| First Author | Welc SS | Year | 2012 |
| Journal | Am J Physiol Cell Physiol | Volume | 303 |
| Issue | 4 | Pages | C455-66 |
| PubMed ID | 22673618 | Mgi Jnum | J:191346 |
| Mgi Id | MGI:5461583 | Doi | 10.1152/ajpcell.00028.2012 |
| Citation | Welc SS, et al. (2012) Hyperthermia increases interleukin-6 in mouse skeletal muscle. Am J Physiol Cell Physiol 303(4):C455-66 |
| abstractText | Skeletal muscles produce and contribute to circulating levels of IL-6 during exercise. However, when core temperature is reduced, the response is attenuated. Therefore, we hypothesized that hyperthermia may be an important and independent stimulus for muscle IL-6. In cultured C2C12 myotubes, hyperthermia (42 degrees C) increased IL-6 gene expression 14-fold after 1 h and 35-fold after 5 h of 37 degrees C recovery; whereas exposure to 41 degrees C resulted in a 2.6-fold elevation at 1 h. IL-6 protein was secreted and significantly elevated in the cell supernatant. Similar but reduced responses to heat were seen in C2C12 myoblasts. Isolated soleus muscles from mice, exposed ex vivo to 41 degrees C for 1 h, yielded similar IL-6 gene responses (>3-fold) but without a significant effect on protein release. When whole animals were exposed to passive hyperthermia, such that core temperature increased to 42.4 degrees C, IL-6 mRNA in soleus increased 5.4-fold compared with time matched controls. Interestingly, TNF-alpha gene expression was routinely suppressed at all levels of hyperthermia (40.5-42 degrees C) in the isolated models, but TNF-alpha was elevated (4.2-fold) in the soleus taken from intact mice exposed, in vivo, to hyperthermia. Muscle HSP72 mRNA increased as a function of the level of hyperthermia, and IL-6 mRNA responses increased proportionally with HSP72. In cultured C2C12 myotubes, when heat shock factor was pharmacologically blocked with KNK437, both HSP72 and IL-6 mRNA elevations, induced by heat, were suppressed. These findings implicate skeletal muscle as a "heat stress sensor" at physiologically relevant hyperthermia, responding with a programmed cytokine expression pattern characterized by elevated IL-6. |
