| First Author | Pryce BR | Year | 2024 |
| Journal | Cell Rep | Volume | 43 |
| Issue | 11 | Pages | 114925 |
| PubMed ID | 39475511 | Mgi Jnum | J:359777 |
| Mgi Id | MGI:7790358 | Doi | 10.1016/j.celrep.2024.114925 |
| Citation | Pryce BR, et al. (2024) Muscle inflammation is regulated by NF-kappaB from multiple cells to control distinct states of wasting in cancer cachexia. Cell Rep 43(11):114925 |
| abstractText | Although cancer cachexia is classically characterized as a systemic inflammatory disorder, emerging evidence indicates that weight loss also associates with local tissue inflammation. We queried the regulation of this inflammation and its causality to cachexia by exploring skeletal muscle, whose atrophy strongly associates with poor outcomes. Using multiple mouse models and patient samples, we show that cachectic muscle is marked by enhanced innate immunity. Nuclear factor kappaB (NF-kappaB) activity in multiple cells, including satellite cells, myofibers, and fibro-adipogenic progenitors, promotes macrophage expansion equally derived from infiltrating monocytes and resident cells. Moreover, NF-kappaB-activated cells and macrophages undergo crosstalk; NF-kappaB(+) cells recruit macrophages to inhibit regeneration and promote atrophy but, interestingly, also protect myofibers, while macrophages stimulate NF-kappaB(+) cells to sustain an inflammatory feedforward loop. Together, we propose that NF-kappaB functions in multiple cells in the muscle microenvironment to stimulate macrophages that both promote and protect against muscle wasting in cancer. |
