Loading…
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...
Saved in:
Published in: | American journal of physiology: endocrinology and metabolism 2017-12, Vol.313 (6), p.E681-E689 |
---|---|
Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c1156-af4631f1920ebdc4bdb4ab8f959c7e8ab5c76c947b2e971e27a6ab1739beccd93 |
---|---|
cites | cdi_FETCH-LOGICAL-c1156-af4631f1920ebdc4bdb4ab8f959c7e8ab5c76c947b2e971e27a6ab1739beccd93 |
container_end_page | E689 |
container_issue | 6 |
container_start_page | E681 |
container_title | American journal of physiology: endocrinology and metabolism |
container_volume | 313 |
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 |
format | article |
fullrecord | <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1152_ajpendo_00157_2017</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>28811296</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1156-af4631f1920ebdc4bdb4ab8f959c7e8ab5c76c947b2e971e27a6ab1739beccd93</originalsourceid><addsrcrecordid>eNo9kMlOwzAQhi0EomV5AQ5oHoAU21kcH6uyShVICM6RlwmkTeJiJ5X6MLwrCRROHs83_2j0EXLB6IyxlF-r1QZb62aUslTMOGXigEwHwCOWpukhmVIm44jliZyQkxBWlFKRJvyYTHieM8ZlNiVfc2jdFmu4AQ7P0Hll0EOD3Yez0Dn47FXbVeUOXp7m0PV-HPagAijQlWuUXw9fV4LFcY8DX2kXhn494ndsMVThCqoWtlXn3U-l2mrkjbNYD0y1dux-9I1qIayxxm6kfTA1npGjUtUBz_fvKXm7u31dPETL5_vHxXwZmUFEFqkyyWJWMskpamsSbXWidF7KVBqBudKpEZmRidAcpWDIhcqUZiKWGo2xMj4l_Hev8S4Ej2Wx8cORflcwWoyui73r4sd1MboeQpe_oU2vG7T_kT-58TfRXH5n</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><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</title><source>American Physiological Society Free</source><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</creator><creatorcontrib>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</creatorcontrib><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.</description><identifier>ISSN: 0193-1849</identifier><identifier>EISSN: 1522-1555</identifier><identifier>DOI: 10.1152/ajpendo.00157.2017</identifier><identifier>PMID: 28811296</identifier><language>eng</language><publisher>United States</publisher><subject>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</subject><ispartof>American journal of physiology: endocrinology and metabolism, 2017-12, Vol.313 (6), p.E681-E689</ispartof><rights>Copyright © 2017 the American Physiological Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1156-af4631f1920ebdc4bdb4ab8f959c7e8ab5c76c947b2e971e27a6ab1739beccd93</citedby><cites>FETCH-LOGICAL-c1156-af4631f1920ebdc4bdb4ab8f959c7e8ab5c76c947b2e971e27a6ab1739beccd93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28811296$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brook, M S</creatorcontrib><creatorcontrib>Wilkinson, D J</creatorcontrib><creatorcontrib>Mitchell, W K</creatorcontrib><creatorcontrib>Lund, J L</creatorcontrib><creatorcontrib>Phillips, B E</creatorcontrib><creatorcontrib>Szewczyk, N J</creatorcontrib><creatorcontrib>Kainulainen, H</creatorcontrib><creatorcontrib>Lensu, S</creatorcontrib><creatorcontrib>Koch, L G</creatorcontrib><creatorcontrib>Britton, S L</creatorcontrib><creatorcontrib>Greenhaff, P L</creatorcontrib><creatorcontrib>Smith, K</creatorcontrib><creatorcontrib>Atherton, P J</creatorcontrib><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</title><title>American journal of physiology: endocrinology and metabolism</title><addtitle>Am J Physiol Endocrinol Metab</addtitle><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.</description><subject>Animals</subject><subject>Biomarkers - metabolism</subject><subject>Cell Line</subject><subject>Deuterium Oxide</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Mice</subject><subject>Physical Conditioning, Animal</subject><subject>Quadriceps Muscle - metabolism</subject><subject>Rats</subject><subject>Resistance Training</subject><subject>Ribose - metabolism</subject><subject>Ribosomes - metabolism</subject><subject>RNA - biosynthesis</subject><subject>Tandem Mass Spectrometry</subject><subject>Young