Monocytes mediate homing of circulating microvesicles to the pulmonary vasculature during low‐grade systemic inflammation. Issue 1 (5th January 2020)

• Record Type: Journal Article
• Authors: O'Dea, Kieran P.; Tan, Ying Ying; Shah, Sneh; V Patel, Brijesh; C Tatham, Kate; Wilson, Mike R.; Soni, Sanooj; Takata, Masao
• Is Part Of: Journal of extracellular vesicles. Volume 9:Issue 1(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-01-05
• Subjects: Extracellular vesicles -- microvesicles -- monocytes -- systemic inflammation -- pulmonary vasculature; Cells -- Mechanical properties -- Periodicals; Transport Vesicles; Cells -- Mechanical properties; Periodicals; Fulltext; Internet Resources; Periodicals; Electronic journals; Periodicals; 571.63
• DOI: 10.1080/20013078.2019.1706708
• Languages: English
• ISSNs: 2001-3078

Abstract

ABSTRACT: Microvesicles (MVs), a plasma membrane‐derived subclass of extracellular vesicles, are produced and released into the circulation during systemic inflammation, yet little is known of cell/tissue‐specific uptake of MVs under these conditions. We hypothesized that monocytes contribute to uptake of circulating MVs and that their increased margination to the pulmonary circulation and functional priming during systemic inflammation produces substantive changes to the systemic MV homing profile. Cellular uptake of i.v.‐injected, fluorescently labelled MVs (J774.1 macrophage‐derived) in vivo was quantified by flow cytometry in vascular cell populations of the lungs, liver and spleen of C57BL6 mice. Under normal conditions, both Ly6C high and Ly6C low monocytes contributed to MV uptake but liver Kupffer cells were the dominant target cell population. Following induction of sub‐clinical endotoxemia with low‐dose i.v. LPS, MV uptake by lung‐marginated Ly6C high monocytes increased markedly, both at the individual cell level (~2.5‐fold) and through substantive expansion of their numbers (~8‐fold), whereas uptake by splenic macrophages was unchanged and uptake by Kupffer cells actually decreased (~50%). Further analysis of MV uptake within the pulmonary vasculature using a combined model approach of in vivo macrophage depletion, ex vivo isolated perfused lungs and in vitro lung perfusate cell‐based assays, indicated that Ly6C high monocytes possess a high MV uptake capacity (equivalent to Kupffer cells), that is enhanced directly by endotoxemia and ablated in the presence of phosphatidylserine (PS)‐enriched liposomes and β3 integrin receptor blocking peptide. Accordingly, i.v.‐injected PS‐enriched liposomes underwent a redistribution of cellular uptake during endotoxemia similar to MVs, with enhanced uptake by Ly6C high monocytes and reduced uptake by Kupffer cells. These findings indicate that monocytes, particularly lung‐marginated Ly6C high subset monocytes, become a dominant target cell population for MVs during systemic inflammation, with significant implications for the function and targeting of endogenous and therapeutically administered MVs, lending novel insights into the pathophysiology of pulmonary vascular inflammation.