PTEN secretion in exosomes

• Published in: Methods (San Diego, Calif.) Vol. 77-78; pp. 157 - 163
• Main Authors: Putz, Ulrich, Mah, Sophia, Goh, Choo-Peng, Low, Ley-Hian, Howitt, Jason, Tan, Seong-Seng
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.05.2015
• Subjects: Animals; Cell Line, Tumor; Exosomes; Exosomes - secretion; HEK293 Cells; Humans; Mice; Ndfip1; PTEN Phosphohydrolase - secretion; PTEN secretion; Tumor Suppressor Proteins - secretion; Exosomes; Ndfip1; PTEN secretion
• ISSN: 1046-2023; 1095-9130
• DOI: 10.1016/j.ymeth.2014.12.016

•Exosomes are extracellular microvesicles for intercellular communication.•PTEN is found in exosomes and its recruitment into exosomes requires the Ndfip1/Nedd4 ubiquitination system.•PTEN export in exosomes may provide a means for transferring PTEN.•PTEN in exosomes can be internalized by surrounding recipient cells. PTEN was discovered as a membrane-associated tumor suppressor protein nearly two decades ago, but the concept that it can be secreted and taken up by recipient cells is revolutionary. Since then, various laboratories have reported that PTEN is indeed secreted and available for uptake by other cells in at least two different guises. First, PTEN may be packaged and exported within extracellular vesicles (EV) called exosomes. Second, PTEN may also be secreted as a naked protein in a longer isoform called PTEN-long. While the conditions favouring the secretion of PTEN-long remain unknown, PTEN secretion in exosomes is enhanced by the Ndfip1/Nedd4 ubiquitination system. In this report, we describe conditions for packaging PTEN in exosomes and their potential use for mediating non cell-autonomous functions in recipient cells. We suggest that this mode of PTEN transfer may potentially provide beneficial PTEN for tumor suppression, however it may also propagate deleterious versions of mutated PTEN causing tumorigenesis.