autologous IgG binding and complement fixation, thus favouring the phagocytosis of ZnCl2/BS3 treated cells by macrophages. The extension of red blood cell opsonization can be easily modulated by changing the ZnCl2 concentration in the 0.1-1.0 mM range thus providing an effective way to affect blood cell recognition by macrophages. In fact, murine erythrocytes treated with increasing ZnCl2 concentrations have proportionally reduced survivals when reinjected into the animal. Furthermore, the organ sequestration of ZnCl2/BS3 treated cells strongly resembles the typical distribution of the senescent cells. Since the ZnCl2/BS3 treatment can also be performed on red blood cells loaded with drugs or other substances, this procedure is an effective drug-targeting system to be used for the delivery of molecules to peritoneal, liver and spleen macrophages. More... »

PAGES

53-59

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00926740

DOI

http://dx.doi.org/10.1007/bf00926740

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1044109978

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/7791745


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