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An Extract of the Tapeworm, Hymenolepis diminuta, Inhibits Neutrophil Migration in vitro

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Advisor
McKay, Derek
Gilleard, John
Author
Graves, Nicholas
Committee Member
Yipp, Bryan
Finney, Constance
Other
neutrophils
helminth
parasite
reactive oxygen species
Subject
Immunology
Type
Thesis
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Abstract
Neutrophils are not typically the first cell that comes to mind when the immune response to infection with helminths is considered. However, data are emerging showing that these cells may play an overlooked role in response to helminths perhaps early in the infection and particularly those species that cause tissue damage (e.g. Nippostrongylus brasiliensis - a gut nematode (roundworm)). Additionally, different helminth products have been shown to directly activate neutrophils in vitro (e.g. crude extracts of the porcine cestode Cysticercus cellulosae) and directly induce their chemotaxis (e.g. excretory/secretory products of the sheep nematode Haemonchus contortus). Hymenolepis diminuta crude extract (HdE) has been shown to inhibit dinitrobenzene sulfonic acid-induced colitis. Intraperitoneal injection of this crude extract recruited a population of peritoneal exudate cells dominated by neutrophils at 4h post-injection. Remarkably, these neutrophil-predominant PECs evoked increased production of the anti-inflammatory cytokine IL-10 from co-cultures of activated murine splenic CD4+ T cells. HdE did not directly induce murine neutrophil chemotaxis in vitro and direct application of HdE to neutrophils was not preferentially cytotoxic as assessed by trypan blue staining and LDH release. HdE did however induce Ca2+ mobilization and respiratory burst by murine neutrophils in vitro. In contrast to its ability to recruit neutrophils to the peritoneal cavity, HdE inhibited neutrophil chemotaxis in response to WKYMVm and keratinocyte derived chemokine (KC). HdE was unable to modulate neutrophil migration towards leukotriene B4. Biochemical characterizations (boiling, trypsinization, acidification, and sodium metaperiodate treatment) suggested that an acid-stable glycoprotein was responsible for its ability to block migration towards WKYMVm. The ability of HdE to block migration towards WKYMVm appears to be independent of the phosphorylation of the mitogen-activated protein kinase, p38. HdE did not directly induce production of the cytokines, IL-10, TNF-α, and KC. It also did not modulate production of these cytokines induced by other activators. In conclusion: (1) HdE activated neutrophils to mobilize Ca2+ into the cytoplasm and produce ROS; and, (2) an acid-stable glycoprotein component of the HdE inhibited neutrophil migration towards WKYMVm.
Corporate
University of Calgary
Faculty
Graduate Studies
Doi
http://dx.doi.org/10.5072/PRISM/24897
Uri
http://hdl.handle.net/11023/4240
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