Metabolic protein replacement drives tissue turnover in adult mice

2006 ◽  
Vol 84 (7) ◽  
pp. 992-1002 ◽  
Author(s):  
Lynne S. Arneson ◽  
Stephen MacAvoy ◽  
Ethan Basset

Stable isotopes are increasingly being used to examine ecological and physiological questions, such as dietary choices, migration routes and timing, and physiological condition. To address these questions in the field, laboratory experiments must be done to determine diet–tissue discrimination values and turnover rates for stable isotopes in tissues. In this study, we examined the carbon and nitrogen turnover rates of whole blood, skeletal muscle, liver, kidney, heart, and brain, as well as the sulfur turnover rate of whole blood, skeletal muscle, and liver in Mus musculus L., 1758 following a diet change. By examining tissue isotope change in two groups of mice fed different diets, we found that tissues turnover at different rates (in order of fastest to slowest — liver, kidney, heart, brain, whole blood, skeletal muscle), but that carbon, nitrogen, and sulfur isotopes turned over with similar half-lives within a single tissue. By using a diet with different nutrient isotopic values, we also calculated that up to approximately 90%–95% of carbon in newly synthesized tissue was contributed by dietary protein. These results will provide field researchers with additional tissue isotopic half-lives to elucidate dietary history with a greater degree of certainty. The tissue sulfur half-lives provide an extra stable isotope that may be used in situations where carbon and nitrogen values do not differ between old and new nutrient sources.

2010 ◽  
Vol 88 (10) ◽  
pp. 961-967 ◽  
Author(s):  
Rachel L. DeMots ◽  
James M. Novak ◽  
Karen F. Gaines ◽  
Aaron J. Gregor ◽  
Christopher S. Romanek ◽  
...  

Stable isotope analysis has become an increasingly valuable tool in investigating animal ecology. Here we document the turnover rates for carbon in the liver, muscle, and whole blood tissue, as well as the tissue–diet discrimination values for carbon and nitrogen isotopes in the liver, whole blood, muscle, and hair, of the white-footed mouse ( Peromyscus leucopus (Rafinesque, 1818)). A 168-day diet-switching experiment was conducted with a laboratory population of white-footed mice. The δ13C values for all tissues deviated less than 1‰ from those of the diet except for whole blood, which had a slightly higher tissue–diet discrimination factor of 1.8‰. All tissues were enriched in 15N by approximately 3‰ relative to the diet except for liver tissue, which was 4.5‰ higher than the dietary δ15N value. Turnover rates for tissues of white-footed mice were ranked liver > whole blood > muscle. The half-lives calculated for liver tissue differed significantly between the two diet switches performed in this experiment. We demonstrate that there is potential for variation in tissue–diet discrimination values and tissue turnover rates between even closely related species. These findings highlight the importance of determining species-specific estimates of these parameters prior to the use of stable isotope analysis in field investigations of animal ecology.


2009 ◽  
Vol 23 (2) ◽  
pp. 319-326 ◽  
Author(s):  
Aaron T. Fisk ◽  
Kim Sash ◽  
John Maerz ◽  
William Palmer ◽  
John P. Carroll ◽  
...  

2004 ◽  
Vol 52 (6) ◽  
pp. 635 ◽  
Author(s):  
Marcel Klaassen ◽  
Michele Thums ◽  
Ian D. Hume

Carbon (C) and nitrogen (N) stable isotopes offer a powerful tool for assessing the extent of tissue assimilation of dietary components. However, the method relies on knowledge of diet–tissue isotopic discrimination and how quickly diet shifts become apparent in various tissues. In the present study, blood plasma and blood cells, tissues that are easily obtained under field conditions, were used to validate the stable isotope method over a period of 4–5 weeks using captive long-nosed bandicoots (Perameles nasuta). Diet–tissue discrimination effects appeared to be small. For C, derived diet–tissue isotopic discriminations were 1.4‰ for blood plasma and –0.2‰ for blood cells. For N the values were 2.8‰ and 2.1‰, respectively, and were independent of the nitrogen content of the food. C and N turnover measurements in the blood plasma and cells of the bandicoots indicated that blood plasma provides dietary information integrated over a period of ~3 weeks, whereas blood cells give an impression of the assimilated diet over a period of as much as half a year. These turnover rates were low compared with the little information available for birds and eutherian mammals, and probably relate to the typically low metabolic rate of marsupials.


2005 ◽  
Vol 83 (5) ◽  
pp. 631-641 ◽  
Author(s):  
Stephen E MacAvoy ◽  
Stephen A Macko ◽  
Lynne S Arneson

Stable-isotope signatures in animal tissues presumably reflect the local food web. However, that assumption may be complicated by differential nutrient routing, fractionation, and the possibility that large organisms are not in isotopic equilibrium with seasonally available food sources. Additionally, the rate at which organisms incorporate the isotopic signature of a food is largely unknown. In this study we assessed the rate of carbon- and nitrogen-isotope turnover in liver, muscle, and blood in mice (Mus musculus L., 1758) following a diet change. We report the proportion of tissue turnover caused by growth versus that caused by metabolic tissue replacement. Growth accounted for approximately 10% of observed tissue turnover in adult mice. Blood carbon had the shortest half-life (16.9 days), followed by muscle carbon (23.9 days). Liver carbon turnover, which was slower than blood and muscle carbon turnovers, was not as well described by the exponential decay equations. All tissues primarily reflect the protein carbon signature rather than the carbohydrate carbon signature. The nitrogen signature in all tissues was enriched by 3‰–5‰ over their diets' nitrogen signature, depending on tissue type, and the isotopic turnover rates of nitrogen in blood and muscle were comparable with those observed for carbon.


Function ◽  
2021 ◽  
Author(s):  
Leslie M Baehr ◽  
David C Hughes ◽  
Sarah A Lynch ◽  
Delphi Van Haver ◽  
Teresa Mendes Maia ◽  
...  

Abstract MuRF1 (TRIM63) is a muscle-specific E3 ubiquitin ligase and component of the ubiquitin proteasome system. MuRF1 is transcriptionally upregulated under conditions that cause muscle loss, in both rodents and humans, and is a recognized marker of muscle atrophy. In this study, we used in vivo electroporation to determine if MuRF1 overexpression alone can cause muscle atrophy and, in combination with ubiquitin proteomics, identify the endogenous MuRF1 substrates in skeletal muscle. Overexpression of MuRF1 in adult mice increases ubiquitination of myofibrillar and sarcoplasmic proteins, increases expression of genes associated with neuromuscular junction instability, and causes muscle atrophy. A total of 169 ubiquitination sites on 56 proteins were found to be regulated by MuRF1. MuRF1-mediated ubiquitination targeted both thick and thin filament contractile proteins, as well as, glycolytic enzymes, deubiquitinases, p62, and VCP. These data reveal a potential role for MuRF1 in not only the breakdown of the sarcomere, but also the regulation of metabolism and other proteolytic pathways in skeletal muscle.


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