Török E, Pollok J M, Ma P X, Kaufmann P M, Dandri M, Petersen J, Burda M R, Kluth D, Perner F, Rogiers X
Department of Surgery, University of Hamburg, Germany.
Cells Tissues Organs. 2001;169(1):34-41. doi: 10.1159/000047858.
We hypothesize that in vitro conditioning of hepatocytes within biodegradable poly-L-lactic acid (PLLA) polymer matrices prior to implantation may increase hepatocyte survival and function after transplantation. The purpose of this study was to optimize the culture conditions of hepatocytes in a pulsatile flow bioreactor. PLLA discs were seeded with rat hepatocytes in a concentration of 2.5, 5, 10, 20 and 40 x 10(6) cells/ml. Seeded discs were exposed to recirculated perpendicular flow of 0, 7, 15, 24, 32, 52 ml/min of supplemented Williams' Medium E and harvested after 6 days in flow culture. Only under flow conditions the hepatocytes formed spheroidal aggregates (SphA) of 50-260 microm in diameter with a liver-like morphology and active metabolic function. The number of SphA was examined by phase contrast microscopy and the reductive enzyme function of the hepatocytes was tested using MTT. Hematoxylin and eosin histology showed vital hepatocytes within the SphA less than 200 microm in diameter but central necrosis in the SphA exceeding this size. Immunohistochemical staining confirmed albumin production of hepatocytes within the SphA. The optimal cell seeding concentration was 10 x 10(6) cells/ml with a flow speed of 24 ml/min. SphA of hepatocytes cultured with this flow bioreactor method may prove useful as a functional unit for tissue engineering of an in vivo liver substitute.
我们假设,在植入前于可生物降解的聚-L-乳酸(PLLA)聚合物基质内对肝细胞进行体外预处理,可能会提高移植后肝细胞的存活率和功能。本研究的目的是优化搏动流生物反应器中肝细胞的培养条件。将PLLA圆盘以2.5、5、10、20和40×10⁶个细胞/毫升的浓度接种大鼠肝细胞。接种后的圆盘暴露于补充了Williams' Medium E的0、7、15、24、32、52毫升/分钟的再循环垂直流中,并在流动培养6天后收获。仅在流动条件下,肝细胞形成直径为50 - 260微米的球形聚集体(SphA),具有类似肝脏的形态和活跃的代谢功能。通过相差显微镜检查SphA的数量,并使用MTT测试肝细胞的还原酶功能。苏木精和伊红组织学显示,直径小于200微米的SphA内有存活的肝细胞,但直径超过此大小的SphA中央出现坏死。免疫组织化学染色证实SphA内的肝细胞产生白蛋白。最佳细胞接种浓度为10×10⁶个细胞/毫升,流速为24毫升/分钟。用这种流动生物反应器方法培养的肝细胞SphA可能被证明是体内肝替代组织工程的有用功能单元。