Bone Morphogenetic Proteins in Bone Stimulate Osteoclasts and Osteoblasts During Bone Development

@article{Okamoto2006BoneMP,
  title={Bone Morphogenetic Proteins in Bone Stimulate Osteoclasts and Osteoblasts During Bone Development},
  author={Mina Okamoto and Junko Murai and Hideki Yoshikawa and Noriyuki Tsumaki},
  journal={Journal of Bone and Mineral Research},
  year={2006},
  volume={21}
}
In this study, overexpression of noggin, a BMP antagonist, in developing bone caused significantly decreased osteoclast number as well as bone formation rate, resulting in increased bone mass with immature bone quality. BMP signaling plays important roles in normal bone development and regulation of bone resorption. 

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  • Biology, Medicine
    Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
  • 2008
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BMP-6 and mesenchymal stem cell differentiation.

...

References

SHOWING 1-10 OF 36 REFERENCES

Skeletal overexpression of noggin results in osteopenia and reduced bone formation.

Transgenic mice overexpressing noggin in the bone microenvironment have decreased trabecular bone volume and impaired osteoblastic function, leading to osteopenia and fractures.

Bone Morphogenetic Protein Type IA Receptor Signaling Regulates Postnatal Osteoblast Function and Bone Remodeling*

Bone morphogenetic proteins (BMPs) function during various aspects of embryonic development including skeletogenesis. However, their biological functions after birth are less understood. To

Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton.

Excess BMP activity in the absence of Noggin antagonism may enhance the recruitment of cells into cartilage, resulting in oversized growth plates; chondrocytes are also refractory to joint-inducing positional cues.

The Bone Morphogenetic Proteins Antagonist Noggin Inhibits Membranous Ossification

It is shown that Noggin can modify bone formation in vivo in the adult animal and, thus, indirectly, that BMP signaling is indispensable in this process.

Bone morphogenetic protein receptor signaling is necessary for normal murine postnatal bone formation

The effects of alterations in BMP receptor function targeted to the osteoblast lineage are shown and a necessary role of B MP receptor signaling in postnatal bone growth and bone formation in vivo is demonstrated.

Essential Requirement of BMPs‐2/4 for Both Osteoblast and Osteoclast Formation in Murine Bone Marrow Cultures from Adult Mice: Antagonism by Noggin

  • E. AbeMatsuo Yamamoto S. Manolagas
  • Biology, Medicine
    Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
  • 2000
It is suggested that BMP‐2 and −4 are expressed in the bone marrow in postnatal life and serve to maintain the continuous supply of osteoblasts and osteoclasts, and that, in fact, B MP‐2/4‐induced commitment to the osteoblastic lineage is a prerequisite for osteoclast development.

Impaired osteoblastic differentiation, reduced bone formation, and severe osteoporosis in noggin-overexpressing mice.

The results provide compelling evidence that noggin, expressed in mature osteoblasts, inhibits osteoblast differentiation and bone formation, and the overproduction of noggins during biological aging may result in impaired osteoblow formation and function and hence, net bone loss.

Stimulatory effect of bone morphogenetic protein‐2 on osteoclast‐like cell formation and bone‐resorbing activity

  • M. KanataniT. Sugimoto K. Chihara
  • Biology, Medicine
    Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
  • 1995
The present data are the first to indicate that BMP‐2 stimulates bone resorption through both direct stimulation of osteoclast formation and activation of mature osteoclasts, possibly via stromal cells, in vitro.