TLR4 Deletion Improves Cognitive Brain Function and Structure in Aged Mice

• Published in: Neuroscience Vol. 492; pp. 1 - 17
• Main Authors: Fei, Xiaowei, Dou, Ya-nan, Lv, Weihao, Ding, Boyun, Wei, Jialiang, Wu, Xiuquan, He, Xin, Fei, Zhou, Fei, Fei
• Format: Journal Article
• Language: English
• Published: United States Elsevier Ltd 01.06.2022
• Subjects: blood–brain barrier; cerebral blood flow; inflammatory factors; learning and memory; neurobehavioral function; TLR4; MWM; BBB; CBF; WB; ICH; PTSD; Aβ; blood–brain barrier; PD; learning and memory; ANOVA; cerebral blood flow; TBI; neurobehavioral function; HE; TLR4; inflammatory factors; PCR; TLRs
• ISSN: 0306-4522; 1873-7544
• DOI: 10.1016/j.neuroscience.2022.04.007

•TLR4 deletion improves behavioral dysfunction in aged mice.•TLR4 deletion enhanced the learning and memory ability of aged mice.•TLR4 deletion improves the integrity of blood–brain barrier in aged mice.•TLR4 deletion inhibits the release of proinflammatory factors in aged mice.•TLR4 deletion had no effect on the visual acuity of aged mice. Toll-like receptor-4 (TLR4), a member of the TLR family, plays a key role in inflammation-related diseases of the nervous system. TLR4 knockout mice are widely used in various neurological disease studies, and there is a clear correlation between inflammation and behavior. Therefore, elucidating the effect of TLR4 on neurobehavioral function is essential, and the related mechanisms need to be explored. Male TLR4 knockout (TLR4−/−) and wild-type (TLR4+/+) mice of different ages (4, 8, and 16 months) were used for behavioral experiments. Synaptic spine, blood–brain barrier (BBB) integrity, memory regulatory proteins, cortical blood flow, and inflammatory factor examinations were also conducted to explore the possible mechanism by which TLR4 works. Here, we found that compared with 16-m-old TLR4+/+ mice, age-matched TLR4−/− mice had better learning and memory abilities, increased expression of neuronal synaptic spines, and increased memory-related regulatory proteins in the hippocampus. TLR4 knockout significantly attenuated the fear response in 16-m-old mice. The TLR4−/− mice also had better blood–brain barrier integrity, increased expression of tight junction-associated proteins, increased cerebral cortical blood flow and reduced proinflammatory cytokine expression in the cortex and cerebrospinal fluid. Our results suggest that TLR4 deletion ameliorates significant neurobehavioral dysfunction during the aging stage, as well as multiple abnormalities in brain function and structure due to alterations in tight junction-associated proteins and inflammatory factors.