Abstract

Hippocampal neurogenesis is linked with a cognitive process under a normal physiological condition including learning, memory, pattern separation, and cognitive flexibility. Hippocampal neurogenesis is altered by multiple factors such as the systemic metabolic changes. NADPH oxidase 4 (NOX4) has been implicated in the regulation of brain function. While the role of NOX4 plays in the brain, the mechanism by which NOX4 regulates hippocampal neurogenesis under metabolic stress is unclear. In this case, we show that NOX4 deficiency exacerbates the impairment of hippocampal neurogenesis by inhibiting neuronal maturation by a chronic high fat diet (HFD). NOX4 deficiency resulted in less hippocampal neurogenesis by decreasing doublecortin (DCX)-positive neuroblasts, a neuronal differentiation marker, and their branched-dendrites. Notably, NOX4 deficiency exacerbates the impairment of hippocampal neurogenesis by chronic HFD. Moreover, NOX4 deficiency had a significant reduction of Cystatin C levels, which is critical for hippocampal neurogenesis, under chronic HFD as well as normal chow (NC) diet. Furthermore, the reduction of Cystatin C levels was correlated with the impairment of hippocampal neurogenesis in NOX4 deficient and wild-type (WT) mice under chronic HFD. Our results suggest that NOX4 regulates the impairment of Cystatin C-dependent hippocampal neurogenesis under chronic HFD.

Highlights

  • Hippocampal neurogenesis is critical for learning and memory function in the brain

  • To investigate the role of NADPH oxidase 4 (NOX4) in hippocampal neurogenesis under chronic high fat diet (HFD), we examined whether genetic deficiency of NOX4 could affect the impairment of hippocampal neurogenesis by chronic HFD

  • We examined whether NOX4 deficiency could reduce fat accumulation in epididymal white adipose tissue

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Summary

Introduction

Hippocampal neurogenesis is regulated by cell proliferation, neuronal differentiation, and cell survival in the granular cell layer (GCL) of the dentate gyrus (DG) and the adjacent sub-granular zone (SGZ) [1]. These three critical components of neurogenesis can be modulated by multiple factors [2,3]. These factors can depend on human behavior or the environmental factor and can increase or decrease the formation of new neurons during adulthood [2] They are critical for understanding the relevance of adult neurogenesis on a functional basis, either behaviorally, cognitively, or clinically [2]

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