RESUMEN
Transforming growth factor ß (TGFß) signaling plays an important role in skeletal development. We previously demonstrated that the loss of TGFß receptor II (Tgfbr2) in Osterix-Cre-expressing mesenchyme results in defects in bones and teeth due to reduced proliferation and differentiation in pre-osteoblasts and pre-odontoblasts. These Osterix-Cre;Tgfbr2f/f mice typically die within approximately four weeks for unknown reasons. To investigate the cause of death, we performed extensive pathological analysis on Osterix-Cre- (Cre-), Osterix-Cre+;Tgfbr2f/wt (HET), and Osterix-Cre+;Tgfbr2f/f (CKO) mice. We also crossed Osterix-Cre mice with the ROSA26mTmG reporter line to identify potential off-target Cre expression. The findings recapitulated published skeletal and tooth abnormalities and revealed previously unreported osteochondral dysplasia throughout both the appendicular and axial skeletons in the CKO mice, including the calvaria. Alterations to the nasal area and teeth suggest a potentially reduced capacity to sense and process food, while off-target Cre expression in the gastrointestinal tract may indicate an inability to absorb nutrients. Additionally, altered nasal passages and unexplained changes in diaphragmatic muscle support the possibility of hypoxia. We conclude that these mice likely died due to a combination of breathing difficulties, malnutrition, and starvation resulting primarily from skeletal deformities that decreased their ability to sense, gather, and process food.
Asunto(s)
Osteogénesis/genética , Receptor Tipo II de Factor de Crecimiento Transformador beta/genética , Esqueleto/anomalías , Factor de Transcripción Sp7/genética , Animales , Huesos/anomalías , Huesos/fisiopatología , Diferenciación Celular/genética , Modelos Animales de Enfermedad , Regulación del Desarrollo de la Expresión Génica/genética , Humanos , Integrasas/genética , Mesodermo/crecimiento & desarrollo , Mesodermo/metabolismo , Ratones , Osteoblastos/metabolismo , Osteoblastos/patología , Transducción de Señal/genética , Esqueleto/diagnóstico por imagen , Esqueleto/metabolismo , Esqueleto/fisiopatologíaRESUMEN
Literature describes different patterns of calcaneal facets for the talus in terms of whether some calcaneal facets are connected or separated from each other or completely absent. The aim of this study was to establish the patterns of calcaneal facets for the talus, to calculate their total area, and to analyse the data with respect to gender. The study involved 59 calcanei which were photographed. The patterns of calcaneal facets noted in this study were compared with the patterns from the literature. ImageJ program was used to measure different parameters on calcanei. The pattern 1 was the most commonly found in the study sample (45.76%), then the pattern 2 (40.68%), and finally the pattern 3 (13.56%). That order of frequencies is the same in both sexes. The patterns 1 and 2 have a larger contact surface for the talus in comparison to the pattern 3. Male bones have a larger contact surface for the talus than female bones. The sum of the pattern 1 and pattern 3 frequencies was high. Knowing the frequency of different patterns of calcaneal facets for the talus in a certain population is important for orthopaedic surgeons when performing foot osteotomy.
Asunto(s)
Artritis/diagnóstico por imagen , Calcáneo/diagnóstico por imagen , Astrágalo/diagnóstico por imagen , Articulación Cigapofisaria/diagnóstico por imagen , Artritis/fisiopatología , Calcáneo/fisiopatología , Calcáneo/cirugía , Femenino , Humanos , Masculino , Procedimientos Ortopédicos , Pakistán/epidemiología , Serbia/epidemiología , Esqueleto/diagnóstico por imagen , Esqueleto/fisiopatología , Esqueleto/cirugía , Astrágalo/fisiopatología , Astrágalo/cirugía , Articulación Cigapofisaria/fisiopatología , Articulación Cigapofisaria/cirugíaRESUMEN
Spaceflight is a unique environment that includes at least two factors which can negatively impact skeletal health: microgravity and ionizing radiation. We have previously shown that a diet supplemented with dried plum powder (DP) prevented radiation-induced bone loss in mice. In this study, we investigated the capacity of the DP diet to prevent bone loss in mice following exposure to simulated spaceflight, combining microgravity (by hindlimb unloading) and radiation exposure. The DP diet was effective at preventing most decrements in bone micro-architectural and mechanical properties due to hindlimb unloading alone and simulated spaceflight. Furthermore, we show that the DP diet can protect osteoprogenitors from impairments resulting from simulated microgravity. Based on our findings, a dietary supplementation with DP could be an effective countermeasure against the skeletal deficits observed in astronauts during spaceflight.
