
ACS Applied Materials & Interfaces, Journal Year: 2025, Volume and Issue: unknown
Published: April 15, 2025
Self-assembling peptides (SAPs) are fully defined nanobiomaterials offering unprecedented opportunities to control nanostructure and chemical attributes investigate manipulate cellular signals. To the influence of morphological characteristics on inflammatory signaling in native immunity, we designed five β-sheet SAPs: EFEFKFEFK (EF8), YEFEFKFEFK (YEF8), EFEFKFEFKY (EF8Y), YEFEFKFEFKY (YEF8Y), EYEFKFEFK (EYF8) (F: phenylalanine; E: glutamic acid; K: lysine, Y: tyrosine). The position tyrosine peptide sequence dictated self-assembly into nanostructures, with all SAPs self-assembling thin constituent nanofibers d ≈ 3.8 ± 0.4 nm, sequences YEF8 EF8 showing a propensity for associative bundling. These distinct induced contrasting responses monocytic model THP-1 cells-derived macrophages (MΦs). Presence soluble (at 2 mM) an anti-inflammatory response polarization toward M2 state, whereas displayed tendency inducing pro-inflammatory M1 state. EF8Y, YEF8Y, EYF8 did not induce our models. results were validated using peripheral blood mononuclear cells (PBMCs)-derived MΦs from human donors, confirming critical role as possible orchestrators repair tissues or inducers respectively. same THP-1-derived cultured 20 mM hydrogels obtained. findings will facilitate utilization this family immunomodulatory potentially changing course inflammation during progression various diseases.
Language: Английский