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10.1016/j.jim.2014.06.007 http://scihub22266oqcxt.onion/10.1016/j.jim.2014.06.007 C4260336!4260336 !24952243     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\24952243 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       J+Immunol+Methods 2014 ; 411 (ä): 55-65 Nephropedia Template TP {{tp|p=24952243 |t=2014. Isolation of biologically-active exosomes from human plasma |pdf=|usr=}}{{24952243 }} gab.com Text Isolation of biologically-active exosomes from human plasma JO: J Immunol Methods http://www.kidney.de/pget.php?&tw=1&pmid=24952243 #FOAvip Effects of exosomes present in human plasma on immune cells have not been examined in detail. Immunological studies with plasma-derived exosomes require their isolation by procedures involving ultracentrifugation. These procedures were largely developed using supernatants of cultured cells. To test biologic activities of plasma-derived exosomes, methods are necessary that ensure adequate recovery of exosome fractions free of contaminating larger vesicles, cell fragments and protein/nucleic acid aggregates. Here, an optimized method for exosome isolation from human plasma/serum specimens of normal controls (NC) or cancer patients and its advantages and pitfalls are described. To remove undesirable plasma-contaminating components, ultrafiltration of differentially-centrifuged plasma/serum followed by size-exclusion chromatography prior to ultracentrifugation facilitated the removal of contaminants. Plasma or serum was equally acceptable as a source of exosomes based on the recovered protein levels (in ?g protein/mL plasma) and TEM image quality. Centrifugation on sucrose density gradients led to large exosome losses. Fresh plasma was the best source of morphologically-intact exosomes, while the use of frozen/thawed plasma decreased exosome purity but not their biologic activity. Treatments of frozen plasma with DNAse, RNAse or hyaluronidase did not improve exosome purity and are not recommended. Cancer patients' plasma consistently yielded more isolated exosomes than did NCs' plasma. Cancer patients' exosomes also mediated higher immune suppression as evidenced by decreased CD69 expression on responder CD4+ T effector cells. Thus, the described procedure yields biologically-active, morphologically-intact exosomes that have reasonably good purity without large protein losses and can be used for immunological, biomarker and other studies. Twit Text FOAVip Isolation of biologically-active exosomes from human plasma ????J Immunol Methods http://www.kidney.de/pget.php?&tw=1&pmid=24952243 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24952243 #FOAvip English Wikipedia <ref>{{Cite pmid|24952243 }}</ref> Isolation of biologically-active exosomes from human plasma #MMPMID24952243 Muller L ; Hong CS ; Stolz DB ; Watkins SC ; Whiteside TL J Immunol Methods 2014[Sep]; 411 (ä): 55-65 PMID24952243 show ga Effects of exosomes present in human plasma on immune cells have not been examined in detail. Immunological studies with plasma-derived exosomes require their isolation by procedures involving ultracentrifugation. These procedures were largely developed using supernatants of cultured cells. To test biologic activities of plasma-derived exosomes, methods are necessary that ensure adequate recovery of exosome fractions free of contaminating larger vesicles, cell fragments and protein/nucleic acid aggregates. Here, an optimized method for exosome isolation from human plasma/serum specimens of normal controls (NC) or cancer patients and its advantages and pitfalls are described. To remove undesirable plasma-contaminating components, ultrafiltration of differentially-centrifuged plasma/serum followed by size-exclusion chromatography prior to ultracentrifugation facilitated the removal of contaminants. Plasma or serum was equally acceptable as a source of exosomes based on the recovered protein levels (in ?g protein/mL plasma) and TEM image quality. Centrifugation on sucrose density gradients led to large exosome losses. Fresh plasma was the best source of morphologically-intact exosomes, while the use of frozen/thawed plasma decreased exosome purity but not their biologic activity. Treatments of frozen plasma with DNAse, RNAse or hyaluronidase did not improve exosome purity and are not recommended. Cancer patients' plasma consistently yielded more isolated exosomes than did NCs' plasma. Cancer patients' exosomes also mediated higher immune suppression as evidenced by decreased CD69 expression on responder CD4+ T effector cells. Thus, the described procedure yields biologically-active, morphologically-intact exosomes that have reasonably good purity without large protein losses and can be used for immunological, biomarker and other studies. |*Exosomes/chemistry/immunology/metabolism/ultrastructure [MESH] |*Neoplasms/blood/immunology/pathology [MESH] |Antigens, CD/biosynthesis/chemistry/immunology [MESH] |Antigens, Differentiation, T-Lymphocyte/biosynthesis/chemistry/immunology [MESH] |Blood Buffy Coat/immunology/metabolism/pathology [MESH] |CD4-Positive T-Lymphocytes/immunology/metabolism/pathology [MESH] |Cells, Cultured [MESH] |Deoxyribonucleases/chemistry [MESH] |Female [MESH] |Gene Expression Regulation, Neoplastic [MESH] |Humans [MESH] |Hyaluronoglucosaminidase/chemistry [MESH] |Lectins, C-Type/biosynthesis/chemistry/immunology [MESH] |Male [MESH] |Microscopy, Electron, Transmission [MESH] |Neoplasm Proteins/chemistry/immunology/metabolism [MESH]Isolation of biologically-active exosomes from human plasma (epmc).pdf DeepDyve Pubget Overpricing