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. Author manuscript; available in PMC: 2018 Nov 10.
Published in final edited form as: Circ Res. 2017 Oct 11;121(11):1251–1262. doi: 10.1161/CIRCRESAHA.117.311819

Table 1.

Activity of canonical pathways in hiPSC-vSMCs after stimulation with lactate or hypoxia

Ingenuity Canonical Pathways SMC-hypoxia SMC-lac
EIF2 Signaling −2.940 −6.021
HIPPO signaling 2.496 3.051
ILK Signaling 2.111 3.015
mTOR Signaling 3.266 1.633
p70S6K Signaling 1.964 1.528
CREB Signaling 1.698 1.698
AMPK Signaling 2.000 1.000
Calcium Signaling 1.155 1.155
PAK Signaling 0.447 1.789
Signaling by Rho family GTPases 0.866 1.155
Telomerase Signaling 1.213 0.728
Regulation of eIF4 and p70S6K Signaling 0.943 0.943
Ephrin B Signaling 0.905 0.905
Protein Kinase A Signaling −0.745 −1.044
Insulin Receptor Signaling −0.218 −1.528
GNRH Signaling 0.853 0.853
Rho A Signaling −0.667 −1.000
JAK/Stat Signaling 1.069 −0.535
Granzyme B Signaling 0.378 1.134
PTEN Signaling −0.447 −0.894
Apoptosis Signaling −1.091 −0.218
Acute Phase Response Signaling 1.091 −0.218
CDK5 Signaling −0.218 −1.091
Rac Signaling −0.378 −0.756
VEGF Signaling 0.000 1.069
IGF-1 Signaling 0.535 0.535
Agrin Interactions at Neuromuscular Junction 0.258 0.775
PI3K/AKT Signaling 0.343 0.686
PDGF Signaling −0.728 −0.243
ERK/MAPK Signaling 0.000 0.354

Proteins in hiPSC-vSMCs that were quantitatively changed by L+ culture conditions or hypoxia were identified via proteomics analysis and then evaluated with Ingenuity Pathway Analysis software. The results for pathways that regulate cell proliferation, survival, and migration; protein synthesis; gene transcription; and synthetic SMC differentiation are displayed.