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Biology subjects

Morgan, E. F.

Publications and source records attributed to Morgan, E. F..

2 recordsLinked to original sources

Aging-related mechanical degradation of cortical bone is driven by microstructural changes in addition to porosity

This study aims to gain mechanistic understanding of how aging-related changes in the microstructure of cortical bone drive mechanical consequences at the macroscale. To that end, cortical bone was modeled as a bundle of elastic-plastic, parallel fibers loaded in uniaxial tension, which comprised osteons and interstitial tissue. Distinct material properties were assigned to each fiber in either the osteon or interstitial fiber "families." Models representative of mature (20-60 yrs.) bone, and elderly (60+) bone were created. Aging-related changes were modeled along three independent dimensions: (i) increased porosity, (ii) increased ratio of osteon fibers relative to interstitial fibers, and (iii) a change in fiber material properties. The model captured decreases in modulus, yield stress, yield strain, ultimate stress, ultimate strain, and toughness with age of 14%, 11%, 8%, 6%, 20%, and 30%, respectively. In both mature and elderly bundles, rupture of the interstitial fibers drove the initial loss of strength following the ultimate point. Plasticity and more gradual rupture of the osteons drove the remainder of the response. Both the onset and completion of interstitial fiber rupture occurred at lower strains in the elderly vs. mature case. Changes along all three dimensions were required for the model to capture aging-related decline in the strength, ductility, and toughness of cortical bone. These findings point to the importance of studying microstructural changes beyond porosity, such as the area fraction of osteons and the microconstituent material properties of osteon and interstitial tissue, in order to further our understanding of aging-related changes in bone.

bioengineering↗

Identification of known and novel long non-coding RNAs potentially responsible for the effects of BMD GWAS loci

Osteoporosis, characterized by low bone mineral density (BMD), is the most common complex disease affecting bone and constitutes a major societal health problem. Genome-wide association studies (GWASs) have identified over 1100 associations influencing BMD. It has been shown that perturbations to long non-coding RNAs (lncRNAs) influence BMD and the activities of bone cells; however, the extent to which lncRNAs are involved in the genetic regulation of BMD is unknown. Here, we combined the analysis of allelic imbalance (AI) in human acetabular bone fragments with a transcriptome-wide association study (TWAS) and expression quantitative trait loci (eQTL) colocalization analysis using data from the Genotype-Tissue Expression (GTEx) project to identify lncRNAs potentially responsible for GWAS associations. We identified 27 lncRNAs in bone that are located in proximity to a BMD GWAS association and harbor SNPs demonstrating AI. Using GTEx data we identified an additional 31 lncRNAs whose expression was associated (FDR correction<0.05) with BMD through TWAS and had a colocalizing eQTL (regional colocalization probability (RCP)>0.1). The 58 lncRNAs are located in 43 BMD associations. To further support a causal role for the identified lncRNAs, we show that 23 of the 58 lncRNAs are differentially expressed as a function of osteoblast differentiation. Our approach identifies lncRNAs that are potentially responsible for BMD GWAS associations and suggest that lncRNAs play a role in the genetics of osteoporosis.

genomics↗