Mechanical stretch suppresses BMP4 induction of stem cell adipogenesis via upregulating ERK but not through downregulating Smad or p38

被引:30
作者
Lee, Jeong Soon [1 ]
Ha, Ligyeom [1 ]
Park, Jin-Hee [1 ]
Lim, Jung Yul [1 ,2 ]
机构
[1] Univ Nebraska Lincoln, Dept Mech & Mat Engn, Lincoln, NE 68588 USA
[2] Kyung Hee Univ, Grad Sch Dent, Seoul, South Korea
关键词
Mesenchymal stem cells; Adipogenesis; Bone morphogenetic proteins; Cell stretch; Smad; p38; ERK; Obesity; BONE MORPHOGENETIC PROTEIN-4; ACTIVATED-RECEPTOR-GAMMA; MARROW STROMAL CELLS; OSTEOGENIC DIFFERENTIATION; ADIPOCYTE DIFFERENTIATION; INHIBITS ADIPOGENESIS; METABOLIC SYNDROME; COMMITMENT; LINEAGE; PATHWAY;
D O I
10.1016/j.bbrc.2012.01.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Bone morphogenetic proteins (BMPs) are also implicated in the commitment of mesenchymal stem cells (MSCs) toward adipocytes. We tested that stretching of cells may downregulate BMP4 induction of MSC adipogenesis. C3H10T1/2 MSCs were pretreated with BMP4 and induced to differentiate to adipocytes using adipogenic hormonal inducers. To test the stretch effect on BMP4 function, cells were exposed to cyclic tensile stretch (10% strain, 0.25 Hz, 120 min/day) during the BMP4 pretreatment period. BMP4 induced MSC adipocytic commitment. Stretching during the BMP4 exposure could suppress BMP4 induction of MSC adipogenesis, as assessed by downregulated adipogenic transcription factors (PPAR gamma, C/EBP alpha, aP2) and decreased lipid accumulation. BMP4 signaled through Smad1/5/8 and p38MAPK, whereas cell stretch did not affect BMP4-induced activation in Smad or p38. On the other hand, cell stretch triggered significant ERK1/2 phosphorylation relative to BMP4 treatment alone cells. Further, stretch suppression of BMP4-induced MSC adipogenesis was significantly deteriorated if cells were stretched with ERK blocked by PD98059. Combined, these suggest that cell stretch suppresses the BMP4 induction of MSC adipogenesis potentially via upregulating ERK but not through the downregulation of Smad or p38. Our data on inhibiting MSC adipogenesis will be of significant interest for obesity and developmental mechanobiology studies. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:278 / 283
页数:6
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