Saturday, March 21, 2020

200328 Identifying Potential Therapeutics for Modulating Neutrophil Inflammation

Title:
Identifying Potential Therapeutics for Modulating Neutrophil Inflammation

Speaker:
許翊輝 (Alan Y. Hsu), PhD student, Purdue University

Time:
03/28 (Sat.) 3 pm PDT, 4 pm MDT, 5 pm CDT, 6 pm EDT
03/29 (Sun.) 6 am Taiwan

Keywords:
Biological sciences, Cell biology/immunology, Neutrophil, Cell migration, Inflammation, MicroRNA, Zebrafish



Abstract:
Neutrophils are the first cells recruited to an immune stimulus stemming from infection or sterile injuries via a mixture of chemoattractant cues. In addition to eliminating pathogens, neutrophils coordinate the overall inflammation by activating and producing inflammatory signals in the tissue while modulating the activation of other immune cells which in some cases leads to adverse tissue damage. Over amplified or chronic neutrophil recruitment directly leads to autoimmune diseases including rheumatic arthritis, diabetes, neurodegenerative diseases, and cancer. Dampening neutrophil recruitment is a strategy to intervene in neutrophil-orchestrated chronic inflammation. Despite intensive research, clinical studies targeting neutrophil migration have been largely unsuccessful, possibly due to the prominent redundancy of adhesion receptors and chemokines. Additional challenges lie in the balance of dampening detrimental inflammation while preserving immunity. We thus performed a neutrophil-specific microRNA (miRNA) overexpression screen in zebrafish and identified 9 miRNAs as potent suppressors of neutrophil migration.

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