TY - JOUR
T1 - Three Months of Strength Training Changes the Gene Expression of Inflammation-Related Genes in PBMC of Older Women
T2 - A Randomized Controlled Trial
AU - Liberman, Keliane
AU - Njemini, Rose
AU - Forti, Louis Nuvagah
AU - Cools, Wilfried
AU - Debacq-Chainiaux, Florence
AU - Kooijman, Ron
AU - Beyer, Ingo
AU - Bautmans, Ivan
N1 - Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/2/1
Y1 - 2022/2/1
N2 - Here, we investigate changes in inflammation-related gene-expression in peripheral mon-onuclear 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: 3×10rep at 80% 1RM), strength endurance training (SET: 2×30reps at 40% 1RM) or control (CON: 3×30sec stretching). Dif-ferentially 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 (n = 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 in-flammation. None of the altered pathways overlapped between IST and SET. Liver X Receptor/Ret-inoid 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.
AB - Here, we investigate changes in inflammation-related gene-expression in peripheral mon-onuclear 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: 3×10rep at 80% 1RM), strength endurance training (SET: 2×30reps at 40% 1RM) or control (CON: 3×30sec stretching). Dif-ferentially 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 (n = 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 in-flammation. None of the altered pathways overlapped between IST and SET. Liver X Receptor/Ret-inoid 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.
KW - Aged
KW - Gene expression
KW - Inflammation
KW - Leukocytes
KW - Resistance training
UR - http://www.scopus.com/inward/record.url?scp=85123873565&partnerID=8YFLogxK
U2 - 10.3390/cells11030531
DO - 10.3390/cells11030531
M3 - Article
C2 - 35159340
AN - SCOPUS:85123873565
SN - 2073-4409
VL - 11
JO - Cells
JF - Cells
IS - 3
M1 - 531
ER -