Development of pyrrole-imidazole polyamide targeting Fc receptor common gamma chain for the treatment of immune-complex related renal disease

Mamiko Kajiwara, Takahiro Ueno, Noboru Fukuda, Hiroyuki Matsuda, Toshibumi Shimokawa, Maki Kitai, Akiko Tsunemi, Yoshinobu Fuke, Takayuki Fujita, Koichi Matsumoto, Yoshiaki Matsumoto, Chisei Ra, Masayoshi Soma

研究成果: ジャーナルへの寄稿記事査読

3 被引用数 (Scopus)

抄録

Fcγ receptors I and III are thought to be involved in the development of lupus nephritis. Expression of Fc receptor common gamma chain (FcRγ) is necessary for the stable expression of Fcγ receptors I and III. The aim of this study was to develop a novel agent for the treatment of immune complex related renal disease using a gene regulator, pyrrole(Py)-imidazole(Im) (PI) polyamide, targeting the mouse FcRγ gene promoter. Two PI polyamides targeting FcRγ promoters were designed and synthesized. The effect of the PI polyamides on FcRγ mRNA expression was evaluated in J774.A cells by real-time polymerase chain reaction (PCR), and CD16/32 protein expression was determined by immunocytochemical analysis and flow cytometry. The effects of these polyamides on FcRγ gene expression and CD16/32 protein expression were evaluated in mouse peripheral blood mononuclear cells (PBMCs). One milligram per kilogram body weight of PI polyamide was injected via the tail vein every 2d for 1 week and PBMCs were collected and analyzed. PI polyamide showed a specific binding to the target DNA in a gel mobility shift assay. Treatment of J774.A cells with 1.0μM PI polyamide 1 significantly reduced FcRγ mRNA expression and CD16/32 surface protein expression in J774.A cells. Similarly, PI polyamide significantly decreased expression of FcRγ mRNA and CD16/32 in the PBMCs of C57B6 mice. PI polyamide designed to bind the FcRγ promoter decreased FcRγ gene and CD16/32 protein expression. PI polyamide targeting the FcRγ gene may be a novel gene regulator for the prevention of lupus nephritis or other immune complex-related disease.

本文言語英語
ページ(範囲)2028-2035
ページ数8
ジャーナルBiological and Pharmaceutical Bulletin
35
11
DOI
出版ステータス出版済み - 11月 2012

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