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  4. Human parvovirus B19 antibodies induce altered membrane protein expression and apoptosis of BeWo trophoblasts
 
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Human parvovirus B19 antibodies induce altered membrane protein expression and apoptosis of BeWo trophoblasts

Journal
Molecular Medicine Reports
Date Issued
2016-11-01
Author(s)
BOR-SHOW TZANG  
TSAI-CHING HSU  
DOI
10.3892/mmr.2016.5787
URI
https://www.scopus.com/pages/publications/84992416940
https://scholars.csmu.edu.tw/handle/123456789/23379
Abstract
Human parvovirus B19 (B19) is harmful during pregnancy since it can be vertically transmitted to the developing fetus. In addition, the anti-B19 antibodies induced by B19 infection are believed to have a cytopathic role in B19 transmission; however, knowledge regarding the effects of anti-B19 antibodies during pregnancy is limited. To investigate the possible roles of anti-B19 antibodies during pregnancy, the present study examined the effects of anti-B19-VP1 unique region (VP1u), anti-B19-VP2 and anti-B19-nonstructural protein 1 (NS1) immunoglobulin G (IgG) antibodies on BeWo trophoblasts. Briefly, BeWo trophoblasts were incubated with purified IgG against B19-VP1u, B19-VP2 and B19-NS1. Subsequently, the expression of surface proteins and apoptotic molecules were assessed in BeWo trophoblasts using flow cytometry, ELISA and western blotting. The expression levels of human leukocyte antigen (HLA)-G were significantly increased on BeWo trophoblasts treated with rabbit anti-B19-VP1u IgG, and were unchanged in those treated with rabbit anti-B19-NS1 and anti-B19-VP2 IgG, as compared with the control group. Furthermore, the expression levels of globoside (P blood group antigen) and cluster of differentiation (CD)29 (-1 integrin) were significantly increased in BeWo trophoblasts treated with rabbit anti-B19-NS1 and anti-B19-VP2 IgG, whereas only CD29 was also significantly increased in cells treated with anti-B19-VP1u IgG. In addition, the number of cells at sub-G1 phase; caspase-3 activity; and the expression of intrinsic and extrinsic apoptotic molecules, including Fas-associated death domain protein, activated caspase-8, activated caspase-3, B-cell lymphoma 2-associated X protein, cytochrome c, apoptotic peptidase activating factor 1 and activated caspase-9, were significantly increased in BeWo trophoblasts treated with anti-B19-VP1u and anti-B19-NS1 IgG. In conclusion, the present study demonstrated that antibodies against B19 may have a crucial role in pathological processes during pregnancy. These findings may help to elucidate the mechanisms underlying transmission of the B19 virus during pregnancy.
Type
journal article
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