Intraventricular IL-17A administration activates microglia and alters their localization in the mouse embryo cerebral cortex
Viral infection during pregnancy has been suggested to increase the probability of autism spectrum disorder (ASD) in offspring via the phenomenon of maternal immune activation (MIA). This has been modeled in rodents. Maternal T helper 17 cells and the effector cytokine, interleukin 17A (IL-17A), play a central role in MIA-induced behavioral abnormalities and cortical dysgenesis, termed cortical patch. However, it is unclear how IL-17A acts on fetal brain cells to cause ASD pathologies. To assess the effect of IL-17A on cortical development, we directly administered IL-17A into the lateral ventricles of the fetal mouse brain. We analyzed injected brains focusing on microglia, which express IL-17A receptors. We found that IL-17A activated microglia and altered their localization in the cerebral cortex. Our data indicate that IL-17A activates cortical microglia, which leads to a cascade of ASD-related brain pathologies, including excessive phagocytosis of neural progenitor cells in the ventricular zone.

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Posted 03 Jun, 2020
On 16 Jun, 2020
On 03 Jun, 2020
Received 31 May, 2020
On 28 May, 2020
Invitations sent on 28 May, 2020
On 26 May, 2020
On 25 May, 2020
On 25 May, 2020
Received 15 May, 2020
On 15 May, 2020
Received 06 May, 2020
On 02 May, 2020
Invitations sent on 02 May, 2020
On 02 May, 2020
On 28 Apr, 2020
On 27 Apr, 2020
On 27 Apr, 2020
On 24 Apr, 2020
Intraventricular IL-17A administration activates microglia and alters their localization in the mouse embryo cerebral cortex
Posted 03 Jun, 2020
On 16 Jun, 2020
On 03 Jun, 2020
Received 31 May, 2020
On 28 May, 2020
Invitations sent on 28 May, 2020
On 26 May, 2020
On 25 May, 2020
On 25 May, 2020
Received 15 May, 2020
On 15 May, 2020
Received 06 May, 2020
On 02 May, 2020
Invitations sent on 02 May, 2020
On 02 May, 2020
On 28 Apr, 2020
On 27 Apr, 2020
On 27 Apr, 2020
On 24 Apr, 2020
Viral infection during pregnancy has been suggested to increase the probability of autism spectrum disorder (ASD) in offspring via the phenomenon of maternal immune activation (MIA). This has been modeled in rodents. Maternal T helper 17 cells and the effector cytokine, interleukin 17A (IL-17A), play a central role in MIA-induced behavioral abnormalities and cortical dysgenesis, termed cortical patch. However, it is unclear how IL-17A acts on fetal brain cells to cause ASD pathologies. To assess the effect of IL-17A on cortical development, we directly administered IL-17A into the lateral ventricles of the fetal mouse brain. We analyzed injected brains focusing on microglia, which express IL-17A receptors. We found that IL-17A activated microglia and altered their localization in the cerebral cortex. Our data indicate that IL-17A activates cortical microglia, which leads to a cascade of ASD-related brain pathologies, including excessive phagocytosis of neural progenitor cells in the ventricular zone.

Figure 1

Figure 2

Figure 3

Figure 4