Sex differences in prenatal epigenetic programing of stress pathways

被引:165
作者
Bale, Tracy L. [1 ]
机构
[1] Univ Penn, Dept Anim Biol, Sch Vet Med, Philadelphia, PA 19104 USA
来源
STRESS-THE INTERNATIONAL JOURNAL ON THE BIOLOGY OF STRESS | 2011年 / 14卷 / 04期
关键词
Brain; masculinization; neurodevelopmental disorders; placenta; prenatal stress; sex differences; PITUITARY-ADRENAL AXIS; CORTICOTROPIN-RELEASING HORMONE; ANTENATAL MATERNAL EXPOSURE; FOLIC-ACID SUPPLEMENTATION; JUVENILE RHESUS-MONKEYS; GENE-EXPRESSION; FEMALE RAT; GLUCOCORTICOID-RECEPTOR; PLACENTAL DEVELOPMENT; BEHAVIORAL-RESPONSES;
D O I
10.3109/10253890.2011.586447
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Maternal stress experience is associated with neurodevelopmental disorders including schizophrenia and autism. Recent studies have examined mechanisms by which changes in the maternal milieu may be transmitted to the developing embryo and potentially translated into programing of the epigenome. Animal models of prenatal stress have identified important sex- and temporal-specific effects on offspring stress responsivity. As dysregulation of stress pathways is a common feature in most neuropsychiatric diseases, molecular and epigenetic analyses at the maternal--embryo interface, especially in the placenta, may provide unique insight into identifying much-needed predictive biomarkers. In addition, as most neurodevelopmental disorders present with a sex bias, examination of sex differences in the inheritance of phenotypic outcomes may pinpoint gene targets and specific windows of vulnerability in neurodevelopment, which have been disrupted. This review discusses the association and possible contributing mechanisms of prenatal stress in programing offspring stress pathway dysregulation and the importance of sex.</.
引用
收藏
页码:348 / 356
页数:9
相关论文
共 116 条
[31]   NEUROENDOCRINE MECHANISMS MEDIATING SUPPRESSION OF CIRCULATING TESTOSTERONE LEVELS ASSOCIATED WITH CHRONIC STRESS IN MALE RATS [J].
GRAY, GD ;
SMITH, ER ;
DAMASSA, DA ;
EHRENKRANZ, JRL ;
DAVIDSON, JM .
NEUROENDOCRINOLOGY, 1978, 25 (04) :247-256
[32]   SRY RECOGNIZES CONSERVED DNA SITES IN SEX-SPECIFIC PROMOTERS [J].
HAQQ, CM ;
KING, CY ;
DONAHOE, PK ;
WEISS, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (03) :1097-1101
[33]   Epigenetic landscape required for placental development [J].
Hemberger, M. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2007, 64 (18) :2422-2436
[34]   A critical time window of Sry action in gonadal sex determination in mice [J].
Hiramatsu, Ryuji ;
Matoba, Shogo ;
Kanai-Azuma, Masami ;
Tsunekawa, Naoki ;
Katoh-Fukui, Yuko ;
Kurohmaru, Masamichi ;
Morohashi, Ken-ichirou ;
Wilhelm, Dagmar ;
Koopman, Peter ;
Kanai, Yoshiakira .
DEVELOPMENT, 2009, 136 (01) :129-138
[35]   Stress in Pregnancy: A Role for Neuroactive Steroids in Protecting the Fetal and Neonatal Brain [J].
Hirst, Jonathan J. ;
Walker, David W. ;
Yawno, Tamara ;
Palliser, Hannah K. .
DEVELOPMENTAL NEUROSCIENCE, 2009, 31 (05) :363-377
[36]   Interleukin-6 regulation of the human DNA methyltransferase (HDNMT) gene in human erythroleukemia cells [J].
Hodge, DR ;
Xiao, WH ;
Clausen, PA ;
Heidecker, G ;
Szyf, M ;
Farrar, WL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (43) :39508-39511
[37]  
HUTTUNEN MO, 1978, ARCH GEN PSYCHIAT, V35, P429
[38]   Rethinking schizophrenia [J].
Insel, Thomas R. .
NATURE, 2010, 468 (7321) :187-193
[39]   Hippocampal Dysfunction and Cognitive Impairments Provoked by Chronic Early-Life Stress Involve Excessive Activation of CRH Receptors [J].
Ivy, Autumn S. ;
Rex, Christopher S. ;
Chen, Yuncai ;
Dube, Celine ;
Maras, Pamela M. ;
Grigoriadis, Dimitri E. ;
Gall, Christine M. ;
Lynch, Gary ;
Baram, Tallie Z. .
JOURNAL OF NEUROSCIENCE, 2010, 30 (39) :13005-13015
[40]   NEONATAL SEX-STEROID HORMONES AND COGNITIVE-ABILITIES AT 6 YEARS [J].
JACKLIN, CN ;
WILCOX, KT ;
MACCOBY, EE .
DEVELOPMENTAL PSYCHOBIOLOGY, 1988, 21 (06) :567-574