Alfonso-Rodríguez C A, González-Andrades E, Jaimes-Parra B D, Fernández-Valadés R, Campos A, Sánchez-Quevedo M C, Alaminos M, Garzón I
Department of Histology (Tissue Engineering Group), University of Granada and Instituto de Investigación Biosanitaria ibs and PhD program in Biomedicine, University of Granada, Granada, Spain.
Department of Histology (Tissue Engineering Group), University of Granada and Instituto de Investigación Biosanitaria ibs, Granada, Spain.
Histol Histopathol. 2015 Nov;30(11):1321-32. Epub 2015 May 13.
Novel oral mucosa substitutes have been developed in the laboratory using human umbilical cord Wharton's jelly stem cells -HWJSC- as an alternative cell source. In the present work, we have generated human oral mucosa substitutes with oral mucosa keratinocytes and HWJSC to determine the influence of these cell sources on stromal differentiation. First, acellular and cellular stroma substitutes and bilayered oral mucosa substitutes with an epithelial layer consisting of oral mucosa keratinocytes -OM samples- or HWJSC -hOM- were generated. Then, tissues were analyzed by light and electron microscopy, histochemistry and immunohistochemistry to quantify all major extracellular matrix components after 1, 2 and 3 weeks of ex vivo development, and OM and hOM were also analyzed after in vivo grafting. The results showed that bioengineered oral mucosa stromas displayed an adequate fibrillar mesh. Synthesis of abundant collagen fibers was detected in OM and hOM after 3 weeks, and in vivo grafting resulted in an increased collagen synthesis. No elastic or reticular fibers were found. Glycoprotein synthesis was found at the epithelial-stromal layer when samples were grafted in vivo. Finally, proteoglycans, decorin, versican and aggrecan were strongly dependent on the in vivo environment and the presence of a well-structured epithelium on top. The use of HWJSC was associated to an increased synthesis of versican. These results confirm the usefulness of fibrin-agarose biomaterials for the generation of an efficient human oral mucosa stroma substitute and the importance of the in vivo environment and the epithelial-mesenchymal interaction for the adequate differentiation of the bioengineered stroma.
实验室已利用人脐带华通氏胶干细胞(HWJSC)作为替代细胞来源开发出新型口腔黏膜替代物。在本研究中,我们用口腔黏膜角质形成细胞和HWJSC生成了人口腔黏膜替代物,以确定这些细胞来源对基质分化的影响。首先,生成了无细胞和有细胞的基质替代物以及双层口腔黏膜替代物,其上皮层由口腔黏膜角质形成细胞(OM样本)或HWJSC(hOM)组成。然后,通过光学和电子显微镜、组织化学和免疫组织化学对组织进行分析,以量化离体培养1、2和3周后所有主要细胞外基质成分,并且在体内移植后也对OM和hOM进行了分析。结果表明,生物工程口腔黏膜基质呈现出合适的纤维网。3周后在OM和hOM中检测到大量胶原纤维的合成,并且体内移植导致胶原合成增加。未发现弹性纤维或网状纤维。当样本在体内移植时,在上皮层-基质层发现了糖蛋白合成。最后,蛋白聚糖、核心蛋白聚糖、多功能蛋白聚糖和聚集蛋白聚糖强烈依赖于体内环境以及顶部结构良好的上皮的存在。HWJSC的使用与多功能蛋白聚糖合成增加有关。这些结果证实了纤维蛋白-琼脂糖生物材料在生成高效人口腔黏膜基质替代物方面的有用性,以及体内环境和上皮-间充质相互作用对生物工程基质充分分化的重要性。