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在兔颅骨成骨动态可控模型中鉴定类H型血管

Identification of Type-H-like Blood Vessels in a Dynamic and Controlled Model of Osteogenesis in Rabbit Calvarium.

作者信息

Marger Laurine, Liaudet Nicolas, Scherrer Susanne S, Brembilla Nicolo-Constantino, Preynat-Seauve Olivier, Manoil Daniel, Mekki Mustapha, Durual Stéphane

机构信息

Biomaterials Laboratory, Division of Fixed Prosthodontics and Biomaterials, University Clinics of Dental Medicine, University of Geneva, 1 Rue Michel Servet, 1204 Geneva, Switzerland.

Bioimaging Core Facility, University of Geneva, 1204 Geneva, Switzerland.

出版信息

Materials (Basel). 2022 Jul 5;15(13):4703. doi: 10.3390/ma15134703.

Abstract

Angiogenesis and bone regeneration are closely interconnected processes. Whereas type-H blood vessels are abundantly found in the osteogenic zones during endochondral long bone development, their presence in flat bones' development involving intramembranous mechanisms remains unclear. Here, we hypothesized that type-H-like capillaries that highly express CD31 and Endomucin (EMCN), may be present at sites of intramembranous bone development and participate in the control of osteogenesis. A rabbit model of calvarial bone augmentation was used in which bone growth was controlled over time (2-4 weeks) using a particulate bone scaffold. The model allowed the visualization of the entire spectrum of stages throughout bone growth in the same sample, i.e., active ossification, osteogenic activity, and controlled inflammation. Using systematic mRNA hybridization, the formation of capillaries subpopulations (CD31-EMCN staining) over time was studied and correlated with the presence of osteogenic precursors (Osterix staining). Type-H-like capillaries strongly expressing CD31 and EMCN were identified and described. Their presence increased gradually from the regenerative zone up to the osteogenic zone, at 2 and 4 weeks. Type-H-like capillaries may thus represent the initial vascular support encountered in flat bones' development and which organize osteogenic niches.

摘要

血管生成与骨再生是紧密相连的过程。在软骨内长骨发育过程中,H型血管大量存在于成骨区域,然而其在涉及膜内机制的扁骨发育中的存在情况尚不清楚。在此,我们假设高表达CD31和内皮粘蛋白(EMCN)的类H型毛细血管可能存在于膜内骨发育部位,并参与成骨控制。我们使用了兔颅骨增大模型,其中使用颗粒状骨支架随时间(2 - 4周)控制骨生长。该模型能够在同一样本中观察到骨生长全过程的各个阶段,即活跃骨化、成骨活性和可控炎症。通过系统的mRNA杂交,研究了毛细血管亚群(CD31 - EMCN染色)随时间的形成情况,并将其与成骨前体的存在(osterix染色)相关联。我们鉴定并描述了强表达CD31和EMCN的类H型毛细血管。在2周和4周时,它们的存在从再生区域到成骨区域逐渐增加。因此,类H型毛细血管可能代表了扁骨发育中最初遇到的血管支持,并构建了成骨微环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c009/9267487/ef2b25e0c509/materials-15-04703-g001.jpg

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