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用于生物人工肝的猪肝细胞球体的形成。

Formation of porcine hepatocyte spheroids for use in a bioartificial liver.

作者信息

Lazar A, Peshwa M V, Wu F J, Chi C M, Cerra F B, Hu W S

机构信息

Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis 55455-0132, USA.

出版信息

Cell Transplant. 1995 May-Jun;4(3):259-68. doi: 10.1177/096368979500400303.

Abstract

Xenogeneic hepatocytes have recently been used in a bioartificial liver device as a potential short-term extracorporeal support of acute liver failure. Scaling up the system requires large quantities of viable and highly active cells. Hepatocytes grown as spheroids manifest higher metabolic activities for longer time periods as compared to those in monolayer cultures. Use of hepatocyte spheroids for application in a bioartificial liver can possibly alleviate the need of scaling up. Porcine hepatocytes when cultured under stirred conditions, from multicellular spheroids in a defined culture medium. Spheroids were formed 24 h after cell inoculation with an efficiency of 80-90% and a mean diameter of about 135 microns. Scanning electron microscopy revealed numerous microvilli projecting from the entire surface of the spheroids. Transmission electron microscopy revealed differentiated hepatocytes which displayed well-developed cytoplasmic structures separated by bile canaliculus-like structures. The morphological studies show a resemblance between cells in the spheroids and in the liver in vivo. Urea-genesis by spheroids was twice as active and was sustained for a longer culture period than that by hepatocytes cultured as monolayers. Preparation of porcine hepatocyte spheroids in an agitated vessel is simple efficient and reproducible. It will allow for preparation of large quantities of spheroids to be employed in a bioartificial liver device as well as in liver metabolism studies.

摘要

异种肝细胞最近已被用于生物人工肝装置中,作为急性肝衰竭潜在的短期体外支持。扩大该系统需要大量有活力且高度活跃的细胞。与单层培养的肝细胞相比,以球体形式生长的肝细胞在更长时间段内表现出更高的代谢活性。将肝细胞球体应用于生物人工肝可能会缓解扩大规模的需求。猪肝细胞在搅拌条件下于特定培养基中培养形成多细胞球体。细胞接种后24小时形成球体,效率为80 - 90%,平均直径约为135微米。扫描电子显微镜显示球体整个表面有许多微绒毛突出。透射电子显微镜显示分化的肝细胞,其具有由胆小管样结构分隔的发育良好的细胞质结构。形态学研究表明球体中的细胞与体内肝脏中的细胞相似。球体的尿素生成活性是单层培养肝细胞的两倍,且在更长的培养期内持续保持。在搅拌容器中制备猪肝细胞球体简单、高效且可重复。这将使得能够制备大量球体,用于生物人工肝装置以及肝脏代谢研究。

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