The complex heterogeneity of immune cell signatures across wasting tissues with C26 and 5-fluorouracil-induced cachexia
Brandon N. VanderVeen, Thomas D. Cardaci, Brooke M. Bullard, Alexander R. Huss, Sierra J. McDonald, Ahmed D. Muhammed, Jason L. Kubinak, Daping Fan, E. Angela Murphy
Abstract
Despite being an immune-driven condition, our understanding of skeletal muscle and adipose tissue immune cells with cachexia is limited. Here, we identified immune cell populations in tumors, skeletal muscle, and adipose tissue in C26 tumor-bearing mice with/without 5-fluorouracil (5FU). C26 and C26 + 5FU had increased skeletal muscle profibrotic macrophages, but 5FU reduced inflammatory myeloid cells without sparing mass. Tumor presence and chemotherapy have contrasting effects on certain immune cells, which appeared not necessary for wasting.
Topics & Concepts
WastingCachexiaImmune systemWasting SyndromeCancer researchBiologyImmunologyMedicineInternal medicineCancerNutrition and Health in AgingVitamin C and Antioxidants ResearchMesenchymal stem cell research