Alberto Sols Biomedical Research Institute (IIBm), Consejo Superior de Investigaciones Científicas/Universidad Autónoma de Madrid (CSIC/UAM), Madrid, Spain
Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, (CSIC) Madrid, Spain.
J Lipid Res. 2018 Dec;59(12):2308-2320. doi: 10.1194/jlr.M085209. Epub 2018 Oct 23.
Tyrosine hydroxylase (TH) catalyzes the first step in catecholamines synthesis. We studied the impact of reduced TH in brown adipose tissue (BAT) activation. In adult heterozygous ( ) mice, dopamine and noradrenaline (NA) content in BAT decreased after cold exposure. This reduced catecholaminergic response did not impair cold adaptation, because these mice induced uncoupling protein 1 (UCP-1) and maintained BAT temperature to a similar extent than controls ( ). Possible compensatory mechanisms implicated were studied. and expression, key genes in BAT activation, were elevated in mice at thermoneutrality from day 18.5 of embryonic life. Likewise, plasma FGF21 and liver mRNA were increased. Analysis of endoplasmic reticulum (ER) stress, a process that triggers elevations in FGF21, showed higher phospho-IRE1, phospho-JNK, and CHOP in BAT of mice at thermoneutrality. Also, increased lipolysis in BAT of cold-exposure mice was demonstrated by increased phosphorylation of hormone-sensitive lipase (HSL), as well as diacylglycerol (DAG) and FFA content. Overall, these results indicate that the mild effects of haploinsufficiency on BAT function are likely due to compensatory mechanisms involving elevations in and and through adaptive changes in the lipid profile.
酪氨酸羟化酶(TH)催化儿茶酚胺合成的第一步。我们研究了棕色脂肪组织(BAT)激活中 TH 减少的影响。在成年杂合子()小鼠中,BAT 中的多巴胺和去甲肾上腺素(NA)含量在暴露于寒冷后减少。这种减少的儿茶酚胺反应并没有损害对寒冷的适应,因为这些小鼠诱导解偶联蛋白 1(UCP-1)并将 BAT 温度维持在与对照组相似的水平()。研究了可能涉及的代偿机制。在胚胎生命第 18.5 天的常温下,BAT 激活的关键基因和的表达在 小鼠中升高。同样,血浆 FGF21 和肝脏 mRNA 也增加。内质网(ER)应激分析,一种触发 FGF21 升高的过程,显示常温下 BAT 中的磷酸化 IRE1、磷酸化 JNK 和 CHOP 在 小鼠中增加。此外,通过增加激素敏感脂肪酶(HSL)的磷酸化以及二酰基甘油(DAG)和游离脂肪酸(FFA)含量,证明了寒冷暴露的 小鼠中 BAT 的脂肪分解增加。总的来说,这些结果表明,TH 单倍不足对 BAT 功能的轻微影响可能归因于涉及和表达升高的代偿机制,以及通过脂质谱的适应性变化。