Sánchez-Marco Javier, Martínez-Beamonte Roberto, Diego Alicia De, Herrero-Continente Tania, Barranquero Cristina, Arnal Carmen, Surra Joaquín, Navarro María A, Osada Jesús
Departamento de Bioquímica y Biología Molecular y Celular, Facultad de Veterinaria, Instituto de Investigación Sanitaria de Aragón-Universidad de Zaragoza, E-50013 Zaragoza, Spain.
Instituto Agroalimentario de Aragón, CITA-Universidad de Zaragoza, E-50013 Zaragoza, Spain.
Biomedicines. 2022 Mar 18;10(3):709. doi: 10.3390/biomedicines10030709.
Thioredoxin domain containing 5 (TXNDC5) is a protein disulfide isomerase involved in several diseases related to oxidative stress, energy metabolism and cellular inflammation. In a previous manuscript, a negative association between fatty liver development and hepatic expression was observed. To study the role of TXNDC5 in the liver, we generated -deficient mice. The absence of the protein caused an increased metabolic need to gain weight along with a bigger and fatter liver. RNAseq was performed to elucidate the putative mechanisms, showing a substantial liver overexpression of serum amyloid genes (, ) with no changes in hepatic protein, but discrete plasma augmentation by the gene inactivation. Higher levels of malonyldialdehyde, apolipoprotein A1 and platelet activating factor-aryl esterase activity were also found in serum from -deficient mice. However, no difference in the distribution of high-density lipoproteins (HDL)-mayor components and SAA was found between groups, and even the reactive oxygen species decreased in HDL coming from -deficient mice. These results confirm the relation of this gene with hepatic steatosis and with a fasting metabolic derive remedying an acute phase response. Likewise, they pose a new role in modulating the nature of HDL particles, and SAA-containing HDL particles are not particularly oxidized.
含硫氧还蛋白结构域5(TXNDC5)是一种蛋白质二硫键异构酶,与多种与氧化应激、能量代谢和细胞炎症相关的疾病有关。在之前的一篇论文中,观察到脂肪肝发展与肝脏表达之间存在负相关。为了研究TXNDC5在肝脏中的作用,我们构建了基因敲除小鼠。该蛋白的缺失导致体重增加的代谢需求增加,同时肝脏更大更胖。进行RNA测序以阐明可能的机制,结果显示血清淀粉样蛋白基因( )在肝脏中大量过表达,肝脏蛋白无变化,但基因失活导致血浆中该蛋白有明显增加。在基因敲除小鼠的血清中还发现丙二醛、载脂蛋白A1和血小板活化因子 - 芳基酯酶活性水平更高。然而,两组之间高密度脂蛋白(HDL)主要成分和血清淀粉样蛋白A(SAA)的分布没有差异,甚至基因敲除小鼠来源的HDL中的活性氧物质减少。这些结果证实了该基因与肝脂肪变性以及与纠正急性期反应的空腹代谢之间的关系。同样,它们在调节HDL颗粒的性质方面发挥了新作用,并且含SAA的HDL颗粒没有特别被氧化。