Asunto(s)
Enfermedades Óseas Metabólicas/prevención & control , Radiación Cósmica/efectos adversos , Suspensión Trasera/efectos adversos , Prunus domestica , Vuelo Espacial , Animales , Densidad Ósea/fisiología , Densidad Ósea/efectos de la radiación , Enfermedades Óseas Metabólicas/diagnóstico , Enfermedades Óseas Metabólicas/etiología , Enfermedades Óseas Metabólicas/fisiopatología , Modelos Animales de Enfermedad , Alimentos en Conserva , Suspensión Trasera/fisiología , Humanos , Masculino , Ratones , Esqueleto/diagnóstico por imagen , Esqueleto/fisiopatología , Esqueleto/efectos de la radiación , Microtomografía por Rayos XRESUMEN
Pulsed electromagnetic fields (PEMFs) and whole-body vibration (WBV) are proved to partially preserve bone mass/strength in hindlimb-unloaded and ovariectomized animals. However, the potential age-dependent skeletal response to either PEMF or WBV has not been fully investigated. Moreover, whether the coupled "mechano-electro-magnetic" signals can induce greater osteogenic potential than single stimulation remains unknown. Herein, 5-month-old or 20-month-old rats were assigned to the Control, PEMF, WBV, and PEMF + WBV groups. After 8-week treatment, single PEMF/WBV enhanced bone mass, strength, and anabolism in 5-month-old rats, but not in 20-month-old rats. PEMF + WBV induced greater increase of bone quantity, quality, and anabolism than single PEMF/WBV in young adult rats. PEMF + WBV also inhibited bone loss in elderly rats by primarily improving osteoblast and osteocyte activity, but had no effects on bone resorption. PEMF + WBV upregulated the expression of various canonical Wnt ligands and downstream molecules (p-GSK-3ß and ß-catenin), but had no impacts on noncanonical Wnt5a expression in aged skeleton, revealing the potential involvement of canonical Wnt signaling in bone anabolism of PEMF + WBV. This study not only reveals much weaker responsiveness of aged skeleton to single PEMF/WBV relative to young adult skeleton, but also presents a novel noninvasive approach based on combinatorial treatment with PEMF + WBV for improving bone health and preserving bone quantity/quality (especially for age-related osteoporosis) with stronger anabolic effects.
Asunto(s)
Envejecimiento , Magnetoterapia , Osteoporosis , Esqueleto , Vibración , Animales , Masculino , Osteoporosis/metabolismo , Osteoporosis/fisiopatología , Osteoporosis/terapia , Ratas , Ratas Sprague-Dawley , Esqueleto/metabolismo , Esqueleto/fisiopatologíaRESUMEN
Cyclophilins are a type of peptidyl-prolyl cis-trans isomerases. CWC27, one of the known human cyclophilins, is recruited by the spliceosome for the pre-mRNA splicing process. Biallelic deleterious variants in CWC27 lead to a spectrum of overlapping phenotypes including retinal degeneration, skeletal anomalies, short stature, and neurological defects. The present work reports a woman showing these clinical features, in addition to hypergonadotropic hypogonadism, hypoplastic/agenesic teeth, and cataracts, not previously associated with such phenotypic spectrum. Whole exome sequencing on this patient identified a novel CWC27 homozygous variant predicted to originate a severely truncated protein and the consequent loss of functionality. The clinical and genetic characterization of such patient could provide further insight into the underlying causes of the spliceosomopathies.
Asunto(s)
Anomalías Múltiples/genética , Ciclofilinas/genética , Secuenciación del Exoma , Anomalías Múltiples/fisiopatología , Enanismo/genética , Enanismo/fisiopatología , Femenino , Humanos , Lactante , Fenotipo , Empalme del ARN/genética , Degeneración Retiniana/genética , Degeneración Retiniana/fisiopatología , Esqueleto/anomalías , Esqueleto/fisiopatologíaRESUMEN
Limb-length inequality in a child can be a complex condition for patients, parents, and medical providers. Managing these patients and explaining the treatment options to families requires knowledge of the potential risks associated with leaving a discrepancy untreated and a thorough understanding of skeletal growth. The provider must also be familiar with the available growth prediction methods as treatment is influenced by the anticipated discrepancy at skeletal maturity. This article provides an overview to skeletal growth, assessing skeletal maturity and growth prediction to help providers develop an organized and thoughtful approach to treating pediatric patients with limb-length inequalities.
