Preferent Diaphragmatic Involvement in TK2 Deficiency: An Autopsy Case Study
Our goal was to analyze <i>post</i><i>mortem</i> tissues of an adult patient with late-onset thymidine kinase 2 (TK2) deficiency who died of respiratory failure. Compared with control tissues, we found a low mtDNA content in the patient’s skeletal muscle, liver, kidney, small...
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doaj-acffa3f428ed4d09b1c0b948adb982b92021-06-01T01:04:27ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-05-01225598559810.3390/ijms22115598Preferent Diaphragmatic Involvement in TK2 Deficiency: An Autopsy Case StudySara Laine-Menéndez0Cristina Domínguez-González1Alberto Blázquez2Aitor Delmiro3Inés García-Consuegra4Miguel Fernández-de la Torre5Aurelio Hernández-Laín6Javier Sayas7Miguel Ángel Martín8María Morán9Mitochondrial and Neuromuscular Diseases Laboratory, Instituto de Investigación Sanitaria Hospital ‘12 de Octubre’ (‘imas12’), 28041 Madrid, SpainMitochondrial and Neuromuscular Diseases Laboratory, Instituto de Investigación Sanitaria Hospital ‘12 de Octubre’ (‘imas12’), 28041 Madrid, SpainMitochondrial and Neuromuscular Diseases Laboratory, Instituto de Investigación Sanitaria Hospital ‘12 de Octubre’ (‘imas12’), 28041 Madrid, SpainMitochondrial and Neuromuscular Diseases Laboratory, Instituto de Investigación Sanitaria Hospital ‘12 de Octubre’ (‘imas12’), 28041 Madrid, SpainMitochondrial and Neuromuscular Diseases Laboratory, Instituto de Investigación Sanitaria Hospital ‘12 de Octubre’ (‘imas12’), 28041 Madrid, SpainMitochondrial and Neuromuscular Diseases Laboratory, Instituto de Investigación Sanitaria Hospital ‘12 de Octubre’ (‘imas12’), 28041 Madrid, SpainDepartment of Pathology (Neuropathology), Hospital 12 de Octubre, 28041 Madrid, SpainDepartment of Pneumology, Ventilation Unit, Hospital 12 de Octubre, 28041 Madrid, SpainMitochondrial and Neuromuscular Diseases Laboratory, Instituto de Investigación Sanitaria Hospital ‘12 de Octubre’ (‘imas12’), 28041 Madrid, SpainMitochondrial and Neuromuscular Diseases Laboratory, Instituto de Investigación Sanitaria Hospital ‘12 de Octubre’ (‘imas12’), 28041 Madrid, SpainOur goal was to analyze <i>post</i><i>mortem</i> tissues of an adult patient with late-onset thymidine kinase 2 (TK2) deficiency who died of respiratory failure. Compared with control tissues, we found a low mtDNA content in the patient’s skeletal muscle, liver, kidney, small intestine, and particularly in the diaphragm, whereas heart and brain tissue showed normal mtDNA levels. mtDNA deletions were present in skeletal muscle and diaphragm. All tissues showed a low content of OXPHOS subunits, and this was especially evident in diaphragm, which also exhibited an abnormal protein profile, expression of non-muscular β-actin and loss of GAPDH and α-actin. MALDI-TOF/TOF mass spectrometry analysis demonstrated the loss of the enzyme fructose-bisphosphate aldolase, and enrichment for serum albumin in the patient’s diaphragm tissue. The TK2-deficient patient’s diaphragm showed a more profound loss of OXPHOS proteins, with lower levels of catalase, peroxiredoxin 6, cytosolic superoxide dismutase, p62 and the catalytic subunits of proteasome than diaphragms of ventilated controls. Strong overexpression of TK1 was observed in all tissues of the patient with diaphragm showing the highest levels. TK2 deficiency induces a more profound dysfunction of the diaphragm than of other tissues, which manifests as loss of OXPHOS and glycolytic proteins, sarcomeric components, antioxidants and overactivation of the TK1 salvage pathway that is not attributed to mechanical ventilation.https://www.mdpi.com/1422-0067/22/11/5598mitochondrial diseasesdiaphragmthymidine kinase 2respiratory failure |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sara Laine-Menéndez Cristina Domínguez-González Alberto Blázquez Aitor Delmiro Inés García-Consuegra Miguel Fernández-de la Torre Aurelio Hernández-Laín Javier Sayas Miguel Ángel Martín María Morán |
spellingShingle |
Sara Laine-Menéndez Cristina Domínguez-González Alberto Blázquez Aitor Delmiro Inés García-Consuegra Miguel Fernández-de la Torre Aurelio Hernández-Laín Javier Sayas Miguel Ángel Martín María Morán Preferent Diaphragmatic Involvement in TK2 Deficiency: An Autopsy Case Study International Journal of Molecular Sciences mitochondrial diseases diaphragm thymidine kinase 2 respiratory failure |
author_facet |
Sara Laine-Menéndez Cristina Domínguez-González Alberto Blázquez Aitor Delmiro Inés García-Consuegra Miguel Fernández-de la Torre Aurelio Hernández-Laín Javier Sayas Miguel Ángel Martín María Morán |
author_sort |
Sara Laine-Menéndez |
title |
Preferent Diaphragmatic Involvement in TK2 Deficiency: An Autopsy Case Study |
title_short |
Preferent Diaphragmatic Involvement in TK2 Deficiency: An Autopsy Case Study |
title_full |
Preferent Diaphragmatic Involvement in TK2 Deficiency: An Autopsy Case Study |
title_fullStr |
Preferent Diaphragmatic Involvement in TK2 Deficiency: An Autopsy Case Study |
title_full_unstemmed |
Preferent Diaphragmatic Involvement in TK2 Deficiency: An Autopsy Case Study |
title_sort |
preferent diaphragmatic involvement in tk2 deficiency: an autopsy case study |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1661-6596 1422-0067 |
publishDate |
2021-05-01 |
description |
Our goal was to analyze <i>post</i><i>mortem</i> tissues of an adult patient with late-onset thymidine kinase 2 (TK2) deficiency who died of respiratory failure. Compared with control tissues, we found a low mtDNA content in the patient’s skeletal muscle, liver, kidney, small intestine, and particularly in the diaphragm, whereas heart and brain tissue showed normal mtDNA levels. mtDNA deletions were present in skeletal muscle and diaphragm. All tissues showed a low content of OXPHOS subunits, and this was especially evident in diaphragm, which also exhibited an abnormal protein profile, expression of non-muscular β-actin and loss of GAPDH and α-actin. MALDI-TOF/TOF mass spectrometry analysis demonstrated the loss of the enzyme fructose-bisphosphate aldolase, and enrichment for serum albumin in the patient’s diaphragm tissue. The TK2-deficient patient’s diaphragm showed a more profound loss of OXPHOS proteins, with lower levels of catalase, peroxiredoxin 6, cytosolic superoxide dismutase, p62 and the catalytic subunits of proteasome than diaphragms of ventilated controls. Strong overexpression of TK1 was observed in all tissues of the patient with diaphragm showing the highest levels. TK2 deficiency induces a more profound dysfunction of the diaphragm than of other tissues, which manifests as loss of OXPHOS and glycolytic proteins, sarcomeric components, antioxidants and overactivation of the TK1 salvage pathway that is not attributed to mechanical ventilation. |
topic |
mitochondrial diseases diaphragm thymidine kinase 2 respiratory failure |
url |
https://www.mdpi.com/1422-0067/22/11/5598 |
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