GPR30 Deficiency Causes Increased Bone Mass, Mineralization, and Growth Plate Proliferative Activity in Male Mice
2011

GPR30 Deficiency Increases Bone Mass and Growth in Male Mice

Sample size: 40 publication 15 minutes Evidence: high

Author Information

Author(s): Ford Jeffery, Hajibeigi Asghar, Long Michael, Hahner Lisa, Gore Crystal, Hsieh Jer-Tseng, Clegg Deborah, Zerwekh Joseph, Öz Orhan K

Primary Institution: University of Texas Southwestern Medical Center at Dallas

Hypothesis

Does GPR30 deficiency affect bone mass and growth plate activity in male mice?

Conclusion

GPR30 deficiency in male mice leads to increased bone mass, size, and growth plate proliferation without altering circulating IGF-1 levels.

Supporting Evidence

  • Gpr30 KO mice had increased body weight and nasal-anal length compared to wild-type mice.
  • Femur length and bone mineral density were significantly greater in Gpr30 KO mice.
  • BrdU labeling indicated higher proliferation in the growth plate of Gpr30 KO mice.
  • Dynamic histomorphometry showed increased mineralized surface in Gpr30 KO mice.

Takeaway

When male mice don't have GPR30, they grow bigger bones and have more active growth plates, which helps them grow taller.

Methodology

The study involved comparing GPR30 knockout mice with wild-type mice, measuring body weight, bone density, and growth plate activity using various imaging and histological techniques.

Potential Biases

Potential bias due to the specific genetic background of the mice used in the study.

Limitations

The study was conducted only on male mice, and the findings may not be generalizable to females or other species.

Participant Demographics

Adult male mice, specifically Gpr30 knockout and wild-type strains.

Statistical Information

P-Value

p<0.001

Statistical Significance

p<0.001

Digital Object Identifier (DOI)

10.1002/jbmr.209

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