Megan Jackson
  • 0 Author merit


Ph.D, Queen's University Belfast, Northern Ireland, 2014

Current position

Postdoctoral research fellow, Centre for Experimental Medicine, Queen's University Belfast, Northern Ireland


  1. Jackson, M. V., Morrison, T. J., Doherty, D. F., McAuley, D. F., Matthay, M. A., Kissenpfennig, A., O'Kane, C. M. and Krasnodembskaya, A. D. (2016). Mitochondrial Transfer via Tunneling Nanotubes is an Important Mechanism by Which Mesenchymal Stem Cells Enhance Macrophage Phagocytosis in the In Vitro and In Vivo Models of ARDS. Stem Cells 34(8): 2210-2223.
    Figure from paper chosen for front cover for Stem Cells Aug 2016 edition ( and 4th most downloaded manuscript in 2016 (Jan Nolta, Editor, Stem Cells
  2. Jackson, M. V., Morrison, T., McAuley, D., O'Kane, C., Matthay, M., Krasnodembskaya, A. (2016). Mesenchymal stromal cells (MSC) anti-microbial effect in acute respiratory distress syndrome (ARDS) is mediated in part by enhanced alveolar macrophage phagocytosis through cell contact-dependent mitochondrial transfer leading to improved macrophage bioenergetics. European Respiratory Journal 48: PA939.
  3. Jackson, M. V., Morrison, T. J., McAuley, F. D., Matthay, A. M., O'Kane, C. M. and Krasnodembskaya, A. D. (2016). Mitochondrial Transfer Via Tunnelling Nanotubes (TNT) Is A Novel Mechanism By Which Mesenchymal Stromal Cells Enhance Macrophage Phagocytosis In In Vivo Models Of Acute Lung Injury. Am J Respir Crit Care Med 193: A6607.
  4. Jackson, M. V., Morrison, T. J., O’Kane, C. M., McAuley, D. F. and Krasnodembskaya, A. D. (2015). Mitochondrial transfer is an important mechanism by which Mesenchymal Stromal Cells (MSC) facilitate macrophage phagocytosis in the in vitro and in vivo models of Acute Respiratory Distress Syndrome (ARDS). Thorax 70: A1-A2.
  5. O'Kane, D., Jackson, M. V., Kissenpfennig, A., Spence, S., Damkat-Thomas, L., Tolland, J. P., Smyth, A. E., Denton, C. P., Stuart Elborn, J., McAuley, D. F. and O'Kane, C. M. (2014). SMAD inhibition attenuates epithelial to mesenchymal transition by primary keratinocytes in vitro. Exp Dermatol 23(7): 497-503.
  6. Jackson, M. V., Tunney, M. M., Elborn, J. S. and O'Kane, C. M. (2013). A clinical isolate of Prevotella histicola drives MMP-9 secretion through mitogen activated protein kinase dependent mechanisms in Monocytes. Pediatr Pulmonol 48(S36): 319.
  7. Jackson, M. V., O'Kane, C. M., Tunney, M. M. and Elborn, J. S. (2012). WS9.1 Clinical isolates of Prevotella histicola drive MMP-9 secretion by mononuclear cells. J Cyst Fibros 11: S19.
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