The regulatory role of cytokines on neurodevelopment and behaviour during the early postnatal period : An investigation on the impact of TNF on mouse behaviour in the early postnatal period and a novel approach of data analysis applied to the immune activation mouse model of autism

Overview & Synopsis

Both preclinical and clinical studies have shown that immune activation and inflammation during the early stages of neurodevelopment increase the risk of neurodevelopment disorders and behaviour abnormalities in adults. While the underlying mechanisms have only been partially elucidated, experiments in the maternal immune activation mouse model (MIA) – in which pregnant dams are injected with the viral mimic poly(I:C) – have demonstrated the critical role of two cytokines: interleukin (IL)-6 and IL-17A. However, the vast majority of the studies performed to date have used behavioural tests in adult mice as a read out to study the impact of cytokines on neurodevelopment. Therefore, it is not clear whether altered levels of other cytokines during the perinatal period could impact neurodevelopment and behaviour in infant mice. To address this issue, we have analysed the progeny of several cohorts of poly(I:C)- and saline-injected mothers for behaviour between postnatal day 5 (P5) and P15 and serum cytokine levels at P15. Because both perinatal neurodevelopment and cytokine production are known or believed to be impacted by many environmental variables, we analysed our data using a multivariable statistical model to identify features associated with being born to a poly(I:C)-injected mother (as opposed to being born to a saline-injected mother). We found that the drop of body weight and temperature of the mother after poly(I:C) injection, the litter size, the pup weight at P15, the number of ultrasonic vocalizations (USV) emitted by the pup at P6, the distance travelled by the pup and the time it spent mobile at P13, as well as serum levels of Tumour Necrosis Factor (TNF), IL-5, IL-15 and C-X-C motif chemokine (CXCL)10 were all associated with altered odds of being born to a poly(I:C)-injected mother. To further explore the role of TNF during the early postnatal period, we injected mouse pups daily from P1 to P5 and assessed these animals for both developmental milestones and behaviour from P8 to P15. Unexpectedly, injection of recombinant TNF did not have a detrimental impact on neurodevelopment but rather promoted sensorimotor reflexes acquisition and exploratory behaviour. Altogether, our results confirm that cytokines play a critical role during neurodevelopment and that altered levels of specific cytokines, and in particular TNF, could regulate the acquisition of developmental milestones and behaviour in infant mice. While we have only obtained preliminary insights into underlying mechanisms, the protocols that we have developed provide a framework for further studies.