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1.
J Clin Invest ; 134(15)2024 Jun 17.
Artículo en Inglés | MEDLINE | ID: mdl-38885336

RESUMEN

Osteogenesis imperfecta (OI) type V is the second most common form of OI, distinguished by hyperplastic callus formation and calcification of the interosseous membranes, in addition to the bone fragility. It is caused by a recurrent, dominant pathogenic variant (c.-14C>T) in interferon-induced transmembrane protein 5 (IFITM5). Here, we generated a conditional Rosa26-knockin mouse model to study the mechanistic consequences of the recurrent mutation. Expression of the mutant Ifitm5 in osteo-chondroprogenitor or chondrogenic cells resulted in low bone mass and growth retardation. Mutant limbs showed impaired endochondral ossification, cartilage overgrowth, and abnormal growth plate architecture. The cartilage phenotype correlates with the pathology reported in patients with OI type V. Surprisingly, expression of mutant Ifitm5 in mature osteoblasts caused no obvious skeletal abnormalities. In contrast, earlier expression in osteo-chondroprogenitors was associated with an increase in the skeletal progenitor cell population within the periosteum. Lineage tracing showed that chondrogenic cells expressing the mutant Ifitm5 had decreased differentiation into osteoblastic cells in diaphyseal bone. Moreover, mutant IFITM5 disrupted early skeletal homeostasis in part by activating ERK signaling and downstream SOX9 protein, and inhibition of these pathways partially rescued the phenotype in mutant animals. These data identify the contribution of a signaling defect altering osteo-chondroprogenitor differentiation as a driver in the pathogenesis of OI type V.


Asunto(s)
Diferenciación Celular , Sistema de Señalización de MAP Quinasas , Osteoblastos , Osteogénesis Imperfecta , Factor de Transcripción SOX9 , Animales , Femenino , Masculino , Ratones , Proteínas de la Membrana/genética , Proteínas de la Membrana/metabolismo , Ratones Transgénicos , Mutación , Osteoblastos/metabolismo , Osteoblastos/patología , Osteogénesis/genética , Osteogénesis Imperfecta/genética , Osteogénesis Imperfecta/patología , Osteogénesis Imperfecta/metabolismo , Factor de Transcripción SOX9/genética , Factor de Transcripción SOX9/metabolismo , Células Madre/metabolismo , Células Madre/patología , Quinasas MAP Reguladas por Señal Extracelular
2.
J Hand Surg Am ; 36(2): 238-45, 2011 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-21276887

RESUMEN

PURPOSE: To compare the biomechanical characteristics of screw versus plate versus both screw and plate fixation for large, type 3 O'Driscoll coronoid fractures. METHODS: Synthetic ulnas had 70% of their coronoids cut. Fixation was performed with either a cannulated screw, a plate, or both a screw and a plate. Energy to failure, force at failure, first cycle stiffness, and stiffness at failure were measured on a servohydraulic testing machine under cyclic posterior axial loading. RESULTS: The combination of a plate and screw had significantly greater energy to failure (83 Nm), force required to cause failure (634 N), and stiffness at failure (387 N/mm) compared to either an isolated plate (38 Nm, 474 N, 237 N/mm, respectively) or a screw (10 Nm, 279 N, 149 N/mm, respectively). For energy to failure and force required to cause failure, the plate group significantly outperformed the screw group. There was no significant difference in stiffness at the time of failure between the plate and screw groups. CONCLUSIONS: For type 3 O'Driscoll coronoid fractures or nonunions when both a screw and a plate can be placed, the combination of these 2 fixation devices appears to produce significantly greater biomechanical stability than either fixation device alone.


Asunto(s)
Placas Óseas , Tornillos Óseos , Fijación Interna de Fracturas/instrumentación , Fenómenos Biomecánicos , Fijación Interna de Fracturas/métodos , Fracturas Óseas/cirugía , Humanos , Modelos Anatómicos , Sensibilidad y Especificidad , Resistencia a la Tracción
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