Hyaluronan mediates the adhesion of porcine peripheral blood mononuclear cells to poly (I:C)-treated intestinal cells and modulates their cytokine production

• Published in: Veterinary immunology and immunopathology Vol. 184; pp. 8 - 17
• Main Authors: Docampo, María José, Cabrera, Jennifer, Bassols, Anna
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01-02-2017
• Subjects: Animals; Cell Adhesion - drug effects; Cell Line; Cytokines; Cytokines - metabolism; Hyaluronan; Hyaluronic Acid - pharmacology; Inflammation; Intestinal cells; Intestinal Mucosa - cytology; Intestinal Mucosa - drug effects; Intestinal Mucosa - metabolism; Intestines - cytology; Intestines - drug effects; Intestines - metabolism; Leukocytes, Mononuclear; PBMCs; Pig; Poly (I:C); Poly I-C - pharmacology; Swine; Hyaluronan; Cytokines; Poly (I:C); Inflammation; PBMCs; Intestinal cells; Pig
• ISSN: 0165-2427; 1873-2534
• DOI: 10.1016/j.vetimm.2016.12.008

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•Poly (I:C) induces the deposition of hyaluronan in the surface of porcine intestinal cells.•Poly (I:C)-induced hyaluronan coats in intestinal cells are adhesive for porcine PBMCs.•Low molecular weight hyaluronan fragments promote the secretion of proinflammatory cytokines in porcine PBMCs.
Hyaluronan (HA), a major component of the extracellular matrix (ECM), has been increasingly recognized as a regulator of inflammation. Its role is complex since it has pro- and anti-inflammatory actions by modulating the expression of inflammatory genes, the recruitment of inflammatory cells and the production of inflammatory cytokines, but also by attenuating the course of inflammation and providing protection against tissue damage. Certain viruses and other inflammatory stimuli induce organization of HA into cable-like structures, which may be responsible for leukocyte recruitment and, on the other hand, low molecular weight fragments of HA have been shown to activate various inflammatory responses.
The aim of the present study was to analyze the effects of a simulated infection with the viral mimetic Poly (I:C) on HA deposition on different porcine intestinal cells (primary colonic muscular smooth muscle cells (SMC), and epithelial IPEC-J2 and IPI-2I cell lines) and on the recruitment of peripheral blood mononuclear cells (PBMC) to intestinal cell layers. We show that Poly (I:C) treatment induces the formation of an HA-based pericellular matrix coat in muscular SMC and in intestinal epithelial cells (IECs) and that, on differentiated IPEC-J2 cells, HA accumulates in the basolateral membrane. Porcine PBMCs bind to Poly (I:C)-treated cells and this binding is dependent on HA, since the increase in adhesion is abolished by hyaluronidase treatment of the cell layers. A second goal was to study the effect of different molecular weight HA forms on the production of pro-inflammatory cytokines and chemokines (TNF-α, IL-1β and IL-8) by porcine PBMCs. Low molecular weight HA fragments (100–150kDa), in contrast to high molecular weight HA (2500kDa), stimulate the release of these pro-inflammatory mediators by porcine PBMCs. Our results suggest that HA is involved in the inflammatory response against pathogenic insults to the porcine gut.