通过功能化水凝胶实现异位工程化骨软骨组织的软骨内骨化的空间限制诱导。

Spatially confined induction of endochondral ossification by functionalized hydrogels for ectopic engineering of osteochondral tissues.

机构信息

Department of Biomedicine, University Hospital Basel, University of Basel, Basel, Switzerland.

Department of Obstetrics, University Hospital Zürich, University of Zürich, Zürich, Switzerland; Institute of Bioengineering, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.

出版信息

Biomaterials. 2018 Jul;171:219-229. doi: 10.1016/j.biomaterials.2018.04.025. Epub 2018 Apr 21.

Abstract

Despite the various reported approaches to generate osteochondral composites by combination of different cell types and materials, engineering of templates with the capacity to autonomously and orderly develop into cartilage-bone bi-layered structures remains an open challenge. Here, we hypothesized that the embedding of cells inducible to endochondral ossification (i.e. bone marrow derived mesenchymal stromal cells, BMSCs) and of cells capable of robust and stable chondrogenesis (i.e. nasal chondrocytes, NCs) adjacent to each other in bi-layered hydrogels would develop directly in vivo into osteochondral tissues. Poly(ethylene glycol) (PEG) hydrogels were functionalized with TGFβ3 or BMP-2, enzymatically polymerized encapsulating human BMSCs, combined with a hydrogel layer containing human NCs and ectopically implanted in nude mice without pre-culture. The BMSC-loaded layers reproducibly underwent endochondral ossification and generated ossicles containing bone and marrow. The NC-loaded layers formed cartilage tissues, which (under the influence of BMP-2 but not of TGFβ3 from the neighbouring layer) remained phenotypically stable. The proposed strategy, resulting in orderly connected osteochondral composites, should be further assessed for the repair of osteoarticular defects and will be useful to model developmental processes leading to cartilage-bone interfaces.

摘要

尽管已经报道了多种方法通过结合不同的细胞类型和材料来生成软骨 - 骨复合材料,但具有自主且有序地发展为软骨 - 骨双层结构的模板工程仍然是一个开放性挑战。在这里,我们假设将诱导性向软骨内骨化(即骨髓间充质基质细胞,BMSCs)和具有强大且稳定的软骨生成能力(即鼻软骨细胞,NCs)的细胞分层嵌入双层水凝胶中,会直接在体内发育成软骨 - 骨组织。聚乙二醇(PEG)水凝胶通过 TGFβ3 或 BMP-2 功能化,酶聚合包封人 BMSCs,与含有人 NCs 的水凝胶层结合,并在没有预培养的情况下异位植入裸鼠中。负载 BMSC 的层可重复地经历软骨内骨化,并生成包含骨和骨髓的骨赘。负载 NC 的层形成软骨组织,其(在相邻层的 BMP-2 的影响下,但不受 TGFβ3 的影响)保持表型稳定。这种导致有序连接的软骨 - 骨复合材料的策略应该进一步评估用于修复骨关节炎缺陷,并将有助于模拟导致软骨 - 骨界面的发育过程。

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