A PI3K p110 beta-Rac signalling loop mediates Pten-loss-induced perturbation of haematopoiesis and leukaemogenesis

作者：Yuzugullu Haluk; Baitsch Lukas; Thanh Von; Steiner Allison; Tong Haoxuan; Ni Jing; Clayton Linda K; Bronson Roderick; Roberts Thomas M^*; Gritsman Kira; Zhao Jean J

来源：Nature Communications, 2015, 6(1): 8501.

DOI：10.1038/ncomms9501

The tumour suppressor PTEN, which antagonizes PI3K signalling, is frequently inactivated in haematologic malignancies. In mice, deletion of PTEN in haematopoietic stem cells (HSCs) causes perturbed haematopoiesis, myeloproliferative neoplasia (MPN) and leukaemia. Although the roles of the PI3K isoforms have been studied in PTEN-deficient tumours, their individual roles in PTEN-deficient HSCs are unknown. Here we show that when we delete PTEN in HSCs using the Mx1-Cre system, p110 beta ablation prevents MPN, improves HSC function and suppresses leukaemia initiation. Pharmacologic inhibition of p110 beta in PTEN-deficient mice recapitulates these genetic findings, but suggests involvement of both Akt-dependent and -independent pathways. Further investigation reveals that a p110 beta-Rac signalling loop plays a critical role in PTEN-deficient HSCs. Together, these data suggest that myeloid neoplasia driven by PTEN loss is dependent on p110 beta via p110 beta-Rac-positive-feedback loop, and that disruption of this loop may offer a new and effective therapeutic strategy for PTEN-deficient leukaemia.

• 出版日期2015-10