TY - JOUR
T1 - Polymerase delta-interacting protein 2 regulates collagen accumulation via activation of the Akt/mTOR pathway in vascular smooth muscle cells
AU - Fujii, Masakazu
AU - Amanso, Angélica
AU - Abrahão, Thalita B.
AU - Lassègue, Bernard
AU - Griendling, Kathy K.
N1 - Funding Information:
Sources of funding: This work was supported by National Institutes of Health grants HL38206 and HL095070 .
PY - 2016/3/1
Y1 - 2016/3/1
N2 - Objectives: Polymerase delta interacting protein 2 (Poldip2) has previously been implicated in migration, proliferation and extracellular matrix (ECM) production in vascular smooth muscle cells. To better understand the role of Poldip2 in ECM regulation, we investigated the mechanism responsible for collagen I accumulation in Poldip2+/- mouse aortic smooth muscle cells (MASMs). Approach and results: Protein degradation and protein synthesis pathways were investigated. Depletion of Poldip2 had no effect on proteasome activity, but caused a partial reduction in autophagic flux. However, the rate of collagen I degradation was increased in Poldip2+/- vs. Poldip2+/+ MASMs. Conversely, activation of the PI3K/Akt/mTOR signaling pathway, involved in regulation of protein synthesis, was significantly elevated in Poldip2+/- MASMs as was β1-integrin expression. Suppressing mTOR signaling using Akt inhibitor or rapamycin and reducing β1-integrin expression using siRNA prevented the increase in collagen I production. While collagen I and fibronectin were increased in Poldip2+/- MASMs, overall protein synthesis was not different from that in Poldip2+/+MASMs, suggesting selectivity of Poldip2 for ECM proteins. Conclusions: Poldip2+/- MASMs exhibit higher β1-integrin expression and activity of the PI3K/Akt/mTOR signaling pathway, leading to increased ECM protein synthesis. These findings have important implications for vascular diseases in which ECM accumulation plays a role.
AB - Objectives: Polymerase delta interacting protein 2 (Poldip2) has previously been implicated in migration, proliferation and extracellular matrix (ECM) production in vascular smooth muscle cells. To better understand the role of Poldip2 in ECM regulation, we investigated the mechanism responsible for collagen I accumulation in Poldip2+/- mouse aortic smooth muscle cells (MASMs). Approach and results: Protein degradation and protein synthesis pathways were investigated. Depletion of Poldip2 had no effect on proteasome activity, but caused a partial reduction in autophagic flux. However, the rate of collagen I degradation was increased in Poldip2+/- vs. Poldip2+/+ MASMs. Conversely, activation of the PI3K/Akt/mTOR signaling pathway, involved in regulation of protein synthesis, was significantly elevated in Poldip2+/- MASMs as was β1-integrin expression. Suppressing mTOR signaling using Akt inhibitor or rapamycin and reducing β1-integrin expression using siRNA prevented the increase in collagen I production. While collagen I and fibronectin were increased in Poldip2+/- MASMs, overall protein synthesis was not different from that in Poldip2+/+MASMs, suggesting selectivity of Poldip2 for ECM proteins. Conclusions: Poldip2+/- MASMs exhibit higher β1-integrin expression and activity of the PI3K/Akt/mTOR signaling pathway, leading to increased ECM protein synthesis. These findings have important implications for vascular diseases in which ECM accumulation plays a role.
UR - http://www.scopus.com/inward/record.url?scp=84961307487&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84961307487&partnerID=8YFLogxK
U2 - 10.1016/j.yjmcc.2016.01.016
DO - 10.1016/j.yjmcc.2016.01.016
M3 - Article
C2 - 26801741
AN - SCOPUS:84961307487
VL - 92
SP - 21
EP - 29
JO - Journal of Molecular and Cellular Cardiology
JF - Journal of Molecular and Cellular Cardiology
SN - 0022-2828
ER -