Journalartikel
Autorenliste: Paddenberg, Renate; Tiefenbach, Martina; Faulhammer, Petra; Goldenberg, Anna; Gries, Barbara; Pfeil, Uwe; Lips, Katrin S.; Piruat, Jose I.; Lopez-Barneo, Jose; Schermuly, Ralph T.; Weissmann, Norbert; Kummer, Wolfgang
Jahr der Veröffentlichung: 2012
Seiten: 702-710
Zeitschrift: Cardiovascular Research
Bandnummer: 93
Heftnummer: 4
ISSN: 0008-6363
Open Access Status: Bronze
DOI Link: https://doi.org/10.1093/cvr/cvr359
Verlag: Oxford University Press
Alveolar hypoxia acutely elicits contraction of pulmonary arteries, leading to a rise in pulmonary arterial pressure (PAP) and shifting blood to better ventilated areas of the lung. The molecular mechanisms underlying this hypoxic pulmonary vasoconstriction (HPV) are still incompletely understood. Here, we investigated the role of succinate dehydrogenase (SDH; synonymous to mitochondrial complex II) in HPV, with particular emphasis on regional differences along the vascular bed and consequences for PAP and perfusion-to-ventilation matching, using mutant mice heterozygous for the SDHD subunit of complex II (SDHD/). Western blots revealed reduced protein content of complex II subunits SDHA, SDHB, and SDHC in lungs of SDHD/ mice, despite unaffected mRNA content as determined by real-time PCR. Hypoxic pulmonary vasoconstriction of small (2050 m) intra-acinar and larger (51100 m) pre-acinar arteries was evaluated by videomorphometric analysis of precision-cut lung slices. The hypoxic response was detectable in pre-acinar arteries but absent from intra-acinar arteries of SDHD/ mice. In isolated perfused lungs, basal PAP and its hypoxia-induced increase were indistinguishable between both mouse strains. Arterial oxygenation was measured after provocation of regional ventilatory failure by tracheal fluid instillation in anaesthetized mice, and it declined more in SDHD/ than in wild-type mice. SDHD is required for the formation of a stable mitochondrial complex II and it is selectively important for HPV of intra-acinar vessels. This specialized vascular segment participates in perfusion-to-ventilation matching but does not significantly contribute to the acute hypoxic rise in PAP that results from more proximal vasoconstriction.
Abstract:
Zitierstile
Harvard-Zitierstil: Paddenberg, R., Tiefenbach, M., Faulhammer, P., Goldenberg, A., Gries, B., Pfeil, U., et al. (2012) Mitochondrial complex II is essential for hypoxia-induced pulmonary vasoconstriction of intra- but not of pre-acinar arteries, Cardiovascular Research, 93(4), pp. 702-710. https://doi.org/10.1093/cvr/cvr359
APA-Zitierstil: Paddenberg, R., Tiefenbach, M., Faulhammer, P., Goldenberg, A., Gries, B., Pfeil, U., Lips, K., Piruat, J., Lopez-Barneo, J., Schermuly, R., Weissmann, N., & Kummer, W. (2012). Mitochondrial complex II is essential for hypoxia-induced pulmonary vasoconstriction of intra- but not of pre-acinar arteries. Cardiovascular Research. 93(4), 702-710. https://doi.org/10.1093/cvr/cvr359
Schlagwörter
Complex II; CUT LUNG SLICES; ENZYMATIC-ACTIVITY; HEREDITARY PARAGANGLIOMA; HYDROXYLASES; HYPOXIC PULMONARY VASOCONSTRICTION; Intra-acinar artery; RESPIRATORY-CHAIN; SDHD GENE; SMOOTH-MUSCLE-CELLS; Succinate dehydrogenase; SUCCINATE-DEHYDROGENASE