TY - JOUR
T1 - Novel function of transglutaminase 2 in extracellular histone-induced acute lung injury
AU - Mizuno, Tomohiro
AU - Nagano, Fumihiko
AU - Ito, Yoshimasa
AU - Tatsukawa, Hideki
AU - Shinoda, Yoshiki
AU - Takeuchi, Taishu
AU - Takahashi, Kazuo
AU - Tsuboi, Naotake
AU - Nagamatsu, Tadashi
AU - Yamada, Shuhei
AU - Maruyama, Shoichi
AU - Hitomi, Kiyotaka
N1 - Publisher Copyright:
© 2023 Elsevier Inc.
PY - 2023/10/20
Y1 - 2023/10/20
N2 - Extracellular histones induce endothelial damage, resulting in lung haemorrhage; however, the underlying mechanism remains unclear. Factor XIII, as a Ca2+-dependent cross-linking enzyme in blood, mediates fibrin deposition. As another isozyme, transglutaminase 2 (TG2) has a catalytic activity distributing in most tissues. Herein, we investigated whether TG2 promotes fibrin deposition and mediates the adhesion of platelets to ECs in histone-induced acute lung injury (ALI). We evaluated the lung histology and the adhesion of platelets to endothelial cells (ECs) after injecting histones to wild-type (WT) C57BL/6J and TG2 knockout (TG2−/−) mice, and administered a TG2 inhibitor (NC9) to WT mice. Pulmonary haemorrhage was more severe in TG2−/− mice than that in WT mice. The area of fibrin deposition and the proportion of CD41+CD31+ cells were lower in TG2−/− mice than in WT mice. Pre-treatment of NC9 decreased the area of fibrin deposition and the proportion of CD41+CD31+ cells in WT mice. These results suggest that TG2 prevents from pulmonary haemorrhage in ALI by promoting the adhesion of platelets to ECs and the fibrin deposition.
AB - Extracellular histones induce endothelial damage, resulting in lung haemorrhage; however, the underlying mechanism remains unclear. Factor XIII, as a Ca2+-dependent cross-linking enzyme in blood, mediates fibrin deposition. As another isozyme, transglutaminase 2 (TG2) has a catalytic activity distributing in most tissues. Herein, we investigated whether TG2 promotes fibrin deposition and mediates the adhesion of platelets to ECs in histone-induced acute lung injury (ALI). We evaluated the lung histology and the adhesion of platelets to endothelial cells (ECs) after injecting histones to wild-type (WT) C57BL/6J and TG2 knockout (TG2−/−) mice, and administered a TG2 inhibitor (NC9) to WT mice. Pulmonary haemorrhage was more severe in TG2−/− mice than that in WT mice. The area of fibrin deposition and the proportion of CD41+CD31+ cells were lower in TG2−/− mice than in WT mice. Pre-treatment of NC9 decreased the area of fibrin deposition and the proportion of CD41+CD31+ cells in WT mice. These results suggest that TG2 prevents from pulmonary haemorrhage in ALI by promoting the adhesion of platelets to ECs and the fibrin deposition.
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U2 - 10.1016/j.bbrc.2023.08.051
DO - 10.1016/j.bbrc.2023.08.051
M3 - Article
C2 - 37643535
AN - SCOPUS:85168715536
SN - 0006-291X
VL - 678
SP - 179
EP - 185
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
ER -