Some studies found an increase in the expression of the microglial marker Iba-1 in the brains of alcoholic individuals (see figure 2) (He and Crews 2008), suggesting that microglia contribute to the neurobiology of alcoholism. Microglia in postmortem human alcoholic brain and chronic alcohol-treated mouse and rat brain show increased MHC gene expression, but not the bushy or phagocytic activation profiles associated with marked brain damage. Chronic ethanol treatment also increases microglial TLR4 expression (Vetreno et al. 2013). Thus, microglia are the only immune cells in healthy brain and are integrated into the brain’s responses to both neurotransmitters and neuroimmune signals. They also seem to contribute to chronic alcohol-induced responses.