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A novel D 2 O tracer method to quantify RNA turnover as a biomarker of de novo ribosomal biogenesis, in vitro, in animal models, and in human skeletal muscle

Current methods to quantify in vivo RNA dynamics are limited. Here, we developed a novel stable isotope (D O) methodology to quantify RNA synthesis (i.e., ribosomal biogenesis) in cells, animal models, and humans. First, proliferating C2C12 cells were incubated in D O-enriched media and myotubes ±50...

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Published in:American journal of physiology: endocrinology and metabolism 2017-12, Vol.313 (6), p.E681-E689
Main Authors: Brook, M S, Wilkinson, D J, Mitchell, W K, Lund, J L, Phillips, B E, Szewczyk, N J, Kainulainen, H, Lensu, S, Koch, L G, Britton, S L, Greenhaff, P L, Smith, K, Atherton, P J
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container_title American journal of physiology: endocrinology and metabolism
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creator Brook, M S
Wilkinson, D J
Mitchell, W K
Lund, J L
Phillips, B E
Szewczyk, N J
Kainulainen, H
Lensu, S
Koch, L G
Britton, S L
Greenhaff, P L
Smith, K
Atherton, P J
description Current methods to quantify in vivo RNA dynamics are limited. Here, we developed a novel stable isotope (D O) methodology to quantify RNA synthesis (i.e., ribosomal biogenesis) in cells, animal models, and humans. First, proliferating C2C12 cells were incubated in D O-enriched media and myotubes ±50 ng/ml IGF-I. Second, rat quadriceps (untrained, = 9; 7-wk interval-"like" training, = 13) were collected after ~3-wk D O (70 atom %) administration, with body-water enrichment monitored via blood sampling. Finally, 10 (23 ± 1 yr) men consumed 150-ml D O followed by 50 ml/wk and undertook 6-wk resistance exercise (6 × 8 repetitions, 75% 1-repetition maximum 3/wk) with body-water enrichment monitored by saliva sampling and muscle biopsies (for determination of RNA synthesis) at 0, 3, and 6 wk. Ribose mole percent excess (r-MPE) from purine nucleotides was analyzed via GC-MS/MS. Proliferating C2C12 cell r-MPE exhibited a rise to plateau, whereas IGF-I increased myotube RNA from 76 ± 3 to 123 ± 3 ng/μl and r-MPE by 0.39 ± 0.1% (both < 0.01). After 3 wk, rat quadriceps r-MPE had increased to 0.25 ± 0.01% ( < 0.01) and was greater with running exercise (0.36 ± 0.02%; < 0.01). Human muscle r-MPE increased to 0.06 ± 0.01 and 0.13 ± 0.02% at 3/6 wk, respectively, equating to synthesis rates of ~0.8%/day, increasing with resistance exercise to 1.7 ± 0.3%/day ( < 0.01) and 1.2 ± 0.1%/day ( < 0.05) at 3/6 wk, respectively. Therefore, we have developed and physiologically validated a novel technique to explore ribosomal biogenesis in a multimodal fashion.
doi_str_mv 10.1152/ajpendo.00157.2017
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After 3 wk, rat quadriceps r-MPE had increased to 0.25 ± 0.01% ( &lt; 0.01) and was greater with running exercise (0.36 ± 0.02%; &lt; 0.01). Human muscle r-MPE increased to 0.06 ± 0.01 and 0.13 ± 0.02% at 3/6 wk, respectively, equating to synthesis rates of ~0.8%/day, increasing with resistance exercise to 1.7 ± 0.3%/day ( &lt; 0.01) and 1.2 ± 0.1%/day ( &lt; 0.05) at 3/6 wk, respectively. 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After 3 wk, rat quadriceps r-MPE had increased to 0.25 ± 0.01% ( &lt; 0.01) and was greater with running exercise (0.36 ± 0.02%; &lt; 0.01). Human muscle r-MPE increased to 0.06 ± 0.01 and 0.13 ± 0.02% at 3/6 wk, respectively, equating to synthesis rates of ~0.8%/day, increasing with resistance exercise to 1.7 ± 0.3%/day ( &lt; 0.01) and 1.2 ± 0.1%/day ( &lt; 0.05) at 3/6 wk, respectively. Therefore, we have developed and physiologically validated a novel technique to explore ribosomal biogenesis in a multimodal fashion.</abstract><cop>United States</cop><pmid>28811296</pmid><doi>10.1152/ajpendo.00157.2017</doi></addata></record>
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subjects Animals
Biomarkers - metabolism
Cell Line
Deuterium Oxide
Female
Humans
Male
Mice
Physical Conditioning, Animal
Quadriceps Muscle - metabolism
Rats
Resistance Training
Ribose - metabolism
Ribosomes - metabolism
RNA - biosynthesis
Tandem Mass Spectrometry
Young Adult
title A novel D 2 O tracer method to quantify RNA turnover as a biomarker of de novo ribosomal biogenesis, in vitro, in animal models, and in human skeletal muscle
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