Induction of lactoferrin expression in murine ES cells by retinoic acid and estrogen

Experimental Cell Research

Volumn 245, Issue 1, 1998, Pages 214-220

  Geng, Ke ^a   Li, Ying ^a   Bezault, Joann ^a   Furmanski, Philip ^a  

^a NEW YORK UNIVERSITY   (United States)

Author keywords

9 cis retinoic acid (9 cis RA); Diethylstilbestrol (DES); Embryonic stem (ES) cells; Reverse transcription polymerase chain reaction (RT PCR); estradiol

Indexed keywords

ESTROGEN; LACTOFERRIN; MESSENGER RNA; RETINOIC ACID;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; ENZYME LINKED IMMUNOSORBENT ASSAY; HORMONAL REGULATION; HORMONE DETERMINATION; IMMUNOBLOTTING; IMMUNOFLUORESCENCE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN INDUCTION; RNA ANALYSIS;

ANIMALIA; MAMMALIA; MURINAE;

EID: 0031772727     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1006/excr.1998.4266     Document Type: Article

References (35)

1. Arnold, R. R., Cole, M. F., and McGhee, J. R. (1977). A bactericidal effect for human lactoferrin. Science 197, 263-265.
2. Lu, I., Hangoc, G., Oliff, A., Chen, L. T., Shen, R. N., and Broxmeyer, H. E. (1987). Protective influence of lactoferrin on mice infected with polycythemia-inducing strain of Friend virus complex. Cancer Res. 47, 4184-4188.
3. Broxmeyer, H. E., Williams, D. E., Hangoc, G., Cooper, S., Gentile, P., Shen, R. N., Ralph, P., Gillis, S., and Bicknell, D. C. (1987). The opposing actions in vivo on murine myelopoiesis of purified preparations of lactoferrin and the colony stimulating factors. Blood Cells 13, 31-48.
4. Birgens, H. S. (1984). The biological significance of lactoferrin in haematology. Scand. J. Haematol. 33, 225-230.
5. Bezault, J., Bhimani, R., Wiprovnik, J., and Furmanski, P. (1994) Human lactoferrin inhibits growth of solid tumors and development of experimental metastases in mice. Cancer Res. 54, 2310-2312.
6. He, J., and Furmanski, P. (1995). Sequence specificity and transcriptional activation in the binding of lactoferrin to DNA. Nature 373, 721-724.
7. Lee, M. O., Liu, Y., and Zhang, X. K. (1995). A retinoic acid response element that overlaps an estrogen response element mediates multihormonal sensitivity in transcriptional activation of the binding to lactoferrin gene. Mol. Cell. Biol. 15, 4194-4207.
8. Mason, D. Y., and Taylor, C. R. (1978). Distribution of transferrin, ferritin, and lactoferrin in human tissues. J. Clin. Pathol. 31, 316-327.
9. Pentecost, B. T., and Teng, C. T. (1987). Lactotransferrin is the major estrogen inducible protein of mouse uterine secretions. J. Biol. Chem. 262, 10134-10139.
10. Masson, P. L., Heremans, J. F., and Schonne, E. (1969). Lactoferrin, an iron-binding protein in neutriphilic leukocytes. J. Exp. Med. 130, 643-658.
11. Pryzwansky, K. B., Martin, L. E., and Spitznagel, J. K. (1978). Immunocytochemical localization of myeloperoxidase, lactoferrin, lysozyme and neutral proteases in human monocytes and neutrophilic granulocytes. J. Reticuloendothel. Soc. 24, 295-310.
12. Kreider, B. L., and Rovera, G. (1992). The immediate early gene response to a differentiative stimulus is disrupted by the v-abl and v-ras oncogenes. Oncogene 7, 135-140.
13. Evans, M. J., and Kaufman, M. H. (1981). Establishment in culture of pluripotential cells from mouse embryos. Nature 292, 154-156.
14. Martin, G. R. (1981) Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells. Proc. Natl. Acad. Sci. USA 78, 7634-7638.
15. Bradley, A., Evans, M., Kaufman, M. H., and Robertson, E. (1984). Formation of germ-line chimeras from embryo-derived teratocarcinoma cell lines. Nature 309, 255-256.
16. Nagy, A., Rossant, J., Nagy, R., Abramow-Newerly, W., and Roder, J. C. (1993). Derivation of completely cell culture-derived mice from early-passage embryonic stem cells. Proc. Natl. Acad. Sci. USA 90, 8424-8428.
