Journal Article

Morphodensitometric analysis of protein kinase C β<sub>II</sub> expression in rat colon: modulation by diet and relation to <i>in situ</i> cell proliferation and apoptosis

Laurie A. Davidson, Roxanne E. Brown, Wen-Chi L. Chang, Jeffrey S. Morris, Naisyin Wang, Raymond J. Carroll, Nancy D. Turner, Joanne R. Lupton and Robert S. Chapkin

in Carcinogenesis

Volume 21, issue 8, pages 1513-1519
Published in print August 2000 | ISSN: 0143-3334
Published online August 2000 | e-ISSN: 1460-2180 | DOI:
Morphodensitometric analysis of protein kinase C βII expression in rat colon: modulation by diet and relation to in situ cell proliferation and apoptosis

More Like This

Show all results sharing this subject:

  • Clinical Cytogenetics and Molecular Genetics


Show Summary Details


We have recently demonstrated that overexpression of PKC βII renders transgenic mice more susceptible to carcinogen-induced colonic hyperproliferation and aberrant crypt foci formation. In order to further investigate the ability of PKC βII to modulate colonocyte cytokinetics, we determined the localization of PKC βII with respect to cell proliferation and apoptosis along the entire colonic crypt axis following carcinogen and diet manipulation. Rats were provided diets containing either corn oil [containing n-6 polyunsaturated fatty acids (PUFA)] or fish oil (containing n-3 PUFA), cellulose (non-fermentable fiber) or pectin (fermentable fiber) and injected with azoxymethane (AOM) or saline. After 16 weeks, an intermediate time point when no macroscopic tumors are detected, colonic sections were utilized for immunohistochemical image analysis and immunoblotting. Cell proliferation was measured by incorporation of bromodeoxyuridine into DNA and apoptosis by terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end-labeling. In the distal colon, PKC βII staining was localized to the upper portion of the crypt. In comparison, proximal crypts had more (P < 0.05) staining in the lower tertile. AOM enhanced (P < 0.05) PKC βII expression in all regions of the distal colonic crypt (upper, middle and lower tertiles). There was also an interaction (P < 0.05) between dietary fat and fiber on PKC βII expression (corn/pectin > fish/cellulose, fish/pectin > corn/cellulose) in all regions of the distal colonic crypt. With respect to colonic cell kinetics, proliferation paralleled the increase in PKC βII expression in carcinogen-treated animals. In contrast, apoptosis at the lumenal surface was inversely proportional to PKC βII expression in the upper tertile. These results suggest that an elevation in PKC βII expression along the crypt axis in the distal colon is linked to enhancement of cell proliferation and suppression of apoptosis, predictive intermediate biomarkers of tumor development. Therefore, select dietary factors may confer protection against colon carcinogenesis in part by blocking carcinogen-induced PKC βII expression.

Keywords: AOM, azoxymethane; BrdU, bromodeoxyuridine; BT, biotinyl tyramide/amplification diluent; DAG, diacylglycerol; PBS, phosphate-buffered saline; PKC, protein kinase C; PUFA, polyunsaturated fatty acids; SA-HRP, streptavidin-conjugated horseradish peroxidase.

Journal Article.  5763 words.  Illustrated.

Subjects: Clinical Cytogenetics and Molecular Genetics

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.