Novel Hedgehog Agonists Promote Osteoblast Differentiation in Mesenchymal Stem Cells

被引:52
作者
Nakamura, Takashi [1 ,2 ]
Naruse, Masahiro [1 ]
Chiba, Yuta [1 ]
Komori, Toshihisa [3 ]
Sasaki, Keiichi [2 ]
Iwamoto, Masahiro [4 ]
Fukumoto, Satoshi [1 ]
机构
[1] Dept Oral Hlth & Dev Sci, Div Pediat Dent, Sendai, Miyagi, Japan
[2] Tohoku Univ, Grad Sch Dent, Liaison Ctr Innovat Dent, Sendai, Miyagi 9808575, Japan
[3] Nagasaki Univ, Grad Sch Biomed Sci, Dept Cell Biol, Unit Basic Med Sci, Nagasaki 852, Japan
[4] Childrens Hosp Philadelphia, Div Orthoped Res Surg, Philadelphia, PA 19104 USA
基金
日本学术振兴会;
关键词
BONE MORPHOGENETIC PROTEIN-2; CLEIDOCRANIAL DYSPLASIA; CLINICAL-APPLICATIONS; MUTATION ANALYSIS; FACTOR EPIPROFIN; MINERAL DENSITY; GENE; RUNX2; OSTERIX; CBFA1;
D O I
10.1002/jcp.24823
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Hedgehog (Hh) family members are involved in multiple cellular processes including proliferation, migration, differentiation, and cell fate determination. Recently, the novel Hh agonists Hh-Ag 1.3 and 1.7 were identified in a high-throughput screening of small molecule compounds that activate the expression of Gli1, a target of Hh signaling. This study demonstrates that Hh-Ag 1.3 and 1.7 strongly activate the expression of endogenous Gli1 and promote osteoblast differentiation in the mesenchymal stem cell line C3H10T1/2. Both compounds stimulated alkaline phosphatase activity in a dose-dependent manner, and induced osteoblast marker gene expression in C3H10T1/2 cells, which indicated that they had acquired an osteoblast identity. Of the markers, the expression of osterix/Sp7, a downstream target of runt-related transcription factor (Runx)2, was induced by Hh-Ag 1.7, which also rescued the osteoblast differentiation defect of RD-127, a mesenchymal cell line from Runx2-deficient mice. Hh-Ags also activated canonical Wnt signaling and synergized with low doses of BMP-2 to enhance osteoblastic potential. Thus, Hh-Ag 1.7 could be useful for bone healing in individuals with abnormalities in osteogenesis, such as osteoporosis patients and the elderly, and can contribute to the development of novel therapeutics for the treatment of bone fractures and defects. (C) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:922 / 929
页数:8
相关论文
共 40 条
[1]
Tissue repair and stem cell renewal in carcinogenesis [J].
Beachy, PA ;
Karhadkar, SS ;
Berman, DM .
NATURE, 2004, 432 (7015) :324-331
[2]
Promoter 2-1025 T/C polymorphism in the RUNX2 gene is associated with femoral neck BMD in Spanish postmenopausal women [J].
Bustamante, Mariona ;
Nogues, Xavier ;
Agueda, Lidia ;
Jurado, Susana ;
Wesselius, Anke ;
Caceres, Enrique ;
Carreras, Ramon ;
Ciria, Manel ;
Mellibovsky, Leonardo ;
Balcells, Susana ;
Diez-Perez, Adolfo ;
Grinberg, Daniel .
CALCIFIED TISSUE INTERNATIONAL, 2007, 81 (04) :327-332
[3]
Calori GM, 2009, INJURY, V40, P67
[4]
Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function [J].
Chiang, C ;
Ying, LTT ;
Lee, E ;
Young, KE ;
Corden, JL ;
Westphal, H ;
Beachy, PA .
NATURE, 1996, 383 (6599) :407-413
[5]
Severe Cleidocranial Dysplasia and Hypophosphatasia in a Child With Microdeletion of the C-Terminal Region of RUNX2 [J].
El-Gharbawy, Areeg H. ;
Peeden, Joseph N., Jr. ;
Lachman, Ralph S. ;
Graham, John M., Jr. ;
Moore, Stephen R. ;
Rimoin, David L. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (01) :169-174
[6]
Hedgehog proteins stimulate chondrogenic cell differentiation and cartilage formation [J].
Enomoto-Iwamoto, M ;
Nakamura, T ;
Aikawa, T ;
Higuchi, Y ;
Yuasa, T ;
Yamaguchi, A ;
Nohno, T ;
Noji, S ;
Matsuya, T ;
Kurisu, K ;
Koyama, E ;
Pacifici, M ;
Iwamoto, M .
JOURNAL OF BONE AND MINERAL RESEARCH, 2000, 15 (09) :1659-1668
[7]
Gene therapy for bone healing [J].
Evans, Christopher H. .
EXPERT REVIEWS IN MOLECULAR MEDICINE, 2010, 12
[8]
Frank-Kamenetsky Maria, 2002, J Biol, V1, P10, DOI 10.1186/1475-4924-1-10
[9]
Communicating with Hedgehogs [J].
Hooper, JE ;
Scott, MP .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (04) :306-317
[10]
Sequential roles of Hedgehog and Wnt signaling in osteoblast development [J].
Hu, HL ;
Hilton, MJ ;
Tu, XL ;
Yu, K ;
Ornitz, DM ;
Long, F .
DEVELOPMENT, 2005, 132 (01) :49-60