Title of article
Membrane damages under high pressure of human erythrocytes agglutinated by concanavalin A
Author/Authors
Yamaguchi، نويسنده , , Takeo and Tajiri، نويسنده , , Keita and Murata، نويسنده , , Kunihiko and Nagadome، نويسنده , , Shigemi، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2014
Pages
5
From page
695
To page
699
Abstract
Human erythrocytes are agglutinated by lectins such as concanavalin A (Con A). The behaviors of agglutinated erythrocytes under pressure are less well understood. Here, we report the effects of erythrocyte agglutination on pressure-induced membrane damages. Small clumps of intact erythrocytes by Con A were dissociated by a pressure of 200 MPa. Further, the observation by scanning electron microscopy demonstrated the generation of vesicles, fragmented particles, and membrane hole. On the other hand, large clumps of trypsin-digested erythrocytes by Con A seemed to be stable against 200 MPa. However, the erythrocytes dissociated from such pressure-treated clumps by methyl α-mannopyranoside also showed the existence of vesicles and fragmented particles except for the membrane hole. Pressure-induced hemolysis was greatly suppressed in such large clumps. Similar suppressive effects were observed in erythrocytes packed by centrifugation. However, the hemolysis occurred when the erythrocytes dissociated from 200 MPa-treated large clumps by methyl α-mannopyranoside were incubated at 0 °C and atmospheric pressure. Pyrene excimer fluorescence due to spectrin denaturation was observed in Con A-agglutinated ghosts that were exposed to a pressure of 200 MPa. These results suggest that upon pressure treatment of tightly agglutinated erythrocytes, the hemolysis is greatly suppressed, but membrane damages occur such as spectrin denaturation and vesiculation.
Keywords
erythrocyte , Concanavalin A , Hemolysis , Agglutination , Vesiculation , Spectrin
Journal title
Colloids and Surfaces B Biointerfaces
Serial Year
2014
Journal title
Colloids and Surfaces B Biointerfaces
Record number
1978313
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