体外培养过程中MSCS与血单个核细胞的相互作用在模拟再生骨组织的三维人工基质中共同培养

Kristina A. Yurova, I. K. Norkin, O. G. Khaziakhmatova, V. V. Malashchenko, O. B. Melashchenko, P. A. Ivanov, D. D. Ligatyuk, I. A. Khlusov, L. S. Litvinova
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引用次数: 0

摘要

骨组织的修复和再生是一个涉及许多细胞、受多种因素控制的复杂过程。免疫细胞和细胞因子在调节骨形成和骨吸收平衡中起着至关重要的作用。然而,骨再生的免疫调节机制尚不清楚。然而,免疫活性细胞和间充质干细胞(MSCs)的相互调节作用是众所周知的。MSCs和免疫能力细胞分泌各种细胞因子、生长因子和细胞外基质分子,在调节造血、血管生成、免疫和炎症反应中发挥重要作用。多项研究证实,MSCs表达的不同分子可诱导淋巴细胞增殖。因此,在体外共培养过程中,即使在模拟再生骨组织的人工基质存在的情况下,研究间充质干细胞和血单核细胞的相互影响是相关的和有利的。在这个实验系列中,研究在活体和非活体基质阶段的界面上进行,从而模拟再生骨/造血微环境系统。在塑料表面(2D培养模型)和模拟再生骨组织的三维人工基质(3D培养模型)上进行了一系列分离的时间实验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interaction between MSCS and blood mononuclear cells during <i>in vitro</i> co-cultivation in the presence of a three-dimensional artificial matrix mimicking regenerating bone tissue
Bone tissue repair and regeneration is a complex process involving many cells and controlled by multiple factors. Immune cells and cytokines play a crucial role in regulating the balance of bone formation and resorption. However, the immunomodulatory mechanism of bone regeneration is still unclear. Nevertheless, the reciprocal regulatory influence of immunocompetent cells and mesenchymal stem cells (MSCs) is well known. MSCs and immunocompetent cells secrete various cytokines, growth factors, and extracellular matrix molecules that play important roles in regulating hematopoiesis, angiogenesis, immune and inflammatory responses. Several studies confirm that different molecules expressed by MSCs may induce lymphocyte proliferation. Therefore, the study of the mutual influence of MSCs and blood mononuclear cells during in vitro co-cultivation, even in the presence of an artificial matrix mimicking regenerating bone tissue, is relevant and expedient. In this experimental series, the studies were performed at the interface between living and non-living substrate phases thus mimicking the regenerating bone / hematopoietic microenvironment system. A series of separated in time experiments was performed on a plastic surface (2D culture model) and in the presence of three-dimensional artificial matrices mimicking regenerating bone tissue (3D culture model).
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