The fluorescent ligand bTVBT2 reveals increased p-tau uptake by retinal microglia in Alzheimer’s disease patients and App NL−F/NL−F mice

Abstract Background Amyloid beta (Aβ) deposits and hyperphosphorylated tau (p-tau) accumulation have been identified in the retina of Alzheimer’s disease (AD) patients and transgenic AD mice. Previous studies have shown that retinal microglia engulf Aβ, but this property decreases in AD patients. Wh...

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Main Authors: Cristina Nuñez-Diaz, Emelie Andersson, Nina Schultz, Dovilė Pocevičiūtė, Oskar Hansson, The Netherlands Brain Bank, K Peter R. Nilsson, Malin Wennström
Format: Article
Language:English
Published: BMC 2024-01-01
Series:Alzheimer’s Research & Therapy
Subjects:
Online Access:https://doi.org/10.1186/s13195-023-01375-7
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author Cristina Nuñez-Diaz
Emelie Andersson
Nina Schultz
Dovilė Pocevičiūtė
Oskar Hansson
The Netherlands Brain Bank
K Peter R. Nilsson
Malin Wennström
author_facet Cristina Nuñez-Diaz
Emelie Andersson
Nina Schultz
Dovilė Pocevičiūtė
Oskar Hansson
The Netherlands Brain Bank
K Peter R. Nilsson
Malin Wennström
author_sort Cristina Nuñez-Diaz
collection DOAJ
description Abstract Background Amyloid beta (Aβ) deposits and hyperphosphorylated tau (p-tau) accumulation have been identified in the retina of Alzheimer’s disease (AD) patients and transgenic AD mice. Previous studies have shown that retinal microglia engulf Aβ, but this property decreases in AD patients. Whether retinal microglia also take up p-tau and if this event is affected in AD is yet not described. In the current study, we use the p-tau-specific thiophene-based ligand bTVBT2 to investigate the relationship between disease progression and p-tau uptake by microglia in the retina of AD patients and App NL−F/NL−F knock-in mice, an AD mouse model known to demonstrate extracellular Aβ plaques and dystrophic neurites in the brain from 6 months of age. Methods Evaluation of bTVBT2 specificity and its presence within microglia was assessed by immunofluorescent staining of hippocampal sections and flat-mount retina samples from non-demented controls, AD patients, 3-, 9-, and 12-month-old App NL−F/NL−F knock-in mice and 12- and 18-month-old wild type (WT) mice. We used ImageJ to analyze the amount of bTVBT2 inside Iba1-positive microglia. Co-localization between the ligand and p-tau variant Ser396/Ser404 (PHF-1), Aβ, phosphorylated TAR DNA binding protein 43 (pTDP-43), and islet amyloid polypeptide (IAPP) in the brain and retina was analyzed using confocal imaging. Results Confocal imaging analysis showed that bTVBT2 binds to PHF-1- and AT8-positive aggregates inside retinal microglia, and not to Aβ, pTDP-43, or IAPP. The density of bTVBT2-positive microglia was higher in cases with a high Aβ load compared to those with a low Aβ load. This density correlated with the neurofibrillary tangle load in the brain, but not with retinal levels of high molecular weight (aggregated) Aβ40 or Aβ42. Analysis of App NL−F/NL−F knock-in mouse retina further showed that 50% of microglia in 3-month-old App NL−F/NL−F knock-in mice contained bTVBT2. The percentage significantly increased in 9- and 12-month-old mice. Conclusion Our study suggests that the microglial capability to uptake p-tau in the retina persists and intensifies with AD progression. These results also highlight bTVBT2 as a ligand of interest in future monitoring of retinal AD pathology.
