Parvalbumin interneurons in human ventromedial prefrontal cortex: a comprehensive post-mortem study of myelination and perineuronal nets in neurotypical individuals and depressed suicides with and without a history of child abuse

Cereb Cortex. 2024 May 2;34(5):bhae197. doi: 10.1093/cercor/bhae197.

Abstract

Cortical parvalbumin interneurons (PV+) are major regulators of excitatory/inhibitory information processing, and their maturation is associated with the opening of developmental critical periods (CP). Recent studies reveal that cortical PV+ axons are myelinated, and that myelination along with perineuronal net (PNN) maturation around PV+ cells is associated with the closures of CP. Although PV+ interneurons are susceptible to early-life stress, their relationship between their myelination and PNN coverage remains unexplored. This study compared the fine features of PV+ interneurons in well-characterized human post-mortem ventromedial prefrontal cortex samples (n = 31) from depressed suicides with or without a history of child abuse (CA) and matched controls. In healthy controls, 81% of all sampled PV+ interneurons displayed a myelinated axon, while a subset (66%) of these cells also displayed a PNN, proposing a relationship between both attributes. Intriguingly, a 3-fold increase in the proportion of unmyelinated PV+ interneurons with a PNN was observed in CA victims, along with greater PV-immunofluorescence intensity in myelinated PV+ cells with a PNN. This study, which is the first to provide normative data on myelination and PNNs around PV+ interneurons in human neocortex, sheds further light on the cellular and molecular consequences of early-life adversity on cortical PV+ interneurons.

Keywords: child abuse; myelin; parvalbumin; perineuronal nets; post-mortem ventromedial prefrontal cortex.

MeSH terms

  • Adult
  • Aged
  • Autopsy
  • Child Abuse / psychology
  • Female
  • Humans
  • Interneurons* / metabolism
  • Interneurons* / pathology
  • Male
  • Middle Aged
  • Myelin Sheath / metabolism
  • Myelin Sheath / pathology
  • Parvalbumins* / metabolism
  • Prefrontal Cortex* / metabolism
  • Prefrontal Cortex* / pathology
  • Suicide
  • Young Adult