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. 2017 Dec 15;196(12):1510-1518.
doi: 10.1164/rccm.201612-2457PP.

Extracellular Vesicle Biology in the Pathogenesis of Lung Disease

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Extracellular Vesicle Biology in the Pathogenesis of Lung Disease

Serge P Nana-Sinkam et al. Am J Respir Crit Care Med. .
No abstract available

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Figures

Figure 1.
Figure 1.
Extracellular vesicle biogenesis. Extracellular vesicles are divided into three main types: exosomes, microvesicles, and apoptotic bodies. Exosomes are formed in multivesicular endosomes and contain molecules including nucleic acids, proteins, lipids, and metabolites. The exosomal content can be transferred to other cells through different processes, including endocytosis, phagocytosis, macropinocytosis, or direct membrane fusion.
Figure 2.
Figure 2.
Applications for extracellular vesicles in lung disease. COPD = chronic obstructive pulmonary disease; EMT = epithelial–mesenchymal transition; SOCS = suppressor of cytokine protein signaling; STAT = signal transducers and activators of transcription; TLR = Toll-like receptor.

References

    1. Araldi E, Krämer-Albers EM, Hoen EN, Peinado H, Psonka-Antonczyk KM, Rao P, van Niel G, Yáñez-Mó M, Nazarenko I. International Society for Extracellular Vesicles: first annual meeting, April 17–21, 2012: ISEV-2012. J Extracell Vesicles. 2012;1:19995. - PMC - PubMed
    1. Aucamp J, Bronkhorst AJ, Badenhorst CP, Pretorius PJ. A historical and evolutionary perspective on the biological significance of circulating DNA and extracellular vesicles. Cell Mol Life Sci. 2016;73:4355–4381. - PMC - PubMed
    1. Pan BT, Johnstone RM. Fate of the transferrin receptor during maturation of sheep reticulocytes in vitro: selective externalization of the receptor. Cell. 1983;33:967–978. - PubMed
    1. Buschow SI, Nolte-’t Hoen EN, van Niel G, Pols MS, ten Broeke T, Lauwen M, Ossendorp F, Melief CJ, Raposo G, Wubbolts R, et al. MHC II in dendritic cells is targeted to lysosomes or T cell–induced exosomes via distinct multivesicular body pathways. Traffic. 2009;10:1528–1542. - PubMed
    1. Millimaggi D, Mari M, D’Ascenzo S, Carosa E, Jannini EA, Zucker S, Carta G, Pavan A, Dolo V. Tumor vesicle–associated CD147 modulates the angiogenic capability of endothelial cells. Neoplasia. 2007;9:349–357. - PMC - PubMed

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