Frailty in Ageing Research Group (FRIA), Gerontology Department, Vrije Universiteit Brussel (VUB), B-1090 Brussels, Belgium.
Interfaculty Center Data Processing and Statistics (ICDS), Vrije Universiteit Brussel (VUB), B-1090 Brussels, Belgium.
Cells. 2022 Feb 3;11(3):531. doi: 10.3390/cells11030531.
Here, we investigate changes in inflammation-related gene-expression in peripheral mononuclear blood cells (PBMC) by strength training. A total of 14 women aged ≥65 years were randomized into 3 months of either 3×/week intensive strength training (IST: 3×10 rep at 80% 1RM), strength endurance training (SET: 2×30 reps at 40% 1RM) or control (CON: 3×30 sec stretching). Differentially expressed genes (fold change ≤0.67 or ≥1.5) were identified by targeted RNA-sequencing of 407 inflammation-related genes. A total of 98 genes ( = 61 pro-inflammatory) were significantly affected. IST and SET altered 14 genes in a similar direction and 19 genes in the opposite direction. Compared to CON, IST changed the expression of 6 genes in the same direction, and 17 genes in the SET. Likewise, 18 and 13 genes were oppositely expressed for, respectively, IST and SET compared to CON. Changes in gene expression affected 33 canonical pathways related to chronic inflammation. None of the altered pathways overlapped between IST and SET. Liver X Receptor/Retinoid X Receptor Activation (LXR/RXR) and Triggering Receptor Expressed On Myeloid Cells 1 (TREM1) pathways were enriched oppositely in both training groups. We conclude that three months IST and SET can induce changes in CLIP-related gene expression in PBMC, but by affecting different genes and related pathways.
在这里,我们通过力量训练研究了外周血单核细胞(PBMC)中与炎症相关的基因表达变化。共有 14 名年龄≥65 岁的女性被随机分为 3 个月的高强度力量训练(IST:3×10 次,强度为 80%1RM)、力量耐力训练(SET:2×30 次,强度为 40%1RM)或对照组(CON:3×30 秒伸展)。通过靶向 RNA-seq 对 407 个与炎症相关的基因进行检测,确定差异表达基因(倍数变化≤0.67 或≥1.5)。共有 98 个基因(=61 个促炎基因)受到显著影响。IST 和 SET 以相似的方向改变了 14 个基因,以相反的方向改变了 19 个基因。与 CON 相比,IST 使 6 个基因的表达方向相同,SET 使 17 个基因的表达方向相同。同样,与 CON 相比,IST 和 SET 分别有 18 个和 13 个基因的表达方向相反。基因表达的变化影响了 33 个与慢性炎症相关的经典途径。IST 和 SET 之间没有重叠的改变途径。肝 X 受体/视黄酸 X 受体激活(LXR/RXR)和髓样细胞表达的触发受体 1(TREM1)途径在两组中均呈相反富集。我们得出结论,三个月的 IST 和 SET 可以诱导 PBMC 中与 CLIP 相关的基因表达变化,但通过影响不同的基因和相关途径。