TY - JOUR
T1 - Three-dimensional ultrastructure of capillary endothelial glycocalyx under normal and experimental endotoxemic conditions
AU - Okada, Hideshi
AU - Takemura, Genzou
AU - Suzuki, Kodai
AU - Oda, Kazumasa
AU - Takada, Chihiro
AU - Hotta, Yasuaki
AU - Miyazaki, Nagisa
AU - Tsujimoto, Akiko
AU - Muraki, Isamu
AU - Ando, Yoshiaki
AU - Zaikokuji, Ryogen
AU - Matsumoto, Atsumu
AU - Kitagaki, Hiroki
AU - Tamaoki, Yuto
AU - Usui, Takahiro
AU - Doi, Tomoaki
AU - Yoshida, Takahiro
AU - Yoshida, Shozo
AU - Ushikoshi, Hiroaki
AU - Toyoda, Izumi
AU - Ogura, Shinji
N1 - Publisher Copyright:
© 2017 The Author(s).
PY - 2017/10/23
Y1 - 2017/10/23
N2 - Background: Sugar-protein glycocalyx coats healthy endothelium, but its ultrastructure is not well described. Our aim was to determine the three-dimensional ultrastructure of capillary endothelial glycocalyx in the heart, kidney, and liver, where capillaries are, respectively, continuous, fenestrated, and sinusoidal. Methods: Tissue samples were processed with lanthanum-containing alkaline fixative, which preserves the structure of glycocalyx. Results: Scanning and transmission electron microscopy revealed that the endothelial glycocalyx layer in continuous and fenestrated capillaries was substantially thicker than in sinusoids. In the heart, the endothelial glycocalyx presented as moss- or broccoli-like and covered the entire luminal endothelial cell surface. In the kidney, the glycocalyx appeared to nearly occlude the endothelial pores of the fenestrated capillaries and was also present on the surface of the renal podocytes. In sinusoids of the liver, glycocalyx covered not only the luminal side but also the opposite side, facing the space of Disse. In a mouse lipopolysaccharide-induced experimental endotoxemia model, the capillary endothelial glycocalyx was severely disrupted; that is, it appeared to be peeling off the cells and clumping. Serum concentrations of syndecan-1, a marker of glycocalyx damage, were significantly increased 24 h after administration of lipopolysaccharide. Conclusions: In the present study, we visualized the three-dimensional ultrastructure of endothelial glycocalyx in healthy continuous, fenestrated, and sinusoidal capillaries, and we also showed their disruption under experimental endotoxemic conditions. The latter may provide a morphological basis for the microvascular endothelial dysfunction associated with septic injury to organs.
AB - Background: Sugar-protein glycocalyx coats healthy endothelium, but its ultrastructure is not well described. Our aim was to determine the three-dimensional ultrastructure of capillary endothelial glycocalyx in the heart, kidney, and liver, where capillaries are, respectively, continuous, fenestrated, and sinusoidal. Methods: Tissue samples were processed with lanthanum-containing alkaline fixative, which preserves the structure of glycocalyx. Results: Scanning and transmission electron microscopy revealed that the endothelial glycocalyx layer in continuous and fenestrated capillaries was substantially thicker than in sinusoids. In the heart, the endothelial glycocalyx presented as moss- or broccoli-like and covered the entire luminal endothelial cell surface. In the kidney, the glycocalyx appeared to nearly occlude the endothelial pores of the fenestrated capillaries and was also present on the surface of the renal podocytes. In sinusoids of the liver, glycocalyx covered not only the luminal side but also the opposite side, facing the space of Disse. In a mouse lipopolysaccharide-induced experimental endotoxemia model, the capillary endothelial glycocalyx was severely disrupted; that is, it appeared to be peeling off the cells and clumping. Serum concentrations of syndecan-1, a marker of glycocalyx damage, were significantly increased 24 h after administration of lipopolysaccharide. Conclusions: In the present study, we visualized the three-dimensional ultrastructure of endothelial glycocalyx in healthy continuous, fenestrated, and sinusoidal capillaries, and we also showed their disruption under experimental endotoxemic conditions. The latter may provide a morphological basis for the microvascular endothelial dysfunction associated with septic injury to organs.
KW - Capillary
KW - Endothelial cell
KW - Glycocalyx
KW - Sepsis
KW - Ultrastructure
KW - Vascular endothelial injury
UR - http://www.scopus.com/inward/record.url?scp=85032874083&partnerID=8YFLogxK
U2 - 10.1186/s13054-017-1841-8
DO - 10.1186/s13054-017-1841-8
M3 - 学術論文
C2 - 29058634
AN - SCOPUS:85032874083
SN - 1364-8535
VL - 21
JO - Critical Care
JF - Critical Care
IS - 1
M1 - 261
ER -