# Morphological and Hyperphosphorylation Transitions of Nanoscale Tau Aggregates in Alzheimer's Disease

## TL;DR

The study uses super-resolution microscopy to show how nano-sized tau aggregates change in shape and chemical marks in Alzheimer's disease and related conditions.

## Contribution

The study reveals distinct morphological and hyperphosphorylation transitions of tau nano-aggregates in Alzheimer's disease progression.

## Key findings

- Hyperphosphorylated tau nano-aggregates at p-T231 and p-T181 are present in control cases, while p-S202/T205 aggregates are specific to Alzheimer's disease.
- Nano-aggregates increase in size and complexity in advanced Alzheimer's disease and contain multiple phosphorylation sites.
- Morphological and phosphorylation signatures distinguish physiological from pathological tau nano-aggregates.

## Abstract

Tau aggregation plays a critical role in Alzheimer's Disease (AD), where neurofibrillary tangles (NFTs) are a pathological hallmark. While much attention is given to NFTs, emerging evidence highlights nano‐sized tau oligomers as toxic entities. Using super‐resolution microscopy, we visualized nano‐sized tau aggregates (nano‐aggregates) in human postmortem brain tissues from intermediate and advanced AD, Primary Age‐Related Tauopathy (PART), and controls lacking tau pathology. Surprisingly, tau nano‐aggregates hyperphosphorylated at threonine 231 (p‐T231) and threonine 181 (p‐T181)are detected in control cases, whereas hyperphosphorylated serine 202/threonine 205 (p‐S202/T205)nano‐aggregates are specifically associated with AD and, to a lesser extent, observed in PART. This finding suggests that distinct hyperphosphorylation signatures distinguish physiological from pathological nano‐aggregates. Moreover, nano‐aggregates exhibit morphological differences between AD and non‐AD conditions, increasing in size and complexity in AD. In advanced AD, nano‐aggregates typically contain multiple distinct hyperphosphorylated residues, whereas intermediate AD nano‐aggregates are predominantly marked by a single hyperphosphorylated residue. These findings reveal novel transitions in the morphology and hyperphosphorylation states of tau nano‐aggregates as they shift from physiological to pathological forms. The ability to detect and profile physiological and pathological nanoscale tau aggregates in human brain tissues opens new avenues for studying the molecular underpinnings of tauopathies.

Super‐resolution microscopy identifies nano‐sized tau aggregates (nano‐aggregates) and reveals distinct transitions in their morphology and phosphorylation profiles across control, Primary Age‐Related Tauopathy, and Alzheimer's disease brains. Morphology and hyperphosphorylation signatures distinguish physiological from pathological forms, with nano‐aggregates growing in size and complexity as disease advances. These findings provide new avenues for studying protein aggregates in tauopathies.