[No authors listed]
A disintegrin and metalloproteinase with thrombospondin motifs 7 (ADAMTSâ7) has been revealed to serve an important role in inflammationâassociated diseases. However, the role of ADAMTSâ7 in spontaneous abortion (SA) remains unclear. In the present study, human and mouse decidual tissues were used to detect the expression of ADAMTSâ7 and cartilage oligomeric matrix protein (COMP) in mice with lipopolysaccharide (LPS)âinduced abortion (10Â mice/group), and in SA humans and the corresponding control group (21 participants in the SA group and 15 participants in the control group). The results revealed that ADAMTSâ7 expression was upregulated and that COMP expression was downregulated in the mouse decidual tissue of the LPSâinduced abortion group, when compared with that of the normal control group. The results were further confirmed by western blot analysis and reverse transcriptionâquantitative polymerase chain reaction (RTâqPCR) analysis, which revealed increased ADAMTSâ7 and decreased COMP expression at the protein and mRNA levels in mice treated with LPS. Additionally, the expression of ADAMTSâ7 was negatively correlated with the expression of COMP in mice, with a correlation coefficient of â0.936 (P<0.001). In addition, the expression of ADAMTSâ7 and COMP exhibited was similar in the decidual tissue of SA patients when compared with the levels observed in the tissues of the normal control participants, as demonstrated by increased ADAMTSâ7 expression and decreased COMP expression. Western blotting and RTâqPCR analysis revealed that ADAMTSâ7 was increased and COMP was decreased in the decidual tissue of SA subjects. The correlation analysis of ADAMTSâ7 and COMP in human decidual tissue also revealed a similar result, with a correlation coefficient of â0.836 (P<0.001). The results of the present study demonstrated that ADAMTSâ7 was upregulated and COMP was downregulated in the decidual tissues of humans and mice with SA, and a negative correlation was identified between the expression levels of ADAMTSâ7 and COMP, thereby providing novel evidence for a better understanding of the pathogenesis of SA, which may lead to improvements in the clinical pregnancy outcomes of these individuals.
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