The overall objective of the proposed research is the study of the growth regulation of intestinal epithelial cells in vitro, and their expression of differential properties. We will focus, in particular, on the regulation of proliferation of these cells by cell density, hormones, growth factors, serum factors. The effect of glucocorticoids will be studied in detail to determine the mechanism of the growth inhibition caused by these hormones, and to examine the possibility that the striking morphological changes and the synthesis of new proteins they induce in the cultural intestinal epithelial cells represent the expression of differentiated cell properties characteristics of intestinal villus cells. Cell-substrate interactions will be investigated by studying the effect of different collagen types, desposited in the cultured dishes, on the adhesion of the epithelial cells, the role played by fibronectin in this interaction, and the collagen type(s) synthesized by the epithelial cells in the presence of ascorbate. In the course of these studies, we will determine growth rates, DNA synthesis, duration of cell cycle phases, kinetics of growth inhibition and/or stimulation in the presence or absence of the various hormones and other factors. Morphological and ultrastructural studies will be performed by transmission and scanning electron microscopy. Collagen synthesis will be studied by internal labeling with radioactive proline and analysis of the labeled proteins with established biochemical techniques.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
3R01DK032656-04S1
Application #
3231032
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1982-12-01
Project End
1987-03-31
Budget Start
1985-09-01
Budget End
1987-03-31
Support Year
4
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Cornell University
Department
Type
Earth Sciences/Resources
DUNS #
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Paul, E C; Quaroni, A (1993) Identification of a 102 kDa protein (cytocentrin) immunologically related to keratin 19, which is a cytoplasmically derived component of the mitotic spindle pole. J Cell Sci 106 ( Pt 3):967-81
Quaroni, A; Paul, E C; Nichols, B L (1993) Intracellular degradation and reduced cell-surface expression of sucrase-isomaltase in heat-shocked Caco-2 cells. Biochem J 292 ( Pt 3):725-34
Calnek, D; Quaroni, A (1993) Differential localization by in situ hybridization of distinct keratin mRNA species during intestinal epithelial cell development and differentiation. Differentiation 53:95-104
Quaroni, A; Nichols, B L; Quaroni, E et al. (1992) Expression and different polarity of aminopeptidase N in normal human colonic mucosa and colonic tumors. Int J Cancer 51:404-11
Rings, E H; Buller, H A; de Boer, P A et al. (1992) Messenger RNA sorting in enterocytes. Co-localization with encoded proteins. FEBS Lett 300:183-7
Calnek, D; Quaroni, A (1992) Changes in keratin expression during fetal and postnatal development of intestinal epithelial cells. Biochem J 285 ( Pt 3):939-46
Cross, H S; Quaroni, A (1991) Inhibition of sucrose-isomaltase expression by EGF in the human colon adenocarcinoma cells Caco-2. Am J Physiol 261:C1173-83
Beaulieu, J F; Quaroni, A (1991) Clonal analysis of sucrase-isomaltase expression in the human colon adenocarcinoma Caco-2 cells. Biochem J 280 ( Pt 3):599-608
Quaroni, A; Calnek, D; Quaroni, E et al. (1991) Keratin expression in rat intestinal crypt and villus cells. Analysis with a panel of monoclonal antibodies. J Biol Chem 266:11923-31
Daniele, B; Quaroni, A (1991) Effects of epidermal growth factor on diamine oxidase expression and cell growth in Caco-2 cells. Am J Physiol 261:G669-76

Showing the most recent 10 out of 15 publications