Department of Anatomy and Clinical Anatomy, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Laboratory for Mineralized Tissues, Center for Translational and Clinical Research, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Int J Mol Sci. 2022 Jan 12;23(2):785. doi: 10.3390/ijms23020785.
Bone morphogenetic proteins (BMPs) have a major role in tissue development. BMP3 is synthesized in osteocytes and mature osteoblasts and has an antagonistic effect on other BMPs in bone tissue. The main aim of this study was to fully characterize cortical bone and trabecular bone of long bones in both male and female mice. To investigate the effect of from birth to maturity, we compared mice with wild-type littermates at the following stages of postnatal development: 1 day (P0), 2 weeks (P14), 8 weeks and 16 weeks of age. deletion was confirmed using X-gal staining in P0 animals. Cartilage and bone tissue were examined in P14 animals using Alcian Blue/Alizarin Red staining. Detailed long bone analysis was performed in 8-week-old and 16-week-old animals using micro-CT. The reporter signal was localized in bone tissue, hair follicles, and lungs. Bone mineralization at 2 weeks of age was increased in long bones of mice. deletion was shown to affect the skeleton until adulthood, where increased cortical and trabecular bone parameters were found in young and adult mice of both sexes, while delayed mineralization of the epiphyseal growth plate was found in adult mice.
骨形态发生蛋白(BMPs)在组织发育中起着重要作用。BMP3 在骨细胞和成骨细胞中合成,对骨组织中的其他 BMP 具有拮抗作用。本研究的主要目的是全面描述雄性和雌性小鼠长骨的皮质骨和小梁骨。为了研究从出生到成熟的影响,我们在以下几个阶段比较了从出生到成熟的 和野生型同窝仔鼠:1 天(P0)、2 周(P14)、8 周和 16 周龄。在 P0 动物中使用 X-gal 染色确认 缺失。在 P14 动物中使用 Alcian Blue/Alizarin Red 染色检查软骨和骨组织。在 8 周龄和 16 周龄动物中使用 micro-CT 进行详细的长骨分析。 报告基因信号定位于骨组织、毛囊和肺部。2 周龄时, 鼠长骨中的骨矿化增加。 缺失被证明会影响骨骼直到成年,在两性的年轻和成年 鼠中发现皮质骨和小梁骨参数增加,而成年 鼠的骺板矿化延迟。