Ostrovidov Serge, Jiang Jinlan, Sakai Yasuyuki, Fujii Teruo
LIMMS/CNRS-IIS, University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8505, Japan.
Biomed Microdevices. 2004 Dec;6(4):279-87. doi: 10.1023/B:BMMD.0000048560.96140.ca.
To improve primary adult rat hepatocyte cultures, two types of PDMS microbioreactors containing a membrane, used as a scaffold for the attachment of cells, were built: one with a commercially-available polyester membrane, the other with a PDMS membrane (5 x 5 microm hole sizes) made in our laboratory. In that way, the relative surface area between blood perfusion and hepatocytes seen in vivo was mimicked and as cells were bathed in both sides by the culture medium they expressed much higher functions. A new technique to build such PDMS membrane was created. With this technique we could build various PDMS membranes with down to 5 x 5 microm holes and with thickness even below 20 microm. During the fifteen days of perfusion in these microbioreactors, good cell attachment then cell reorganization was observed. Moreover compared to static cultures in tissue-culture-treated dishes and in cultures in inserts with the same polyester membranes, seven and two times increases in the albumin secretion by the cultured primary rat adult hepatocyte were demonstrated, respectively. Ammonium removal also increased 7 times in perfused cultures compared to static cultures. These new microbioreactors, which closely mimic the in vivo liver architecture, revealed themselves to be very promising tools towards future applications in drug screening or liver tissue engineering.
为了改进原代成年大鼠肝细胞培养,构建了两种含膜的聚二甲基硅氧烷(PDMS)微生物反应器,该膜用作细胞附着的支架:一种使用市售聚酯膜,另一种使用我们实验室制作的PDMS膜(孔径5×5微米)。通过这种方式,模拟了体内血液灌注与肝细胞之间的相对表面积,并且由于细胞两侧都被培养基浸润,它们表现出更高的功能。创建了一种构建此类PDMS膜的新技术。利用该技术,我们可以构建孔径低至5×5微米且厚度甚至低于20微米的各种PDMS膜。在这些微生物反应器中灌注的15天内,观察到细胞良好附着并随后发生细胞重组。此外,与在经组织培养处理的培养皿中的静态培养以及在具有相同聚酯膜的插入物中的培养相比,原代成年大鼠肝细胞培养物的白蛋白分泌分别增加了7倍和2倍。与静态培养相比,灌注培养中的氨去除也增加了7倍。这些紧密模拟体内肝脏结构的新型微生物反应器,显示出它们在未来药物筛选或肝组织工程应用中极具前景。