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The expression of RAGE and EN-RAGE in leprosy

Authors
 M-H. Kim  ;  Y.W. Choi  ;  H.Y. Choi  ;  K.B. Myung  ;  S.N. Cho 
Citation
 BRITISH JOURNAL OF DERMATOLOGY, Vol.154(4) : 594-601, 2006 
Journal Title
BRITISH JOURNAL OF DERMATOLOGY
ISSN
 0007-0963 
Issue Date
2006
MeSH
Enzyme-Linked Immunosorbent Assay/methods ; Humans ; Immunoenzyme Techniques ; Leprosy/metabolism* ; Microscopy, Confocal ; Mycobacterium Infections, Nontuberculous/metabolism ; Receptor for Advanced Glycation End Products ; Receptors, Immunologic/biosynthesis ; Receptors, Immunologic/metabolism* ; S100 Proteins/biosynthesis ; S100 Proteins/metabolism* ; S100A12 Protein ; Sarcoidosis/metabolism ; Skin/metabolism
Keywords
atypical mycobacterial infection ; EN‐RAGE ; leprosy ; RAGE ; S100A12 ; sarcoidosis
Abstract
BACKGROUND: Extracellular newly identified RAGE-binding protein (EN-RAGE) is a ligand of the receptor for advanced glycation endproducts (RAGE) and has been termed S100A12. The ligation of EN-RAGE with RAGE on the endothelium, mononuclear phagocytes and lymphocytes triggers cellular activation with the generation of the key proinflammatory mediators interleukin (IL)-1beta and tumour necrosis factor (TNF)-alpha.
OBJECTIVES: The aim of this study was to investigate the presence of RAGE and EN-RAGE, their spatial localization and their coexpression in leprosy lesions.
METHODS: Immunohistochemistry and confocal laser scanning microscopy were used to evaluate the expression of RAGE and EN-RAGE in leprosy. By enzyme-linked immunosorbent assay, RAGE and EN-RAGE were detected in the serum.
RESULTS: (1) In the multibacillary (MB) and paucibacillary (PB) groups, the level of RAGE production was significantly higher than in patients with atypical mycobacterial infection or sarcoidosis (P < 0.01). In the MB group, the production of RAGE was higher than in the PB group (P < 0.01), and it was higher in patients without the lepra reaction than in patients with the lepra reaction (P < 0.05). (2) In MB, PB and atypical mycobacterial infection, the level of EN-RAGE production was significantly higher than in sarcoidosis (P < 0.01). (3) In the confocal laser scanning microscopic examination, the RAGE and EN-RAGE proteins were detected in lepromatous leprosy. These proteins are spatially colocalized along the cell surface, which is in agreement with their receptor-ligand interaction. (4) A comparable amount of EN-RAGE was detected in the serum of the MB and PB groups. Patients with the reaction showed a higher level of EN-RAGE than patients without the reaction in leprosy.
CONCLUSIONS: Our data suggest that in leprosy, RAGE and EN-RAGE may be involved in the proinflammatory process rather than the antimycobacterial activity, especially during the lepra reaction. The blockade of the interaction of RAGE and EN-RAGE at the early stage of the inflammatory process may minimize the inflammatory response and consequent tissue damage or the sequelae of leprosy.
Full Text
http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2133.2005.07112.x/abstract
DOI
10.1111/j.1365-2133.2005.07112.x
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Microbiology (미생물학교실) > 1. Journal Papers
Yonsei Authors
Cho, Sang Nae(조상래)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/109866
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