Abstract
Recent studies suggest that interleukin 6 (IL-6) is released from contracting skeletal muscles; however, the cellular origin, secretion kinetics, and signaling mechanisms regulating IL-6 secretion are unknown. To address these questions, we developed imaging methodology to study IL-6 in fixed mouse muscle fibers and in live animals in vivo. Using confocal imaging to visualize endogenous IL-6 protein in fixed muscle fibers, we found IL-6 in small vesicle structures distributed throughout the fibers under basal (resting) conditions. To determine the kinetics of IL-6 secretion, intact quadriceps muscles were transfected with enhanced green fluorescent protein (EGFP)-tagged IL-6 (IL-6-EGFP), and 5 days later anesthetized mice were imaged before and after muscle contractions in situ. Contractions decreased IL-6-EGFP-containing vesicles and protein by 62% (P
| Original language | English |
|---|---|
| Journal | Diabetes |
| Volume | 62 |
| Issue number | 9 |
| Pages (from-to) | 3081-92 |
| Number of pages | 12 |
| ISSN | 0012-1797 |
| DOIs | |
| Publication status | Published - Sept 2013 |
Keywords
- Aminoimidazole Carboxamide
- Animals
- Green Fluorescent Proteins
- Interleukin-6
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Microscopy, Confocal
- Muscle Contraction
- Muscle Fibers, Skeletal
- Ribonucleotides
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