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Biol Med Case Rep 2017 | Volume 1 Issue 2

November 06-07, 2017 | New Orleans, USA

Nanomedicine & Healthcare

Global Meet on

Human mast cell response to nanosurfaces: Balancing innate and adaptive immunity

Marianna Kulka

National Institute for Nanotechnology, Canada

L

ocatedatmucosal surfacesandsurroundingbloodvesselsand

nerves, human mast cells are uniquely situated to regulate

the function of the vasculature, to initiate the recruitment and

activation of leukocytes into tissues and to trigger physiological

responses that are mediated by the nervous system. Mast

cells are primarily responsible for the acute allergic response

to allergen exposure, including bronchoconstriction and

edema. Mast cells and immunoglobulin E (IgE) are also felt to

be important in the evolution of allergic late phase responses,

which are largely responsible for the pathogenesis of chronic

allergic diseases such as asthma, atopic dermatitis and rhinitis.

Our recent research has shown that human mast cells respond

to a vast array of proteins, each of which activates a unique

signaling pathway through specific surface receptors. Our

laboratory is interested inmodulating humanmast cell function

using proteins, lipid nanoparticles and silver oxysalt nanofibers

with the goal of producing hypoallergenic nanosurfaces. In

one of our projects, we have focused on complement and

specific complement protein receptors. The anaphylatoxin C5a

regulates diverse innate and adaptive immune responses by

chemoattracting and activating immune cells, such asmast cells

(MC). It is postulated that C5a regulates human MC function by

activating a G protein-coupled receptor (GPCR) However, C5a

can bind to C5aR, a G protein-coupled receptor, or C5L2, not

coupled to G proteins and thought to activate distinct signaling

cascades. The presence and role of C5L2 in human MC remain

unknown. Using a human mast cell model that expresses

C5L2 but not C5aR, we have shown that C5L2 is a functional

receptor, capable of modulating specific mast cell responses.

C5a activates LAD2 cytokine and chemokine production and

initiates adhesion and migration by human mast cells. Our

research suggests that functionalizing surfaces with specific

proteins may be an effective way of modulating human mast

cell responses and regulating allergic inflammation.

Speaker Biography

Marianna Kulka is currently a Group Leader and Project Leader at the National Institute

for Nanotechnology located at the University of Alberta, Edmonton, Canada. She is also

an Adjunct Professor in the Department of Medical Microbiology and Immunology at

the University of Alberta. Currently, she is investigating the role of G protein-coupled

receptors in inflammatory disease and mast cell activation pathways. Her focus is on

activation pathways of human mast cells and their regulation of human inflammatory

diseases. Her work aims to use novel nano-packaging strategies to manipulate these

pathways. She has published numerous articles in peer-reviewed journals and serves

on several review panels, including national and international granting agencies.

e:

marianna.kulka@nrc-cnrc.gc.ca