Single BMSC-derived cartilage organoids for gradient heterogeneous osteochondral regeneration by leveraging native vascular microenvironment.

IF 10.6 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Zhenying Chen, Qitao Bo, Chao Wang, Yong Xu, Xiang Fei, Ru Chen
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引用次数: 0

Abstract

Heterogeneous osteochondral regeneration remains a significant challenge due to the distinct microenvironments across the cartilage, calcified cartilage, and subchondral bone layers. The natural gradient of vascularization from the superficial to deep layers of osteochondral tissue plays a critical role in guiding the differentiation of bone marrow stem cells (BMSCs) into chondrocytes and osteoblasts. In this study, we propose a strategy for gradient heterogeneous osteochondral regeneration using cartilage organoids derived from single BMSCs, leveraging the natural vascularization gradient within osteochondral tissue. We successfully isolated BMSCs from rabbits and generated cartilage organoids via in vitro three-dimensional chondrogenic culture. To mimic the pro-vascular microenvironment, we introduced vascular endothelial growth factor, which promoted the hypertrophic differentiation of the cartilage organoids. We then prepared cartilage organoid/GelMA complexes, with or without the anti-vascular drug Axitinib, and implanted them subcutaneously in nude mice. The vascularized subcutaneous microenvironment induced osteogenic differentiation, while Axitinib treatment created an anti-vascular microenvironment, inhibiting osteogenesis and preserving chondrogenesis within the complexes. Both in vitro and in vivo data demonstrated the crucial role of the vascular microenvironment in regulating osteogenic differentiation of cartilage organoids. Finally, organoid/GelMA cylinders were implanted into a rabbit osteochondral defect, where the gradient vascularization at the defect site guided the organoids to differentiate into both cartilage and bone. This single BMSC-derived cartilage organoid approach enables precise gradient heterogeneous osteochondral regeneration, guided by the natural microenvironment within the osteochondral defect site, representing a significant advancement for clinical applications.

利用原生血管微环境,单骨髓间充质干细胞衍生软骨类器官实现梯度异质骨软骨再生。
由于软骨、钙化软骨和软骨下骨层的微环境不同,异质骨软骨再生仍然是一个重大挑战。骨软骨组织血管形成的自然梯度在引导骨髓干细胞向软骨细胞和成骨细胞分化中起着关键作用。在这项研究中,我们提出了一种梯度异质骨软骨再生策略,利用单一骨髓间充质干细胞衍生的软骨类器官,利用骨软骨组织内的自然血管化梯度。我们成功地从家兔体内分离出骨髓间充质干细胞,并通过体外三维软骨培养生成软骨类器官。为了模拟促血管微环境,我们引入血管内皮生长因子,促进软骨类器官的肥厚分化。然后,我们制备软骨类器官/GelMA复合物,含或不含抗血管药物阿西替尼,并将其植入裸鼠皮下。血管化的皮下微环境诱导成骨分化,而阿西替尼治疗创造了一个抗血管微环境,抑制成骨并保留复合物内的软骨形成。体外和体内数据均证明了血管微环境在软骨类器官成骨分化调控中的重要作用。最后,将类器官/GelMA圆柱体植入兔骨软骨缺损,缺损部位梯度血管化引导类器官分化为软骨和骨。这种单一的骨髓间充质干细胞衍生的软骨类器官方法在骨软骨缺损部位的自然微环境引导下,实现了精确的梯度异质骨软骨再生,代表了临床应用的重大进步。
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来源期刊
Journal of Nanobiotechnology
Journal of Nanobiotechnology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
13.90
自引率
4.90%
发文量
493
审稿时长
16 weeks
期刊介绍: Journal of Nanobiotechnology is an open access peer-reviewed journal communicating scientific and technological advances in the fields of medicine and biology, with an emphasis in their interface with nanoscale sciences. The journal provides biomedical scientists and the international biotechnology business community with the latest developments in the growing field of Nanobiotechnology.
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