骨结合需要成对相关同源框 1 阳性细胞

Xi Feng, Haicheng Wang, Yuteng Weng, Yongliang Chen, Jie Huang, Zuolin Wang
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引用次数: 0

摘要

目的:探讨成对相关同源染色体 1 阳性细胞对成人牙槽骨种植体诱导的骨结合过程的贡献及其潜在的内在机制:在小鼠牙种植模型中进行了Cre重组酶诱导的品系追踪和细胞消融。使用划痕和跨孔试验评估配对相关同源染色体 1 过度表达后 MC3T3-E1 细胞的迁移。应用单细胞RNA测序鉴定参与配对相关同源染色体1阳性细胞驱动成骨的潜在基因:结果:观察到成对相关homeobox 1-阳性细胞以时间依赖性的方式在种植体周围区域聚集。这些细胞的数量在第 14 天达到最大值。消减配对相关同源染色体 1 阳性细胞后,小鼠的骨结合明显受损。此外,研究还发现配对相关同形体 1 能促进 MC3T3- E1 细胞迁移,而这一过程是种植体周围组织健全愈合所不可或缺的。最后,在配对相关同源框 1 阳性的细胞中检测到了大量表达的semaphorin 3C。在配对相关同工酶 1- 阳性细胞中敲除 Semaphorin 3C 会显著削弱其成骨潜能:我们的数据表明,配对相关同工酶1阳性细胞在应力刺激下有助于骨结合过程,而半aphorin 3C 可能在配对相关同工酶1阳性细胞驱动的成骨过程中发挥关键作用。配对相关同源框 1 能显著促进 MC3T3-E1 细胞迁移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Paired-Related Homeobox 1-Positive Cells Are Needed for Osseointegration.

Purpose: To explore the contribution of paired-related homeobox 1-positive (Prrx1+) cells to the implant-induced osseointegration process in adult alveolar bone and the potential underlying mechanisms.

Materials and methods: Crerecombinase-induced lineage tracing and cell ablation were conducted in a murine dental implant model. Scratch and transwell assays were used to assess MC3T3-E1 cell migration after paired-related homeobox 1 overexpression. Single-cell RNA sequencing was applied to identify potential genes involved in Prrx1+ cell-driven osteogenesis.

Results: Prrx1+ cells were observed to accumulate in the peri-implant area in a time-dependent manner; the number of these cells was found to reach its maximum on day 14. Osseointegration in mice was noticeably impaired after ablation of Prrx1+ cells. Further, it was discovered that Prrx1 promotes MC3T3-E1 cell migration, a process which is indispensable for sound healing of peri-implant tissue. Finally, semaphorin 3C (Sema3C) was detected exclusively and abundantly expressed by Prrx1+ cells. Knockdown of Sema3C in Prrx1+ cells significantly weakened their osteogenic potential.

Conclusions: Our data suggest that Prrx1+ cells contribute to the osseointegration process under stress stimulation and Sema3C may play a critical role in Prrx1+ cell-driven osteogenesis. Prrx1 could significantly promote MC3T3-E1 cell migration.

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