“…When in this polarization state, microglia induce neuroinflammation by producing proinflammatory cytokines, nitric oxide (NO), and reactive oxygen species (ROS), which can lead to neural damage and impaired neurogenesis. , Moreover, M1 microglia can trigger astrocyte infiltration and activation (astrogliosis) . This can result in glial scar formation, which can form a barrier surrounding the injured region that prevents neuronal/axonal extension. , In contrast, M2 microglia are activated by interleukin 4 (IL-4) and IL-13, which induce neurogenesis and brain tissue regeneration by secreting anti-inflammatory neurotrophic factors such as IL-10, transforming growth factor-β (TGF-β), insulin-like growth factor 1 (IGF-1), basic fibroblast growth factor (bFGF), and brain-derived neurotrophic factor (BDNF). ,,, The shift from M2 microglia to M1 microglia has been associated with increased injury progression in stroke and TBI. , Hence, modulating microglial polarization from M1 toward M2 is considered as a potential therapeutic strategy for CNS regeneration and disease treatment. ,, …”