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Peter Tong, Zayna A. Khayat, Carol Huang, Nish Patel, Atsunori Ueyama, Amira Klip
Published in Volume 108, Issue 3
J Clin Invest. 2001; 108(3):371–381 doi:10.1172/JCI12348
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Figure 9

Insulin resistance caused by chronic high glucose and insulin impairs insulin-stimulated, GLUT4 externalization and actin remodeling. L6 GLUT4myc myotubes were maintained in high insulin (100 nM) and high glucose (25 mM) for 24 hours before serum deprivation for 4 hours. Myotubes were then treated with or without 100 nM insulin for 30 minutes (a) or 10 minutes (be) at 37°C. (a) Quantification of cell-surface GLUT4myc was performed, as described in Methods. Results are expressed as the fold change relative to basal cells in the untreated control (mean ± SEM of four independently performed experiments). *P < 0.05 compared with respective control in the absence of high insulin/high glucose. (be) Cells were fixed and stained for F-actin using Oregon Green-phalloidin as described in Figure 1. Arrows indicate regions of remodeled (c) or partially remodeled (e) actin filaments. The images are representative of four experiments. Scale bar = 50 μm.