Bouland Cyril, Philippart Pierre, Dequanter Didier, Corrillon Florent, Loeb Isabelle, Bron Dominique, Lagneaux Laurence, Meuleman Nathalie
Department of Stomatology and Maxillofacial Surgery, Saint-Pierre Hospital, Brussels, Belgium.
Laboratory of Clinical Cell Therapy, Jules Bordet Institute, Université Libre de Bruxelles, Brussels, Belgium.
Front Cell Dev Biol. 2021 May 13;9:674084. doi: 10.3389/fcell.2021.674084. eCollection 2021.
Bone regeneration is a complex, well-orchestrated process based on the interactions between osteogenesis and angiogenesis, observed in both physiological and pathological situations. However, specific conditions (e.g., bone regeneration in large quantity, immunocompromised regenerative process) require additional support. Tissue engineering offers novel strategies. Bone regeneration requires a cell source, a matrix, growth factors and mechanical stimulation. Regenerative cells, endowed with proliferation and differentiation capacities, aim to recover, maintain, and improve bone functions. Vascularization is mandatory for bone formation, skeletal development, and different osseointegration processes. The latter delivers nutrients, growth factors, oxygen, minerals, etc. The development of mesenchymal stromal cells (MSCs) and endothelial progenitor cells (EPCs) cocultures has shown synergy between the two cell populations. The phenomena of osteogenesis and angiogenesis are intimately intertwined. Thus, cells of the endothelial line indirectly foster osteogenesis, and conversely, MSCs promote angiogenesis through different interaction mechanisms. In addition, various studies have highlighted the importance of the microenvironment via the release of extracellular vesicles (EVs). These EVs stimulate bone regeneration and angiogenesis. In this review, we describe (1) the phenomenon of bone regeneration by different sources of MSCs. We assess (2) the input of EPCs in coculture in bone regeneration and describe their contribution to the osteogenic potential of MSCs. We discuss (3) the interaction mechanisms between MSCs and EPCs in the context of osteogenesis: direct or indirect contact, production of growth factors, and the importance of the microenvironment via the release of EVs.
骨再生是一个复杂且精心编排的过程,基于成骨作用与血管生成之间的相互作用,在生理和病理情况下均可观察到。然而,特定条件(例如大量骨再生、免疫受损的再生过程)需要额外的支持。组织工程提供了新的策略。骨再生需要细胞来源、基质、生长因子和机械刺激。具有增殖和分化能力的再生细胞旨在恢复、维持和改善骨功能。血管化对于骨形成、骨骼发育以及不同的骨整合过程至关重要。后者输送营养物质、生长因子、氧气、矿物质等。间充质基质细胞(MSCs)和内皮祖细胞(EPCs)共培养的发展已显示出这两种细胞群体之间的协同作用。成骨作用和血管生成现象紧密相连。因此,内皮系细胞间接促进成骨作用,反之,MSCs通过不同的相互作用机制促进血管生成。此外,各种研究强调了通过细胞外囊泡(EVs)释放所形成的微环境的重要性。这些EVs刺激骨再生和血管生成。在本综述中,我们描述(1)不同来源的MSCs的骨再生现象。我们评估(2)EPCs在骨再生共培养中的作用,并描述它们对MSCs成骨潜力的贡献。我们讨论(3)在成骨作用背景下MSCs和EPCs之间的相互作用机制:直接或间接接触、生长因子的产生以及通过EVs释放所形成的微环境的重要性。