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固定稳定性决定了骨折修复过程中骨膜祖细胞的分化途径。

Fixation stability dictates the differentiation pathway of periosteal progenitor cells in fracture repair.

作者信息

Hagiwara Yusuke, Dyment Nathaniel A, Jiang Xi, Jiang Ping Huang, Ackert-Bicknell Cheryl, Adams Douglas J, Rowe David W

机构信息

Department of Orthopedic Surgery, Nippon Medical School Hospital, Tokyo, 113, Japan.

Center for Regenerative Medicine and Skeletal Development, School of Dental Medicine, University of Rochester School of Medicine, Rochester, New York, 14642.

出版信息

J Orthop Res. 2015 Jul;33(7):948-56. doi: 10.1002/jor.22816. Epub 2015 May 13.

Abstract

This study compared fracture repair stabilized by intramedullary pin (IMP) or external fixation (EF) in GFP reporter mice. A modified IMP was used as control while EF utilized six needles inserted transversely through the tibia and into a segment of a syringe barrel. X-rays taken at days 0, 14, and 35 showed that IMP resulted in significant three-dimensional deformity with a large callus while EF showed minimal deformity and callus formation. Cryohistological analysis of IMP at day 14 confirmed a large ColX-RFPchry+ callus surrounded by woven bone (Col3.6-GFPcyan) and TRAP+ osteoclasts with mature bone (hOC-GFPtpz) at the base. By day 35, cartilaginous components had been resorbed and an outer cortical shell (OCS) showed evidence of inward modeling. In contrast, the EF at day 14 showed no evidence of cartilage formation. Instead, periosteal-derived osteoblasts (Col3.6-GFPcyan) entered the fracture cleft and formed woven bone that spanned the marrow space. By day 35, mature bone had formed that was contiguous with the opposing cortical bone. Fracture site stability greatly affects the cellular response during repair and must be considered in the preclinical models that test therapies for improving fracture healing.

摘要

本研究比较了髓内针(IMP)或外固定(EF)稳定骨折修复在绿色荧光蛋白(GFP)报告基因小鼠中的情况。使用改良的髓内针作为对照,而外固定则使用六根针横向穿过胫骨并插入一段注射器筒中。在第0天、14天和35天拍摄的X射线显示,髓内针导致明显的三维畸形并伴有大量骨痂,而外固定显示出最小的畸形和骨痂形成。在第14天对髓内针进行的冷冻组织学分析证实,有一个大的X型胶原-红色荧光蛋白阳性(ColX-RFPchry+)骨痂,周围是编织骨(Col3.6-绿色荧光蛋白青色,Col3.6-GFPcyan),底部有抗酒石酸酸性磷酸酶阳性(TRAP+)破骨细胞和成熟骨(人破骨细胞-绿色荧光蛋白tpz,hOC-GFPtpz)。到第35天,软骨成分已被吸收,外层皮质壳(OCS)显示出向内塑形的迹象。相比之下,第14天的外固定没有软骨形成的迹象。相反,骨膜来源的成骨细胞(Col3.6-绿色荧光蛋白青色)进入骨折裂隙并形成跨越骨髓腔的编织骨。到第35天,已形成与对侧皮质骨连续的成熟骨。骨折部位的稳定性在很大程度上影响修复过程中的细胞反应,在测试改善骨折愈合疗法的临床前模型中必须予以考虑。

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