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Signal pathway of 17beta-estradiol-induced MUC5B expression in human airway epithelial cells. | LitMetric

AI Article Synopsis

  • - The study investigates how the hormone 17beta-estradiol (E2) regulates the expression of MUC5B, a key mucin in the human respiratory system, particularly in airway diseases.
  • - It finds that E2 triggers MUC5B overexpression through its interaction with the estrogen receptor alpha (ERalpha) and activation of the ERK1/2-MAPK signaling pathway.
  • - Using an ER antagonist blocked E2's effects on MUC5B expression, highlighting the roles of RSK1, CREB, and other signaling cascades in the regulation of this gene, which helps explain abnormal mucin secretion due to hormonal changes.

Article Abstract

MUC5B is a major mucin of the human respiratory tract, and it is not clear how MUC5B expression is regulated in various airway diseases. The goal of this study was to determine the mechanisms by which 17beta-estradiol induces MUC5B gene expression in airway epithelial cells. It was found that E2, a sex hormone, stimulates MUC5B gene overexpression by interaction with estrogen receptor alpha (ERalpha) and by acting through extracellular signal-regulated kinase 1/2 (ERK1/2)-mitogen-activated protein kinase (MAPK). Pretreatment with ER antagonist ICI 182,780 blocked both E2-induced ERK1/2-MAPK activation and MUC5B gene expression. It was also found that the activation of p90 ribosomal S 6 protein kinase 1 (RSK1), cAMP-response element-binding protein (CREB), and cAMP-response element (CRE) (-956 region of the MUC5B promoter)-responsive signaling cascades via ERK1/2 MAPK are crucial aspects of the intracellular mechanisms that mediate MUC5B gene expression. Taken together, these studies give additional insights into the molecular mechanism of hormone-induced MUC5B gene expression and enhance our understanding of abnormal mucin secretion in response to hormonal imbalances.

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Source
http://dx.doi.org/10.1165/rcmb.2007-0377OCDOI Listing

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