A probe for NIR-II imaging and multimodal analysis of early Alzheimer's disease by targeting CTGF.
Cao LuCong MengYuying LiJinling YuanXiaojun RenLiang GaoDongdong SuKai CaoMeng-Chao CuiQing YuanXueyun GaoPublished in: Nature communications (2024)
To date, earlier diagnosis of Alzheimer's disease (AD) is still challenging. Recent studies revealed the elevated expression of connective tissue growth factor (CTGF) in AD brain is an upstream regulator of amyloid-beta (Aβ) plaque, thus CTGF could be an earlier diagnostic biomarker of AD than Aβ plaque. Herein, we develop a peptide-coated gold nanocluster that specifically targets CTGF with high affinity (KD ~ 21.9 nM). The probe can well penetrate the blood-brain-barrier (BBB) of APP/PS1 transgenic mice at early-stage (earlier than 3-month-old) in vivo, allowing non-invasive NIR-II imaging of CTGF when there is no appearance of Aβ plaque deposition. Notably, this probe can also be applied to measuring CTGF on postmortem brain sections by multimodal analysis, including fluorescence imaging, peroxidase-like chromogenic imaging, and ICP-MS quantitation, which enables distinguishment between the brains of AD patients and healthy people. This probe possesses great potential for precise diagnosis of earlier AD before Aβ plaque formation.
Keyphrases
- fluorescence imaging
- photodynamic therapy
- growth factor
- living cells
- high resolution
- early stage
- coronary artery disease
- quantum dots
- fluorescent probe
- mass spectrometry
- end stage renal disease
- ms ms
- cognitive decline
- ejection fraction
- multiple sclerosis
- poor prognosis
- newly diagnosed
- chronic kidney disease
- hydrogen peroxide
- blood brain barrier
- peritoneal dialysis
- drug delivery
- single cell
- radiation therapy
- liquid chromatography tandem mass spectrometry
- risk assessment
- single molecule
- human health