The Regulatory Role of the Adrenergic Agonists Phenylephrine and Isoproterenol on Fetal Hemoglobin Expression and Erythroid Differentiation
Author(s) -
Yun Mei,
Naida Yin,
Xia Jin,
Jiangyan He,
Zhan Yin
Publication year - 2013
Publication title -
endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.674
H-Index - 257
eISSN - 1945-7170
pISSN - 0013-7227
DOI - 10.1210/en.2013-1535
Subject(s) - endocrinology , medicine , erythropoiesis , biology , k562 cells , agonist , mapk/erk pathway , adrenergic agonist , fetal hemoglobin , adrenergic receptor , signal transduction , microbiology and biotechnology , chemistry , receptor , fetus , anemia , leukemia , genetics , pregnancy
It has been reported that various endocrine hormones exert prominent effects on erythropoiesis. We conducted experiments to identify the mechanisms involved in the regulatory functions of adrenergic signaling on erythroid differentiation and the expression of hemoglobin genes. The reactivation of fetal hemoglobin (HbF) expression is also an important therapeutic option in patients with hemoglobin disorders. We determined that the adrenergic agonists phenylephrine (PE) and isoproterenol (ISO) can induce the production of β-hemoglobin embryonic 1 (hbbe1) mRNA and protein in adult zebrafish erythrocytes. Elevated levels of HbF mRNA and protein were also observed in human K562 cells after the adrenergic agonist treatments. In addition, elevated levels of histone acetylation were observed in both the PE- and the ISO-treated K562 cells. Additionally, our data further indicate that the induction effects of the adrenergic agonists on HbF synthesis and erythroid differentiation in K562 cells are mainly mediated by the p38 MAPK/cAMP response element binding pathway. In summary, the present study identifies the role of the adrenergic agonists PE and ISO on p38 MAPK and ERK signaling for the stimulation of HbF production and erythroid differentiation.
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