2.Application of fetal DNA in maternal plasma in noninvasive prenatal diagnosis.
Journal of Huazhong University of Science and Technology (Medical Sciences) 2004;24(1):59-61
To explore the application of fetal DNA in maternal plasma for noninvasive prenatal diagnosis, the DNA template was extracted by hydroxybenzene-chloroform from 44 maternal (7-41 weeks) plasma. The Fetus-derived Y sequence DYZ-1 gene (149bp) was chosen to be amplified by PCR. The fragment was identified in all the plasma of male bearing pregnant women with the diagnostic accordance rate being 100.00%. Two of the 22 female bearing pregnant women had false positive results. Among the 44 pregnant women, the diagnostic accordance rate was 88.89% at early pregnant stage, 100.00% at medium pregnant stage, and 96.55% at late stage respectively. The final accuracy of 95.45% was obtained in all cases. It was concluded that by means of hydroxybenzene-chloroform extraction the authors of this article promoted the concentration and purity of the DNA template, and diagnosed more accurately. The results showed that free fetal DNA in the maternal plasma could be regarded as the gene resource for noninvasive prenatal diagnosis.
DNA/*blood
;
DNA Primers
;
Fetus
;
Maternal-Fetal Exchange
;
Pregnancy/*blood
;
Prenatal Diagnosis/*methods
;
*Sex Determination (Genetics)
3.Research advances of natural killer cells at the maternal-fetal interface.
Acta Physiologica Sinica 2021;73(1):103-114
Natural killer (NK) cells are the main immune cells at the maternal-fetal interface and accumulate in the uterine decidua in early pregnancy. Many studies have shown that NK cells at the maternal-fetal interface have unique phenotypes and play critical roles in various processes, including immune tolerance during pregnancy, decidualization, invasion of trophoblasts, remodeling of the uterine spiral artery, formation of the placenta and growth of embryo. However, specific functions of NK cells and their mechanism remain to be fully elucidated. This review summarizes the research progress of NK cells at the maternal-fetal interface and their roles in the pregnancy-related disorders in recent years. The aims of this review are to gain deep insight of the function of NK cells at the maternal-fetal interface and provide new ideas for intervention of pregnancy-related diseases.
Decidua
;
Female
;
Humans
;
Killer Cells, Natural
;
Maternal-Fetal Exchange
;
Placenta
;
Pregnancy
;
Trophoblasts
;
Uterus
5.Exposure profile of mercury, lead, cadmium, arsenic, antimony, copper, selenium and zinc in maternal blood, cord blood and placenta: the Tohoku Study of Child Development in Japan.
Miyuki IWAI-SHIMADA ; Satomi KAMEO ; Kunihiko NAKAI ; Kozue YAGINUMA-SAKURAI ; Nozomi TATSUTA ; Naoyuki KUROKAWA ; Shoji F NAKAYAMA ; Hiroshi SATOH
Environmental Health and Preventive Medicine 2019;24(1):35-35
BACKGROUND:
The effects of prenatal exposure to toxic elements on birth outcomes and child development have been an area of concern. This study aimed to assess the profile of prenatal exposure to toxic elements, arsenic (As), bismuth (Bi), cadmium (Cd), mercury (total mercury (THg), methylmercury (MHg), inorganic mercury (IHg)), lead (Pb), antimony (Sb) and tin (Sn), and essential trace elements, copper (Cu), selenium (Se) and zinc (Zn), using the maternal blood, cord blood and placenta in the Tohoku Study of Child Development of Japan (N = 594-650).
METHODS:
Inductively coupled plasma mass spectrometry was used to determine the concentrations of these elements (except mercury). Levels of THg and MeHg were measured using cold vapour atomic absorption spectrophotometry and a gas chromatograph-electron capture detector, respectively.
RESULTS:
Median concentrations (25th-75th) of As, Cd, Pb, Sb, Sn and THg in the maternal blood were 4.06 (2.68-6.81), 1.18 (0.74-1.79), 10.8 (8.65-13.5), 0.2 (0.06-0.40) and 0.2 (0.1-0.38) ng mL and 5.42 (3.89-7.59) ng g, respectively. Median concentrations (25th-75th) of As, Cd, Pb, Sb, Sn and THg in the cord blood were 3.68 (2.58-5.25), 0.53 (0.10-1.25), 9.89 (8.02-12.5), 0.39 (0.06-0.92) and 0.2 (0.2-0.38) ng mL and 9.96 (7.05-13.8) ng g, respectively.
CONCLUSIONS
THg and Sb levels in the cord blood were twofold higher than those in the maternal blood. Cord blood to maternal blood ratios for As, Cd and Sb widely varied between individuals. To understand the effects of prenatal exposure, further research regarding the variations of placental transfer of elements is necessary.
Adult
;
Female
;
Fetal Blood
;
chemistry
;
Humans
;
Japan
;
Maternal Exposure
;
statistics & numerical data
;
Maternal-Fetal Exchange
;
Metals
;
blood
;
Placenta
;
chemistry
;
Pregnancy
;
blood
;
Trace Elements
;
blood
;
Urban Health
6.Application of fetal DNA in maternal plasma in noninvasive prenatal diagnosis.
