The gut microbiome has sexually dimorphic effects on bone tissue energy metabolism and multiscale bone quality in C57BL/6J mice

Abstract

AbstractThe gut microbiome impacts bone mass, implying a disruption to bone homeostasis, yet significant uncertainty remains regarding the impacts of the gut microbiome on remodeling bone cells. The gut microbiome is thought to be essential for normal biomineralization, but the specific consequences of the absent gut microbiome on tissue mineralization and multiscale bone quality are not determined. We hypothesized that bone homeostasis and tissue-scale metabolism, tissue mineralization, and whole-bone biomechanics are altered in germ-free (GF) C57BL/6J mice. Further, because many characteristics of the gut microbiome are sexually dimorphic, we hypothesized that the gut microbiome would show important sex differences with regards to its impact on bone quality. Differences between GF and conventional mouse bone extended from bone tissue metabolism to whole bone biomechanics. Cortical bone tissue from male mice had a greater signature of amino acid metabolism whereas female cells had a greater signature of lipid metabolism. These sex differences were also present in GF mice and were indeed even more stark. GF increased cortical femur bone formation for both sexes and decreased bone resorption and osteoclast density only in females. GF similarly increased cortical femur tissue mineralization and altered collagen structure for both sexes but led to greater gains in distal femur trabecular microarchitecture for males. Whole femur strength was similarly increased with GF for both sexes, but males had a greater increase in modulus. GF did not impact fracture toughness for either sex. The altered bone quality with GF is multifactorial and is likely contributed to by differences in tissue-scale composition as well as lower cortical porosity. Together, these data demonstrate that the gut microbiome influences bone cells and multiscale bone quality, but that the specific relationships that underlie these effects to bone are different for females and males.