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Hydroxyethyl Starch 130/0.4 Binds to Neutrophils Impairing Their Chemotaxis through a Mac-1 Dependent Interaction

Title: Hydroxyethyl Starch 130/0.4 Binds to Neutrophils Impairing Their Chemotaxis through a Mac-1 Dependent Interaction
Authors: Trentini, Alessandro; Murganti, Francesca; Rosta, Valentina; Cervellati, Carlo; Manfrinato, Maria Cristina; Spadaro, Savino; Dallocchio, Franco; Volta, Carlo Alberto; Bellini, Tiziana
Contributors: Trentini, Alessandro; Murganti, Francesca; Rosta, Valentina; Cervellati, Carlo; Manfrinato, Maria Cristina; Spadaro, Savino; Dallocchio, Franco; Volta, Carlo Alberto; Bellini, Tiziana
Publication Year: 2019
Collection: Università degli Studi di Ferrara: CINECA IRIS
Subject Terms: Chemotaxis; FMLP; Hydroxyethyl Starch; IL-8; Integrin; Neutrophil; Volume replacement solutions
Description: Several studies showed that hydroxyethyl starch (HES), a synthetic colloid used in volume replacement therapies, interferes with leukocyte-endothelium interactions. Although still unclear, the mechanism seems to involve the inhibition of neutrophils' integrin. With the aim to provide direct evidence of the binding of HES to neutrophils and to investigate the influence of HES on neutrophil chemotaxis, we isolated and treated the cells with different concentrations of fluorescein-conjugated HES (HES-FITC), with or without different stimuli (N-Formylmethionine-leucyl-phenylalanine, fMLP, or IL-8). HES internalization was evaluated by trypan blue quenching and ammonium chloride treatment. Chemotaxis was evaluated by under-agarose assay after pretreatment of the cells with HES or a balanced saline solution. The integrin interacting with HES was identified by using specific blocking antibodies. Our results showed that HES-FITC binds to the plasma membrane of neutrophils without being internalized. Additionally, the cell-associated fluorescence increased after stimulation of neutrophils with fMLP (p < 0.01) but not IL-8. HES treatment impaired the chemotaxis only towards fMLP, event mainly ascribed to the inhibition of CD-11b (Mac-1 integrin) activity. Therefore, the observed effect mediated by HES should be taken into account during volume replacement therapies. Thus, HES treatment could be advantageous in clinical conditions where a low activation/recruitment of neutrophils may be beneficial, but may be harmful when unimpaired immune functions are mandatory.
Document Type: article in journal/newspaper
File Description: STAMPA
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/30769810; info:eu-repo/semantics/altIdentifier/wos/WOS:000460805400025; volume:20; issue:4; firstpage:817-1; lastpage:817-16; numberofpages:16; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; https://hdl.handle.net/11392/2400213
DOI: 10.3390/ijms20040817
Availability: https://hdl.handle.net/11392/2400213; https://doi.org/10.3390/ijms20040817; https://www.mdpi.com/1422-0067/20/4/817/pdf; https://www.mdpi.com/1422-0067/20/4/817
Rights: info:eu-repo/semantics/openAccess ; license:Creative commons ; license uri:http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.A50AE3AC
Database: BASE