Schofer Markus Dietmar, Boudriot Ulrich, Wack Christina, Leifeld Irini, Gräbedünkel Christian, Dersch Roland, Rudisile Markus, Wendorff Joachim Heinz, Greiner Andreas, Paletta Jürgen Rudolf Josef, Fuchs-Winkelmann Susanne
Department of Orthopedics, University of Marburg, Baldingerstrasse, 35043, Marburg, Germany.
J Mater Sci Mater Med. 2009 Mar;20(3):767-74. doi: 10.1007/s10856-008-3634-8. Epub 2008 Nov 6.
The aim of this study was to compare biological collagen I (ColI) and synthetic poly-(L: -lactide) (PLLA) nanofibers concerning their stability and ability to promote growth and osteogenic differentiation of human mesenchymal stem cells in vitro. Matrices were seeded with human stem cells and cultivated over a period of 28 days under growth and osteoinductive conditions and analyzed during the course. During this time the PLLA nanofibers remained stable while the presence of cells resulted in an attenuation of the ColI nanofiber mesh. Although there was a tendency for better growth and osteoprotegerin production of stem cells when cultured on collagen nanofibers, there was no significant difference compared to PLLA nanofibers or controls. The gene expression of alkaline phosphate, osteocalcin and collagen I diminished in the initial phase of cultivation independent of the polymer used. In the case of PLLA fibers, this gene expression normalized during the course of cultivation, whereas the presence of collagen nanofibers resulted in an increased gene expression of osteocalcin and collagen during the course of the experiment. Taken together the PLLA fibers were easier to produce, more stable and did not compromise growth and differentiation of stem cells over the course of experiment. On the other hand, collagen nanofibers supported the differentiation process to some extent. Nevertheless, the need for fixation as well as the missing stability during cell culture requires further work.
本研究的目的是比较生物胶原蛋白I(ColI)和合成聚(L-丙交酯)(PLLA)纳米纤维在体外的稳定性以及促进人间充质干细胞生长和成骨分化的能力。将人间充质干细胞接种到基质上,并在生长和骨诱导条件下培养28天,在此期间进行分析。在此期间,PLLA纳米纤维保持稳定,而细胞的存在导致ColI纳米纤维网衰减。虽然在胶原纳米纤维上培养时干细胞有更好的生长和骨保护素产生的趋势,但与PLLA纳米纤维或对照相比没有显著差异。无论使用何种聚合物,碱性磷酸酶、骨钙素和胶原蛋白I的基因表达在培养初期都会降低。对于PLLA纤维,这种基因表达在培养过程中恢复正常,而胶原纳米纤维的存在导致在实验过程中骨钙素和胶原蛋白的基因表达增加。综上所述,PLLA纤维更容易制备,更稳定,并且在实验过程中不会损害干细胞的生长和分化。另一方面,胶原纳米纤维在一定程度上支持分化过程。然而,细胞培养过程中需要固定以及缺乏稳定性需要进一步研究。