Lung-derived exosome uptake into and epigenetic modulation of marrow progenitor/stem and differentiated cells

Journal of Extracellular Vesicles

Volumn 4, Issue 1, 2015, Pages

  Aliotta, Jason M ^a   Pereira, Mandy ^a   Sears, Edmund H ^a   Dooner, Mark S ^a   Wen, Sicheng ^a   Goldberg, Laura R ^a   Quesenberry, Peter J ^a  

^a BROWN UNIVERSITY   (United States)

Author keywords

Bone marrow cells; Extracellular vesicles; Pulmonary epithelial cells

Indexed keywords

CARBOXYFLUORESCEIN DIACETATE SUCCINIMIDYL ESTER; SURFACTANT;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; B CELL CULTURE; BONE MARROW PROGENITOR CELL; CELL DIFFERENTIATION; CELL ISOLATION; CELL SEPARATION; EPIGENETICS; ERYTHROID CELL; EXOSOME; FLOW CYTOMETRY; FLUORESCENCE MICROSCOPY; GENE EXPRESSION; GRANULOCYTE; HEMATOPOIETIC STEM CELL; LUNG ALVEOLUS CELL; LUNG EPITHELIUM; MALE; MOUSE; NONHUMAN; PROTEIN EXPRESSION; RAT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SPECIES DIFFERENCE; TRANSCRIPTION INITIATION;

EID: 84978768856     PISSN: None     EISSN: 20013078     Source Type: Journal    
DOI: 10.3402/jev.v4.26166     Document Type: Article

References (24)

1. Ratajczak J, Wysoczynski M, Hayek F, Janowska-Wieczorek A, Ratajczak MZ. Membrane-derived microvesicles: important and underappreciated mediators of cell-to-cell communication. Leukemia. 2006;20:1487-95
2. Chargaff E, West R. The biological significance of the thromboplastic protein of blood. J Biol Chem. 1946;166: 189-97
3. Wolf P. The nature and significance of platelet products in human plasma. Br J Haematol. 1967;13:269-88
4. Warren BA, Vales O. The release of vesicles from platelets following adhesion to vessel walls in vitro. Br J Exp Pathol. 1972;53:206-15
5. Del Conde I, Shrimpton CN, Thiagarajan P, Lopez JA. Tissuefactor bearing microvesicles arise from lipid rafts and fuse with activated platelets to initiate coagulation. Blood. 2005;106: 1604-11
6. Mackman N. Tissue-specific hemostasis in mice. Arterioscler Thromb Vasc Biol. 2005;25:2273-81
7. Falati S, Liu Q, Gross P, Merrill-Skoloff G, Chou J, Vandendries E, et al. Accumulation of tissue factor into developing thrombi in vivo is dependent upon microparticle P-selectin glycoprotein ligand 1 and platelet P-selectin. J Exp Med. 2003;197:1585-98
8. Hrachovinova I, Cambien B, Hafezi-Moghadam A, Kappelmayer J, Camphausen RT, Widom A, et al. Interaction of P-selectin and PSGL-1 generates microparticles that correct hemostasis in a mouse model of hemophilia A. Nat Med. 2003;9:1020-5
9. Andre P, Hartwell D, Hrachovinova I, Saffaripour S, Wagner DD. Pro-coagulant state resulting from high levels of soluble P-selectin in blood. Proc Natl Acad Sci USA. 2000; 97:13835-40
10. Cambien B, Wagner DD. A new role in hemostasis for the adhesion receptor P-selectin. Trends Mol Med. 2004;10: 179-86
11. Mallat Z, Hugel B, Ohan J, Leseche G, Freyssinet JM, Tedgui A. Shed membrane microparticles with procoagulant potential in human atherosclerotic plaques: a role for apoptosis in plaque thrombogenicity. Circulation. 1999;99:348-53
12. Keller S, Sanderson MP, Stoeck A. Exosomes: from biogenesis and secretion to biological function. Immunol Lett. 2006;107: 102-8
13. Morel O, Toti F, Hugel B, Freyssinet JM. Cellular microparticles: a disseminated storage pool of bioactive vascular effectors. Curr Opin Hematol. 2004;11:156-64
14. Wood CR, Huang K, Diener DR, Rosenbaum JL. The cilium secretes bioactive ectosomes. Curr Biol. 2013;23:906-11
15. Heijnen HF, Schiel AE, Fijnheer R, Geuze HJ, Sixma JJ. Activated platelets release two types of membrane vesicles: microvesicles by surface shedding and exosomes derived from exocytosis of multivesicular bodies and alpha-granules. Blood. 1999;94:3791-9
16. Lorizate M, Sachsenheimer T, Glass B, Habermann A, Gerl MJ, Kräusslich HG, et al. Comparative lipidomics analysis of HIV-1 particles and their producer cell membrane in different cell lines. Cell Microbiol. 2013;15:292-304
17. Schiller M, Heyder P, Ziegler S, Niessen A, Claben L, Lauffer A, et al. During apoptosis HMGb1 is translocated into apoptotic cell-derived membraneous vesicles. Autoimmunity. 2013;46:342-6
18. Thery C, Ostrowski M, Segura E. Membrane vesicles as conveyors of immune responses. Nat Rev Immunol. 2009;9: 581-93
19. Aliotta JM, Keaney P, Passero M, Dooner MS, Pimentel J, Greer D, et al. Bone marrow production of lung cells: the impact of G-CSF, cardiotoxin, graded doses of irradiation, and subpopulation phenotype. Exp Hematol. 2006;34:230-41
20. Aliotta JM, Sanchez-Guijo FM, Dooner GJ, Johnson KW, Dooner MS, Greer KA, et al. Alteration of marrow cell gene expression, protein production, and engraftment into lung by lung-derived microvesicles: a novel mechanism for phenotype modulation. Stem Cells. 2007;25:2245-56
21. Aliotta JM, Pereira M, Johnson KW, de Paz N, Dooner MS, Puente N, et al. Microvesicle entry into marrow cells mediates tissue-specific changes in mRNA by direct delivery of mRNA and induction of transcription. Exp Hematol. 2010;38:233-45
22. Aliotta JM, Pereira M, Amaral A, Dooner MS, Sears EH, Brilliant K, et al. Stable cell fate changes in marrow cells induced by lung-derived microvesicles. J Extracell Vesicles. 2012;1:18163, doi: http://dx.doi.org/10.3402/jev.v1i0.18163
23. Aliotta JM, Pereira M, Amaral A, Sorokina A, Igbinoba Z, Hasslinger A, et al. Induction of pulmonary hypertensive changes by extracellular vesicles from monocrotaline-treated mice. Cardiovasc Res. 2013;100:354-62
24. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-delta delta C(T)) method. Methods. 2001;25:402-8