Adult</subject><issn>0193-1849</issn><issn>1522-1555</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNo9kMlOwzAQhi0EomV5AQ5oHoAU21kcH6uyShVICM6RlwmkTeJiJ5X6MLwrCRROHs83_2j0EXLB6IyxlF-r1QZb62aUslTMOGXigEwHwCOWpukhmVIm44jliZyQkxBWlFKRJvyYTHieM8ZlNiVfc2jdFmu4AQ7P0Hll0EOD3Yez0Dn47FXbVeUOXp7m0PV-HPagAijQlWuUXw9fV4LFcY8DX2kXhn494ndsMVThCqoWtlXn3U-l2mrkjbNYD0y1dux-9I1qIayxxm6kfTA1npGjUtUBz_fvKXm7u31dPETL5_vHxXwZmUFEFqkyyWJWMskpamsSbXWidF7KVBqBudKpEZmRidAcpWDIhcqUZiKWGo2xMj4l_Hev8S4Ej2Wx8cORflcwWoyui73r4sd1MboeQpe_oU2vG7T_kT-58TfRXH5n</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Brook, M S</creator><creator>Wilkinson, D J</creator><creator>Mitchell, W K</creator><creator>Lund, J L</creator><creator>Phillips, B E</creator><creator>Szewczyk, N J</creator><creator>Kainulainen, H</creator><creator>Lensu, S</creator><creator>Koch, L G</creator><creator>Britton, S L</creator><creator>Greenhaff, P L</creator><creator>Smith, K</creator><creator>Atherton, P J</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20171201</creationdate><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</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1156-af4631f1920ebdc4bdb4ab8f959c7e8ab5c76c947b2e971e27a6ab1739beccd93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Biomarkers - metabolism</topic><topic>Cell Line</topic><topic>Deuterium Oxide</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Mice</topic><topic>Physical Conditioning, Animal</topic><topic>Quadriceps Muscle - metabolism</topic><topic>Rats</topic><topic>Resistance Training</topic><topic>Ribose - metabolism</topic><topic>Ribosomes - metabolism</topic><topic>RNA - biosynthesis</topic><topic>Tandem Mass Spectrometry</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brook, M S</creatorcontrib><creatorcontrib>Wilkinson, D J</creatorcontrib><creatorcontrib>Mitchell, W K</creatorcontrib><creatorcontrib>Lund, J L</creatorcontrib><creatorcontrib>Phillips, B E</creatorcontrib><creatorcontrib>Szewczyk, N J</creatorcontrib><creatorcontrib>Kainulainen, H</creatorcontrib><creatorcontrib>Lensu, S</creatorcontrib><creatorcontrib>Koch, L G</creatorcontrib><creatorcontrib>Britton, S L</creatorcontrib><creatorcontrib>Greenhaff, P L</creatorcontrib><creatorcontrib>Smith, K</creatorcontrib><creatorcontrib>Atherton, P J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>American journal of physiology: endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brook, M S</au><au>Wilkinson, D J</au><au>Mitchell, W K</au><au>Lund, J L</au><au>Phillips, B E</au><au>Szewczyk, N J</au><au>Kainulainen, H</au><au>Lensu, S</au><au>Koch, L G</au><au>Britton, S L</au><au>Greenhaff, P L</au><au>Smith, K</au><au>Atherton, P J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>American journal of physiology: endocrinology and metabolism</jtitle><addtitle>Am J Physiol Endocrinol Metab</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>313</volume><issue>6</issue><spage>E681</spage><epage>E689</epage><pages>E681-E689</pages><issn>0193-1849</issn><eissn>1522-1555</eissn><abstract>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.</abstract><cop>United States</cop><pmid>28811296</pmid><doi>10.1152/ajpendo.00157.2017</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0193-1849 |
ispartof | American journal of physiology: endocrinology and metabolism, 2017-12, Vol.313 (6), p.E681-E689 |
issn | 0193-1849 1522-1555 |
language | eng |
recordid | cdi_crossref_primary_10_1152_ajpendo_00157_2017 |
source | American Physiological Society Free |
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 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T02%3A45%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20novel%20D%202%20O%20tracer%20method%20to%20quantify%20RNA%20turnover%20as%20a%20biomarker%20of%20de%20novo%20ribosomal%20biogenesis,%20in%20vitro,%20in%20animal%20models,%20and%20in%20human%20skeletal%20muscle&rft.jtitle=American%20journal%20of%20physiology:%20endocrinology%20and%20metabolism&rft.au=Brook,%20M%20S&rft.date=2017-12-01&rft.volume=313&rft.issue=6&rft.spage=E681&rft.epage=E689&rft.pages=E681-E689&rft.issn=0193-1849&rft.eissn=1522-1555&rft_id=info:doi/10.1152/ajpendo.00157.2017&rft_dat=%3Cpubmed_cross%3E28811296%3C/pubmed_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c1156-af4631f1920ebdc4bdb4ab8f959c7e8ab5c76c947b2e971e27a6ab1739beccd93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/28811296&rfr_iscdi=true |