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Mendelsohn, Daniel H. ; Niedermair, Tanja ; Walter, Nike ; Alt, Volker ; Rupp, Markus ; Brochhausen, Christoph

Ultrastructural Evidence of Mitochondrial Dysfunction in Osteomyelitis Patients

Mendelsohn, Daniel H. , Niedermair, Tanja, Walter, Nike , Alt, Volker , Rupp, Markus und Brochhausen, Christoph (2023) Ultrastructural Evidence of Mitochondrial Dysfunction in Osteomyelitis Patients. International Journal of Molecular Sciences 24 (6), S. 5709.

Veröffentlichungsdatum dieses Volltextes: 11 Mai 2023 05:34
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.54196


Zusammenfassung

Osteomyelitis is a difficult-to-treat disease with high chronification rates. First studies suggest increases in mitochondrial fission and mitochondrial dysfunction as possible contributors to the accumulation of intracellular reactive oxygen species and thereby to the cell death of infected bone cells. The aim of the present study is to analyze the ultrastructural impact of bacterial infection ...

Osteomyelitis is a difficult-to-treat disease with high chronification rates. First studies suggest increases in mitochondrial fission and mitochondrial dysfunction as possible contributors to the accumulation of intracellular reactive oxygen species and thereby to the cell death of infected bone cells. The aim of the present study is to analyze the ultrastructural impact of bacterial infection on osteocytic and osteoblastic mitochondria. Human infected bone tissue samples were visualized via light microscopy and transmission electron microscopy. Osteoblasts, osteocytes and their mitochondria were analyzed histomorphometrically and compared with the control group of noninfectious human bone tissue samples. The results depicted swollen hydropic mitochondria including depleted cristae and a decrease in matrix density in the infected samples. Furthermore, perinuclear clustering of mitochondria could also be observed regularly. Additionally, increases in relative mitochondrial area and number were found as a correlate for increased mitochondrial fission. In conclusion, mitochondrial morphology is altered during osteomyelitis in a comparable way to mitochondria from hypoxic tissues. This gives new perspectives on the treatment strategies since the manipulation of mitochondrial dynamics may improve bone cell survival as a potential new target for the therapy of osteomyelitis.



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Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftInternational Journal of Molecular Sciences
Verlag:MDPI
Ort der Veröffentlichung:BASEL
Band:24
Nummer des Zeitschriftenheftes oder des Kapitels:6
Seitenbereich:S. 5709
Datum16 März 2023
InstitutionenMedizin > Lehrstuhl für Unfallchirurgie
Medizin > Lehrstuhl für Pathologie
Identifikationsnummer
WertTyp
10.3390/ijms24065709DOI
Stichwörter / KeywordsISCHEMIA-REPERFUSION INJURY; ROS; OXYGEN; TRANSPLANTATION; HYPOXIA; osteomyelitis; mitochondria; mitochondrial ultrastructure; mitochondrial dysfunction; mitochondrial dynamics
Dewey-Dezimal-Klassifikation600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenJa
URN der UB Regensburgurn:nbn:de:bvb:355-epub-541963
Dokumenten-ID54196

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