Abstract

Altered dendritic morphology is common in neurodevelopmental disorders (NDDs), many of which show sex biases in prevalence, onset and/or severity. However, whether dendritic morphology varies as a function of sex in juvenile mice or primary neuronal cell cultures is largely unknown even though both are widely used models for studying NDDs. To address this gap, we quantified dendritic morphology in CA1 pyramidal hippocampal and adjacent somatosensory pyramidal cortical neurons from male and female postnatal day (P)28 C57BL/6J mice. As determined by Sholl analysis of Golgi-stained brain sections, dendritic arbors of male hippocampal neurons are more complex than females. Conversely, dendritic morphology of female cortical neurons is more complex than males. In primary neuron-glia co-cultures from P0 mouse hippocampi, male neurons have more complex dendritic arbors than female neurons. Sex differences are less pronounced in cortical cultures. In vitro sex differences in dendritic morphology are driven in part by estrogen-dependent mechanisms, as evidenced by decreased dendritic complexity in male hippocampal neurons cultured in phenol red-free media or in the presence of an estrogen receptor antagonist. Evidence that sex influences dendritic morphogenesis in two models of neurodevelopment in a region-specific manner has significant mechanistic implications regarding sex biases in NDDs.

Highlights

  • While neurodevelopmental disorders (NDDs) such as autism spectrum disorder (ASD), attention deficit and hyperactivity disorder (ADHD) and schizophrenia affect both sexes[1, 2], they show a clear sex bias in onset, severity and/or prevalence[3, 4]

  • Our preliminary studies of Golgi-stained neurons in the hippocampus of P28 C57BL/6J mice suggested that the basilar dendritic arbor of CA1 pyramidal hippocampal neurons is significantly more complex in male compared to female hippocampal neurons[45]

  • We used Golgi staining to visualize individual pyramidal neurons in the CA1 hippocampus and adjacent somatosensory cortex of P28 male and female juvenile mice, an age previously examined for effects of early life stresses, including environmental exposures, on neurodevelopment[43, 48, 49]

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Summary

Introduction

While neurodevelopmental disorders (NDDs) such as autism spectrum disorder (ASD), attention deficit and hyperactivity disorder (ADHD) and schizophrenia affect both sexes[1, 2], they show a clear sex bias in onset, severity and/or prevalence[3, 4]. More recent data demonstrate sex differences in brain structure, and in neuronal cytoarchitecture, the morphology of dendrites This is critically important because dendritic morphology is a major determinant of neuronal connectivity[36,37,38], which is often perturbed in NDDs8, 30, 31, 39, 40. Our preliminary studies of Golgi-stained neurons in the hippocampus of P28 C57BL/6J mice suggested that the basilar dendritic arbor of CA1 pyramidal hippocampal neurons is significantly more complex in male compared to female hippocampal neurons[45] We extend those studies to further characterize sex differences in the dendritic morphology of CA1 pyramidal hippocampal neurons and determine whether sex differences are generalized to pyramidal neurons in the somatosensory cortex of P28 mice. To determine whether sex differences are observed in vitro, we quantified dendritic arborization in primary cell cultures derived from the hippocampus and neocortex of male versus female mouse pups at P0, which are widely used models for characterizing factors that influence dendritic arborization[46, 47]

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