Journal Article

Critical role for PI3-kinase in regulating the use of proteins as an amino acid source

Palm, Wilhelm, Araki, Jingwen, King, Bryan, Thompson, Craig B., DeMatteo, Raymond G.

2017

Overview

Ras-transformed cells can grow in amino acid-poor environments by recovering amino acids through macropinocytosis and lysosomal catabolism of extracellular proteins. However, when studying nontransformed fibroblasts, we found that Ras GTPases are dispensable for growth-factor–stimulated macropinocytosis and lysosomal catabolism of extracellular proteins. Instead, we establish a critical role for phosphatidylinositol 3-kinase (PI3-kinase) signaling in cell proliferation that is supported by protein macropinocytosis. Downstream of PI3-kinase, distinct effectors have opposing roles in regulating uptake and catabolism of extracellular proteins. Rac1 and PLC are required for nutritional use of extracellular proteins. In contrast, Akt suppresses lysosomal catabolism of ingested proteins when free amino acids are abundant. The interplay between these pathways allows cells with oncogenic PIK3CA mutations or PTEN deletion to grow using diverse amino acid sources. Thus, the prevalence of PI3-kinase and PTEN mutations in cancer may result in part because they allow cells to cope with fluctuating nutrient availability.

• Publisher: National Academy of Sciences
• Subject: 1-Phosphatidylinositol 3-kinase / AKT protein / Amino acids / Biological Sciences / Cancer / Catabolism / Cell Biology / Cell proliferation / Clonal deletion / Fibroblasts / Kinases / Metabolism / Mutation / Nutrient availability / PNAS Plus / Proteins / PTEN protein / Rac1 protein / Ras protein / Signaling / Transformed cells