Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention  AACR Conference on Molecular Diagnostics - 2008
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[Cancer Research 38, 1539-1549, June 1, 1978]
© 1978 American Association for Cancer Research

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Ultrastructure of Adult Rat Hepatocytes Cultured on Floating Collagen Membranes1

Carol A. Sattler2, George Michalopoulos3, Gerald L. Sattler and Henry C. Pitot

Departments of Oncology [C. A. S., G. M., G. L. S., H. C. P.] and Pathology [G. M., H. C. P.], McArdle Laboratory for Cancer Research, University of Wisconsin, Madison, Wisconsin 53706

The ultrastructure of primary hepatocytes cultured for 2 to 17 days on floating collagen membranes was evaluated. A pellet of the hepatic cell suspension used to in0culate the collagen membranes contained some single cells and many aggregates of two, three, or four cells. Desmosomes were spilt during the perfusion, but tight junctions and gap junctions remained intact. By 2 days in culture, the hepatocytes had formed a monolayer of cells of polygonal shape with newly synthesized desmosomes between cells. Since the flexible floating collagen membrane decreases in size as the monolayer forms, the hepatocytes do not flatting out, as is characteristic of cells cultured on a right substrate. Hepatocytes in culture for 10 days or less exhibited large lamellar arrays of rough endoplasmic reticulum, well developed Golgi complexes, and structures resembling bile canallcull, which possess tight junctions and desmosomes separating them from the intercellular space. Microfilaments oriented parallel to the plasma membranes of adjoining cells and in an intermeshed network at the edge of the monolayer and beneath the plasma membrane bordering the medium increased in size and number in older cultures. After 17 days in culture, the cells maintained tight junctions, desmosomes, Golgi complexes, and rough endoplasmic reticulum in small lamellar stacks and in small vesicles. Since hepatocytes on the floating collagen membrane retain most of the subcellular structural elements characteristic of normal functioning hepatocytes for 2.5 weeks, this system may be valulable for future experiments involving drug metabolism and carcinogenesis in vitro.

1 This study was supported in part by Grant CA-02575 from the National Cancer Institute.

2 To whom requests for reprints should be addressed.

3 Postdoctoral trainee in biochemical pathology of the National Institute of General Medical Sciences (GM-00130). Present address: Department of Pathology, Duke University School of Medicine, Durham. N. C.

Received 11/10/77. Accepted 3/ 2/78.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1978 by the American Association for Cancer Research.