Blair Lab

University of South Florida

BIOCHEMISTRY

Tampa · United States

NIH-funded
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NIH R01 · 2025

The hsp90 Cochaperone FKBP51 Regulates tau Structure and Function

Project Summary/Abstract Neuropsychiatric symptoms (NPS), like depression, are common early in Alzheimer’s disease (AD) and correlate with a faster decline in patients. NPS and cognitive deficits in AD have been linked with the accumulation of tau protein. Two independent studies associated an allelic variant in the 51kDa FK506-binding protein (FKBP51) with increased risk for depression in AD. FKBP51 also regulates tau accumulation and toxicity to nerve cells. We will use transgenic mouse models to determine if either removing or inhibiting FKBP51 in mice will be protective against tau accumulation. We will also study whether mice that have this risk variant in combination with tau…

From the public funding record at NIH RePORTER. Describes the funded project, not the reviews below.

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