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Artikel: Prior Fc Receptor activation primes macrophages for increased sensitivity to IgG via long term and short term mechanisms.

Bond, Annalise / Fiaz, Sareen / Rollins, Kirstin R / Nario, Jazz Elaiza Q / Rosen, Samuel J / Granados, Alyssa / Wilson, Maxwell Z / Morrissey, Meghan A

bioRxiv : the preprint server for biology

2023  

Abstract: Macrophages measure the 'eat-me' signal IgG to identify targets for phagocytosis. We wondered if prior encounters with IgG influence macrophage appetite. IgG is recognized by the Fc Receptor. To temporally control Fc Receptor activation, we engineered an ...

Abstract Macrophages measure the 'eat-me' signal IgG to identify targets for phagocytosis. We wondered if prior encounters with IgG influence macrophage appetite. IgG is recognized by the Fc Receptor. To temporally control Fc Receptor activation, we engineered an Fc Receptor that is activated by light-induced oligomerization of Cry2, triggering phagocytosis. Using this tool, we demonstrate that Fc Receptor activation primes macrophages to be more sensitive to IgG in future encounters. Macrophages that have previously experienced Fc Receptor activation eat more IgG-bound cancer cells. Increased phagocytosis occurs by two discrete mechanisms - a short- and long-term priming. Long term priming requires new protein synthesis and Erk activity. Short term priming does not require new protein synthesis and correlates with an increase in Fc Receptor mobility. Our work demonstrates that IgG primes macrophages for increased phagocytosis, suggesting that therapeutic antibodies may become more effective after initial priming doses.
Sprache Englisch
Erscheinungsdatum 2023-11-14
Erscheinungsland United States
Dokumenttyp Preprint
DOI 10.1101/2023.11.14.567059
Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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