Glycomic analysis of human mast cells, eosinophils and basophils

North, Simon J; von Gunten, Stephan; Antonopoulos, Aristotelis; Trollope, Alana; MacGlashan, Donald W; Jang-Lee, Jihye; Dell, Anne; Metcalfe, Dean D; Kirshenbaum, Arnold S; Bochner, Bruce S; Haslam, Stuart M (2012). Glycomic analysis of human mast cells, eosinophils and basophils. Glycobiology, 22(1), pp. 12-22. Oxford: Oxford University Press 10.1093/glycob/cwr089

[img]
Preview
Text
cwr089.pdf - Published Version
Available under License Creative Commons: Attribution-Noncommercial (CC-BY-NC).

Download (620kB) | Preview

In allergic diseases such as asthma, eosinophils, basophils and mast cells, through release of preformed and newly generated mediators, granule proteins and cytokines, are recognized as key effector cells. While their surface protein phenotypes, mediator release profiles, ontogeny, cell trafficking and genomes have been generally explored and compared, there has yet to be any thorough analysis and comparison of their glycomes. Such studies are critical to understand the contribution of carbohydrates to the induction and regulation of allergic inflammatory responses and are now possible using improved technologies for detecting and characterizing cell-derived glycans. We thus report here the application of high-sensitivity mass spectrometric-based glycomics methodologies to the analysis of N-linked glycans derived from isolated populations of human mast cells, eosinophils and basophils. The samples were subjected to matrix-assisted laser desorption ionization (MALDI) time-of-flight (TOF) screening analyses and MALDI-TOF/TOF sequencing studies. Results reveal substantive quantities of terminal N-acetylglucosamine containing structures in both the eosinophil and the basophil samples, whereas mast cells display greater relative quantities of sialylated terminal epitopes. For the first time, we characterize the cell surface glycan structures of principal allergic effector cells, which by interaction with glycan-binding proteins (e.g. lectins) have the possibility to dictate cellular functions, and might thus have important implications for the pathogenesis of inflammatory and allergic diseases.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Pre-clinic Human Medicine > Institute of Pharmacology

UniBE Contributor:

von Gunten, Stephan

ISSN:

0959-6658

Publisher:

Oxford University Press

Language:

English

Submitter:

Factscience Import

Date Deposited:

04 Oct 2013 14:18

Last Modified:

20 Dec 2022 12:37

Publisher DOI:

10.1093/glycob/cwr089

PubMed ID:

21725073

Web of Science ID:

000297864400004

BORIS DOI:

10.48350/5465

URI:

https://boris.unibe.ch/id/eprint/5465 (FactScience: 210212)

Actions (login required)

Edit item Edit item
Provide Feedback