Use of in situ hybridization to identify collagen and albumin mRNAs in isolated mouse hepatocytes.

M. A. Saber, Mark A Zern, D. A. Shafritz

Research output: Contribution to journalArticle

32 Citations (Scopus)

Abstract

We present a simple and improved method for in situ localization of albumin and collagen mRNAs in isolated mouse hepatocytes. The cells were isolated by collagenase perfusion, mincing, and differential centrifugation. Nick-translated 3H-labeled mouse albumin cDNA (pmalb-2) and chicken pro-alpha 2(I) collagen cDNA (pCg45) probes were then hybridized with the cells in silane-treated microcentrifuge tubes. The cells were transferred and fixed to a microscope slide and hybridization was evaluated semiquantitatively by counting exposure of grains in autoradiographic emulsion placed over the cells. With this method of in situ hybridization, all hepatocytes appear to have significant, but highly variable, amounts of albumin mRNA. In addition, type I procollagen mRNA appears to be present at low abundance in hepatocytes. These results indicate that in situ hybridization can effectively demonstrate the presence of specific low- or high-abundance mRNAs in isolated well-differentiated eukaryotic cells.

Original languageEnglish (US)
Pages (from-to)4017-4020
Number of pages4
JournalProceedings of the National Academy of Sciences of the United States of America
Volume80
Issue number13
StatePublished - Jul 1983
Externally publishedYes

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In Situ Hybridization
Hepatocytes
Albumins
Collagen
Messenger RNA
Collagen Type I
Complementary DNA
Silanes
Eukaryotic Cells
Collagenases
Emulsions
Centrifugation
Chickens
Perfusion

ASJC Scopus subject areas

  • General
  • Genetics

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Use of in situ hybridization to identify collagen and albumin mRNAs in isolated mouse hepatocytes. / Saber, M. A.; Zern, Mark A; Shafritz, D. A.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 80, No. 13, 07.1983, p. 4017-4020.

Research output: Contribution to journalArticle

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