Gilmore Jennifer L, Riese David J
Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University School of Pharmacy, West Lafayette, IN 47907-1333, USA.
Oncol Res. 2004;14(11-12):589-602. doi: 10.3727/0965040042707907.
ErbB4 is a member of the ErbB family of receptor tyrosine kinases. Because of a paucity of appropriate pharmacologic tools, little is known about ErbB4 functions in vivo. In response to this need, we hypothesized that a recombinant form of the extracellular domain of ErbB4 would antagonize ligand-induced receptor tyrosine phosphorylation and subsequent downstream signaling and could be used to probe ErbB4 function. Indeed, we show here that one such ErbB4 protein, secErbB4-26/549, is a potent inhibitor of ligand-induced ErbB4 tyrosine phosphorylation and of ligand-induced ErbB4 coupling to biological responses. Furthermore, we demonstrate that secErbB4-26/549 antagonizes ligand-induced ErbB4 signaling by acting as a ligand sink. Thus, secErbB4-26/549 is suitable for elucidating the effects of ErbB4 ligand-induced ErbB signaling in a variety of biological contexts.
ErbB4是受体酪氨酸激酶ErbB家族的成员之一。由于缺乏合适的药理学工具,人们对ErbB4在体内的功能了解甚少。为满足这一需求,我们推测ErbB4细胞外结构域的重组形式会拮抗配体诱导的受体酪氨酸磷酸化及随后的下游信号传导,并可用于探究ErbB4的功能。事实上,我们在此表明,一种这样的ErbB4蛋白,即secErbB4-26/549,是配体诱导的ErbB4酪氨酸磷酸化以及配体诱导的ErbB4与生物学反应偶联的有效抑制剂。此外,我们证明secErbB4-26/549通过充当配体阱来拮抗配体诱导的ErbB4信号传导。因此,secErbB4-26/549适用于阐明在多种生物学背景下ErbB4配体诱导的ErbB信号传导的作用。