Development of gene silencing pyrrole-imidazole polyamide targeting the TGF-β1 promoter for treatment of progressive renal diseases

被引:101
作者
Fukuda, Noboru
Ueno, Takahiro
Tahira, Yoshiko
Ayame, Hirohito
Zhang, Wen
Bando, Toshikazu
Sugiyama, Hiroshi
Saito, Satoshi
Matsumoto, Koichi
Mugishima, Hideo
Serie, Kazuo
机构
[1] Nihon Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 1738610, Japan
[2] Nihon Univ, Dept Adv Med, Tokyo 1738610, Japan
[3] Nihon Univ, Adv Res Inst Sci & Humanities, Tokyo 1738610, Japan
[4] Kyoto Univ, Grad Sch Sci, Dept Chem, Kyoto, Japan
[5] Gentier Biosyst Inc, Tokyo, Japan
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2006年 / 17卷 / 02期
关键词
D O I
10.1681/ASN.2005060650
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Pyrrole-imidazole (Py-Im) polyamides are nuclease-resistant novel compounds that inhibit gene expression by binding to the minor groove of DNA. A Py-Im polyamide that targets rat TGF-beta 1 was designed as a gene-silencing agent for progressive renal diseases, and the distribution and the effects of this polyamide on renal injury were examined in Dahl-salt sensitive (Dahl-S) rats. For identification of transcription factor binding elements for activation of the rat TGF-beta 1 gene, recombinant TGF-beta 1 reporter plasmids were transfected into HEK-293 cells, and promoter activity was measured. Py-Im polyamide was designed to the activator protein-1 binding site of the rat TGF-beta 1 promoter. This Py-Im polyamide showed strong, fast, and specific binding to the target DNA in gel mobility shift and Biacore assays. Py-Im polyamide significantly inhibited TGF-beta 1 promoter activity and expression of TGF-beta 1 mRNA and protein in rat mesangial cells. Intravenously administered fluorescein-labeled polyamide distributed to the kidney of rats. Py-Im polyamide significantly inhibited expression of TGF-beta 1 mRNA and protein in the renal cortex of Dahl-S rats and reduced the increase in urinary protein and albumin in Dahl-S rats independent of changes in blood pressure. These results indicate that Py-Im polyamide that targets TGF-beta 1 will be a novel gene-silencing agent for the TGF-beta 1-associated diseases, including progressive renal diseases.
引用
收藏
页码:422 / 432
页数:11
相关论文
共 40 条
[1]   Duplication of the genome in normal and cancer cell cycles [J].
Bandura, JL ;
Calvi, BR .
CANCER BIOLOGY & THERAPY, 2002, 1 (01) :8-13
[2]   Cellular uptake of N-methylpyrrole/N-methylimidazole polyamide-dye conjugates [J].
Belitsky, JM ;
Leslie, SJ ;
Arora, PS ;
Beerman, TA ;
Dervan, PB .
BIOORGANIC & MEDICINAL CHEMISTRY, 2002, 10 (10) :3313-3318
[3]   Nuclear localization of pyrrole-imidazole polyamide-fluorescein conjugates in cell culture [J].
Best, TP ;
Edelson, BS ;
Nickols, NG ;
Dervan, PB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (21) :12063-12068
[4]   TRANSFORMING GROWTH-FACTOR TYPE-BETA SPECIFICALLY STIMULATES SYNTHESIS OF PROTEOGLYCAN IN HUMAN ADULT ARTERIAL SMOOTH-MUSCLE CELLS [J].
CHEN, JK ;
HOSHI, H ;
MCKEEHAN, WL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (15) :5287-5291
[5]   Antihypertensive effects of chronic anti-TGF-β antibody therapy in Dahl S rats [J].
Dahly, AJ ;
Hoagland, KM ;
Flasch, AK ;
Jha, S ;
Ledbetter, SR ;
Roman, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2002, 283 (03) :R757-R767
[6]   Molecular recognition of DNA by small molecules [J].
Dervan, PB .
BIOORGANIC & MEDICINAL CHEMISTRY, 2001, 9 (09) :2215-2235
[7]   Inhibition of RNA polymerase II transcription in human cells by synthetic DNA-binding ligands [J].
Dickinson, LA ;
Gulizia, RJ ;
Trauger, JW ;
Baird, EE ;
Mosier, DE ;
Gottesfeld, JM ;
Dervan, PB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :12890-12895
[8]   Sequence-specific protection of plasmid DNA from restriction endonuclease hydrolysis by pyrrole-imidazole-cyclopropapyrroloindole conjugates [J].
Fujimoto, K ;
Iida, H ;
Kawakami, M ;
Bando, T ;
Tao, ZF ;
Sugiyama, H .
NUCLEIC ACIDS RESEARCH, 2002, 30 (17) :3748-3753
[9]   CHARACTERIZATION OF THE MOUSE TRANSFORMING GROWTH FACTOR-BETA-1 PROMOTER AND ACTIVATION BY THE HA-RAS ONCOGENE [J].
GEISER, AG ;
KIM, SJ ;
ROBERTS, AB ;
SPORN, MB .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (01) :84-92
[10]   Renal expression of transforming growth factor-β inducible gene-h3 (βig-h3) in normal and diabetic rats [J].
Gilbert, RE ;
Wilkinson-Berka, JL ;
Johnson, DW ;
Cox, A ;
Soulis, T ;
Wu, LL ;
Kelly, DJ ;
Jerums, G ;
Pollock, CA ;
Cooper, ME .
KIDNEY INTERNATIONAL, 1998, 54 (04) :1052-1062