Herzog David Paul Eric, Dohle Eva, Bischoff Iris, Kirkpatrick Charles James
Institute of Pathology, University Medical Center, Johannes Gutenberg University, Langenbeckstraße 1, 55101 Mainz, Germany.
Biomed Res Int. 2014;2014:320123. doi: 10.1155/2014/320123. Epub 2014 Apr 22.
Bone tissue is a highly vascularized and dynamic system with a complex construction. In order to develop a construct for implant purposes in bone tissue engineering, a proper understanding of the complex dependencies between different cells and cell types would provide further insight into the highly regulated processes during bone repair, namely, angiogenesis and osteogenesis, and might result in sufficiently equipped constructs to be beneficial to patients and thereby accomplish their task. This study is based on an in vitro coculture model consisting of outgrowth endothelial cells and primary osteoblasts and is currently being used in different studies of bone repair processes with special regard to angiogenesis and osteogenesis. Coculture systems of OECs and pOBs positively influence the angiogenic potential of endothelial cells by inducing the formation of angiogenic structures in long-term cultures. Although many studies have focused on cell communication, there are still numerous aspects which remain poorly understood. Therefore, the aim of this study is to investigate certain growth factors and cell communication molecules that are important during bone repair processes. Selected growth factors like VEGF, angiopoietins, BMPs, and IGFs were investigated during angiogenesis and osteogenesis and their expression in the cultures was observed and compared after one and four weeks of cultivation. In addition, to gain a better understanding on the origin of different growth factors, both direct and indirect coculture strategies were employed. Another important focus of this study was to investigate the role of "gap junctions," small protein pores which connect adjacent cells. With these bridges cells are able to exchange signal molecules, growth factors, and other important mediators. It could be shown that connexins, the gap junction proteins, were located around cell nuclei, where they await their transport to the cell membrane. In addition, areas in which two cells formed gap junctions were found.
骨组织是一个高度血管化且结构复杂的动态系统。为了开发用于骨组织工程植入目的的构建体,正确理解不同细胞和细胞类型之间复杂的相互依存关系,将有助于进一步深入了解骨修复过程中高度受调控的过程,即血管生成和骨生成,并且可能产生装备充分的构建体,对患者有益,从而完成其使命。本研究基于一个由内皮祖细胞和原代成骨细胞组成的体外共培养模型,目前该模型正用于关于血管生成和骨生成的骨修复过程的不同研究中。内皮祖细胞和成骨细胞的共培养系统通过在长期培养中诱导血管生成结构的形成,对内皮细胞的血管生成潜力产生积极影响。尽管许多研究聚焦于细胞通讯,但仍有许多方面了解甚少。因此,本研究的目的是探究在骨修复过程中重要的某些生长因子和细胞通讯分子。在血管生成和骨生成过程中研究了如血管内皮生长因子(VEGF)、血管生成素、骨形态发生蛋白(BMPs)和胰岛素样生长因子(IGFs)等选定的生长因子,并在培养1周和4周后观察并比较它们在培养物中的表达。此外,为了更好地了解不同生长因子的来源,采用了直接和间接共培养策略。本研究的另一个重要重点是研究“间隙连接”的作用,间隙连接是连接相邻细胞的小蛋白质通道。通过这些通道,细胞能够交换信号分子、生长因子和其他重要介质。结果表明,间隙连接蛋白连接蛋白位于细胞核周围,在那里等待转运到细胞膜。此外,还发现了两个细胞形成间隙连接的区域。