Evidence map›Paper›PMID 39915794›Full record

ArticleProteome science2025

MiR-18a-LncRNA NONRATG-022419 pairs targeted PRG-1 regulates diabetic induced cognitive impairment by regulating NGF\BDNF-Trkb signaling pathway.

Qiong Xiang, Hu Lin, Jia-Sheng Tao, Chuan-Jun Fu, Li-Ni Liu, Jing Deng, Xian-Hui Li

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Article in Proteome science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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5 · Who and what money

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7 authors.

Qiong XiangInstitute of Medicine, Medical Research Center, Jishou University, Hunan, China.
Hu Lin *Institute of Medicine, Jishou University, Ren min south road 120#, Jishou, Hunan, 416000, China.
Jia-Sheng Tao *Institute of Medicine, Medical Research Center, Jishou University, Hunan, China.
Chuan-Jun Fu *Institute of Medicine, Medical Research Center, Jishou University, Hunan, China.
Li-Ni LiuInstitute of Medicine, Medical Research Center, Jishou University, Hunan, China.
Jing DengInstitute of Medicine, Medical Research Center, Jishou University, Hunan, China.
Xian-Hui LiInstitute of Medicine, Jishou University, Ren min south road 120#, Jishou, Hunan, 416000, China. lxh_surgeon@yeah.net.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetic encephalopathy (DE) is considered as one of the complications of diabetes,which is associated with cognitive impairment in the pathological process of development. Up to now, phospholipid phosphatase related 4 (Plppr4), also known as plasticity related gene 1 (PRG-1) has been revealed its important role in neuroplasticity. However, the underlying mechanisms of Plppr4 on the basis of diabetic-induced cognitive dysfunction (DCD) are still unknown. The aim of current study was to provide insight into molecular mechanism and cellular heterogeneity underlying DCD, and investigate the functional role of PRG-1 involved in this process.

methodsCombined Single-cell RNA sequencing (scRNA-seq) and RNA transcriptome analysis, the distinct sub-populations, functional heterogeneity as well as potential enriched signaling pathways of hippocampal cells could be elucidated.

resultsWe identified the sub-cluster of type I spiral ganglion neurons expressed marker gene as Amigo2 in cluster8 and Cnr1 in cluster 9 of hippocampal cells from DCD and the effect of those on neuronal cells interaction. We also found that PRG-1 was involved in the synaptic plasticity regulation of hippocampus via NGF\BDNF-Trkb signaling pathway. In high glucose induced HT22 cells injury model in vitro, we investigated that down-regulated PRG-1 along with down-regulated BDNF and also decreased expression of synapsin-1, PSD-95, SYN which are related to synaptic plasticity; Meanwhile, the Prg-1 targeted miR-18a-LncRNA NONRATG-022419 pairs related with significantly down-regulated expression of PRG-1.

conclusionThis study revealed the synaptic plasticity regulation of PRG-1 in DCD, and might provide the therapeutic target and potential biomarkers for early interventions in DCD patients.

Indexed as

Diabetic encephalopathyDiabetic induced cognitive dysfunctionHippocampusPRG-1Synaptic plasticity regulationType I spiral ganglion neurons

Identifiers

PMID39915794
PMCPMC11800523

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