TonEBP Haploinsufficiency Attenuates Microglial Activation and Memory Deficits in Middle-Aged and Amyloid β Oligomer-Treated Mice.
Jong Youl LeeEun Ae JeongJaewoong LeeHyun Joo ShinSo Jeong LeeHyeong Seok AnKyung Eun KimWon-Ho KimYong Chul BaeHeeyoung KangGu Seob RohPublished in: Cells (2023)
Age-related microglial activation is associated with cognitive impairment. Tonicity-responsive enhancer-binding protein (TonEBP) is a critical mediator of microglial activation in response to neuroinflammation. However, the precise role of TonEBP in the middle-aged brain is not yet known. We used TonEBP haploinsufficient mice to investigate the role of TonEBP in middle-aged or amyloid β oligomer (AβO)-injected brains and examined the effect of TonEBP knockdown on AβO-treated BV2 microglial cells. Consistent with an increase in microglial activation with aging, hippocampal TonEBP expression levels were increased in middle-aged (12-month-old) and old (24-month-old) mice compared with young (6-month-old) mice. Middle-aged TonEBP haploinsufficient mice showed reduced microglial activation and fewer memory deficits than wild-type mice. Electron microscopy revealed that synaptic pruning by microglial processes was reduced by TonEBP haploinsufficiency. TonEBP haploinsufficiency also reduced dendritic spine loss and improved memory deficits in AβO-treated mice. Furthermore, TonEBP knockdown attenuated migration and phagocytosis in AβO-treated BV2 cells. These findings suggest that TonEBP plays important roles in age-related microglial activation and memory deficits.
Keyphrases
- middle aged
- lipopolysaccharide induced
- lps induced
- inflammatory response
- wild type
- high fat diet induced
- traumatic brain injury
- neuropathic pain
- binding protein
- cognitive impairment
- induced apoptosis
- working memory
- poor prognosis
- metabolic syndrome
- type diabetes
- insulin resistance
- spinal cord injury
- cell proliferation
- cell death
- transcription factor
- signaling pathway
- single cell
- brain injury
- subarachnoid hemorrhage
- blood brain barrier
- electron microscopy
- cerebral ischemia
- cell cycle arrest
- functional connectivity