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Expression of Toll‐like receptors and costimulatory molecules in splenic B cells in a normal and abortion‐prone murine pregnancy model
Author(s) -
Lorek Daria,
Kedzierska Anna Ewa,
Slawek Anna,
ChelmonskaSoyta Anna
Publication year - 2019
Publication title -
american journal of reproductive immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 97
eISSN - 1600-0897
pISSN - 1046-7408
DOI - 10.1111/aji.13148
Subject(s) - cd86 , cd80 , cd40 , tlr2 , biology , immunology , immune system , andrology , medicine , tlr4 , t cell , cytotoxic t cell , genetics , in vitro
Problem The regulatory role of B lymphocytes in the pregnancy‐induced maternal immune response is not well recognized. B lymphocytes function as antigen‐presenting cells (APCs) and regulate Toll‐like receptors and costimulatory molecule expression in response to intrinsic and extrinsic signals. Therefore, the aim of this study was to determine the expression of TLR2, TLR4, TLR9, and MHC class II and the costimulatory molecules CD80, CD86, and CD40 in splenic B cells in a normal and abortion‐prone murine pregnancy model. Methods of study The expression level of these molecules on female splenic B cells was investigated using real‐time PCR and flow cytometry. The analysis was performed on the 3rd and 14th day of normal (CBA/JxBALB/c) and abortion‐prone (CBA/JxDBA/2J) murine pregnancy. Results The expression of Tlr9, Cd86, and H2‐Ab1 in splenic B cells on the 3rd day after mating was upregulated, whereas Tlr2 was downregulated in abortion‐prone females. On day 14, we observed lower expression levels of Tlr4 and Cd80 and higher expression levels of Cd86 in CBA/J females mated with DBA/2J males. At the protein level, the differences were observed only on day 3 of pregnancy. TLR4 and CD40 molecules were upregulated in splenic B cells, while TLR9 and CD86 were downregulated in abortion‐prone mice. Conclusion Differential expression of TLRs and costimulatory molecules in splenic B cells in abortion‐prone and normal pregnancies suggests the involvement of these cells in the regulation of the immune response at the periphery in pregnant females.