Sex-Specific Placental Responses in Fetal Development

被引:341
作者
Rosenfeld, Cheryl S. [1 ]
机构
[1] Univ Missouri, Dept Bond Life Sci Ctr, Genet Area Program, Biomed Sci, Columbia, MO 65211 USA
关键词
GLUCOCORTICOID-RECEPTOR ISOFORMS; HUMAN CHORIONIC-GONADOTROPIN; X-CHROMOSOME INACTIVATION; IN-SITU HYBRIDIZATION; GENE-EXPRESSION; BISPHENOL-A; Y-CHROMOSOME; DEHYDROGENASE TYPE-2; GROWTH RESTRICTION; DNA METHYLATION;
D O I
10.1210/en.2015-1227
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The placenta is an ephemeral but critical organ for the survival of all eutherian mammals and marsupials. It is the primary messenger system between the mother and fetus, where communicational signals, nutrients, waste, gases, and extrinsic factors are exchanged. Although the placenta may buffer the fetus from various environmental insults, placental dysfunction might also contribute to detrimental developmental origins of adult health and disease effects. The placenta of one sex over the other might possess greater ability to respond and buffer against environmental insults. Given the potential role of the placenta in effecting the lifetime health of the offspring, it is not surprising that there has been a resurging interest in this organ, including the Human Placental Project launched by the National Institutes of Child Health and Human Development. In this review, we will compare embryological development of the laboratory mouse and human chorioallantoic placentae. Next, evidence that various species, including humans, exhibit normal sex-dependent structural and functional placental differences will be examined followed by how in utero environmental changes (nutritional state, stress, and exposure to environmental chemicals) might interact with fetal sex to affect this organ. Recent data also suggest that paternal state impacts placental function in a sex-dependent manner. The research to date linking placental maladaptive responses and later developmental origins of adult health and disease effects will be explored. Finally, we will focus on how sex chromosomes and epimutations may contribute to sex-dependent differences in placental function, the unanswered questions, and future directions that warrant further consideration.
引用
收藏
页码:3422 / 3434
页数:13
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