Journal of Huazhong University of Science and Technology (Medical Sciences) 2004;24(1):59-61
To explore the application of fetal DNA in maternal plasma for noninvasive prenatal diagnosis, the DNA template was extracted by hydroxybenzene-chloroform from 44 maternal (7-41 weeks) plasma. The Fetus-derived Y sequence DYZ-1 gene (149bp) was chosen to be amplified by PCR. The fragment was identified in all the plasma of male bearing pregnant women with the diagnostic accordance rate being 100.00%. Two of the 22 female bearing pregnant women had false positive results. Among the 44 pregnant women, the diagnostic accordance rate was 88.89% at early pregnant stage, 100.00% at medium pregnant stage, and 96.55% at late stage respectively. The final accuracy of 95.45% was obtained in all cases. It was concluded that by means of hydroxybenzene-chloroform extraction the authors of this article promoted the concentration and purity of the DNA template, and diagnosed more accurately. The results showed that free fetal DNA in the maternal plasma could be regarded as the gene resource for noninvasive prenatal diagnosis.
Adult
;
DNA
;
blood
;
DNA Primers
;
Female
;
Fetus
;
Humans
;
Male
;
Maternal-Fetal Exchange
;
Pregnancy
;
blood
;
Prenatal Diagnosis
;
methods
;
Sex Determination Processes
7.Maternal and fetal exposure to four carcinogenic environmental metals.
Huai GUAN ; Feng-Yuan PIAO ; Xiao-Wei LI ; Qiu-Juan LI ; Lei XU ; Kazuhito YOKOYAMA
Biomedical and Environmental Sciences 2010;23(6):458-465
OBJECTIVETo examine maternal and fetal exposure levels to four carcinogenic metals, arsenic (As), cadmium (Cd), nickel (Ni), and beryllium (Be), and to investigate their environmental influences.
METHODSMetal concentrations in maternal and umbilical cord blood were measured by inductively coupled plasma-mass spectrometry (ICP-MS). Environmental factors that might play a role in exposure were analyzed using Mann-Whitney nonparametric U-tests and multiple linear regression.
RESULTSThe concentrations of As, Cd, and Ni in umbilical cord blood (5.41, 0.87, and 139.54 μg/L) were significantly lower than those in maternal blood (6.91, 1.93, and 165.93 μg/L). There were significant positive correlations between the maternal and cord concentrations of each carcinogen. Our results showed that: (i) exposures to potentially harmful occupational factors during pregnancy were associated with high levels of maternal As, Cd, and Ni; (ii) living close to major transportation routes (<500 m) or exposure to second-hand smoke during pregnancy increased the maternal Cd levels and (iii) living close to industrial chimneys induced high maternal Ni levels. Multiple linear regression analysis showed that these environmental factors remained significant in models of the influences of these four carcinogens.
CONCLUSIONBoth mothers and fetuses had been exposed to As, Cd, Ni, and Be. The increased levels of these carcinogens in pregnant women were associated with some detrimental environmental factors, such as occupational exposure, contact with second-hand smoke and living close to major transportation routes or industrial chimneys.
Carcinogens, Environmental ; toxicity ; Environmental Exposure ; Environmental Pollutants ; toxicity ; Female ; Humans ; Maternal-Fetal Exchange ; Metals ; toxicity ; Pregnancy ; Time Factors
9.Cytogenetic Effects on Mouse Fetus of Acute and Chronic Transplacental In Vivo Exposure to Carbon Monoxide: Induction of Micronuclei and Sister Chromatid Exchanges.
Hyun Mo KWAK ; Young Ho YANG ; Myeong Seon LEE
Yonsei Medical Journal 1986;27(3):205-212
Carbon monoxide gas is found in the atmosphere whenever society has become industrialized. In addition to the fact that Korea has become industrialized, bituminous coal is used to heat homes here, in heating systems that, if not very carefully maintained, leak this gas, resulting in a number of deaths and near deaths each winter. It has only rarely been reported by investigators that genetic damage may be done transplacentally to a human fetus by a pregnant woman's being poisoned by CO. We explored this by evaluating the damage done to the mouse fetus through an in vivo experiment, using micronucleus and sister chromatid exchange (SCE) tests. Mice were mated and pregnant ones divided into a group that received acute exposures on 3 different days, a group that received chronic exposure, and a control group. In the meantime in the control group the incidence of both micronuclei and SCE was less on the maternal side, in both the acute and chronic exposure groups, whereas the incidences of both micronuclei and SCE were more on the maternal side. However, the incidence on the fetal side was not far behind. Increasing, the dosage of carbon monoxide with gestational age increased the incidence of both micronuclei and SCE in the mother and fetus alike.
Animal
;
Carbon Monoxide/toxicity*
;
Cell Nucleus/drug effects*
;
Female
;
Fetus/drug effects*
;
Maternal-Fetal Exchange
;
Mice
;
Mice, Inbred ICR
;
Mutagens*
;
Pregnancy
;
Sister Chromatid Exchange/drug effects*
10.Noninvasive prenatal diagnosis of single gene disorders through cell-free fetal DNA in maternal blood.
Chinese Journal of Medical Genetics 2009;26(4):410-413
The discovery of cell-free fetal DNA (cff-DNA) in maternal plasma offered a new way to noninvasive prenatal diagnosis for single gene disorders. In the past decade, many techniques such as real-time PCR, pyrophosphorolysis-activated polymerization, mass spectrum and digital PCR have been developed for noninvasive prenatal diagnosis. In this review, the author discuss the principles, applications, advantages and disadvantages of these techniques.
DNA
;
blood
;
genetics
;
Female
;
Fetal Diseases
;
diagnosis
;
genetics
;
Genetic Diseases, Inborn
;
diagnosis
;
genetics
;
Humans
;
Maternal-Fetal Exchange
;
Pregnancy
;
Prenatal Diagnosis
;
methods