کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5040950 | 1473908 | 2017 | 9 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Microglial production of TNF-alpha is a key element of sustained fear memory Microglial production of TNF-alpha is a key element of sustained fear memory](/preview/png/5040950.png)
- Footshock-induced microglial TNF-α production remained high as fear memory retained.
- Microglial TNF-α returned to baseline in the process of fear memory extinction.
- Inhibition of TNF-α facilitated fear memory extinction.
- TNF-α inhibitors might be candidate remedies for posttraumatic stress disorder.
The proinflammatory cytokine productions in the brain are altered in a process of fear memory formation, indicating a possibility that altered microglial function may contribute to fear memory formation. We aimed to investigate whether and how microglial function contributes to fear memory formation. Expression levels of M1- and M2-type microglial marker molecules in microglia isolated from each conditioned mice group were assessed by real-time PCR and immunohistochemistry. Levels of tumor necrosis factor (TNF)-α, but not of other proinflammatory cytokines produced by M1-type microglia, increased in microglia from mice representing retention of fear memory, and returned to basal levels in microglia from mice representing extinction of fear memory. Administration of inhibitors of TNF-α production facilitated extinction of fear memory. On the other hand, expression levels of M2-type microglia-specific cell adhesion molecules, CD206 and CD209, were decreased in microglia from mice representing retention of fear memory, and returned to basal levels in microglia from mice representing extinction of fear memory. Our findings indicate that microglial TNF-α is a key element of sustained fear memory and suggest that TNF-α inhibitors can be candidate molecules for mitigating posttraumatic reactions caused by persistent fear memory.
Journal: Brain, Behavior, and Immunity - Volume 59, January 2017, Pages 313-321