Understanding
how Aβ42 oligomers induce changes
in neurons
from a mechanobiological perspective has important implications in
neuronal dysfunction relevant to neurodegenerative diseases. However,
it remains challenging to profile the mechanical responses of neurons
and correlate the mechanical signatures to the biological properties
of neurons given the structural complexity of cells. Here, we quantitatively
investigate the nanomechanical properties of primary hippocampus neurons
upon exposure to Aβ42 oligomers at the single neuron level by
using atomic force microscopy (AFM). We develop a method termed heterogeneity-load-unload
nanomechanics (HLUN), which exploits the AFM force spectra in the
whole loading–unloading cycle, allowing comprehensive profiling
of the mechanical properties of living neurons. We extract four key
nanomechanical parameters, including the apparent Young’s modulus,
cell spring constant, normalized hysteresis, and adhesion work, that
serve as the nanomechanical signatures of neurons treated with Aβ42
oligomers. These parameters are well-correlated with neuronal height
increase, cortical actin filament strengthening, and calcium concentration
elevation. Thus, we establish an HLUN method-based AFM nanomechanical
analysis tool for single neuron study and build an effective correlation
between the nanomechanical profile of the single neurons and the biological
effects triggered by Aβ42 oligomers. Our finding provides useful
information on the dysfunction of neurons from the mechanobiological
perspective.