Yu Li-qiang, Liu Hong-chen, E Ling-ling, Wu Xia, Wang Dong-sheng
Institute of Stomatology, General Hospital of PLA, Beijing 100853, China.
Zhonghua Kou Qiang Yi Xue Za Zhi. 2009 Nov;44(11):690-4.
To investigate the integrity of multilayer of human periodontal ligament fibroblasts (HPDLF) and human gingival fibroblasts (HGF) on filter membrane of Transwell and to provide basis for the drug transcellular transport by the HPDLF and HGF in the hypothesis of delivering medicine to the periodontium and whole body through the root canal.
HPDLF and HGF derived from the primary culture were seeded on polycarbonate filter membrane of transwell respectively. After 1, 2, 3 and 4 weeks of culture, transepithelial electrical resistance (TEER) was detected and the growth of HPDLF and HGF observed by light microscope. After 2 weeks of culture, section of filter membrane where HPDLF and HGF lived was observed with light microscope and transmission electron microscope (TEM), and the permeability of the drug transport cell models was measured with fluorescein sodium.
HPDLF and HGF converged 1 week after inoculation, and the cells connected each other tightly and completely 2 weeks later. Observation of section of filter membrane by light microscope and TEM revealed a stratified cell growth of HPDLF and HGF 2 weeks after inoculation, and TEER of HPDLF and HGF were (56.14 +/- 7.43) and (57.34 +/- 7.62) ohm.cm(-2) respectively. The values of TEER remained the same level until 4 weeks later. Two weeks after inoculation, the paracellular transport of fluorescein sodium was less than 1% after the cell models were incubated for 30 min.
Stratified cell layers of HPDLF and HGF grown on filter membrane of Transwell are analogous to periodontal membrane and gingiva 2 weeks after inoculation, the test results of permeability and TEER were consistent with the demands of development of cell models. HPDLF and HGF grown on filter membrane of Transwell could be used to study drug transcellular transport by HPDLF and HGF in vitro.
研究人牙周膜成纤维细胞(HPDLF)和人牙龈成纤维细胞(HGF)在Transwell滤膜上多层结构的完整性,为通过根管向牙周组织及全身给药的假说中HPDLF和HGF的药物跨细胞转运提供依据。
将原代培养的HPDLF和HGF分别接种于Transwell的聚碳酸酯滤膜上。培养1、2、3和4周后,检测跨上皮电阻(TEER),并通过光学显微镜观察HPDLF和HGF的生长情况。培养2周后,用光学显微镜和透射电子显微镜(TEM)观察HPDLF和HGF所在滤膜的切片,并用荧光素钠测定药物转运细胞模型的通透性。
接种后1周HPDLF和HGF汇合,2周后细胞彼此紧密且完全连接。接种2周后,通过光学显微镜和TEM观察滤膜切片发现HPDLF和HGF呈分层细胞生长,HPDLF和HGF的TEER分别为(56.14±7.43)和(57.34±7.62)Ω·cm⁻²。直到4周后,TEER值保持在同一水平。接种2周后,细胞模型孵育30分钟后荧光素钠的细胞旁转运小于1%。
接种2周后,在Transwell滤膜上生长的HPDLF和HGF分层细胞层类似于牙周膜和牙龈,通透性和TEER的检测结果符合细胞模型构建的要求。在Transwell滤膜上生长的HPDLF和HGF可用于体外研究HPDLF和HGF的药物跨细胞转运。