Dunn J C, Tompkins R G, Yarmush M L
Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston 02114.
Biotechnol Prog. 1991 May-Jun;7(3):237-45. doi: 10.1021/bp00009a007.
In an effort to reconstruct the cellular polarity normally found in the liver, adult rat hepatocytes were sandwiched between two layers of hydrated rat tail tendon collagen matrix. Functionally, sandwiched hepatocytes maintained the secretion of albumin, transferrin, fibrinogen, bile acids, and urea for at least 6 weeks, whereas cells cultured on a single layer of collagen gel ceased such secretion in 1-2 weeks. After 1 week of culture on a single layer of collagen gel, hepatocytes could still recover these lost functions when a second layer of collagen gel was applied. The exact nature of the substrate for constructing the sandwich system appeared to be unimportant as long as it allowed cellular attachment. Hepatocytes cultured in the sandwich system appeared to maintain a distribution of actin filaments similar to the in vivo state, whereas cells cultured on a single layer of collagen gel showed abnormal formation of stress fibers. These studies suggest that simple manipulations of the configuration of extracellular elements can dramatically alter the behavior of cultured hepatocytes.
为了重建肝脏中正常存在的细胞极性,将成年大鼠肝细胞夹在两层水合大鼠尾腱胶原基质之间。在功能上,夹在中间的肝细胞至少6周维持白蛋白、转铁蛋白、纤维蛋白原、胆汁酸和尿素的分泌,而在单层胶原凝胶上培养的细胞在1-2周内停止这种分泌。在单层胶原凝胶上培养1周后,当应用第二层胶原凝胶时,肝细胞仍可恢复这些丧失的功能。构建三明治系统的底物的确切性质似乎并不重要,只要它允许细胞附着即可。在三明治系统中培养的肝细胞似乎维持了与体内状态相似的肌动蛋白丝分布,而在单层胶原凝胶上培养的细胞则显示出应力纤维的异常形成。这些研究表明,对细胞外成分构型的简单操作可显著改变培养肝细胞的行为。