Research Website
http://web.ics.purdue.edu/~rmain/Main_Lab_Purdue/Home.html
Keywords
Estrogen Receptor, ERβ, Mechanical Loading, Osteocyte, Skeleton, Bone
Presentation Type
Poster
Research Abstract
Estrogen’s biological functions are mediated by estrogen binding to estrogen receptors (ER). Understanding what role both ERα and ERβ have in bone maintenance and formation can contribute to possible treatment of osteoporosis. This study examined osteocyte specific deletion of ERβ in mice. The cross of ERβ-floxed mice with DMP1-8kb-Cre mice provided both experimental knockout mice as well as littermate control mice. At 24 weeks of age the left tibiae of all mice were mechanically loaded five days per week for two weeks to induce bone formation. Analysis of cortical bone was conducted using microcomputed tomography (microCT) to measure load-induced changes in bone density and architecture of both loaded and non-loaded limbs. We found a significant effect of load on cortical bone geometry in both male and female knockout and control mice at 37% and 50% bone length. Based on our findings, osteocyte ERβ appears to play a minor role in determining cortical bone geometry in 24 week old mice. We are still investigating the effect of load and genotype on cancellous bone.
Session Track
Health
Recommended Citation
Julia P. Townsend and Russell P. Main,
"The Role of Osteocyte Estrogen Receptor Beta (ERβ) in Regulating the Skeletal Response to Mechanical Loading"
(August 4, 2016).
The Summer Undergraduate Research Fellowship (SURF) Symposium.
Paper 121.
https://docs.lib.purdue.edu/surf/2016/presentations/121
The Role of Osteocyte Estrogen Receptor Beta (ERβ) in Regulating the Skeletal Response to Mechanical Loading
Estrogen’s biological functions are mediated by estrogen binding to estrogen receptors (ER). Understanding what role both ERα and ERβ have in bone maintenance and formation can contribute to possible treatment of osteoporosis. This study examined osteocyte specific deletion of ERβ in mice. The cross of ERβ-floxed mice with DMP1-8kb-Cre mice provided both experimental knockout mice as well as littermate control mice. At 24 weeks of age the left tibiae of all mice were mechanically loaded five days per week for two weeks to induce bone formation. Analysis of cortical bone was conducted using microcomputed tomography (microCT) to measure load-induced changes in bone density and architecture of both loaded and non-loaded limbs. We found a significant effect of load on cortical bone geometry in both male and female knockout and control mice at 37% and 50% bone length. Based on our findings, osteocyte ERβ appears to play a minor role in determining cortical bone geometry in 24 week old mice. We are still investigating the effect of load and genotype on cancellous bone.
https://docs.lib.purdue.edu/surf/2016/presentations/121