Schistosoma haematobium: Identification of new estrogenic molecules with estradiol antagonistic activity and ability to inactivate estrogen receptor in mammalian cells

被引:31
作者
Botelho, Monica Catarina [1 ,2 ]
Soares, Raquel [3 ]
Vale, Nuno [4 ]
Ribeiro, Ricardo [5 ]
Camilo, Vania [2 ]
Almeida, Raquel [2 ]
Medeiros, Rui [5 ]
Gomes, Paula [4 ]
Machado, Jose Carlos [2 ,6 ]
Correia da Costa, Jose Manuel
机构
[1] INSA, Natl Inst Hlth, CIBP, P-4000055 Oporto, Portugal
[2] Univ Porto, IPATIMUP Inst Pathol & Mol Immunol, P-4100 Oporto, Portugal
[3] Univ Porto, Dept Biochem U38, FMUP, P-4100 Oporto, Portugal
[4] Univ Porto, Fac Sci, Dept Chem & Biochem, CIQUP, P-4100 Oporto, Portugal
[5] Portuguese Inst Oncol, IPO Mol Oncol Grp Lab, Oporto, Portugal
[6] Univ Porto, Fac Med, FMUP Dept Pathol, P-4100 Oporto, Portugal
关键词
Schistosoma haematobium; Estradiol; Estrogen receptor; MCF-7; cells; CHO cells; Estrogenic molecules; Mass spectrometry; TRANSCRIPTIONAL ACTIVITY; MASS-SPECTROMETRY; ALPHA; REPRESSOR;
D O I
10.1016/j.exppara.2010.06.012
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
We have previously identified the expression of an estradiol (E2)-related molecule by Schistosoma haematobium total antigen (Sh). We now show that this molecule has an antagonistic effect of estradiol in vitro. Our results are consistent with the existence of an estrogenic molecule that antagonizes the activity of estradiol. We found evidence for this molecule as we identified and characterized by mass spectrometry new estrogenic molecules previously unknown, present in schistosome worm extracts and sera of Schistosoma-infected individuals. We also show that Sh is able to interact in vitro with estrogen receptor (ER), explaining how host endocrine system can favor the establishment of schistosomes. These findings highlight the exploitation of the host endocrine system by schistosomes and represent an additional regulatory component of schistosome development that defines a novel paradigm enabling host-parasite interactions. The identification of these molecules opens new ways for the development of alternative drugs to treat schistosomiasis. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:526 / 535
页数:10
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