Effects of early life adversity on immediate early gene expression: Systematic review and 3-level meta-analysis of rodent studies

PLoS One. 2022 Jan 13;17(1):e0253406. doi: 10.1371/journal.pone.0253406. eCollection 2022.

Abstract

Early-life adversity (ELA) causes long-lasting structural and functional changes to the brain, rendering affected individuals vulnerable to the development of psychopathologies later in life. Immediate-early genes (IEGs) provide a potential marker for the observed alterations, bridging the gap between activity-regulated transcription and long-lasting effects on brain structure and function. Several heterogeneous studies have used IEGs to identify differences in cellular activity after ELA; systematically investigating the literature is therefore crucial for comprehensive conclusions. Here, we performed a systematic review on 39 pre-clinical studies in rodents to study the effects of ELA (alteration of maternal care) on IEG expression. Females and IEGs other than cFos were investigated in only a handful of publications. We meta-analyzed publications investigating specifically cFos expression. ELA increased cFos expression after an acute stressor only if the animals (control and ELA) had experienced additional hits. At rest, ELA increased cFos expression irrespective of other life events, suggesting that ELA creates a phenotype similar to naïve, acutely stressed animals. We present a conceptual theoretical framework to interpret the unexpected results. Overall, ELA likely alters IEG expression across the brain, especially in interaction with other negative life events. The present review highlights current knowledge gaps and provides guidance to aid the design of future studies.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Animals
  • Brain / metabolism
  • Cytoskeletal Proteins / genetics
  • Early Growth Response Protein 1 / genetics
  • Gene Expression / physiology*
  • Genes, Immediate-Early / genetics*
  • Male
  • Nerve Tissue Proteins / genetics
  • Proto-Oncogene Proteins c-fos / genetics
  • Rodentia
  • Stress, Psychological*

Substances

  • Cytoskeletal Proteins
  • Early Growth Response Protein 1
  • Nerve Tissue Proteins
  • Proto-Oncogene Proteins c-fos
  • activity regulated cytoskeletal-associated protein

Grants and funding

MJ (Consortium of Individual Development, which is funded through the Gravitation program of the Dutch Ministry of Education, Culture, and Science and the Netherlands Organization for Scientific Research; grant number: 024.001.003). RAS (ZoNmW program MKMD; grant number 114024135). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.