Barbosa-Nuñez Jorge Alejandro, Haro-González José Nabor, García-Márquez Eristeo, Espinosa-Andrews Hugo, Padilla-Camberos Eduardo, Herrera-Rodríguez Sara Elisa
Unidad de Tecnología Alimentaría, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco (CIATEJ), Camino Arenero 1227, El Bajío del Arenal, 45019, Zapopan, Jalisco, Mexico.
Unidad Sureste, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco (CIATEJ), Carretera km 5.5, Sierra Papacal-Chuburná, Chuburná, 97302, Mérida, Yucatán, Mexico.
Differentiation. 2025 Jul-Aug;144:100872. doi: 10.1016/j.diff.2025.100872. Epub 2025 May 29.
Bones are living tissues that are periodically renewed through the bone remodeling process. It starts when monocyte-macrophage-type cells begin to proliferate and recruit into the bone tissue due to the action of various proteins. The proteins are generated by the body in response to a lack of calcium in the blood or a damaged bone tissue. Then, other chemical signals promote the differentiation of monocyte-macrophage-type cells into osteoclasts. Finally, osteoclasts carry out a process known as bone resorption in which they degrade bone tissue. After, bone resorption a process known as osteogenesis takes place. In osteogenesis, pluripotent mesenchymal stem cells proliferate and recruit in the bone damaged by bone resorption in response to the action of different compounds. Then, pluripotent mesenchymal stem cells differentiate into osteoblasts due to the effect of specific proteins. Finally, osteoblasts generate new bone tissue, completing the bone remodeling process. This review aims to summarize and provide recent findings of the proteins and chemical signals involved in osteoclast and osteoblast proliferation, recruitment and maturation during the bone resorption and osteogenesis processes. The information found about these molecules could help to better understand all the complex mechanisms that directly or indirectly influence the bone remodeling process. In this sense, the mechanisms of different bone disorders and diseases could be elucidated in a better way, leading to the generation of efficient and specific treatments for each of them in the future.
骨骼是活组织,通过骨重塑过程定期更新。当单核细胞-巨噬细胞型细胞由于各种蛋白质的作用开始增殖并募集到骨组织中时,这个过程就开始了。这些蛋白质是身体在血液中钙缺乏或骨组织受损时产生的。然后,其他化学信号促进单核细胞-巨噬细胞型细胞分化为破骨细胞。最后,破骨细胞进行一个称为骨吸收的过程,在这个过程中它们降解骨组织。之后,骨吸收后会发生一个称为骨生成的过程。在骨生成过程中,多能间充质干细胞在不同化合物的作用下,在因骨吸收而受损的骨骼中增殖并募集。然后,多能间充质干细胞由于特定蛋白质的作用而分化为成骨细胞。最后,成骨细胞生成新的骨组织,完成骨重塑过程。本综述旨在总结并提供在骨吸收和成骨过程中参与破骨细胞和成骨细胞增殖、募集和成熟的蛋白质和化学信号的最新研究结果。关于这些分子的信息有助于更好地理解所有直接或间接影响骨重塑过程的复杂机制。从这个意义上说,可以更好地阐明不同骨疾病和病症的机制,从而在未来为每种疾病开发出高效且特异的治疗方法。