TDAG51 is a crucial regulator of maternal care and depressive-like behavior after parturition

PLoS Genet. 2019 Jun 28;15(6):e1008214. doi: 10.1371/journal.pgen.1008214. eCollection 2019 Jun.

Abstract

Postpartum depression is a severe emotional and mental disorder that involves maternal care defects and psychiatric illness. Postpartum depression is closely associated with a combination of physical changes and physiological stress during pregnancy or after parturition in stress-sensitive women. Although postpartum depression is relatively well known to have deleterious effects on the developing fetus, the influence of genetic risk factors on the development of postpartum depression remains unclear. In this study, we discovered a novel function of T cell death-associated gene 51 (TDAG51/PHLDA1) in the regulation of maternal and depressive-like behavior. After parturition, TDAG51-deficient dams showed impaired maternal behavior in pup retrieving, nursing and nest building tests. In contrast to the normal dams, the TDAG51-deficient dams also exhibited more sensitive depressive-like behaviors after parturition. Furthermore, changes in the expression levels of various maternal and depressive-like behavior-associated genes regulating neuroendocrine factor and monoamine neurotransmitter levels were observed in TDAG51-deficient postpartum brain tissues. These findings indicate that TDAG51 plays a protective role against maternal care defects and depressive-like behavior after parturition. Thus, TDAG51 is a maternal care-associated gene that functions as a crucial regulator of maternal and depressive-like behavior after parturition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism
  • Depressive Disorder / genetics*
  • Depressive Disorder / physiopathology
  • Female
  • Gene Expression Regulation / genetics
  • Humans
  • Maternal Behavior*
  • Mice
  • Mice, Knockout
  • Neurotransmitter Agents / genetics
  • Parturition / genetics*
  • Parturition / physiology
  • Pregnancy
  • Transcription Factors / genetics*

Substances

  • Neurotransmitter Agents
  • Phlda1 protein, mouse
  • Transcription Factors

Grants and funding

This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) and was funded by the Ministry of Education (NRF-2014R1A1A2057884 and NRF-2017R1A2B4007327), by the research fund of Chungnam National University, and by a Ministry of National Defense Foundation grant (ADD: 14-01-06-06). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.