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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Main Authors: 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
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:International Journal of Molecular Sciences
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Online Access:https://www.mdpi.com/1422-0067/22/11/5598
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spelling 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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