When neurons behave like a double-edged sword

If a neuron can be viewed as a battery that stores and discharges electricity, then its intrinsic excitability can be viewed as the battery's storage capacity. While higher energy storage is usually viewed positively, overcharging a battery could cause it to overheat and become damaged.

Like all immune cells,microgliaserve to kill off pathogens and infections, and their activity is known to regulate the intrinsic excitability of neurons. Yet, when microglia are over-stimulated, they can cause inflammation, pain, and other ailments.

"For example, unmanaged intrinsic excitability has been attributed to psychiatric diseases, like mood disorders," explains author Gen Ohtsuki of Kyoto University.

Current knowledge on neuronal regulation comes from experiments analyzingPurkinje cells. These neurons are found in the cerebellum, which is considered an evolutionarily ancient part of the brain and responsible for motor control. Less understood are the effects on the intrinsic excitability ofpyramidal cells, which are neurons found in the cortex: the part of the brain associated with higher-level thinking.

The team observed that calcium-activatedSK ion channelsin pyramidal cells were modulated by microglia, which is the same for Purkinje cells. However, in pyramidal cells, SK channels were upregulated, while they were downregulated in Purkinje cells.

"The effects were completely opposite," notes Ohtsuki.

The pyramidal cells appeared to react to the samecytokine--TNFaortumor necrosis factor alpha-- secreted by activated microglia: one of the most common cytokines released by immune cells in response to an infection.

However, the difference in SK channel regulation resulted in lower intrinsic excitability of pyramidal cells but higher intrinsic excitability of Purkinje cells. These inverted responses ordirectionalitiesto the same input are not uncommon between Purkinje and pyramidal cells and have also been seen withsynaptic plasticity.

Ohtsuki cautions that: "The effects of microglia in one part of the brain should not be generalized to the entire organ. Our findings show that we need to study different brain regions separately to understand how microglia regulate neuronal function and how immunity impairs plasticity of neurons in psychiatric-diseased brains."