Dhondup Yangchen, Sjaastad Ivar, Sandanger Øystein, Aronsen Jan Magnus, Ahmed Muhammad Shakil, Attramadal Håvard, Finsen Alexandra Vanessa, Zhang Lili, Ranheim Trine, Alfsnes Katrine, Aukrust Pål, Christensen Geir, Yndestad Arne, Vinge Leif Erik
Research Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Center for Heart Failure Research, University of Oslo, Oslo, Norway.
Mediators Inflamm. 2017;2017:9450439. doi: 10.1155/2017/9450439. Epub 2017 Apr 11.
. Inflammation is important in heart failure (HF). The role of the immune receptor toll-like receptor 9 (TLR9) in HF is not understood and not investigated in diastolic HF. We investigated the role of TLR9 in a murine diastolic HF model caused by cardiomyocyte SERCA2a excision. . We crossed SERCA2a KO and TLR9 KO mice to generate four mouse lines. Tamoxifen-induced cardiomyocyte SERCA2a gene excision was carried out in mice, causing diastolic HF. After 7.6 weeks, cardiac functions and dimensions were analyzed by echocardiography and heart tissues were processed. HF mice depleted of TLR9 demonstrated reduced survival compared to SERC2a KO mice, with a median life expectancy of 58 days compared to 63 days. Both HF groups displayed increased left atrium size, lung weight, fetal gene expressions, monocyte/macrophage infiltration, and fibrosis. However, there were no significant differences between the groups. . In mice with SERCA2a KO-induced diastolic HF, the absence of TLR9 reduced median life expectancy. The cause remains elusive, as all investigated HF parameters were unaltered. Still, these findings support a salutary role of TLR9 in some subsets of HF conditions and underline the importance for future studies on the mechanisms of TLR9 in diastolic HF.
炎症在心力衰竭(HF)中起着重要作用。免疫受体Toll样受体9(TLR9)在HF中的作用尚不清楚,且未在舒张性HF中进行研究。我们研究了TLR9在由心肌细胞SERCA2a切除引起的小鼠舒张性HF模型中的作用。我们将SERCA2a基因敲除(KO)小鼠和TLR9 KO小鼠杂交,产生了四种小鼠品系。在小鼠中进行他莫昔芬诱导的心肌细胞SERCA2a基因切除,导致舒张性HF。7.6周后,通过超声心动图分析心脏功能和尺寸,并对心脏组织进行处理。与SERCA2a KO小鼠相比,TLR9缺失的HF小鼠存活率降低,中位预期寿命为58天,而SERCA2a KO小鼠为63天。两个HF组的左心房大小、肺重量、胎儿基因表达、单核细胞/巨噬细胞浸润和纤维化均增加。然而,两组之间没有显著差异。在SERCA2a KO诱导的舒张性HF小鼠中,TLR9的缺失降低了中位预期寿命。原因仍然不明,因为所有研究的HF参数均未改变。尽管如此,这些发现支持了TLR9在某些HF情况下的有益作用,并强调了未来研究TLR9在舒张性HF中的机制的重要性。