Traumatic brain injury (TBI) results in disrupted brain function following impact from an external force and is a risk factor for sporadic Alzheimer’s Disease (AD). Though neurological symptoms triggered by mild traumatic brain injuries (mTBI) – the most common form of TBI – typically resolve rapidly, even an isolated mTBI event can increase the risk to develop AD. Aberrant accumulation of amyloid beta peptide (Aβ), a cleaved fragment of amyloid precursor protein (APP), is a key pathological outcome designating the progression of AD following mTBI and has also been linked to impaired axonal transport. However, relationships among mTBI, amyloidogenesis, and axonal transport remain unclear, in part due to the dearth of human models to study the neuronal response following mTBI. Here, we implemented a custom-microfabricated device to deform neurons derived from human induced pluripotent stem cells (hiPSC), derived from a cognitively unimpaired male individual, to mimic the mild stretch experienced by neurons ...