Ortinau Laura, Lei Kevin, Jeong Youngjae, Park Dongsu
Department of Molecular & Human Genetics, Baylor College of Medicine; Center for Skeletal Biology, Baylor College of Medicine.
Department of Molecular & Human Genetics, Baylor College of Medicine.
J Vis Exp. 2020 Sep 16(163). doi: 10.3791/61162.
Periosteal skeletal stem cells (P-SSCs) are essential for lifelong bone maintenance and repair, making them an ideal focus for the development of therapies to enhance fracture healing. Periosteal cells rapidly migrate to an injury to supply new chondrocytes and osteoblasts for fracture healing. Traditionally, the efficacy of a cytokine to induce cell migration has only been conducted in vitro by performing a transwell or scratch assay. With advancements in intravital microscopy using multiphoton excitation, it was recently discovered that 1) P-SSCs express the migratory gene CCR5 and 2) treatment with the CCR5 ligand known as CCL5 improves fracture healing and the migration of P-SSCs in response to CCL5. These results have been captured in real-time. Described here is a protocol to visualize P-SSC migration from the calvarial suture skeletal stem cell (SSC) niche towards an injury after treatment with CCL5. The protocol details the construction of a mouse restraint and imaging mount, surgical preparation of the mouse calvaria, induction of a calvaria defect, and acquisition of time-lapse imaging.
骨膜骨骼干细胞(P-SSCs)对于终身骨骼维持和修复至关重要,这使其成为开发增强骨折愈合疗法的理想研究重点。骨膜细胞会迅速迁移至损伤部位,为骨折愈合提供新的软骨细胞和成骨细胞。传统上,细胞因子诱导细胞迁移的功效仅通过体外进行的Transwell或划痕试验来评估。随着多光子激发活体显微镜技术的进步,最近发现:1)P-SSCs表达迁移基因CCR5;2)用名为CCL5的CCR5配体进行治疗可改善骨折愈合以及P-SSCs对CCL5的迁移反应。这些结果已被实时捕捉。本文描述了一种用于可视化在用CCL5处理后,P-SSC从颅缝骨骼干细胞(SSC)龛向损伤部位迁移的方案。该方案详细介绍了小鼠约束和成像支架的构建、小鼠颅骨的手术准备、颅骨缺损的诱导以及延时成像的采集。