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http://purl.uniprot.org/citations/38161286http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/38161286http://www.w3.org/2000/01/rdf-schema#comment"

Objectives

Chronic hyperglycemia is considered as an important factor to promote the neurodegenerative process of brain, and the synaptic plasticity as well as heterogeneity of hippocampal cells are thought to be associated with cognitive dysfunction in the early process of neurodegeneration. To date, fibronectin type III domain-containing protein 5 (FNDC5) has been highlighted its protective role in multiple neurodegenerative diseases. However, the potential molecular and cellular mechanisms of FNDC5 on synaptic plasticity regulation in cognitive impairment (CI) induced by diabetics are still need to known.

Methods/design

To investigate the heterogeneity and synaptic plasticity of hippocampus in animals with CI state induced by hyperglycemia, and explore the potential role of FNDC5 involved in this process. Firstly, the single cell sequencing was performed based on the hippocampal tissue from db diabetic mice induced CI and normal health control mice by ex vivo experiments; and then the integrated analysis and observations validation using Quantitative Real-time PCR, western blot as well as other in vitro studies.

Results

We observed and clarified the sub-cluster of type IC spiral ganglion neurons expressed marker genes as Trmp3 and sub-cluster of astrocytes with marker gene as Atp1a2 in hippocampal cells from diabetic animals induced CI and the effect of those on neuron-glial communication. We also found that FNDC5\BDNF-Trk axis was involved in the synaptic plasticity regulation of hippocampus. In high glucose induced brain injury model in vitro, we investigated that FNDC5 significantly regulates BDNF expression and that over-expression of FNDC5 up-regulated BDNF expression (p < 0.05) and can also significantly increase the expression of synapsin-1 (p < 0.05), which is related to synaptic plasticity, In addition, the unbalanced methylation level between H3K4 and H3K9 in Fndc5 gene promoter correlated with significantly down-regulated expression of FNDC5 (p < 0.05) in the hyperglycemia state.

Conclusion

The current study revealed that the synaptic plasticity of hippocampal cells in hyperglycemia might be regulated by FNDC5\BDNF-Trk axis, playing the protective role in the process of CI induced by hyperglycemia and providing a target for the early treatment of hyperglycemia induced cognitive dysfunction in clinic."xsd:string
http://purl.uniprot.org/citations/38161286http://purl.org/dc/terms/identifier"doi:10.1002/gps.6047"xsd:string
http://purl.uniprot.org/citations/38161286http://purl.uniprot.org/core/author"Xiang Q."xsd:string
http://purl.uniprot.org/citations/38161286http://purl.uniprot.org/core/author"Deng J."xsd:string
http://purl.uniprot.org/citations/38161286http://purl.uniprot.org/core/author"Liu L.N."xsd:string
http://purl.uniprot.org/citations/38161286http://purl.uniprot.org/core/author"Fu C.J."xsd:string
http://purl.uniprot.org/citations/38161286http://purl.uniprot.org/core/author"Li X.H."xsd:string
http://purl.uniprot.org/citations/38161286http://purl.uniprot.org/core/author"Tao J.S."xsd:string
http://purl.uniprot.org/citations/38161286http://purl.uniprot.org/core/author"Liao L.X."xsd:string
http://purl.uniprot.org/citations/38161286http://purl.uniprot.org/core/date"2024"xsd:gYear
http://purl.uniprot.org/citations/38161286http://purl.uniprot.org/core/name"Int J Geriatr Psychiatry"xsd:string
http://purl.uniprot.org/citations/38161286http://purl.uniprot.org/core/pages"e6047"xsd:string
http://purl.uniprot.org/citations/38161286http://purl.uniprot.org/core/title"The integrated analysis and underlying mechanisms of FNDC5 on diabetic induced cognitive deficits."xsd:string
http://purl.uniprot.org/citations/38161286http://purl.uniprot.org/core/volume"39"xsd:string
http://purl.uniprot.org/citations/38161286http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/38161286
http://purl.uniprot.org/citations/38161286http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/38161286
http://purl.uniprot.org/uniprot/#_Q8K4Z2-mappedCitation-38161286http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/38161286
http://purl.uniprot.org/uniprot/Q8K4Z2http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/38161286