Brown Maria, McGuinness Michael, Wright Terry, Ren Xiaoping, Wang Yang, Boivin Gregory P, Hahn Harvey, Feldman Arthur M, Jones W Keith
Dept. of Pharmacology and Cell Biophysics, 231 Albert Sabin Way, ML0575, Univ. of Cincinnati, Cincinnati, OH 45267-0575, USA.
Am J Physiol Heart Circ Physiol. 2005 Jul;289(1):H466-76. doi: 10.1152/ajpheart.00170.2004. Epub 2005 Feb 4.
The role of NF-kappaB in cardiac physiology and pathophysiology has been difficult to delineate due to the inability to specifically block NF-kappaB signaling in the heart. Cardiac-specific transgenic models have recently been developed that repress NF-kappaB activation by preventing phosphorylation at specific serine residues of the inhibitory kappaB (IkappaB) protein isoform IkappaBalpha. However, these models are unable to completely block NF-kappaB because of a second signaling pathway that regulates NF-kappaB function via Tyr42 phosphorylation of IkappaBalpha. We report the development of transgenic (3M) mouse lines that express the mutant IkappaBalpha(S32A,S36A,Y42F) in a cardiac-specific manner. NF-kappaB activation in cardiomyopathic TNF-1.6 mice is completely blocked by the 3M transgene but only partially blocked (70-80%) by the previously described double-mutant 2M [IkappaBalpha(S32A,S36A)] transgene, which demonstrates the action of two proximal pathways for NF-kappaB activation in TNF-alpha-induced cardiomyopathy. In contrast, after acute stimuli including administration of TNF-alpha and ischemia-reperfusion (I/R), NF-kappaB activation is blocked in both 2M and 3M transgenic mice. This result suggests that phosphorylation of the regulatory Ser32 and Ser36 predominantly mediates NF-kappaB activation in these situations. We show that infarct size after I/R is reduced by 70% in 3M transgenic mice, which conclusively demonstrates that NF-kappaB is involved in I/R injury. In summary, we have engineered novel transgenic mice that allow us to distinguish two major proximal pathways for NF-kappaB activation. Our results demonstrate that the serine and tyrosine phosphorylation pathways are differentially activated during different pathophysiological processes (cardiomyopathy and I/R injury) and that NF-kappaB contributes to infarct development after I/R.
由于无法特异性阻断心脏中的核因子-κB(NF-κB)信号传导,其在心脏生理和病理生理中的作用一直难以明确。最近已开发出心脏特异性转基因模型,该模型通过阻止抑制性κB(IkappaB)蛋白亚型IkappaBalpha特定丝氨酸残基的磷酸化来抑制NF-κB激活。然而,由于第二条信号通路通过IkappaBalpha的Tyr42磷酸化调节NF-κB功能,这些模型无法完全阻断NF-κB。我们报告了以心脏特异性方式表达突变型IkappaBalpha(S32A,S36A,Y42F)的转基因(3M)小鼠品系的开发。3M转基因可完全阻断心肌病TNF-1.6小鼠中的NF-κB激活,但先前描述的双突变2M [IkappaBalpha(S32A,S36A)]转基因只能部分阻断(70-80%),这证明了在TNF-α诱导的心肌病中NF-κB激活的两条近端途径的作用。相比之下,在包括给予TNF-α和缺血再灌注(I/R)在内的急性刺激后,2M和3M转基因小鼠中的NF-κB激活均被阻断。该结果表明,在这些情况下,调节性Ser32和Ser36的磷酸化主要介导NF-κB激活。我们表明,3M转基因小鼠在I/R后的梗死面积减少了70%,这确凿地证明NF-κB参与了I/R损伤。总之,我们构建了新型转基因小鼠,使我们能够区分NF-κB激活的两条主要近端途径。我们的结果表明,丝氨酸和酪氨酸磷酸化途径在不同的病理生理过程(心肌病和I/R损伤)中被差异激活,并且NF-κB促成了I/R后的梗死发展。