Mitochondrial transplantation enhances murine lung viability and recovery after ischemia-reperfusion injury.

Autor:	Moskowitzova K; Department of Cardiac Surgery, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Orfany A; Department of Cardiac Surgery, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Liu K; Department of Pulmonary and Respiratory Diseases, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Ramirez-Barbieri G; Department of Cardiac Surgery, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Thedsanamoorthy JK; Department of Anesthesiology, Critical Care and Pain Medicine, Harvard Medical School, Boston, Massachusetts., Yao R; Department of Anesthesiology, Critical Care and Pain Medicine, Harvard Medical School, Boston, Massachusetts., Guariento A; Department of Cardiac Surgery, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Doulamis IP; Department of Cardiac Surgery, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Blitzer D; Department of Cardiac Surgery, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Shin B; Department of Cardiac Surgery, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Snay ER; Department of Radiology, Division of Nuclear Medicine and Molecular imaging, Boston Children's Hospital, Boston, Massachusetts., Inkster JAH; Department of Radiology, Division of Nuclear Medicine and Molecular imaging, Boston Children's Hospital, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Iken K; Department of Pulmonary and Respiratory Diseases, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Packard AB; Department of Radiology, Division of Nuclear Medicine and Molecular imaging, Boston Children's Hospital, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Cowan DB; Department of Anesthesiology, Critical Care and Pain Medicine, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Visner GA; Department of Pulmonary and Respiratory Diseases, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., Del Nido PJ; Department of Cardiac Surgery, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts., McCully JD; Department of Cardiac Surgery, Harvard Medical School, Boston, Massachusetts.; Harvard Medical School, Boston, Massachusetts.
Jazyk:	angličtina
Zdroj:	American journal of physiology. Lung cellular and molecular physiology [Am J Physiol Lung Cell Mol Physiol] 2020 Jan 01; Vol. 318 (1), pp. L78-L88. Date of Electronic Publication: 2019 Nov 06.
DOI:	10.1152/ajplung.00221.2019
Abstrakt:	The most common cause of acute lung injury is ischemia-reperfusion injury (IRI), during which mitochondrial damage occurs. We have previously demonstrated that mitochondrial transplantation is an efficacious therapy to replace or augment mitochondria damaged by IRI, allowing for enhanced muscle viability and function in cardiac tissue. Here, we investigate the efficacy of mitochondrial transplantation in a murine lung IRI model using male C57BL/6J mice. Transient ischemia was induced by applying a microvascular clamp on the left hilum for 2 h. Upon reperfusion mice received either vehicle or vehicle-containing mitochondria either by vascular delivery (Mito V) through the pulmonary artery or by aerosol delivery (Mito Neb) via the trachea (nebulization). Sham control mice underwent thoracotomy without hilar clamping and were ventilated for 2 h before returning to the cage. After 24 h recovery, lung mechanics were assessed and lungs were collected for analysis. Our results demonstrated that at 24 h of reperfusion, dynamic compliance and inspiratory capacity were significantly increased and resistance, tissue damping, elastance, and peak inspiratory pressure (Mito V only) were significantly decreased ( P < 0.05) in Mito groups as compared with their respective vehicle groups. Neutrophil infiltration, interstitial edema, and apoptosis were significantly decreased ( P < 0.05) in Mito groups as compared with vehicles. No significant differences in cytokines and chemokines between groups were shown. All lung mechanics results in Mito groups except peak inspiratory pressure in Mito Neb showed no significant differences ( P > 0.05) as compared with Sham. These results conclude that mitochondrial transplantation by vascular delivery or nebulization improves lung mechanics and decreases lung tissue injury.
Databáze:	MEDLINE
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