Hirabayashi H, Sato T, Kohno S, Tanaka M, Kobayashi S, Ohta Y, Iguchi T
Graduate School of Integrated Science, Yokohama City University, Yokohama, Japan.
Anat Rec. 1999 Feb 1;254(2):205-13. doi: 10.1002/(SICI)1097-0185(19990201)254:2<205::AID-AR6>3.0.CO;2-K.
Deciduoma induced by mechanical stimulation in pseudopregnant mice is similar to the decidua in normal pregnancy and it undergoes regression after a certain period. Therefore, we examined cell death in deciduomas which were induced by artificial stimulation. To analyze the regression mechanism of artificially induced deciduoma, DNA fragmentation, in situ 3'-DNA nick end labeling, and RT-PCR were performed on day 6 to 14 of pseudopregnancy. DNA fragmentation appeared on day 8 and it increased to day 10 of pseudopregnancy in the traumatized uterine horn. A large number of apoptotic cells were found on day 10 in the periphery of deciduoma at the antimesometrial side. Deciduoma underwent degeneration on day 11 of pseudopregnancy. Expression of tumor necrosis factor-alpha (TNF-alpha) mRNA was high on days 8 and 10, then decreased, whereas the expression increased again on day 14. TNF-alpha protein was expressed from day 8 to day 12, showing a peak expression on day 10 when deciduoma reached maximum weight. Serum progesterone level was high in the traumatized pseudopregnant mice on day 6, then it gradually decreased. Life span of deciduoma was prolonged 4 days more by daily injection of progesterone. A reduction in serum progesterone coincides with TNF-alpha increase, resulting in an increase of apoptotic deciduomal cells at the regression period, and that the life span of deciduoma is prolonged by additive supply of progesterone.
机械刺激诱导假孕小鼠产生的蜕膜瘤与正常妊娠时的蜕膜相似,且在一定时期后会发生退化。因此,我们研究了人工刺激诱导的蜕膜瘤中的细胞死亡情况。为分析人工诱导蜕膜瘤的退化机制,在假孕第6至14天进行了DNA片段化、原位3'-DNA缺口末端标记及逆转录聚合酶链反应。创伤子宫角的DNA片段化在假孕第8天出现,并在第10天增加。在假孕第10天,在蜕膜瘤反系膜侧周边发现大量凋亡细胞。假孕第11天,蜕膜瘤开始退化。肿瘤坏死因子-α(TNF-α)mRNA在第8天和第10天表达较高,随后下降,而在第14天再次升高。TNF-α蛋白从第8天至第12天表达,在蜕膜瘤重量达到最大的第10天出现表达高峰。创伤假孕小鼠第6天血清孕酮水平较高,随后逐渐下降。每天注射孕酮可使蜕膜瘤寿命延长4天。血清孕酮水平降低与TNF-α升高同时出现,导致退化期凋亡蜕膜细胞增加,且补充孕酮可延长蜕膜瘤寿命。