Multimodality imaging reveals angiogenic evolution in vivo during calvarial bone defect healing

IF 9.2 1区 医学 Q1 PERIPHERAL VASCULAR DISEASE Angiogenesis Pub Date : 2023-11-30 DOI:10.1007/s10456-023-09899-0
Yunke Ren, Xinying Chu, Janaka Senarathna, Akanksha Bhargava, Warren L. Grayson, Arvind P. Pathak
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Abstract

The healing of calvarial bone defects is a pressing clinical problem that involves the dynamic interplay between angiogenesis and osteogenesis within the osteogenic niche. Although structural and functional vascular remodeling (i.e., angiogenic evolution) in the osteogenic niche is a crucial modulator of oxygenation, inflammatory and bone precursor cells, most clinical and pre-clinical investigations have been limited to characterizing structural changes in the vasculature and bone. Therefore, we developed a new multimodality imaging approach that for the first time enabled the longitudinal (i.e., over four weeks) and dynamic characterization of multiple in vivo functional parameters in the remodeled vasculature and its effects on de novo osteogenesis, in a preclinical calvarial defect model. We employed multi-wavelength intrinsic optical signal (IOS) imaging to assess microvascular remodeling, intravascular oxygenation (SO2), and osteogenesis; laser speckle contrast (LSC) imaging to assess concomitant changes in blood flow and vascular maturity; and micro-computed tomography (μCT) to validate volumetric changes in calvarial bone. We found that angiogenic evolution was tightly coupled with calvarial bone regeneration and corresponded to distinct phases of bone healing, such as injury, hematoma formation, revascularization, and remodeling. The first three phases occurred during the initial two weeks of bone healing and were characterized by significant in vivo changes in vascular morphology, blood flow, oxygenation, and maturity. Overall, angiogenic evolution preceded osteogenesis, which only plateaued toward the end of bone healing (i.e., four weeks). Collectively, these data indicate the crucial role of angiogenic evolution in osteogenesis. We believe that such multimodality imaging approaches have the potential to inform the design of more efficacious tissue-engineering calvarial defect treatments.

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多模态成像显示颅骨骨缺损愈合过程中血管生成的体内进化。
颅骨骨缺损的愈合是一个迫切的临床问题,涉及到成骨生态位内血管生成和成骨生成之间的动态相互作用。尽管成骨生态位中的结构和功能血管重塑(即血管生成进化)是氧合、炎症和骨前体细胞的重要调节剂,但大多数临床和临床前研究仅限于表征血管和骨的结构变化。因此,我们开发了一种新的多模态成像方法,首次能够在临床前颅骨缺损模型中纵向(即超过四周)和动态表征重建血管的多种体内功能参数及其对新生成骨的影响。我们采用多波长本征光信号(IOS)成像来评估微血管重塑、血管内氧合(SO2)和成骨;激光散斑对比(LSC)成像评估伴随的血流变化和血管成熟度;微计算机断层扫描(μCT)来验证颅骨体积的变化。我们发现血管生成进化与颅骨骨再生密切相关,并与骨愈合的不同阶段相对应,如损伤、血肿形成、血管重建和重塑。前三个阶段发生在骨愈合的最初两周,其特点是血管形态、血流、氧合和成熟度在体内发生了显著变化。总体而言,血管生成进化先于成骨,而成骨仅在骨愈合结束时(即四周)达到稳定。总的来说,这些数据表明血管生成进化在成骨过程中起着至关重要的作用。我们相信,这种多模态成像方法有潜力为设计更有效的组织工程颅骨缺损治疗提供信息。
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来源期刊
Angiogenesis
Angiogenesis PERIPHERAL VASCULAR DISEASE-
CiteScore
21.90
自引率
8.20%
发文量
37
审稿时长
6-12 weeks
期刊介绍: Angiogenesis, a renowned international journal, seeks to publish high-quality original articles and reviews on the cellular and molecular mechanisms governing angiogenesis in both normal and pathological conditions. By serving as a primary platform for swift communication within the field of angiogenesis research, this multidisciplinary journal showcases pioneering experimental studies utilizing molecular techniques, in vitro methods, animal models, and clinical investigations into angiogenic diseases. Furthermore, Angiogenesis sheds light on cutting-edge therapeutic strategies for promoting or inhibiting angiogenesis, while also highlighting fresh markers and techniques for disease diagnosis and prognosis.
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