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C5a Receptor Deficiency Alters Energy Utilization and Fat Storage
OBJECTIVE: To investigate the impact of whole body C5a receptor (C5aR) deficiency on energy metabolism and fat storage. DESIGN: Male wildtype (WT) and C5aR knockout (C5aRKO) mice were fed a low fat (CHOW) or a high fat high sucrose diet-induced obesity (DIO) diet for 14 weeks. Body weight and food i...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3646841/ https://www.ncbi.nlm.nih.gov/pubmed/23667486 http://dx.doi.org/10.1371/journal.pone.0062531 |
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author | Roy, Christian Gupta, Abhishek Fisette, Alexandre Lapointe, Marc Poursharifi, Pegah Richard, Denis Lu, HuiLing Lu, Bao Gerard, Norma Gerard, Craig Cianflone, Katherine |
author_facet | Roy, Christian Gupta, Abhishek Fisette, Alexandre Lapointe, Marc Poursharifi, Pegah Richard, Denis Lu, HuiLing Lu, Bao Gerard, Norma Gerard, Craig Cianflone, Katherine |
author_sort | Roy, Christian |
collection | PubMed |
description | OBJECTIVE: To investigate the impact of whole body C5a receptor (C5aR) deficiency on energy metabolism and fat storage. DESIGN: Male wildtype (WT) and C5aR knockout (C5aRKO) mice were fed a low fat (CHOW) or a high fat high sucrose diet-induced obesity (DIO) diet for 14 weeks. Body weight and food intake were measured weekly. Indirect calorimetry, dietary fatload clearance, insulin and glucose tolerance tests were also evaluated. Liver, muscle and adipose tissue mRNA gene expression were measured by RT-PCR. RESULTS: At week one and 12, C5aRKO mice on DIO had increased oxygen consumption. After 12 weeks, although food intake was comparable, C5aRKO mice had lower body weight (−7% CHOW, −12% DIO) as well as smaller gonadal (−38% CHOW, −36% DIO) and inguinal (−29% CHOW, −30% DIO) fat pads than their WT counterparts. Conversely, in WT mice, C5aR was upregulated in DIO vs CHOW diets in gonadal adipose tissue, muscle and liver, while C5L2 mRNA expression was lower in C5aRKO on both diet. Furthermore, blood analysis showed lower plasma triglyceride and non-esterified fatty acid levels in both C5aRKO groups, with faster postprandial triglyceride clearance after a fatload. Additionally, C5aRKO mice showed lower CD36 expression in gonadal and muscle on both diets, while DGAT1 expression was higher in gonadal (CHOW) and liver (CHOW and DIO) and PPARγ was increased in muscle and liver. CONCLUSION: These observations point towards a role (either direct or indirect) for C5aR in energy expenditure and fat storage, suggesting a dual role for C5aR in metabolism as well as in immunity. |
format | Online Article Text |
id | pubmed-3646841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36468412013-05-10 C5a Receptor Deficiency Alters Energy Utilization and Fat Storage Roy, Christian Gupta, Abhishek Fisette, Alexandre Lapointe, Marc Poursharifi, Pegah Richard, Denis Lu, HuiLing Lu, Bao Gerard, Norma Gerard, Craig Cianflone, Katherine PLoS One Research Article OBJECTIVE: To investigate the impact of whole body C5a receptor (C5aR) deficiency on energy metabolism and fat storage. DESIGN: Male wildtype (WT) and C5aR knockout (C5aRKO) mice were fed a low fat (CHOW) or a high fat high sucrose diet-induced obesity (DIO) diet for 14 weeks. Body weight and food intake were measured weekly. Indirect calorimetry, dietary fatload clearance, insulin and glucose tolerance tests were also evaluated. Liver, muscle and adipose tissue mRNA gene expression were measured by RT-PCR. RESULTS: At week one and 12, C5aRKO mice on DIO had increased oxygen consumption. After 12 weeks, although food intake was comparable, C5aRKO mice had lower body weight (−7% CHOW, −12% DIO) as well as smaller gonadal (−38% CHOW, −36% DIO) and inguinal (−29% CHOW, −30% DIO) fat pads than their WT counterparts. Conversely, in WT mice, C5aR was upregulated in DIO vs CHOW diets in gonadal adipose tissue, muscle and liver, while C5L2 mRNA expression was lower in C5aRKO on both diet. Furthermore, blood analysis showed lower plasma triglyceride and non-esterified fatty acid levels in both C5aRKO groups, with faster postprandial triglyceride clearance after a fatload. Additionally, C5aRKO mice showed lower CD36 expression in gonadal and muscle on both diets, while DGAT1 expression was higher in gonadal (CHOW) and liver (CHOW and DIO) and PPARγ was increased in muscle and liver. CONCLUSION: These observations point towards a role (either direct or indirect) for C5aR in energy expenditure and fat storage, suggesting a dual role for C5aR in metabolism as well as in immunity. Public Library of Science 2013-05-07 /pmc/articles/PMC3646841/ /pubmed/23667486 http://dx.doi.org/10.1371/journal.pone.0062531 Text en © 2013 Roy et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Roy, Christian Gupta, Abhishek Fisette, Alexandre Lapointe, Marc Poursharifi, Pegah Richard, Denis Lu, HuiLing Lu, Bao Gerard, Norma Gerard, Craig Cianflone, Katherine C5a Receptor Deficiency Alters Energy Utilization and Fat Storage |
title | C5a Receptor Deficiency Alters Energy Utilization and Fat Storage |
title_full | C5a Receptor Deficiency Alters Energy Utilization and Fat Storage |
title_fullStr | C5a Receptor Deficiency Alters Energy Utilization and Fat Storage |
title_full_unstemmed | C5a Receptor Deficiency Alters Energy Utilization and Fat Storage |
title_short | C5a Receptor Deficiency Alters Energy Utilization and Fat Storage |
title_sort | c5a receptor deficiency alters energy utilization and fat storage |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3646841/ https://www.ncbi.nlm.nih.gov/pubmed/23667486 http://dx.doi.org/10.1371/journal.pone.0062531 |
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