Targeting glycocalyx of dying and pathological cells

5^th Euro Biosensors & Bioelectronics Conference

June 30-July 02, 2016 Valencia, Spain

Rostyslav Bilyy

Danylo Halysky Lviv National Medical University, Ukraine

Posters & Accepted Abstracts: J Biosens Bioelectron

Abstract :

Every eukaryotic cell is covered with a complex ensemble of glycans attached to both proteins and lipids of plasma membrane altogether comprising cell glycocalyx. Our recent studies demonstrated that cell death is accompanied with dramatical changes in glycocalyx content. One can target these changes for detection of dying cells & modulating immune response against them; moreover, some pathogens also utilize changes in cell glycocalyx to penetrate host cells and colonize them. Apoptotic cells produce of two types of apoptotic cell-derived membranous vesicles (ACMV) (Bilyy, JBC, 2012), each bearing distinct glycosylation patterns, and they posses distinct role in the immune response and host-pathogen interactions. Formation of 2 types of ACMV are related to two active pathways of modification of glycocalyx in dying cells: a) caspase-dependent activation of plasma membrane-associated neuraminidases leads to the formation of desialylated glycoepitopes on ACMV originating from plasma membrane (PM); b) with the aim to compensate membrane surface loss due to apoptotic blebbing dying cells expose on their surface immature membranes of endoplasmic reticulum (ER), bearing a moiety of oligomannosidic glycans. PM-derived ACMV are usually big (>3�¼m) and contain nuclear material (histone and DNA), which actively translocates into the ACMV at the late stages of formation. ER-derived ACMV possess oligomannnosidic glycans, attributable to ER, that represent immunologically novel epitopes rapidly cleared by macrophages. Exposure of ACMV-contained nuclear material may support the formation of anti-nuclear (anti-histone and anti-DNA) antibodies in disorders, associated with impaired clearance, like SLE. At the same time adherent-invasive Escherichia coli (AIEC) cells, causing uropthatogenic infections and Crohnâ��s disease, are known to utilize oligomannose-specific lectin FimH at the tip of their fimbriae to adhere to the host cells. Interaction of AIEC with host cells induces formation of ER-derived ACMV by the latter and fosters bacterial attachment to host cells and their colonization.

Biography :

Email: r.bilyy@gmail.com