Differentiation of Pancreatic Acinar Carcinoma Cells Cultured on Rat Testicular Seminiferous Tubular Basement Membranes

Thomas K. Watanabe, Linnea J. Hansen, Neerad K. Roddy, Yashpal S. Kanwar, Janardan K. Roddy*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

The use of rat testicular seminiferous tubular basement membrane (STBM) segments as a model substratum for the in vitro maintenance of tumor cells dissociated from a transplantable pancreatic acinar rat carcinoma (J. K. Reddy and M. S. Rao, Science (Wash. DC), 198:78-80, 1977) is described. LUtrastruc-turally pure, hollow tubular segments of STBM were prepared by mechanical disaggregation, DNase digestion, and deoxycho-late treatment. Dissociated pancreatic acinar carcinoma cells adhered readily to STBM segments within 1 to 6 3hr, and these 3STBM-tumor cell aggregates were maintained for up to 7 days in serum-free chemically defined medium supplemented with hydrocortisone, insulin, vitamin C, and soybean trypsin inhibitor. The tumor cells formed acinar-like clusters and displayed intercellular junctions and polarization of secretory granules toward the center of these clusters. By 4 days, virtually all cells of this acinar carcinoma maintained on STBM in supplemented chemically defined medium contained numerous secretory granules. Cell replication, as determined by pHJthymidine autoradiography, ceased within 318 hr of attachment of neoplastic cells to STBM; however, all cells incorporated pHJIeucine as evidenced by light and electron microscopic autoradiography. In addition, two-dimensional analysis and fluorography of newly synthesized secretory proteins discharged by these cells in response to carbamyl-choline revealed the presence of M, 24, 000 protein and 19 other secretory proteins characteristic of this tumor (L. J. Hansen, M. K. Reddy, and J. K. Reddy, Proc. Natl. Acad. Sci. USA, 80: 4379-4383, 1983). The culture system utilizing STBM and supplemented chemically defined medium should allow investigation of the effects of a variety of factors on morphogenesis, cytodifferentiation, and gene expression in pancreatic acinar tumors.

Original languageEnglish (US)
Pages (from-to)5361-5368
Number of pages8
JournalCancer Research
Volume44
Issue number11
StatePublished - Nov 1 1984

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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