The PI3K regulatory subunits p55[alpha] and p50[alpha] regulate cell death in vivo

• Published in: Cell death and differentiation Vol. 21; no. 9; p. 1442
• Main Authors: Pensa, S, Neoh, K, Resemann, H K, Kreuzaler, P A, Abell, K, Clarke, N J, Reinheckel, T, Kahn, C R, Watson, C J
• Format: Journal Article
• Language: English
• Published: Rome Nature Publishing Group 01-09-2014
• Subjects: Cell death
• DOI: 10.1038/cdd.2014.59
• EISSN: 1476-5403
• ISSN: 1350-9047

The phosphatidylinositol 3-kinase (PI3K) regulatory subunits p55α and p50α are coordinately transcriptionally upregulated by signal transducer and activator of transcription 3 (Stat3) at the onset of mammary gland involution, a process that requires Stat3. Deletion of both p55α and p50α subunits in vivo abrogated mammary epithelial cell death during involution. This was associated also with reduced cytosolic levels and activity of the cysteine protease cathepsin L, which is implicated in lysosomal-mediated programmed cell death (LM-PCD) and is upregulated in involution. Furthermore, involution is delayed in cathepsin L-deficient mice suggesting that the p55α/p50α subunits mediate cell death in part by elevating the level of cathepsin L resulting in increased cytosolic activity. Surprisingly, we found that p55α/p50α localize to the nucleus where they bind to chromatin and regulate transcription of a subset of inflammatory/acute phase genes that are also Stat3 targets. Our findings reveal a novel role for these PI3K regulatory subunits as regulators of LM-PCD in vivo.