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用于制备骨再生生物活性羟基磷灰石材料的间充质基质细胞单细胞转录组

A single-cell transcriptome of mesenchymal stromal cells to fabricate bioactive hydroxyapatite materials for bone regeneration.

作者信息

Guo Peng, Liu Xizhe, Zhang Penghui, He Zhongyuan, Li Zhen, Alini Mauro, Richards R Geoff, Grad Sibylle, Stoddart Martin J, Zhou Guangqian, Zou Xuenong, Chan Danny, Tian Wei, Chen Dafu, Gao Manman, Zhou Zhiyu, Liu Shaoyu

机构信息

Innovation Platform of Regeneration and Repair of Spinal Cord and Nerve Injury, Department of Orthopaedic Surgery, The Seventh Affiliated Hospital of Sun Yat-sen University, Shenzhen, China.

Guangdong Provincial Key Laboratory of Orthopaedics and Traumatology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.

出版信息

Bioact Mater. 2021 Aug 11;9:281-298. doi: 10.1016/j.bioactmat.2021.08.009. eCollection 2022 Mar.

Abstract

The osteogenic microenvironment of bone-repairing materials plays a key role in accelerating bone regeneration but remains incompletely defined, which significantly limits the application of such bioactive materials. Here, the transcriptional landscapes of different osteogenic microenvironments, including three-dimensional (3D) hydroxyapatite (HA) scaffolds and osteogenic medium (OM), for mesenchymal stromal cells (MSCs) were mapped at single-cell resolution. Our findings suggested that an osteogenic process reminiscent of endochondral ossification occurred in HA scaffolds through sequential activation of osteogenic-related signaling pathways, along with inflammation and angiogenesis, but inhibition of adipogenesis and fibrosis. Moreover, we revealed the mechanism during OM-mediated osteogenesis involves the ZBTB16 and WNT signaling pathways. Heterogeneity of MSCs was also demonstrated. ossification of LRRC75A MSCs was shown to have better utilization of WNT-related ossification process, and PCDH10 MSCs with superiority in hydroxyapatite-related osteogenic process. These findings provided further understanding of the cellular activity modulated by OM conditions and HA scaffolds, providing new insights for the improvement of osteogenic biomaterials. This atlas provides a blueprint for research on MSC heterogeneity and the osteogenic microenvironment of HA scaffolds and a database reference for the application of bioactive materials for bone regeneration.

摘要

骨修复材料的成骨微环境在加速骨再生中起关键作用,但仍未完全明确,这显著限制了此类生物活性材料的应用。在此,以单细胞分辨率绘制了间充质基质细胞(MSCs)在不同成骨微环境中的转录图谱,这些微环境包括三维(3D)羟基磷灰石(HA)支架和成骨培养基(OM)。我们的研究结果表明,通过成骨相关信号通路的顺序激活,HA支架中发生了类似于软骨内成骨的成骨过程,同时伴有炎症和血管生成,但抑制了脂肪生成和纤维化。此外,我们揭示了OM介导的成骨过程中的机制涉及ZBTB16和WNT信号通路。还证明了MSCs的异质性。LRRC75A MSCs的成骨表现出对WNT相关成骨过程的更好利用,而PCDH10 MSCs在与羟基磷灰石相关的成骨过程中具有优势。这些发现进一步加深了对OM条件和HA支架调节的细胞活性的理解,为改善成骨生物材料提供了新的见解。这一图谱为MSCs异质性和HA支架成骨微环境的研究提供了蓝图,并为骨再生生物活性材料的应用提供了数据库参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbbd/8586438/5098890f4ab7/ga1.jpg

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