Department of Physiology & Biophysics, University of Louisville School of Medicine, Louisville, KY, USA.
Department of Electrical Engineering, Fu Foundation School of Engineering and Applied Sciences, Columbia University, New York, NY, USA.
Mol Cell Biochem. 2019 Apr;454(1-2):139-152. doi: 10.1007/s11010-018-3459-9. Epub 2018 Oct 23.
Heart failure (HF) is a functional lack of myocardial performance due to a loss of molecular control over increases in calcium and ROS, resulting in proteolytic degradative advances and cardiac remodeling. Mitochondria are the molecular powerhouse of cells, shifting the sphere of cardiomyocyte stability and performance. Functional mitochondria rely on the molecular abilities of safety factors such as TFAM to maintain physiological parameters. Mitochondrial transcription factor A (TFAM) creates a mitochondrial nucleoid structure around mtDNA, protecting it from mutation, inhibiting NFAT (ROS activator/hypertrophic stimulator), and transcriptionally activates Serca2a to decrease calcium mishandling. Calpain1 and MMP9 are proteolytic degratory factors that play a major role in cardiomyocyte decline in HF. Current literature depicts major decreases in TFAM as HF progresses. We aim to assess TFAM function against Calpain1 and MMP9 proteolytic activity and its role in cardiac remodeling. To this date, no publication has surfaced describing the effects of aortic banding (AB) as a surgical HF model in TFAM-TG mice. HF models were created via AB in TFAM transgenic (TFAM-TG) and C57BLJ-6 (WT) mice. Eight weeks post AB, functional analysis revealed a successful banding procedure, resulting in cardiac hypertrophy as observed via echocardiography. Pulse wave and color doppler show increased aortic flow rates as well as turbulent flow at the banding site. Preliminary results of cardiac tissue immuno-histochemistry of HF-control mice show decreased TFAM and compensatory increases in Serca2a fluorescent expression, along with increased Calpain1 and MMP9 expression. Protein, RNA, and IHC analysis will further assess TFAM-TG results post-banding. Echocardiography shows more cardiac stability and functionality in HF-induced TFAM-TG mice than the control counterpart. These findings complement our published in vitro results. Overall, this suggests that TFAM has molecular therapeutic potential to reduce protease expression.
心力衰竭(HF)是由于钙和 ROS 增加时分子控制丧失导致心肌性能丧失的一种功能不足,导致蛋白水解降解进展和心脏重构。线粒体是细胞的分子动力源,改变了心肌细胞稳定性和功能的范围。功能正常的线粒体依赖于 TFAM 等安全因素的分子能力来维持生理参数。线粒体转录因子 A(TFAM)在 mtDNA 周围创建一个线粒体核区结构,防止其突变,抑制 NFAT(ROS 激活剂/肥大刺激剂),并转录激活 Serca2a 以减少钙处理不当。钙蛋白酶 1 和 MMP9 是蛋白水解降解因子,在 HF 中心肌细胞下降中起主要作用。目前的文献表明,随着 HF 的进展,TFAM 的含量显著下降。我们旨在评估 TFAM 功能对 Calpain1 和 MMP9 蛋白水解活性的影响及其在心脏重构中的作用。迄今为止,没有出版物描述过主动脉缩窄(AB)作为 TFAM-TG 小鼠心力衰竭模型的手术 HF 模型。通过 AB 在 TFAM 转基因(TFAM-TG)和 C57BLJ-6(WT)小鼠中创建 HF 模型。AB 后 8 周,功能分析显示成功的捆绑程序,导致超声心动图观察到的心脏肥大。脉搏波和彩色多普勒显示主动脉血流率增加以及捆绑部位的湍流。HF 对照小鼠心脏组织免疫组织化学的初步结果显示 TFAM 减少,Serca2a 荧光表达代偿性增加,同时 Calpain1 和 MMP9 表达增加。蛋白、RNA 和 IHC 分析将进一步评估捆绑后 TFAM-TG 的结果。与对照组相比,HF 诱导的 TFAM-TG 小鼠中的超声心动图显示出更多的心脏稳定性和功能。这些发现补充了我们已发表的体外结果。总的来说,这表明 TFAM 具有减少蛋白酶表达的分子治疗潜力。