Novel surface expression of reticulocalbin 1 on bone endothelial cells and human prostate cancer cells is regulated by TNF‐α

Year: 2008

Type: article

Abstract: An unbiased cDNA expression phage library derived from bone-marrow endothelial cells was used to identify novel surface adhesion molecules that might participate in metastasis. Herein we report that reticulocalbin 1 (RCN1) is a cell surface-associated protein on both endothelial (EC) and prostate cancer (PCa) cell lines. RCN1 is an H/KDEL protein with six EF-hand, calcium-binding motifs, found in the endoplasmic reticulum. Our data indicate that RCN1 also is expressed on the cell surface of several endothelial cell lines, including human dermal microvascular endothelial cells (HDMVECs), bone marrow endothelial cells (BMEC), and transformed human bone marrow endothelial cells (TrHBMEC). While RCN1 protein levels were highest in lysates from HDMVEC, this difference was not statistically significant compared BMEC and TrHBMEC. Given preferential adhesion of PCa to bone-marrow EC, these data suggest that RCN1 is unlikely to account for the preferential metastasis of PCa to bone. In addition, there was not a statistically significant difference in total RCN1 protein expression among the PCa cell lines. RCN1 also was expressed on the surface of several PCa cell lines, including those of the LNCaP human PCa progression model and the highly metastatic PC-3 cell line. Interestingly, RCN1 expression on the cell surface was upregulated by tumor necrosis factor alpha treatment of bone-marrow endothelial cells. Taken together, we show cell surface localization of RCN1 that has not been described previously for either PCa or BMEC and that the surface expression on BMEC is regulated by pro-inflammatory TNF-alpha.

Source: Journal of Cellular Biochemistry

DOI: 10.1002/jcb.21785

Authors: Carlton R. Cooper, Bianca Graves, Freddie Pruitt, Hassan Chaib, Jill E. Lynch, Andrew Koemeter Cox, Linda Sequeria, Kenneth L. van Golen, Angelo Evans, Kirk Czymmek, Rebecca S. Bullard, Carlton D. Donald, Katia Sol‐Church, James D. Gendernalik, Babette Weksler, Mary C. Farach‐Carson, Jill A. Macoska, Robert A. Sikes, Kenneth J. Pienta

Institutions: University of Delaware, University of Michigan, U-M Rogel Cancer Center, Delaware Biotechnology Institute, Cornell University, Weill Cornell Medicine

Language: English

Topic: Cell Adhesion Molecules Research

Subfield: Immunology and Allergy

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, University of Michigan Comprehensive Cancer Center, National Heart, Lung, and Blood Institute, National Cancer Institute, National Institute of Diabetes and Digestive and Kidney Diseases, National Center for Research Resources

OpenAlex ID: W2129217857