Brandon S. Hughes

ORCID: 0000-0003-0424-2392
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About
Contact & Profiles
Research Areas
  • Exercise and Physiological Responses
  • Autoimmune and Inflammatory Disorders Research
  • IL-33, ST2, and ILC Pathways
  • Immune Cell Function and Interaction
  • Adipose Tissue and Metabolism
  • Muscle Physiology and Disorders

University of California, Irvine
2021-2023

Macrophages are essential for skeletal muscle homeostasis, but how their dysregulation contributes to the development of fibrosis in disease remains unclear. Here, we used single-cell transcriptomics determine molecular attributes dystrophic and healthy macrophages. We identified six clusters unexpectedly found that none corresponded traditional definitions M1 or M2 Rather, predominant macrophage signature was characterized by high expression fibrotic factors, galectin-3 (gal-3) osteopontin...

10.1126/sciadv.add9984 article EN cc-by-nc Science Advances 2023-07-07

Despite the well-accepted view that chronic inflammation contributes to pathogenesis of Duchenne muscular dystrophy (DMD), function and regulation eosinophils remain an unclear facet type II innate immunity in dystrophic muscle. We report observation group 2 lymphoid cells (ILC2s) are present skeletal muscle principal regulators during dystrophy. Eosinophils were elevated DMD patients mice along with interleukin (IL)-5, a major eosinophil survival factor was predominantly expressed by ILC2s....

10.1016/j.celrep.2021.108997 article EN cc-by-nc-nd Cell Reports 2021-04-01
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