De Novo Chemoattractants Form Supramolecular Hydrogels for Immunomodulating Neutrophils In Vivo
Author(s) -
Fan Zhao,
Jingyu Li,
Ning Zhou,
Jiro Sakai,
Yuan Gao,
Junfeng Shi,
Bronia Goldman,
Hayley M. Browdy,
Hongbo R. Luo,
Bing Xu
Publication year - 2014
Publication title -
bioconjugate chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.279
H-Index - 172
eISSN - 1520-4812
pISSN - 1043-1802
DOI - 10.1021/bc5004923
Subject(s) - self healing hydrogels , chemotaxis , innate immune system , chemistry , inflammation , acquired immune system , microbiology and biotechnology , in vivo , immunity , immune system , immunology , biochemistry , biology , receptor , organic chemistry
Most immunomodulatory materials (e.g., vaccine adjuvants such as alum) modulate adaptive immunity, and yet little effort has focused on developing materials to regulate innate immunity, which get mentioned only when inflammation affects the biocompatibility of biomaterials. Traditionally considered as short-lived effector cells from innate immunity primarily for the clearance of invading microorganisms without specificity, neutrophils exhibit a key role in launching and shaping the immune response. Here we show that the incorporation of unnatural amino acids into a well-known chemoattractant-N-formyl-l-methionyl-l-leucyl-l-phenylalanine (fMLF)-offers a facile approach to create a de novo, multifunctional chemoattractant that self-assembles to form supramolecular nanofibrils and hydrogels. This de novo chemoattractant not only exhibits preserved cross-species chemoattractant activity to human and murine neutrophils, but also effectively resists proteolysis. Thus, its hydrogel, in vivo, releases the chemoattractant and attracts neutrophils to the desired location in a sustainable manner. As a novel and general approach to generate a new class of biomaterials for modulating innate immunity, this work offers a prolonged acute inflammation model for developing various new applications.
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