Los F J, Janse H C, Brandenburg H, de Vrij R W, de Bruijn H W
Department of Clinical Genetics, University Hospital Dijkzigt, Erasmus University, Rotterdam, The Netherlands.
Gynecol Obstet Invest. 1995;39(3):149-52. doi: 10.1159/000292398.
Total alpha-fetoprotein (AFP) concentrations and proportions of AFP non-reactive with the lectin concanavalin A (Con A) were studied in extracellular fluid of 22 first-trimester fetuses. Total AFP concentrations were significantly lower in fetuses with Down's syndrome than in those with Mendelian-inherited diseases and normal karyotypes. The proportion of non-Con-A-reactive AFP was low in the fetal compartment (< or = 3.5%) irrespective of the fetal karyotype. So the AFP production in the fetal liver as well as in the yolk sac seems to be reduced in Down's syndrome. The fetus itself contributes only marginally to the non-Con-A-reactive AFP pool of amniotic fluid, which is therefore almost entirely of yolk sac origin. This pool is preserved well into the second trimester of pregnancy, despite cessation of yolk sac AFP production at the end of the first trimester, indicating a very slow rate of disappearance of proteins out of amniotic fluid.
对22例孕早期胎儿的细胞外液中的总甲胎蛋白(AFP)浓度以及与伴刀豆球蛋白A(Con A)无反应的AFP比例进行了研究。唐氏综合征胎儿的总AFP浓度显著低于患有孟德尔遗传疾病和核型正常的胎儿。无论胎儿核型如何,胎儿部分中与Con A无反应的AFP比例都较低(≤3.5%)。因此,唐氏综合征胎儿肝脏以及卵黄囊中AFP的产生似乎减少。胎儿自身对羊水与Con A无反应的AFP库的贡献很小,因此该库几乎完全来源于卵黄囊。尽管在孕早期结束时卵黄囊停止产生AFP,但该库在妊娠中期仍能很好地保留,这表明蛋白质从羊水中消失的速度非常缓慢。