Autophagy and mitochondrial remodelling in mouse mesenchymal stromal cells challenged with Staphylococcus epidermidis |
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| Authors: | Nikolai V Gorbunov Dennis P McDaniel Min Zhai Pei‐Jyun Liao Bradley R Garrison Juliann G Kiang |
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| Affiliation: | 1. Radiation Combined Injury Program, Armed Forces Radiobiology Research Institute, Bethesda, MD, USA;2. Biomedical Instrumentation Center, Uniformed Services University of the Health Sciences, Bethesda, MD, USA;3. Department of Radiation Biology, Uniformed Services University of the Health Sciences, Bethesda, MD, USA;4. Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, USA |
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| Abstract: | The bone marrow stroma constitutes the marrow‐blood barrier, which sustains immunochemical homoeostasis and protection of the haematopoietic tissue in sequelae of systemic bacterial infections. Under these conditions, the bone marrow stromal cells affected by circulating bacterial pathogens shall elicit the adaptive stress‐response mechanisms to maintain integrity of the barrier. The objective of this communication was to demonstrate (i) that in vitro challenge of mesenchymal stromal cells, i.e. colony‐forming unit fibroblasts (CFU‐F), with Staphylococcus epidermidis can activate the autophagy pathway to execute antibacterial defence response, and (ii) that homoeostatic shift because of the bacteria‐induced stress includes the mitochondrial remodelling and sequestration of compromised organelles via mitophagy. Implication of Drp1 and PINK1–PARK2‐dependent mechanisms in the mitophagy turnover of the aberrant mitochondria in mesenchymal stromal cells is investigated and discussed. |
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| Keywords: | mesenchymal stromal cells
Staphylococcus epidermidis
stress response autophagy mitochondria |
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