Superoxide-mediated lysis of erythrocytes: The role of colloid-osmotic forces
✍ Scribed by Dr. Ming-Jie Zhou; Howard R. Petty
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 789 KB
- Volume
- 157
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Although superoxide anions are a well‐known mediator of cytotoxicity, their mechanism of target cell lysis is not clearly understood. In the present study we have used an exogenous source of superoxide to study erythrocyte cytolysis. RBC lysis was studied in buffers containing the cations Li^+^, Na^+^, K^+^, Rb^+^, and Cs^+^; superoxide anions were produced and available in these buffers. During this model superoxide‐dependent cytolytic process, erythrocytes underwent a shape change from biconcave disk to sphere as shown by scanning electron microscopy. Soret band transmitted light microscopy has confirmed this shape change and shown that it precedes cytosolic oxidation. This evidence is consistent with a colloid‐osmotic type lytic mechanism. Erythrocyte lysis was studied by ^51^Crrelease and light scattering methods. Superoxide‐mediated target cytolysis was characterized by: (1) a sigmoidal dose‐response curve and (2) a lag time in cytolysis after superoxide addition in kinetic light scattering experiments. The efficacy of cytolysis followed the rank order Cs^+^ > Rb^+^ > Na^+^, Li^+^ > sucrose = raffinose, which provides additional support for a colloid‐osmotic lytic mechanism. Furthermore, the rank order potency correlates with the cations' hydration numbers. We suggest that oxidative events trigger the formation of colloid‐osmotic pores ∼I nm in diameter. © 1993 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract Microglia‐derived superoxide is critical for the inflammation‐induced selective loss of dopaminergic (DA) neurons, but the underlying mechanisms of microglial activation remain poorly defined. Using neuron‐glia and microglia‐enriched cultures from mice deficient in the MAC1 receptor (MA
Protection of human endothelial cells against complement-mediated lycls 3135 Relative roles of decay-accelerating factor, membrane cofactor protein, and CD59 in the protection of human endothelial cells against complement-mediated lysis\* Human umbilical vein endothelial cells (HUVEC) were found b