The novel role of Kallistatin in linking metabolic syndromes and cognitive memory deterioration by inducing amyloid-β plaques accumulation and tau protein hyperphosphorylation
Weiwei QiiD, Yanlan LongiD, Ziming LiiD, Zhen ZhaoiD, Jinhui Shi, Wanting XieiD, Laijian WangiD, Yandan Tan, Ti ZhouiD, Minting LiangiD, Ping Jiang, Bin JiangiD, Xia YangiD, Guoquan GaoiD
Abstract
Accumulation of amyloid {beta} (A{beta}) peptides and hyperphosphorylated tau proteins in the hippocampus triggers cognitive memory decline in Alzheimers disease (AD). The incidence and mortality of sporadic AD were tightly associated with diabetes and hyperlipidemia, while the exact linked molecular is uncertain. Here, we reported that serum Kallistatin concentrations were meaningfully higher in AD patients, with a higher concentration of fasting blood glucose and triglyceride. In addition, the constructed Kallistatin-transgenic (KAL-TG) mice defined its cognitive memory impairment phenotype and lower LTP in hippocampal CA1 neurons accompanied by increased A{beta} deposition and tau phosphorylation. Mechanistically, Kallistatin could directly bind to the Notch1 receptor and thereby upregulate BACE1 expression by inhibiting PPAR{gamma} signaling, resulting in A{beta} cleavage and production. Besides, Kallistatin could promote the phosphorylation of tau by activating GSK-3{beta}. Fenofibrate, a hypolipidemic drug, could alleviate cognitive memory impairment by down-regulating A{beta} and tau phosphorylation of KAL-TG mice. Collectively, our data clarified a novel mechanism for A{beta} accumulation and tau protein hyperphosphorylation regulation by Kallistatin, which might play a crucial role in linking metabolic syndromes and cognitive memory deterioration, and suggested that fenofibrate might have the potential for treating metabolism-related AD. HighlightsO_LIKallistatin-transgenic (KAL-TG) mice defined its cognitive memory impairment phenotype accompanied by increased A{beta} deposition and tau phosphorylation. C_LIO_LIKallistatin could directly bind to the Notch1 receptor and thereby upregulate BACE1 expression by inhibiting PPAR{gamma} signaling. C_LIO_LIFenofibrate could alleviate cognitive memory impairment and down-regulate the serum Kallistatin level. C_LI
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 1
- FWCI
- 0.65
- Field percentile
- top 31%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Catestatin ameliorates tauopathy and amyloidogenesis via adrenergic inhibition
Suborno Jati, Satadeepa Kal, … Sushil K. Mahata·bioRxiv·Jan 4, 2026
- Ketogenic interventions restore cognition and modulate peripheral metabolic dysfunctions in Alzheimer's disease mouse models
Paule E. H. M’Bra, Laura K. Hamilton, … Karl J. L. Fernandes·bioRxiv·Sep 4, 2024
- Tau accumulation activates STAT1 triggering memory deficits via suppressing NMDA receptor expression
Xiao-Guang Li, Xiao-Yue Hong, … Jian‐Zhi Wang·EMBO ReportsPeer-reviewed·May 13, 2019
- Exenatide reverts the high-fat-diet-induced impairment of BDNF signaling and inflammatory response in an animal model of Alzheimer’s disease
Manuela Bomba, Alberto Granzotto, … Stefano Luca Sensi·Journal of Alzheimer s DiseasePeer-reviewed·Jan 1, 2018
- Impairment of hippocampal astrocyte-mediated striatal dopamine release and locomotion in Alzheimer's disease
Benjamin B. Tournier, Kelly Ceyzériat, … P. Millet·NeuroImagePeer-reviewed·Aug 8, 2024
- TREK1 upregulation is an endogenous mechanism delaying cognitive decline in Alzheimer's Disease
Tuhina Mitra, Ranjit Bhoi, … Swagata Ghatak·bioRxiv·Oct 16, 2025