Carboxy-terminal domain of Cas differentially modulates c-Jun expression, DNA synthesis, and membrane ruffling induced by insulin, EGF, and IGF-1

Anim Cells Syst (Seoul). 2018 Mar 7;22(2):69-75. doi: 10.1080/19768354.2018.1447013. eCollection 2018.

Abstract

p130 Crk-associated substrate (Cas) is an adaptor protein associating with many other signaling proteins and regulates a various biological processes including cell adhesion, migration, and growth factor stimulation. However, the exact functional role of Cas in growth factor signaling pathway was poorly understood. Here we investigated the role of Cas and its domains in the effects of insulin, EGF, and IGF-1 on c-Jun gene expression, DNA synthesis, cytoskeletal reorganization. We found that microinjection of anti-Cas antibody and C-terminal domain of Cas (Cas-CT) specifically inhibited EGF-induced, but not insulin- or IGF-1-induced, c-Jun expression. Cell cycle progression and cytoskeleton reorganization induced by insulin and EGF, but not by IGF-1, were inhibited by microinjected anti-Cas and Cas-CT. In contrast, microinjection of the substate domain (Cas-SD) of Cas did not have any inhibitory effects. These results revealed that the Cas-CT is differentially implicated in insulin and EGF-mediated, but not IGF-1-mediated, c-Jun expression, DNA synthesis and membrane ruffling.

Keywords: Cas; DNA synthesis; EGF; IGF-1; c-Jun expression; insulin; membrane ruffling; microinjection.

Grants and funding

This work was supported by the National Research Foundation of Korea (NRF) [grant number 2017R1C1B2008017 to K.K.] and [grant number 2016R1A6A3A11935271 to S.J.Y.]; the intramural research grant of Chungbuk National University in 2015 to K.K; and BK21 Plus program through the National Research Foundation of Korea [grant number 10Z20130000004 to B.H.J.]