Beta-catenin haplo insufficient male mice do not lose bone in response to hindlimb unloading

Delphine B. Maurel, Peipei Duan, Joshua Farr, An Lin Cheng, Mark L. Johnson, Lynda Bonewald

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

As the β-catenin pathway has been shown to be involved in mechanotransduction, we sought to determine if haploinsufficiency would affect skeletal response to unloading. It has previously been shown that deletion of both alleles of β-catenin in bone cells results in a fragile skeleton highly susceptible to fracture, but deletion of one allele using Dmp1-Cre (Ctnnb1+/loxP ; Dmp1-Cre, cKO HET) has little effect on the 2 mo old skeleton. We found that under normal housing conditions, trabecular bone volume was significantly less in 5 mo old male cKO HET mice compared to controls (Ctrl/HET:Tb. BV/TV = 13.96±2.71/8.92±0.95%, Tb.N. = 4.88±0.51/3.95±0.44/mm, Tb. Sp. = 0.20±0.02/0.26±0.03mm, a 36%, 19% and 30% change respectively) but not in females suggesting an age and gender related effect. Before performing suspension experiments and to control for the environmental effects, animals with the same tail attachment and housing conditions, but not suspended (NS), were compared to normally housed (NH) animals. Attachment and housing resulted in weight loss in both genders and phenotypes. Cortical bone loss was observed in the cKO HET males (NH/NS, Ct BV/TV: 90.45±0.72/89.12±0.56%) and both diaphyseal (0.19±0.01/0.17 ±0.01mm) and metaphyseal (0.10±0.01/0.08±0.01mm) thickness, but not in female cKO HET mice suggesting that male cKO HET mice are susceptible to attachment and housing conditions. These results with transgenic mice emphasizes the importance of proper controls when attributing skeletal responses to unloading. With suspension, cKO HET male mice did not lose bone unlike female cKO HET mice that had greater trabecular bone loss than controls (Ctrl 9%:cKO HET 21% decrease Tb. N; Ctrl 12%:cKO HET 27% increase Tb. Sp.). Suspended and non-suspended mice lost weight compared to normally housed animals. Taken together, the data suggest a protective effect of β-catenin against the effects of stress in males and partial protection against unloading in females.

Original languageEnglish (US)
Article numbere0158381
JournalPLoS One
Volume11
Issue number7
DOIs
StatePublished - Jul 1 2016
Externally publishedYes

Fingerprint

Hindlimb Suspension
beta Catenin
Unloading
Bone
Catenins
bones
Bone and Bones
mice
Animals
Suspensions
Skeleton
skeleton
Alleles
Haploinsufficiency
alleles
animals
Environmental impact
gender
Transgenic Mice
hindlimbs

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

Beta-catenin haplo insufficient male mice do not lose bone in response to hindlimb unloading. / Maurel, Delphine B.; Duan, Peipei; Farr, Joshua; Cheng, An Lin; Johnson, Mark L.; Bonewald, Lynda.

In: PLoS One, Vol. 11, No. 7, e0158381, 01.07.2016.

Research output: Contribution to journalArticle

Maurel, Delphine B. ; Duan, Peipei ; Farr, Joshua ; Cheng, An Lin ; Johnson, Mark L. ; Bonewald, Lynda. / Beta-catenin haplo insufficient male mice do not lose bone in response to hindlimb unloading. In: PLoS One. 2016 ; Vol. 11, No. 7.
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