Hernández-García Frank, Fernández-Iglesias Ángela, Rodríguez Suárez Julián, Gil Peña Helena, López José M, Pérez Rocío Fuente
Departamento de Medicina, Oviedo University, 33003 Oviedo, Spain.
Grupo Investigación Pediatría, Instituto de Investigación Sanitaria del Principado de Asturias, 33011 Oviedo, Spain.
Biomedicines. 2024 Nov 21;12(12):2662. doi: 10.3390/biomedicines12122662.
While the flat bones of the face, most of the cranial bones, and the clavicles are formed directly from sheets of undifferentiated mesenchymal cells, most bones in the human body are first formed as cartilage templates. Cartilage is subsequently replaced by bone via a very tightly regulated process termed endochondral ossification, which is led by chondrocytes of the growth plate (GP). This process requires continuous communication between chondrocytes and invading cell populations, including osteoblasts, osteoclasts, and vascular cells. A deeper understanding of these signaling pathways is crucial not only for normal skeletal growth and maturation but also for their potential relevance to pathophysiological processes in bones and joints. Due to limited information on the communication between chondrocytes and other cell types in developing bones, this review examines the current knowledge of how interactions between chondrocytes and bone-forming cells modulate bone growth.
面部的扁骨、大部分颅骨和锁骨是由未分化的间充质细胞片直接形成的,而人体中的大多数骨骼最初是作为软骨模板形成的。随后,软骨通过一个严格调控的过程被骨替代,这个过程称为软骨内成骨,由生长板(GP)的软骨细胞主导。这个过程需要软骨细胞与包括成骨细胞、破骨细胞和血管细胞在内的侵入细胞群体持续沟通。深入了解这些信号通路不仅对正常骨骼生长和成熟至关重要,而且对它们与骨骼和关节病理生理过程的潜在关联也至关重要。由于关于发育中骨骼软骨细胞与其他细胞类型之间沟通的信息有限,本综述探讨了目前关于软骨细胞与成骨细胞之间相互作用如何调节骨骼生长的知识。