Antisense targeting of TGF-β1 augments BMP-induced upregulation of osteopontin, type I collagen and Cbfa1 in human Saos-2 cells

被引:15
作者
Shen, Zhong-Jian [1 ]
Kim, Sang Kook
Jun, Do Youn
Park, Wan
Kim, Young Ho
Malter, James S.
Moon, Byung Jo
机构
[1] Kyungpook Natl Univ, Coll Nat Sci, Dept Biochem, Taegu 702701, South Korea
[2] Univ Wisconsin, Sch Med & Publ Hlth, Waisman Ctr Dev Disabil, Dept Pathol & Lab Med, Madison, WI 53705 USA
[3] Kyungpook Natl Univ, Inst Genet Engn, Taegu 702701, South Korea
[4] Kyungpook Natl Univ, Coll Nat Sci, Dept Microbiol, Taegu 702701, South Korea
[5] Kyungpook Natl Univ, Coll Nat Sci, Dept Biochem, Taegu 702701, South Korea
关键词
osteoblasts; differentiation; antisense oligonucleotides; TGF; BMP; proliferation; bone; Smad; GROWTH-FACTOR-BETA; BONE MORPHOGENETIC PROTEIN-2; TGF-BETA; OSTEOBLAST DIFFERENTIATION; CLEIDOCRANIAL DYSPLASIA; GENE-EXPRESSION; MESSENGER-RNA; TRANSFORMING GROWTH-FACTOR-BETA-1; OSTEOSARCOMA CELLS; KNOCKOUT MICE;
D O I
10.1016/j.yexcr.2007.01.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite commonalities in signal transduction in osteoblasts from different species, the role of TGF-beta 1 on bone formation remains elusive. In particular, the role of autocrine TGF-beta 1 on human osteoblasts is largely unknown. Here we show the effect of TGF-beta 1 knock-down on the proliferation and differentiation of osteoblasts induced by BMP2. Treatment with antisense TGF-beta 1 moderately increased the rate of cell proliferation, which was completely reversed by the exogenous addition of TGF-beta 1. Notably, TGF-beta 1 blockade significantly enhanced BMP2-induced upregulation of mRNAs encoding osteopontin, type I collagen and Cbfa1, which was suppressed by exogenous TGF-beta 1. Moreover, TGF-beta 1 knock-down increased BMP2-induced phosphorylation of Smad1/5 as well as their nuclear import, which paralleled a reduction of inhibitory Smad6. These data suggest autocrine TGF-beta 1 antagonizes BMP signaling through modulation of inducible Smad6 and the activity of BMP specific Smad1/5. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1415 / 1425
页数:11
相关论文
共 60 条
  • [31] Signal transductions induced by bone morphogenetic protein-2 and transforming growth factor-β in normal human osteoblastic cells
    Lai, CF
    Cheng, SL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (18) : 15514 - 15522
  • [32] The role of Smad signaling in hematopoiesis
    Larsson, J
    Karlsson, S
    [J]. ONCOGENE, 2005, 24 (37) : 5676 - 5692
  • [33] Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia
    Lee, B
    Thirunavukkarasu, K
    Zhou, L
    Pastore, L
    Baldini, A
    Hecht, J
    Geoffroy, V
    Ducy, P
    Karsenty, G
    [J]. NATURE GENETICS, 1997, 16 (03) : 307 - 310
  • [34] Runx2 is a common target of transforming growth factor β1 and bone morphogenetic protein 2, and cooperation between Runx2 and Smad5 induces osteoblast-specific gene expression in the pluripotent mesenchymal precursor cell line C2C12
    Lee, KS
    Kim, HJ
    Li, QL
    Chi, XZ
    Ueta, C
    Komori, T
    Wozney, JM
    Kim, EG
    Choi, JY
    Ryoo, HM
    Bae, SC
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (23) : 8783 - 8792
  • [35] Both the Smad and p38 MAPK pathways play a crucial role in Runx2 expression following induction by transforming growth factor-β and bone morphogenetic protein
    Lee, KS
    Hong, SH
    Bae, SC
    [J]. ONCOGENE, 2002, 21 (47) : 7156 - 7163
  • [36] Smad2 overexpression enhances Smad4 gene expression and suppresses CBFA1 gene expression in osteoblastic osteosarcoma ROS17/2.8 cells and primary rat calvaria cells
    Li, J
    Tsuji, K
    Komori, T
    Miyazono, K
    Wrana, JL
    Ito, Y
    Nifuji, A
    Noda, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (47) : 31009 - 31015
  • [37] Growth factors for bone growth and repair: IGF, TGF beta and BMP.
    Linkhart, TA
    Mohan, S
    Baylink, DJ
    [J]. BONE, 1996, 19 (01) : S1 - S12
  • [38] Morgan D M, 1998, Methods Mol Biol, V79, P179
  • [39] Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
    Mundlos, S
    Otto, F
    Mundlos, C
    Mulliken, JB
    Aylsworth, AS
    Albright, S
    Lindhout, D
    Cole, WG
    Henn, W
    Knoll, JHM
    Owen, MJ
    Mertelsmann, R
    Zabel, BU
    Olsen, BR
    [J]. CELL, 1997, 89 (05) : 773 - 779
  • [40] Smad5 and DPC4 are key molecules in mediating BMP-2-induced osteoblastic differentiation of the pluripotent mesenchymal precursor cell fine C2C12
    Nishimura, R
    Kato, Y
    Chen, D
    Harris, SE
    Mundy, GR
    Yoneda, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (04) : 1872 - 1879