TY - JOUR
T1 - The Endothelial Glycocalyx in Pig-to-Baboon Cardiac Xenotransplantation—First Insights
AU - Bender, Martin
AU - Abicht, Jan Michael
AU - Reichart, Bruno
AU - Leuschen, Maria
AU - Wall, Felicia
AU - Radan, Julia
AU - Neumann, Elisabeth
AU - Mokelke, Maren
AU - Buttgereit, Ines
AU - Michel, Sebastian
AU - Ellgass, Reinhard
AU - Gieseke, Katja
AU - Steen, Stig
AU - Paskevicius, Audrius
AU - Denner, Joachim
AU - Godehardt, Antonia W.
AU - Tönjes, Ralf R.
AU - Hagl, Christian
AU - Ayares, David
AU - Wolf, Eckhard
AU - Schmoeckel, Michael
AU - Brenner, Paolo
AU - Müller, Martin B.
AU - Längin, Matthias
PY - 2024/6
Y1 - 2024/6
N2 - Cardiac xenotransplantation has seen remarkable success in recent years and is emerging as the most promising alternative to human cardiac allotransplantation. Despite these achievements, acute vascular rejection still presents a challenge for long-term xenograft acceptance and new insights into innate and adaptive immune responses as well as detailed characterizations of signaling pathways are necessary. In allotransplantation, endothelial cells and their sugar-rich surface—the endothelial glycocalyx—are known to influence organ rejection. In xenotransplantation, however, only in vitro data exist on the role of the endothelial glycocalyx so far. Thus, in the current study, we analyzed the changes of the endothelial glycocalyx components hyaluronan, heparan sulfate and syndecan-1 after pig-to-baboon cardiac xenotransplantations in the perioperative (n = 4) and postoperative (n = 5) periods. These analyses provide first insights into changes of the endothelial glycocalyx after pig-to-baboon cardiac xenotransplantation and show that damage to the endothelial glycocalyx seems to be comparable or even less pronounced than in similar human settings when current strategies of cardiac xenotransplantation are applied. At the same time, data from the experiments where current strategies, like non-ischemic preservation, growth inhibition or porcine cytomegalovirus (a porcine roseolovirus (PCMV/PRV)) elimination could not be applied indicate that damage of the endothelial glycocalyx also plays an important role in cardiac xenotransplantation.
AB - Cardiac xenotransplantation has seen remarkable success in recent years and is emerging as the most promising alternative to human cardiac allotransplantation. Despite these achievements, acute vascular rejection still presents a challenge for long-term xenograft acceptance and new insights into innate and adaptive immune responses as well as detailed characterizations of signaling pathways are necessary. In allotransplantation, endothelial cells and their sugar-rich surface—the endothelial glycocalyx—are known to influence organ rejection. In xenotransplantation, however, only in vitro data exist on the role of the endothelial glycocalyx so far. Thus, in the current study, we analyzed the changes of the endothelial glycocalyx components hyaluronan, heparan sulfate and syndecan-1 after pig-to-baboon cardiac xenotransplantations in the perioperative (n = 4) and postoperative (n = 5) periods. These analyses provide first insights into changes of the endothelial glycocalyx after pig-to-baboon cardiac xenotransplantation and show that damage to the endothelial glycocalyx seems to be comparable or even less pronounced than in similar human settings when current strategies of cardiac xenotransplantation are applied. At the same time, data from the experiments where current strategies, like non-ischemic preservation, growth inhibition or porcine cytomegalovirus (a porcine roseolovirus (PCMV/PRV)) elimination could not be applied indicate that damage of the endothelial glycocalyx also plays an important role in cardiac xenotransplantation.
KW - endothelial activation
KW - endothelial glycocalyx
KW - heart
KW - organ preservation
KW - orthotopic heart transplantation
KW - xenotransplantation
U2 - 10.3390/biomedicines12061336
DO - 10.3390/biomedicines12061336
M3 - Article
C2 - 38927543
AN - SCOPUS:85197912661
SN - 2227-9059
VL - 12
JO - Biomedicines
JF - Biomedicines
IS - 6
M1 - 1336
ER -