Isaac Emma R, Sherwood Nancy M
Biomedical Research Centre, University of Victoria, Victoria, B.C., Canada V8W 3N5.
Mol Cell Endocrinol. 2008 Jan 2;280(1-2):13-9. doi: 10.1016/j.mce.2007.09.003. Epub 2007 Sep 11.
Mice lacking pituitary adenylate cyclase-activating polypeptide (PACAP) show high mortality during the postnatal period, as well as impaired reproduction in females. This study characterizes the reproductive phenotype in female mice lacking PACAP due to targeted disruption (knockout) of the single copy pacap gene (Adcyap1) to determine the site(s) of action of PACAP in the cascade of reproductive events. PACAP null females showed normal puberty onset, estrous cycles, and seminal plugs when paired with a male of proven fertility. However, significantly fewer PACAP null females (21%) than wild-type females (100%) gave birth following mating. Although a defect was not detected in ovulation, ovarian histology or fertilization of released eggs in PACAP null females, only 13% had implanted embryos 6.5 days after mating. Associated with the decrease in implantation, prolactin and progesterone levels were significantly lower in females lacking PACAP than in wild types on day 6.5 after mating. Our evidence suggests that impaired implantation is the defect responsible for decreased fertility in PACAP null female mice.
缺乏垂体腺苷酸环化酶激活多肽(PACAP)的小鼠在出生后阶段死亡率很高,雌性小鼠的生殖能力也受损。本研究对因单拷贝pacap基因(Adcyap1)靶向破坏(敲除)而缺乏PACAP的雌性小鼠的生殖表型进行了表征,以确定PACAP在生殖事件级联反应中的作用位点。当与具有生育能力的雄性小鼠配对时,PACAP基因敲除的雌性小鼠青春期开始、发情周期和精栓均正常。然而,与野生型雌性小鼠(100%)相比,PACAP基因敲除的雌性小鼠(21%)在交配后分娩的数量明显减少。虽然在PACAP基因敲除的雌性小鼠中未检测到排卵、卵巢组织学或释放卵子的受精缺陷,但只有13%的小鼠在交配后6.5天有植入的胚胎。与植入减少相关的是,在交配后第6.5天,缺乏PACAP的雌性小鼠的催乳素和孕酮水平显著低于野生型小鼠。我们的证据表明,植入受损是导致PACAP基因敲除雌性小鼠生育能力下降的缺陷。