Asunto(s)
Diferencia de Longitud de las Piernas/diagnóstico , Esqueleto/crecimiento & desarrollo , Niño , Humanos , Diferencia de Longitud de las Piernas/fisiopatología , Diferencia de Longitud de las Piernas/terapia , Esqueleto/fisiopatologíaRESUMEN
Life expectancy for a person with Marfan syndrome has essentially doubled over the past four decades. During this period, the clinical histories of the organs managed routinely have improved, and will continue to be. Prominent examples are the eyes, the heart and aorta, and some features of the skeletal system. Meanwhile, the natural histories of organ systems that have not been subjected to treatment need to be described. This is particularly important as due to the improved life span many symptoms and organ systems are only recently being recognized as being intrinsic to Marfan syndrome. Examples are the distal aorta and peripheral arteries, ventricular function, the central nervous system, sleep apnea, and adiposity. As a result, each person with Marfan syndrome will need to be evaluated and followed by more specialists than previously. Moreover, the coordinator of diagnostic testing and clinical referral must be aware of the expanded phenotype as people with Marfan syndrome age and the importance of life-long management of classical and novel features. The benefits of increased longevity and its consequences need to be addressed by investigators, health-care providers, and patients alike.
Asunto(s)
Esperanza de Vida , Longevidad/fisiología , Síndrome de Marfan/fisiopatología , Esqueleto/fisiopatología , Aorta/fisiopatología , Sistema Nervioso Central/fisiopatología , Ojo/fisiopatología , Corazón/fisiopatología , Humanos , Síndrome de Marfan/epidemiologíaRESUMEN
This article is focused on the methodological aspects of the evaluation of the elastic and mechanical strength characteristics of the tissues that form the flexible fibrous and osseous human skeleton. The samples of dura mater and spongy bone (ribs) were subjected to the quantitative analysis for the determination of their bioelemental composition. The study has demonstrated that the force needed to brake dura mater or a rib correlates with the content of biological elements in these tissue, as well as with the age and sex of the human subjects serving as teir sources.
Asunto(s)
Fenómenos Biomecánicos , Duramadre/patología , Elasticidad , Esqueleto , Factores de Edad , Anciano de 80 o más Años , Diagnóstico por Imagen de Elasticidad/métodos , Femenino , Patologia Forense/métodos , Humanos , Masculino , Persona de Mediana Edad , Factores Sexuales , Esqueleto/patología , Esqueleto/fisiopatologíaRESUMEN
Achieving fracture union is highly dependent on the initial inflammatory phase of fracture healing, which is influenced by both the local and systemic inflammatory environments. The rapidly emerging field of osteoimmunology involves the study of the interactions between the immune system and the skeletal system. Recent research has advanced the current state of knowledge regarding the effects of the surrounding soft-tissue injury, fracture hematoma, and the method of fracture fixation on the inflammatory phase of fracture healing. Acute systemic inflammation, as seen in patients with polytrauma, and chronic systemic inflammation, as seen in patients with diabetes or rheumatoid arthritis, affects the inflammatory phase of fracture healing. The use of NSAIDs can influence early fracture healing. Understanding the effects of standard orthopaedic interventions on the local and systemic inflammatory responses and early fracture healing is important for optimizing fracture union.
Asunto(s)
Curación de Fractura/inmunología , Inflamación/inmunología , Esqueleto/inmunología , Traumatismos de los Tejidos Blandos/inmunología , Antiinflamatorios no Esteroideos/farmacología , Fenómenos Biomecánicos , Curación de Fractura/efectos de los fármacos , Curación de Fractura/fisiología , Humanos , Inflamación/fisiopatología , Esqueleto/efectos de los fármacos , Esqueleto/fisiopatología , Traumatismos de los Tejidos Blandos/fisiopatologíaRESUMEN
Type 2 diabetes mellitus (T2DM) is a metabolic disorder associated with obesity and hyperglycemia. Roux-en-Y gastric bypass (RYGB) surgery is a common treatment for severely obese patients and T2DM. Both RYGB and T2DM are linked to increased skeletal fragility, though the exact mechanisms are poorly understood. Our aim was to characterize the structural, mechanical and compositional properties of bones from diet-induced obese and RYGB-treated obese (bypass) mice to elucidate which the exact factors are contributing to the increased skeletal fragility. To achieve this, a combinatory approach including microfocus X-ray computed tomography, 3-point bending, finite element modeling and Raman spectroscopy, was used. Compared to aged-matched lean controls, the obese mice displayed decreased cortical thickness, trabecular bone loss, decreased stiffness and increased Young's modulus. For the bypass mice, these alterations were even more pronounced, and additionally they showed low mineral-to-matrix ratio in the cortical endosteal area. Accumulation of the advanced glycation end-product (AGE) pentosidine was found in the cortex of obese and bypass groups and this accumulation was correlated with an increased Young's modulus. In conclusion, we found that the increased fracture risk in T2DM- and post-RYGB bones is mainly driven by accumulation of AGEs and macro-structural alterations, generating biomechanical dysfunctionality.
