Expression of polydom in dermal neurofibroma and surrounding dermis in von Recklinghausen's disease

被引:0
|
作者
Kamitani, Tomo [1 ]
Murota, Hiroyuki [1 ,2 ]
Arase, Noriko [1 ]
Wataya-Kaneda, Mari [1 ]
Sato-Nishiuchi, Ryoko [3 ]
Sekiguchi, Kiyotoshi [3 ]
Okuzaki, Daisuke [4 ]
Motooka, Daisuke [4 ]
Katayama, Ichiro [1 ,5 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Integrated Med, Dermatol, Osaka, Japan
[2] Nagasaki Univ, Grad Sch Biomed Sci, Dept Dermatol, Nagasaki, Japan
[3] Osaka Univ, Inst Prot Res, Div Matrixome Res & Applicat, Osaka, Japan
[4] Osaka Univ, Genome Informat Res Ctr, Res Inst Microbial Dis, Osaka, Japan
[5] Osaka City Univ, Grad Sch Med, Dept Pigmentat Res & Therapeut, Osaka, Japan
关键词
von Recklinghausen's disease; Neurofibroma; Polydom; Platelet-derived growth factor B; TGF-beta; LUNG-CANCER; GROWTH; CELLS; SVEP1;
D O I
10.1016/j.jdermsci.2019.09.005
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Neurofibromas in von Recklinghausen's disease (vRD) can develop in the dermis. Therefore, we hypothesized that a dermal niche exists that promotes the development of these neurofibromas in subjects with vRD. Objective: The purpose of this study is to examine the function of polydom, known as a ligand for integrin, mediating cell adhesion, and expressed in mouse nerve tissue, in promotion of neurofibroma. Methods: Molecular, transcriptome and immunohistochemical analysis were performed to investigate the association between polydom expression and neurofibroma development. Results: Polydom mRNA levels were significantly higher in neurofibroma tissue than in control tissue. Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) analysis of RNA purified from primary cultured dermal neurofibroma cells demonstrated significantly higher polydom mRNA expression in cells derived from the surrounding dermis of neurofibromas compared to those from normal human dermal fibroblasts. RNA sequencing was used to compare gene expression between cultured cells derived from dermal neurofibroma-surrounding tissue with or without polydom knockdown. Subsequent gene ontology assays revealed that expression of integrin beta 8 (ITGB8), a factor that releases transforming growth factor-beta (TGF-beta) from pro-TGF-beta, was downregulated following polydom knockdown, suggesting upregulation of polydom-mediated TGF-beta production. Furthermore, we observed a strong association between polydom expression and the increase in platelet-derived growth factor B (PDGFB) expression in primary cultured cells from the surrounding dermis of neurofibromas exposed to TGF-beta 1. Conclusion: Our results suggest that increased polydom expression in the dermis surrounding neurofibromas may promote dermal neurofibroma development by activating the TGF-beta signaling pathway. (C) 2019 Published by Elsevier B.V. on behalf of Japanese Society for Investigative Dermatology.
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收藏
页码:73 / 80
页数:8
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