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The umbilical cord suspends the fetus within the amniotic cavity, where fetal dynamics is one of its many functions. Hence, the umbilical cord is a viable index in determining fetal activity. Fetal movements result in mechanical loads that are fundamental for fetal growth. At present, mechanical environment during early human fetal development is still largely unknown. To determine early fetal movement dynamics at given physiological (0.060 m) and pathological umbilical cord lengths (0.030 m, 0.020 m, 0.017 m and 0.014 m) a 2D computational model was created to simulate dynamic movement conditions. Main findings of this computational model revealed the shortest umbilical cord length (0.014 m) with a

ObjectiveHyaline cartilage degenerative pathologies induce morphologic and biomechanical changes resulting in cartilage tissue damage. In pursuit of therapeutic options, electrical and mechanical stimulation have been proposed for improving tissue engineering approaches for cartilage repair. The purpose of this review was to highlight the effect of electrical stimulation and mechanical stimuli in chondrocyte behavior.DesignDifferent information sources and the MEDLINE database were systematically revised to summarize the different contributions for the past 40 years.ResultsIt has been shown that electric stimulation may increase cell proliferation and stimulate the synthesis of molecules associated with the extracellular matrix of the articular cartilage, such as collagen type II, aggrecan and glycosaminoglycans, while mechanical loads trigger anabolic and catabolic responses in chondrocytes.ConclusionThe biophysical stimuli can increase cell proliferation and stimulate molecules associated with hyaline cartilage extracellular matrix maintenance.

Summary Objective The overall aim of this study was to evaluate how supplementation of chondrocyte media with recombinant acid ceramidase (rhAC) influenced cartilage repair in a rat osteochondral defect model. Methods Primary chondrocytes were grown as monolayers in polystyrene culture dishes with and without rhAC (added once at the time of cell plating) for 7 days, and then seeded onto Bio-Gide ® collagen scaffolds and grown for an additional 3 days. The scaffolds were then introduced into osteochondral defects created in Sprague–Dawley rat trochlea by a microdrilling procedure. Analysis was performed 6 weeks post-surgery macroscopically, by micro-CT, histologically, and by immunohistochemistry. Results Treatment with rhAC led to increased cell numbers and glycosaminoglycan (GAG) production (∼2 and 3-fold, respectively) following 7 days of expansion in vitro . Gene expression of collagen 2, aggrecan and Sox-9 also was significantly elevated. After seeding onto Bio-Gide ® , more rhAC treated cells were evident within 4 h. At 6 weeks post-surgery, defects containing rhAC-treated cells exhibited more soft tissue formation at the articular surface, as evidenced by microCT, as well as histological evidence of enhanced cartilage repair. Notably, collagen 2 immunostaining revealed greater surface expression in animals receiving rhAC treated cells as well. Collagen 10 staining was not enhanced. Conclusion The results further demonstrate the positive effects of rhAC treatment on chondrocyte growth and phenotype in vitro , and reveal for the first time the in vivo effects of the treated cells on cartilage repair.

Long bone growth relies on the continuous bone formation from cartilaginous tissue (endochondral ossification). This process starts in the central region (diaphysis) of the forming bone and short before birth, ossification starts in bone extremes (epiphysis). A cartilaginous region known as the growth plate is maintained until adolescence between epiphysis and diaphysis to further contribute to longitudinal growth. Even though there are several biochemical factors controlling this process, there is evidence revealing an important regulatory role of mechanical stimuli. Up to now approaches to understand mechanical effects on ossification have been limited to epiphysis. In this work, based on Carter's mathematical model for epiphyseal ossification, we explored human growth plate response to mechanical loads. We analyzed growth plate stress distribution using finite element method for a generic bone considering different stages of bone development in order to shed light on mechanical contribution to growth plate function. Results obtained revealed that mechanical environment within the growth plate change as epiphyseal ossification progresses. Furthermore, results were compared with physiological behavior, as reported in literature, to analyze the role of mechanical stimulus over development. Our results suggest that mechanical stimuli may play different regulation roles on growth plate behavior through normal long bone development. However, as this approach only took into account mechanical aspects, failed to accurately predict biological behavior in some stages. In order to derive biologically relevant information from computational models it is necessary to consider biological contribution and possible mechanical–biochemical interactions affecting human growth plate physiology. Along these lines, we propose the dilatatorial parameter k used by Carter et al. should assume different values corresponding to the developmental stage in question. Thus, reflecting biochemical contribution changes over time.

The growth plate is a cartilaginous structure located in the metaphysis of long bones, characterized histologically by its stratification and columnar arrangement. It is responsible for assuring longitudinal growth. Evaluation of growth plate histological characteristics has been traditionally performed using qualitative observation; however, some quantitative approaches have been reported using complex techniques. Here, we propose a simple quantitative images based analysis in order to evaluate objectively columnar arrangement within growth plate. For this, we defined six descriptors that were condensated in a geometric tensor. This tensor could be used as a single parameter to evaluate the growth plate organization. Validation of the tensor was performed with growth plate microphotographs of three healthy species (rat, pig and rabbit) and an abnormal one (Csf1tl/Csf1tl rat) found in specialized literature. According to our results, the descriptors and the tensor give a complete picture of the organization of the growth plate, reflecting the expected stratification and columnar arrangement of the cells within the tissue. This methodology could be a reliable tool for evaluation of growth plate structure for research and diagnostic purposes, taking into account that it can be easily implemented.