Expression and Carbonylation of Creatine Kinase in the Quadriceps Femoris Muscles of Patients with Chronic Obstructive Pulmonary Disease
Abstract
Oxidative protein modification involving carbonylation has recently been identified as an important factor in skeletal muscle dysfunction in patients with chronic obstructive pulmonary disease (COPD). However, the exact identity of modified proteins inside limb muscles of patients with COPD remains unknown. We used 2D electrophoresis, immunoblotting, and mass spectrometry to identify carbonylated proteins in the vastus lateralis muscle of 12 patients with COPD and 6 control subjects. Both creatine kinase (CK) and carbonic anhydrase III (CAIII) were identified as being strongly carbonylated in this muscle in both groups of subjects. Total CK activity, CK protein expression, and the intensity of CK carbonylation were significantly greater in the muscles of patients with COPD as compared with control subjects, whereas CAIII protein expression and intensity of carbonylation were similar in the two groups. In patients with COPD, CK activity and protein expression correlated positively with FEV(1) and V O(2)max, whereas the intensity of CK carbonylation correlated negatively with the same parameters. These results indicate that oxygen radicals selectively target CK and CAIII inside limb muscles of humans. The observation that the intensity of CK carbonylation correlates negatively with CK activity in limb muscles of patients with COPD suggests that carbonylation may have a deleterious effect on CK activity, and may contribute to impaired CK function in the limb muscles of these pat…
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Multiple studies point towards increased protein carbonylation in COPD quadriceps compared to healthy controls, including total protein content and specific proteins such as glycolytic enzymes, antioxidant enzymes, and myosin heavy chain.
“Multiple studies point towards an increased protein carbonylation in COPD quadriceps compared to healthy controls, including total protein content but also specific proteins such as glycolytic enzymes (creatine kinase), antioxidant enzymes (glutathione peroxidase), and myosin heavy chain [118,120,121,122].”
From Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting (2023) · cites this paper as [121]
These results point towards an impairment of muscle energy production and are consistent with other studies showing low baseline creatine kinase and ATP concentrations.
“These results point towards an impairment of the muscle energy production and are consistent with other studies showing low baseline creatine kinase and ATP concentrations [121].”
From Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting (2023) · cites this paper as [121]
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Skeletal muscle dysfunction in patients with chronic obstructive pulmonary disease
Hussain, S., Cheol, K., & Mofarrahi, M. (2008) · International Journal of Chronic Obstructive Pulmonary Disease · doi:10.2147/copd.s4480 · Cited by 224 · see citing works
Self-citationThe Mitochondrial Phenotype of Peripheral Muscle in Chronic Obstructive Pulmonary Disease
Picard, M., Godin, R., Sinnreich, M., Baril, J., Bourbeau, J., Perrault, H., Taivassalo, T., & Burelle, Y. (2008) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200807-1005oc · Cited by 95 · see citing works
Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting
Henrot, P., Dupin, I., Schilfarth, P., Esteves, P., Blervaque, L., Zysman, M., Gouzi, F., Hayot, M., Pomiès, P., & Berger, P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076454 · Cited by 85 · see citing works
“These results point towards an impairment of the muscle energy production and are consistent with other studies showing low baseline creatine kinase and ATP concentrations [121].”
ResultInvolvement of Creatine Kinase B in Cigarette Smoke–Induced Bronchial Epithelial Cell Senescence
Hara, H., Araya, J., Takasaka, N., Fujii, S., Kojima, J., Yumino, Y., Shimizu, K., Ishikawa, T., Numata, T., Kawaishi, M., et al. (2012) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2011-0214oc · Cited by 50 · see citing works
- Authors
- Barreiro, E., Gea, J., Matar, G., & Hussain, S. N. A.
- Affiliations
- Universitat Pompeu Fabra (ES)
- Venue
- American Journal of Respiratory Cell and Molecular Biology
- Publisher
- Oxford University Press (OUP)
- Published
- 2005-12-01
- Volume
- 33
- Issue
- 6
- Pages
- 636-642
- ISSN
- 1044-1549 (ISSN-L)
- 1535-4989
- OpenAlex
- W2120787671
- Cited by
- 89
- References
- 0
- Citations by year
- 2026: 2 · 2023: 3 · 2022: 2 · 2021: 2 · 2019: 2 · 2018: 3 · 2017: 8 · 2016: 5 · 2015: 3 · 2014: 2 · 2013: 8 · 2012: 8
- FWCI
- 2.76
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Respiratory Cell and Molecular Biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Chronic Obstructive Pulmonary Disease (COPD) Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Keywords
- creatine kinase, protein carbonylation, chronic obstructive pulmonary disease, protein oxidation, carbonic anhydrase III, vastus lateralis, quadriceps, skeletal muscle dysfunction, oxygen free radicals, creatine kinase activity, FEV1, exercise capacity
- MeSH terms
- Carbon, Creatine Kinase, Forced Expiratory Volume, Humans, Respiratory Function Tests, Mass Spectrometry, Thigh, Immunoblotting, Electrophoresis, Gel, Two-Dimensional, Muscle, Skeletal, Carbonic Anhydrase III, Pulmonary Disease, Chronic Obstructive
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