17. Rudnick, M. A., and McBurney, M. W. (1987). Cell culture methods and induction of differentiation of embryonal carcinoma cell lines. In "Teratocarcinomas and Embryonic Stem Cells" (E. J. Robertson, Ed.), IRL Press, Oxford.
18. Mavilio, F., Simeone, A., Boncinelli, E., and Andrews, P. W. (1988). Activation of four homeobox gene clusters in human embryonal carcinoma cells induced to differentiate by retinoic acid. Differentiation 37, 73-79.
19. Liu, Y., and Teng, C. T. (1991). Characterization of estrogen-responsive mouse lactoferrin promoter. J. Biol. Chem. 266, 21880-21885.
20. Teng, C. T., Pentecost, B. T., Chen, Y. H., Newbold, R. R., Eddy, E. M., and McLachlan, J. A. (1989). Lactotransferrin gene expression in the mouse uterus and mammary gland. Endocrinology 124, 992-999.
21. Furmanski, P., Li, Z. P., Fortuna, M. B., Swamy, C. V., and Das, M. R. (1989). Multiple molecular forms of human lactoferrin: Identification of a class of lactoferrin that possess ribonuclease activity and lack iron-binding capacity. J. Exp. Med. 170, 415-429.
22. Burnette, W. N. (1981). "Western blotting": electrophoretic transfer of proteins from sodium dodecyl sulfate-polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A. Anal. Biochem. 112, 195-203.
23. Ince, B. A., Montano, M. M., and Katzenellenbogen, B. S. (1994). Activation of transcriptionally inactive human estrogen receptors by cyclic adenosine 3′, 5′-monophosphate and ligands including antiestrogens. Mol. Endocrinol. 8, 1397-1406.
24. Kamei, Y., Kawada, T., Mizukami, J., and Sugimoto, E. (1994). The prevention of adipose differentiation of 3T3-L1 cells caused by retinoic acid is elicited through retinoic acid receptor alpha. Life Sci. 55, 307-312.
25. Masson, P. L., and Hermans, J. F. (1971). Lactoferrin in milk from different species. Comp. Biochem. Physiol. 39, 119-129.
26. Arnold, R. R., Russell, J. E., Champion, W. J., Brewer, M., and Gauthier, J. J. (1982). Bactericidal activity of human lactoferrin: differentiation from the stasis of iron deprivation. Inf. Immun. 35, 792-799.
27. Walmer, D. K, Wrona, M. A., Hughes, C. L., and Nelson, K. G. (1992). Lactoferrin expression in the mouse reproductive tract during the natural estrous cycle: correlation with circulating estradiol and progesterone. Endocrinology 131, 1458-1466.
28. Shigeta, H., Newbold, R., McLachlan, J. A., and Teng, C. (1996). Estrogenic effect on the expression of estrogen receptor, COUPTF, and lactoferrin mRNA in developing mouse tissues. Mol. Reprod. Dev. 45, 21-30.
29. Green, M. R., and Pastewka, J. V. (1978). Lactoferrin is a marker for prolactin response in mouse mammary explants. Endocrinology 103, 151-103.
30. Bennett, R. M., and Davis, J. (1982). Lactoferrin interacts with deoxyribonucleic acid: A preferential reactivity with double-stranded DNA and dissociation of DNA-anti-DNA complexes. J. Lab. Clin. Med. 99, 127-138.
31. Bennett, R. M., Davis, J., Campbell, S., and Portnoff, S. (1983). Lactoferrin binds to cell membrane DNA: Association of surface DNA with an enriched population of B cells and monocytes. J. Clin. Invest. 71, 611-618.
32. Furmanski, P., He, J., Ying, L., Bezault, J., Bhimani, R., and K. Ho. (1997). Functional significance of binding of lactoferrin to DNA. In "Lactoferrin: Interaction and Biological Functions (Hutchens, T. w., and B. Lonnerdal, Ed.), Humana Press, Totowa.
33. Andrews, P. W., Gonczol, E., Plotkin, S. A., Dignazio, M., and Oosterhuis, J. W. (1986). Differentiation of TERA-2 human embryonal carcinoma cells into neurons and HCMV-permissive cells: Induction by agents other than retinoic acid. Differentiation 31, 119-126.
34. Furmanski, P., and Li, Z. P. (1990). Multiple forms of lactoferrin in normal and leukemic human granulocytes. Exp. Haematol. 18, 932-935.
35. Siebert, P. D., and Huang, B. C. (1997). Identification of an alternative form of human lactoferrin mRNA that is expressed differently in normal tissues and tumor-derived cell lines. Proc. Natl. Acad. Sci. USA 94, 2198-2203.