Korean J Pediatr.  2004 Nov;47(11):1137-1141.

Role of Mast Cells in Allergic Inflammation and Innate Immunity

Affiliations
  • 1Department of Pediatrics, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea. kmaped@smc.samsung.co.kr

Abstract

Mast cells play a key role in elicitation of the early-phase and late-phase IgE-mediated allergic inflammatory reactions. Mast cells are derived from pluripotent stem cells from the bone marrow. These cells migrate through circulation into connective tissues and mucosal surfaces where they mature. On the cell surfaces, mast cells have high affinity IgE receptor(FcepsilonRI), which react with specific IgE to secrete preformed and newly synthesized mediators within minutes or over a period of hours. For human mast cells, two subtypes have been recognized by the distribution of granular neutral proteases. TC-type mast cells(MCTC) contain tryptase together with chymase, cathepsin-G, and carboxypeptidase, while T-type mast cells(MCT) contain tryptase only. They also produce Th2- type cytokines to persist chronic allergic inflammation in local tissues. Mast cells have been widely studied in the context of allergic reactions and parasite infections, but there is growing evidence that they participate in innate immunity, wound healing, fibrosis, remodelling and autoimmune disease. Much research works are expected to be underwent by the development of in vitro culture system of human mast cells in addition to mast cells obtained from animals, human biopsy or cell lines. In conclusion, it is clear that mast cells are pleiotropic, multipotential and complex. More detailed research remains to be needed for further understanding of biology of mast cells and it will be helpful to develop novel treatment modality in allergic inflammation.

Keyword

Mast cells; Allergy; Immunity

MeSH Terms

Animals
Autoimmune Diseases
Biology
Biopsy
Bone Marrow
Cell Line
Chymases
Connective Tissue
Cytokines
Fibrosis
Humans
Hypersensitivity
Immunity, Innate*
Immunoglobulin E
Inflammation*
Mast Cells*
Parasites
Peptide Hydrolases
Pluripotent Stem Cells
Tryptases
Wound Healing
Chymases
Cytokines
Immunoglobulin E
Peptide Hydrolases
Tryptases
Full Text Links
  • KJP
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr