Journal: The Journal of Heart and Lung Transplantation
Article Title: Respiratory viral infection in lung transplantation induces exosomes that trigger chronic rejection
doi: 10.1016/j.healun.2019.12.009
Figure Lengend Snippet: Exosomes containing 20S proteasome core in LTxRs with RVI and stable LTxRs. Circulatory exosomes isolated from LTxRs with RVI ( n = 5) and stable LTxRs ( n = 4) were used to detect the presence of 20S proteasome subunit α3 using immunoblot. ( A ) The exosomes isolated from patients with RVI showed a significant increase in 20S proteasome compared with exosomes from stable LTxRs (Mean optical density: 1.74 ± 0.6 vs 0.37 ± 0.35, p = 0.0317 ). Alix served as loading control and exosome-specific marker. ( B ) Graphical representation shows optical intensity of 20S proteasome α3 subunit abundance in LTxRs with viral infection and stable LTxRs. The presence of 20S proteasome was compared between stable LTxRs and LTxRs with RVI using Student's t -test. LTxR, lung transplant recipient; RVI, respiratory viral infection.
Article Snippet: 20S proteasome subunit α3 (sc-58414, Santa Cruz Biotechnology), rhinovirus VP3 (MA5-18249, Thermo Fisher Scientific, Waltham, MA), coronavirus (NB100-64754, Novus Biologicals, Littleton, CO), and RSV glycoprotein G (7950-0980, Bio-Rad Laboratories, Hercules, CA) were used as primary Abs; secondary Abs conjugated with horseradish peroxidase (HRP) were used specific to primary Ab.
Techniques: Isolation, Western Blot, Control, Marker, Infection