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DOI 10.1016/j.ajpath.2010.10.005

Медицинская библиотека · The American journal of pathology · 2011

Reduced stathmin-1 expression in natural killer cells associated with spontaneous abortion.

Lin Yi, Li Cui, Shan Bin, Wang Wenjing, Saito Shigeru, Xu Jiehan, Di Jingfang, Zhong Yanmin, Li Da-Jin

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Female CBA/J mice impregnated by male DBA/2J mice (CBA/J×DBA/2J matings) are prone to spontaneous abortion, although the reason for this is unclear. In this study, the stathmin-1 expression pattern was evaluated in uterine natural killer (uNK) cells purified from CBA/J×DBA/2J matings. Results were compared with those in a CBA/J×BALB/c control group that yields successful pregnancies. The mean ± SD percentage of stathmin-1(+) cells in the CD49b(+) uNK cell population was lower in CBA/J×DBA/2J mice (0.7% ± 0.4%) than in control CBA/J×BALB/c mice (4.9% ± 1.5%, P < 0.01) using flow cytometry, and the intracellular stathmin-1 level in uNK cells was lower in CBA/J×DBA/2J mice than in control mice using Western blot analysis. Co-localization of lectin from Dolichos biflorus agglutinin (DBA-lectin) and stathmin-1 was confirmed using multivision immunohistochemical analysis. The frequency of stathmin-1(+)DBA-lectin(+) cells was lower in CBA/J×DBA/2J mice than in CBA/J×BALB/c mice. A similar trend in the frequency of stathmin-1(+)CD56(+) cells was seen in patients with unexplained spontaneous abortion compared with normal early pregnancy. A neutralizing antibody against stathmin-1 further increased the percentage of embryo loss in CBA/J×DBA/2J matings. These results provide evidence that stathmin-1 expression in uNK cells at the maternal-fetal interface may help modulate uNK cell function and may be beneficial for a successful pregnancy.

Для цитирования: Lin Yi, Li Cui, Shan Bin, Wang Wenjing, Saito Shigeru, Xu Jiehan, Di Jingfang, Zhong Yanmin, Li Da-Jin. Reduced stathmin-1 expression in natural killer cells associated with spontaneous abortion.. The American journal of pathology. 2011. DOI: 10.1016/j.ajpath.2010.10.005.

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