Asunto(s)
Huesos/fisiopatología , Diabetes Mellitus Tipo 2/cirugía , Fracturas Óseas/fisiopatología , Productos Finales de Glicación Avanzada/metabolismo , Obesidad/cirugía , Animales , Arginina/análogos & derivados , Arginina/metabolismo , Fenómenos Biomecánicos , Huesos/diagnóstico por imagen , Huesos/metabolismo , Diabetes Mellitus Tipo 2/diagnóstico por imagen , Diabetes Mellitus Tipo 2/metabolismo , Diabetes Mellitus Tipo 2/fisiopatología , Femenino , Fracturas Óseas/diagnóstico por imagen , Fracturas Óseas/metabolismo , Derivación Gástrica/efectos adversos , Humanos , Lisina/análogos & derivados , Lisina/metabolismo , Masculino , Ratones , Ratones Obesos , Obesidad/metabolismo , Obesidad/patología , Esqueleto/fisiopatología , Tomografía Computarizada por Rayos X , Pérdida de PesoRESUMEN
With aging, the skeleton experiences a number of changes, which include reductions in mass and changes in matrix composition, leading to fragility and ultimately an increase of fracture risk. A number of aspects of bone physiology are controlled by genetic factors, including peak bone mass, bone shape, and composition; however, forward genetic studies in humans have largely concentrated on clinically available measures such as bone mineral density (BMD). Forward genetic studies in rodents have also heavily focused on BMD; however, investigations of direct measures of bone strength, size, and shape have also been conducted. Overwhelmingly, these studies of the genetics of bone strength have identified loci that modulate strength via influencing bone size, and may not impact the matrix material properties of bone. Many of the rodent forward genetic studies lacked sufficient mapping resolution for candidate gene identification; however, newer studies using genetic mapping populations such as Advanced Intercrosses and the Collaborative Cross appear to have overcome this issue and show promise for future studies. The majority of the genetic mapping studies conducted to date have focused on younger animals and thus an understanding of the genetic control of age-related bone loss represents a key gap in knowledge.
Asunto(s)
Fracturas Óseas/genética , Osteoporosis/genética , Esqueleto/fisiopatología , Envejecimiento/genética , Envejecimiento/patología , Densidad Ósea , Mapeo Cromosómico , Fracturas Óseas/fisiopatología , Humanos , Osteoporosis/fisiopatologíaRESUMEN
Mitochondrial dysfunction connects metabolic disturbance with numerous pathologies, but the significance of mitochondrial activity in bone remains unclear. We have, therefore, characterized the skeletal phenotype in the Opa3L122P mouse model for Costeff syndrome, in which a missense mutation of the mitochondrial membrane protein, Opa3, impairs mitochondrial activity resulting in visual and metabolic dysfunction. Although widely expressed in the developing normal mouse head, Opa3 expression was restricted after E14.5 to the retina, brain, teeth and mandibular bone. Opa3 was also expressed in adult tibiae, including at the trabecular surfaces and in cortical osteocytes, epiphyseal chondrocytes, marrow adipocytes and mesenchymal stem cell rosettes. Opa3L122P mice displayed craniofacial abnormalities, including undergrowth of the lower mandible, accompanied in some individuals by cranial asymmetry and incisor malocclusion. Opa3L122P mice showed an 8-fold elevation in tibial marrow adiposity, due largely to increased adipogenesis. In addition, femoral length and cortical diameter and wall thickness were reduced, the weakening of the calcified tissue and the geometric component of strength reducing overall cortical strength in Opa3L122P mice by 65%. In lumbar vertebrae reduced vertebral body area and wall thickness were accompanied by a proportionate reduction in marrow adiposity. Although the total biomechanical strength of lumbar vertebrae was reduced by 35%, the strength of the calcified tissue (σmax) was proportionate to a 38% increase in trabecular number. Thus, mitochondrial function is important for the development and maintenance of skeletal integrity, impaired bone growth and strength, particularly in limb bones, representing a significant new feature of the Costeff syndrome phenotype.