Tomoka Hasegawa , Mako Sakakibara , Xuanyu Liu , Hirona Yoshino , Yan Shi , Jiaxin Cui , Mai Haraguchi-Kitakamae , Weisong Li , Wang Haoyu , Tomomaya Yamamoto , Hotaka Ishizu , Tamaki Sekiguchi , Tomohiro Shimizu , Norio Amizuka
{"title":"Alendronate inhibits bone-specific blood vessels in the femoral metaphyses of mice","authors":"Tomoka Hasegawa , Mako Sakakibara , Xuanyu Liu , Hirona Yoshino , Yan Shi , Jiaxin Cui , Mai Haraguchi-Kitakamae , Weisong Li , Wang Haoyu , Tomomaya Yamamoto , Hotaka Ishizu , Tamaki Sekiguchi , Tomohiro Shimizu , Norio Amizuka","doi":"10.1016/j.job.2025.100655","DOIUrl":null,"url":null,"abstract":"<div><div>To determine whether alendronate affects vascular endothelial cells and regulates the interactions between blood vessels and osteoblasts, we have examined the femoral metaphyses of alendronate-administered mice. Following administration, the bone-specific blood vessels exhibited significantly reduced luminal diameters and rough luminal surfaces with numerous small protrusions and vesicles. Although the osteoclast distribution remained unchanged in alendronate-treated mice, osteoblasts were inactivated in the metaphyseal regions where blood vessels had shrunk. Additionally, the expression of genes such as <em>Ephb4</em>/<em>Efnb2</em>, which mediate vascular endothelial cell–osteoblast interactions, was diminished. Therefore, alendronate may primarily affect bone-specific blood vessels, thus leading to osteoblast inactivation.</div></div>","PeriodicalId":45851,"journal":{"name":"Journal of Oral Biosciences","volume":"67 2","pages":"Article 100655"},"PeriodicalIF":2.6000,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Oral Biosciences","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1349007925000441","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0
Abstract
To determine whether alendronate affects vascular endothelial cells and regulates the interactions between blood vessels and osteoblasts, we have examined the femoral metaphyses of alendronate-administered mice. Following administration, the bone-specific blood vessels exhibited significantly reduced luminal diameters and rough luminal surfaces with numerous small protrusions and vesicles. Although the osteoclast distribution remained unchanged in alendronate-treated mice, osteoblasts were inactivated in the metaphyseal regions where blood vessels had shrunk. Additionally, the expression of genes such as Ephb4/Efnb2, which mediate vascular endothelial cell–osteoblast interactions, was diminished. Therefore, alendronate may primarily affect bone-specific blood vessels, thus leading to osteoblast inactivation.