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Tambini, M. D.

Publications and source records attributed to Tambini, M. D..

2 recordsLinked to original sources

Valosin-containing Protein is Cargo in Amyloid Precursor Protein Extracellular Vesicles

The Amyloid Precursor Protein (APP), a genetic cause of Alzheimers disease (AD), is a type-I transmembrane protein that is metabolized by proteolysis in the endolysomal system. APP and its metabolites are secreted by cells in extracellular vesicles (EVs). To study the function of APP-containing EVs, we isolated App-EVs from rat primary neuronal conditioned media and proteomic analysis identified the Valosin-containing protein (Vcp) as molecular cargo. Pharmacological modulation of Vcp activity was found to alter App processing and global EV secretion in rat primary neurons. AD-associated knock-in App mutations were found to alter the abundance of App-EVs and the trafficking of App metabolites within App-EVs, in a manner related to the epitopes generated by the nonamyloidogenic processing of App. The presence of Vcp suggests a role for App-EVs in the clearance of protein aggregates.

cell biology↗

Loss of CDC50A function drives Aβ/p3 production via increased β/α-secretase processing of APP

The Amyloid Precursor Protein (APP) undergoes extensive proteolytic processing to produce several biologically active metabolites which affect Alzheimers disease (AD) pathogenesis. Sequential cleavage of APP by {beta}- and {gamma}-secretases results in A{beta}, while cleavage by - and {gamma}-secretases produces the smaller p3 peptide. Here we report that in cells in which the P4-ATPase flippase subunit CDC50A has been knocked out, large increases in the products of {beta}- and -secretase cleavage of APP (sAPP{beta}/{beta}CTF and sAPP/CTF, respectively) and the downstream metabolites A{beta} and p3 are seen. These data indicate that APP cleavage by {beta}/-secretase are increased and suggest that phospholipid asymmetry plays an important role in APP metabolism and A{beta} production.

molecular biology↗