Erythroid differentiation

Ostareck, D. H., Ostareck-Lederer, A., Shatsky, I. N., and Hentze, M. W. (2001). Lipoxygenase mRNA silencing in erythroid differentiation The 3 UTR regulatory complex controls 60S ribosomal subunit joining. Cell 104, 281-290. 

Weees, I., Mastrandrea, L. D., Haldeman, M., Koury, S. T., Tamburlin, j., Pickart, C. M., and Finley, D. Inducation of ubiquitin-conjugating enzymes during terminal erythroid differentiation. Proc. Natl. Acad. Sci. USA 1995, 92, 4982-86. 

Leder, A. and Leder, P. (1975) Butyric acid, a potent inducer of erythroid differentiation in cultured eryfhroleukemic cells. Cell, 5, 319-322. 

Although the major physiological role of EPO is certainly to promote red blood cell production, EPO mRNA has also been detected in bone marrow macrophages, as well as some multipotential haemopoietic stem cells. Although the physiological relevance is unclear, it is possible that EPO produced by such sources may play a localized paracrine (or autocrine) role in promoting erythroid differentiation. 

Several other cultured cell lines were affected by butyrate (5). These included rat glial C6 cells (12-fold increase) and Friend erythroleukemic cells (4-fold increase). The increase in choleragen receptors in Friend cells was also time dependent (Table III). In addition, butyrate appeared to be specific dimethyl-sulfoxide (DMSO) induces erythroid differentiation (23) as does butyrate (24) but it did not cause an increase in toxin receptors (Table 111)7... 

Crabtree, G. R., Aebersold, R., Geoudine, M. (2004). Dynamic changes in transcription factor complexes during erythroid differentiation revealed by quantitative proteomics. Nat. Struct. 

K. Maruyama, K. Miyata, and A. Yoshimura. Proliferation and erythroid differentiation through the cytoplasmic domain of the erythropoietin receptor. J Biol Chem, 269 (8), 5976-5980, 1994. 

Vuillet-Gaugler, M.H., Breton-Gorius, J., Vainchencker, W., Guichard, J., Leroy, C., Tchernia, G. and Coulombel, L. (1990) Loss of attachment to fibronectin with terminal human erythroid differentiation. Blood 76, 865-873. 

Kilhsch, 1. Steinlein, P. Rbmisch, K. HoUinshead, R. Beug, H. Griffiths, G. Characterization of early and late endocytic compartments of the transferrin cycle transferrin receptor antibody blocks erythroid differentiation by trapping the receptor in the early endosome. J. CeU Sci. 1992, 103,211-232. 

Papayannopoulou T, Abkowitz J, D Andrea A. Biology of erythropoiesis, erythroid differentiation, and maturation. In Hoffman R, Benz EJ, Shattil SJ, et al, eds. Hematology—Basic Principles and Practice. New York, Churchill Livingstone, 2000 202. 

Keywords Apoptosis - Cell cycle Erythroid differentiation Erythroid precursors ... 

H. Fujita, M. Yamamoto, T. Yamagami, N. Hayashi, T.R. Bishop, H. De Verneuil, T. Yoshinaga, S. Shibahara, R. Morimoto, S. Sassa (1991). Sequential activation of genes for heme pathway enzymes during erythroid differentiation of mouse Friend virus-transformed erythroleukemia cells, Biochem. Biophys. Acta, 1090, 311-316. 

P.S. Ebert, I. Wars, D.N. Buell (1976). Erythroid differentiation in cultured Friend leukemia cells treated with metabolic inhibitors. Cancer Res., 36, 1809-1813. 

Rodrigue, C.M., Arous, N., Bachir, D., Smith-Ravin, J., Romeo, P.H., Galacteros, F., and Garel, M.C., Resveratrol, a natural dietary phytoalexin, possesses similar properties to hydroxyurea towards erythroid differentiation, Br. J. Haematol, 113 (2), 500-507,2001. 

Comoe L, Jeannesson P, Trentesaux C, Desoize B, Jardillier JC. The antileukemic alkaloid fagaronine and the human K562 leucemic cells Effects on growth and induction of erythroid differentiation. Leak Res 1987 11 445-51. 

Teiada M, Fujiki H, Marks PA et al. Induction of erythroid differentiation of murine erythtoleu-kemia cells by nicotinamide and related compounds. Proc Natl Acad Sci USA 1979 76(12) 6411-6414. 

Friend C, Scher W, Holland JG, Sato T (1971) Hemoglobin synthesis in murine virus-induced leukemic cells in vitro stimulation of erythroid differentiation by dimethyl sulfoxide. Proc Natl Acad Sci USA 68 378-382... 

Morioka K, Tanaka K, Nokuo T, Ishizawa M, Ono T (1979) Erythroid differentiation and poly-(ADP-ribose) synthesis in Friend leukemia cells. Gann 70 37-46... 

Terada M, Nudel U, Fibach E, Rifkind RA, Marks PA (1978) Changes in DNA associated with induction of erythroid differentiation by dimethyl sulfoxide in mouse erythroleukemic ceHs. Cancer Res 38 835-840... 

Moditication of nuclear proteins by poly(ADP-ribose) has been implicated as an essential step in the differentiation of a number of different systems. However, in some systems a transient rise of poly(ADP-ribose) as a prerequisite of differentiation was deduced from experiments with inhibitors [e.g. mesodermal chick limb cells (1), myoblasts (2) HL 60 cells to macrophages (3) and lymphocytes (4)]. In others, a transient decrease of poly(ADP-ribose) polymerase activity was thought to be required for the induction of differentiation, as inhibitors of poly(ADP-ribosyl)ation were able to replace the inducers [e.g. erythroid differentiation of Friend leukemia cells (5), HL 60 cells to granulocytes (6), murine embryo carcinoma cells (7) and mouse manunary gland differentiation (8)]. 

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