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BMP signaling in mesenchymal stem cell differentiation and bone formation 被引量:28
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作者 Maureen Beederman Joseph D. lamplot +18 位作者 Guoxin Nan Jinhua Wang Xing liu liangjun Yin Ruidong li Wei Shui Hongyu Zhang Stephanie H. Kim Wenwen Zhang Jiye Zhang Yuhan Kong Sahitya Denduluri Mary Rose Rogers Abdullah Pratt Rex C. Haydon Hue H. luu Jovito Angeles lewis l. shi Tong-Chuan He 《Journal of Biomedical Science and Engineering》 2013年第8期32-52,共21页
Bone morphogenetic proteins (BMPs) are members of the TGF-β superfamily and have diverse functions during development and organogenesis. BMPs play a major role in skeletal development and bone formation, and disrupti... Bone morphogenetic proteins (BMPs) are members of the TGF-β superfamily and have diverse functions during development and organogenesis. BMPs play a major role in skeletal development and bone formation, and disruptions in BMP signaling cause a variety of skeletal and extraskeletal anomalies. Several knockout models have provided insight into the mechanisms responsible for these phenotypes. Proper bone formation requires the differentiation of osteoblasts from mesenchymal stem cell (MSC) precursors, a process mediated in part by BMP signaling. Multiple BMPs, including BMP2, BMP6, BMP7 and BMP9, promote osteoblastic differentiation of MSCs both in vitro and in vivo. BMP9 is one of the most osteogenic BMPs, yet it is a poorly characterized member of the BMP family. Several studies demonstrate that the mechanisms controlling BMP9-mediated osteogenesis differ from other osteogenic BMPs, but little is known about these specific mechanisms. Several pathways critical to BMP9-mediated osteogenesis are also important in the differentiation of other cell lineages, including adipocytes and chondrocytes. BMP9 has also demonstrated translational promise in spinal fusion and bone fracture repair. This review will summarize our current knowledge of BMP-mediated osteogenesis, with a focus on BMP9, by presenting recently completed work which may help us to further elucidate these pathways. 展开更多
关键词 BMP BMP9 Bone Regeneration IGF OSTEOGENESIS TGF-β Wnt Signal TRANSDUCTION MESENCHYMAL Stem Cells MSCS
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Corrigendum to “Sox9 augments BMP2-induced chondrogenic differentiation by downregulating Smad7 in mesenchymal stem cells (MSCs)” [Genes & Diseases 4 (2017) 229–239]
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作者 Chen Zhao Wei Jiang +15 位作者 Nian Zhou Junyi liao Mingming Yang Ning Hu Xi liang Wei Xu Hong Chen Wei liu lewis l. shi leonardo Oliveira Jennifer Moriatis Wolf Sherwin Ho Aravind Athiviraham H.M. Tsai Tong-Chuan He Wei Huang 《Genes & Diseases》 SCIE CSCD 2023年第2期624-626,共3页
The authors regret having image assembly errors in Figure 1A and Figure 3A.Specifically,in Figure 1A,the images for"C3H10T1/2",""BMP2"and"Sox9"were erroneously duplicated with the im... The authors regret having image assembly errors in Figure 1A and Figure 3A.Specifically,in Figure 1A,the images for"C3H10T1/2",""BMP2"and"Sox9"were erroneously duplicated with the images from an irrelevant experiment that was conducted at the same time.In Figure 3A,the images for"Col2a1"and"β-actin"were erroneously duplicated with the images from an irrelevant experiment that was conducted at the same time. 展开更多
关键词 SMAD7 FIGURE BMP2
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