Spiral surface growth without desorption

Spiral surface growth is well understood in the limit where the step motion is controlled by the local supersaturation of adatoms near the spiral ridge. In epitaxial thin-film growth, however, spirals can form in a step-flow regime where desorption of adatoms is negligible and the ridge dynamics is governed by the non-local diffusion field of adatoms on the whole surface. We investigate this limit numerically using a phase-field formulation of the Burton-Cabrera-Frank model, as well as analytically. Quantitative predictions, which differ strikingly from those of the local limit, are made for the selected step spacing as a function of the deposition flux, as well as for the dependence of the relaxation time to steady-state growth on the screw dislocation density.Comment: 9 pages, 3 figures, RevTe

Reduction in mesenchymal stem cell numbers in premature aging DNA repair deficient TTD mice

Background: Mice carrying mutations in DNA repair genes often show signs of accelerated ageing and therefore can be used as a model system to study age related diseases like osteoporosis. It has been shown that TTD mice, carrying a mutation in the nucleotide excision repair gene XPD (xeroderma pigmentosa group D), display features of ageing related osteoporosis as well as adipose tissue hypoplasia. Since both cell types involved, osteoblasts as well as adipocytes, arise from the same mesenchymal stem cell population, the aim of the current project was to study the number, proliferation and differentiation potential of these cells in TTD compared to wild type (WT) mice. This might provide us with useful information concerning the mechanism behind age-related osteoporosis and the loss of adipose tissue.Methods: Bone marrow from old TTD and WT mice was cultured under osteogenic or adipogenic conditions and analysed for alkaline phosphatase activity (ALP), mineralisation (osteoblast) and lipid deposition (adipocyte).Results: Under osteogenic conditions the number of ALP-positive colonies after 9 and 14 days of culture was significantly decreased (p=0.02) in TTD compared to WT mice. The rate at which new ALP-positive colonies are formed between day 9 and day 14 of culture has not changed between TTD and WT mice, indicating that the decrease in colony number is not due to a delay in differentiation. Mineralisation of ALP-positive colonies did not seem to be affected, with a borderline significant decrease on day 14 at the onset of mineralisation but no significant changes on day 21 of culture. Lipid deposition was strongly reduced in TTD compared to WT mice (p=0.01) after 35 days of culture.Conclusions: The observed reduction in osteoblast and adipocyte differentiation indicates a reduction of mesenchymal stem cell numbers in TTD mice. This reduction in mesenchymal stem cell numbers and the corresponding decline in osteoblast differentiation could explain the premature osteoporotic features observed in TTD mice. In line with this, the reduction of mesenchymal stem cells and adipocyte differentiation may underlie the adipose tissue hypoplasia observed in TTD mice

Deletion of the ghrelin receptor GHSR corrects the trabecular, but not the cortical bone changes in the femoral head of ob/ob mice

Background: There exists an intriguing and complex relationship between fat and bone cells with respect to aging and osteoporosis, which is mediated in part by leptin. Genetically obese mice (ob/ob), that lack leptin, have aheterogeneous bone phenotype, with differential effects on cortical and trabecular compartments. Besides its role in bone metabolism, leptin is most well known for its anorexigenic properties. Opposed in action to leptin is ghrelin, a potent orexigenic peptide hormone derived from the stomach. Ghrelin and leptin also act as each other’s antagonists in gonadal and immune system function.Objective: To determine if ghrelin opposes leptin action on bone metabolism.Methods: Characterization of femoral micro-architecture in 6 months old male wild type, ob/ob, ghrelin receptor knockout (Ghsr -/-), and ob/ob.Ghsr-/- mice using micro-computed tomography.Results: Deletion of Ghsr alone did not significantly alter bone micro-architecture in wild type mice. Deletion of leptin reduced cortical volume and thickness in the femoral head of wild type mice, while it increased endocortical volume. Tissue volume remained unaffected. Conversely, deletion of leptin increased trabecular bone volume, trabecular number and connectivity in wild type mice. Additional deletion of Ghsr in ob/ob mice restored the changes to wild type levels in trabecular bone, but not in cortical bone (all not significant).Conclusion: We found that leptin deficiency has a negative effect on cortical and a positive effect on trabecular bone micro-architecture, confirming the heterogeneous skeletal effects observed by others in ob/ob mice. Knocking out ghrelin signaling compensates for the effect of leptin deficiency on trabecular bone. These observations demonstrate the positive activity of ghrelin signaling in bone, and suggest that ghrelin and leptin have opposing actions on bone metabolism