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spelling doaj.art-27397dde590844f6a269713b5b3e9bdf2024-01-07T12:14:43ZengBMCAlzheimer’s Research & Therapy1758-91932024-01-0116111210.1186/s13195-023-01375-7The fluorescent ligand bTVBT2 reveals increased p-tau uptake by retinal microglia in Alzheimer’s disease patients and App NL−F/NL−F miceCristina Nuñez-Diaz0Emelie Andersson1Nina Schultz2Dovilė Pocevičiūtė3Oskar Hansson4The Netherlands Brain Bank5K Peter R. Nilsson6Malin Wennström7Cognitive Disorder Research Unit, Department of Clinical Sciences Malmö, Lund UniversityClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund UniversityCognitive Disorder Research Unit, Department of Clinical Sciences Malmö, Lund UniversityCognitive Disorder Research Unit, Department of Clinical Sciences Malmö, Lund UniversityClinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund UniversityNetherlands Institute for NeuroscienceDepartment of Physics, Chemistry and Biology IFM, Linköping UniversityCognitive Disorder Research Unit, Department of Clinical Sciences Malmö, Lund UniversityAbstract Background Amyloid beta (Aβ) deposits and hyperphosphorylated tau (p-tau) accumulation have been identified in the retina of Alzheimer’s disease (AD) patients and transgenic AD mice. Previous studies have shown that retinal microglia engulf Aβ, but this property decreases in AD patients. Whether retinal microglia also take up p-tau and if this event is affected in AD is yet not described. In the current study, we use the p-tau-specific thiophene-based ligand bTVBT2 to investigate the relationship between disease progression and p-tau uptake by microglia in the retina of AD patients and App NL−F/NL−F knock-in mice, an AD mouse model known to demonstrate extracellular Aβ plaques and dystrophic neurites in the brain from 6 months of age. Methods Evaluation of bTVBT2 specificity and its presence within microglia was assessed by immunofluorescent staining of hippocampal sections and flat-mount retina samples from non-demented controls, AD patients, 3-, 9-, and 12-month-old App NL−F/NL−F knock-in mice and 12- and 18-month-old wild type (WT) mice. We used ImageJ to analyze the amount of bTVBT2 inside Iba1-positive microglia. Co-localization between the ligand and p-tau variant Ser396/Ser404 (PHF-1), Aβ, phosphorylated TAR DNA binding protein 43 (pTDP-43), and islet amyloid polypeptide (IAPP) in the brain and retina was analyzed using confocal imaging. Results Confocal imaging analysis showed that bTVBT2 binds to PHF-1- and AT8-positive aggregates inside retinal microglia, and not to Aβ, pTDP-43, or IAPP. The density of bTVBT2-positive microglia was higher in cases with a high Aβ load compared to those with a low Aβ load. This density correlated with the neurofibrillary tangle load in the brain, but not with retinal levels of high molecular weight (aggregated) Aβ40 or Aβ42. Analysis of App NL−F/NL−F knock-in mouse retina further showed that 50% of microglia in 3-month-old App NL−F/NL−F knock-in mice contained bTVBT2. The percentage significantly increased in 9- and 12-month-old mice. Conclusion Our study suggests that the microglial capability to uptake p-tau in the retina persists and intensifies with AD progression. These results also highlight bTVBT2 as a ligand of interest in future monitoring of retinal AD pathology.https://doi.org/10.1186/s13195-023-01375-7RetinaThiophene-based ligandsAlzheimer’s diseaseTauopathy
spellingShingle Cristina Nuñez-Diaz
Emelie Andersson
Nina Schultz
Dovilė Pocevičiūtė
Oskar Hansson
The Netherlands Brain Bank
K Peter R. Nilsson
Malin Wennström
The fluorescent ligand bTVBT2 reveals increased p-tau uptake by retinal microglia in Alzheimer’s disease patients and App NL−F/NL−F mice
Alzheimer’s Research & Therapy
Retina
Thiophene-based ligands
Alzheimer’s disease
Tauopathy
title The fluorescent ligand bTVBT2 reveals increased p-tau uptake by retinal microglia in Alzheimer’s disease patients and App NL−F/NL−F mice
title_full The fluorescent ligand bTVBT2 reveals increased p-tau uptake by retinal microglia in Alzheimer’s disease patients and App NL−F/NL−F mice
title_fullStr The fluorescent ligand bTVBT2 reveals increased p-tau uptake by retinal microglia in Alzheimer’s disease patients and App NL−F/NL−F mice
title_full_unstemmed The fluorescent ligand bTVBT2 reveals increased p-tau uptake by retinal microglia in Alzheimer’s disease patients and App NL−F/NL−F mice
title_short The fluorescent ligand bTVBT2 reveals increased p-tau uptake by retinal microglia in Alzheimer’s disease patients and App NL−F/NL−F mice
title_sort fluorescent ligand btvbt2 reveals increased p tau uptake by retinal microglia in alzheimer s disease patients and app nl f nl f mice
topic Retina
Thiophene-based ligands
Alzheimer’s disease
Tauopathy
url https://doi.org/10.1186/s13195-023-01375-7
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