Cargando…
Skeletal muscle damage and impaired regeneration due to LPL-mediated lipotoxicity
According to the concept of lipotoxicity, ectopic accumulation of lipids in non-adipose tissue induces pathological changes. The most prominent effects are seen in fatty liver disease, lipid cardiomyopathy, non-insulin-dependent diabetes mellitus, insulin resistance and skeletal muscle myopathy. We...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406590/ https://www.ncbi.nlm.nih.gov/pubmed/22825472 http://dx.doi.org/10.1038/cddis.2012.91 |
_version_ | 1782239236288675840 |
---|---|
author | Tamilarasan, K P Temmel, H Das, S K Al Zoughbi, W Schauer, S Vesely, P W Hoefler, G |
author_facet | Tamilarasan, K P Temmel, H Das, S K Al Zoughbi, W Schauer, S Vesely, P W Hoefler, G |
author_sort | Tamilarasan, K P |
collection | PubMed |
description | According to the concept of lipotoxicity, ectopic accumulation of lipids in non-adipose tissue induces pathological changes. The most prominent effects are seen in fatty liver disease, lipid cardiomyopathy, non-insulin-dependent diabetes mellitus, insulin resistance and skeletal muscle myopathy. We used the MCK(m)-hLPL mouse distinguished by skeletal and cardiac muscle-specific human lipoprotein lipase (hLPL) overexpression to investigate effects of lipid overload in skeletal muscle. We were intrigued to find that ectopic lipid accumulation induced proteasomal activity, apoptosis and skeletal muscle damage. In line with these findings we observed reduced Musculus gastrocnemius and Musculus quadriceps mass in transgenic animals, accompanied by severely impaired physical endurance. We suggest that muscle loss was aggravated by impaired muscle regeneration as evidenced by reduced cross-sectional area of regenerating myofibers after cardiotoxin-induced injury in MCK(m)-hLPL mice. Similarly, an almost complete loss of myogenic potential was observed in C2C12 murine myoblasts upon overexpression of LPL. Our findings directly link lipid overload to muscle damage, impaired regeneration and loss of performance. These findings support the concept of lipotoxicity and are a further step to explain pathological effects seen in muscle of obese patients, patients with the metabolic syndrome and patients with cancer-associated cachexia. |
format | Online Article Text |
id | pubmed-3406590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-34065902012-07-27 Skeletal muscle damage and impaired regeneration due to LPL-mediated lipotoxicity Tamilarasan, K P Temmel, H Das, S K Al Zoughbi, W Schauer, S Vesely, P W Hoefler, G Cell Death Dis Original Article According to the concept of lipotoxicity, ectopic accumulation of lipids in non-adipose tissue induces pathological changes. The most prominent effects are seen in fatty liver disease, lipid cardiomyopathy, non-insulin-dependent diabetes mellitus, insulin resistance and skeletal muscle myopathy. We used the MCK(m)-hLPL mouse distinguished by skeletal and cardiac muscle-specific human lipoprotein lipase (hLPL) overexpression to investigate effects of lipid overload in skeletal muscle. We were intrigued to find that ectopic lipid accumulation induced proteasomal activity, apoptosis and skeletal muscle damage. In line with these findings we observed reduced Musculus gastrocnemius and Musculus quadriceps mass in transgenic animals, accompanied by severely impaired physical endurance. We suggest that muscle loss was aggravated by impaired muscle regeneration as evidenced by reduced cross-sectional area of regenerating myofibers after cardiotoxin-induced injury in MCK(m)-hLPL mice. Similarly, an almost complete loss of myogenic potential was observed in C2C12 murine myoblasts upon overexpression of LPL. Our findings directly link lipid overload to muscle damage, impaired regeneration and loss of performance. These findings support the concept of lipotoxicity and are a further step to explain pathological effects seen in muscle of obese patients, patients with the metabolic syndrome and patients with cancer-associated cachexia. Nature Publishing Group 2012-07 2012-07-19 /pmc/articles/PMC3406590/ /pubmed/22825472 http://dx.doi.org/10.1038/cddis.2012.91 Text en Copyright © 2012 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Original Article Tamilarasan, K P Temmel, H Das, S K Al Zoughbi, W Schauer, S Vesely, P W Hoefler, G Skeletal muscle damage and impaired regeneration due to LPL-mediated lipotoxicity |
title | Skeletal muscle damage and impaired regeneration due to LPL-mediated lipotoxicity |
title_full | Skeletal muscle damage and impaired regeneration due to LPL-mediated lipotoxicity |
title_fullStr | Skeletal muscle damage and impaired regeneration due to LPL-mediated lipotoxicity |
title_full_unstemmed | Skeletal muscle damage and impaired regeneration due to LPL-mediated lipotoxicity |
title_short | Skeletal muscle damage and impaired regeneration due to LPL-mediated lipotoxicity |
title_sort | skeletal muscle damage and impaired regeneration due to lpl-mediated lipotoxicity |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406590/ https://www.ncbi.nlm.nih.gov/pubmed/22825472 http://dx.doi.org/10.1038/cddis.2012.91 |
work_keys_str_mv | AT tamilarasankp skeletalmuscledamageandimpairedregenerationduetolplmediatedlipotoxicity AT temmelh skeletalmuscledamageandimpairedregenerationduetolplmediatedlipotoxicity AT dassk skeletalmuscledamageandimpairedregenerationduetolplmediatedlipotoxicity AT alzoughbiw skeletalmuscledamageandimpairedregenerationduetolplmediatedlipotoxicity AT schauers skeletalmuscledamageandimpairedregenerationduetolplmediatedlipotoxicity AT veselypw skeletalmuscledamageandimpairedregenerationduetolplmediatedlipotoxicity AT hoeflerg skeletalmuscledamageandimpairedregenerationduetolplmediatedlipotoxicity |