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
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